
- <Centre d'Information et de documentation du CRA Rhône-Alpes
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Centre d'information et de documentation
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du CRA Rhône-Alpes
Centre Hospitalier le Vinatier
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95, Bd Pinel
69678 Bron CedexLundi au Vendredi
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9h00-12h00 13h30-16h00Tél: +33(0)4 37 91 54 65
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Mention de date : December 1994
Paru le : 01/12/1984 |
[n° ou bulletin]
[n° ou bulletin]
26-6 - December 1994 [Texte imprimé et/ou numérique] . - 1984. Langues : Anglais (eng)
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Code-barres | Cote | Support | Localisation | Section | Disponibilité |
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PER0000255 | PER DMC | Périodique | Centre d'Information et de Documentation du CRA Rhône-Alpes | PER - Périodiques | Exclu du prêt |
Dépouillements


Getting it published / Martin C. O. BAX in Developmental Medicine & Child Neurology, 26-6 (December 1994)
[article]
Titre : Getting it published Type de document : Texte imprimé et/ou numérique Auteurs : Martin C. O. BAX, Auteur Année de publication : 1984 Article en page(s) : p.707-708 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=583
in Developmental Medicine & Child Neurology > 26-6 (December 1994) . - p.707-708[article] Getting it published [Texte imprimé et/ou numérique] / Martin C. O. BAX, Auteur . - 1984 . - p.707-708.
Langues : Anglais (eng)
in Developmental Medicine & Child Neurology > 26-6 (December 1994) . - p.707-708
Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=583 Cerebral palsy and perinatal deaths in geographically defined populations with different perinatal services / Jan ARVIDSSON in Developmental Medicine & Child Neurology, 26-6 (December 1994)
[article]
Titre : Cerebral palsy and perinatal deaths in geographically defined populations with different perinatal services Type de document : Texte imprimé et/ou numérique Auteurs : Jan ARVIDSSON, Auteur ; Roland EKSMYR, Auteur Année de publication : 1984 Article en page(s) : p.709-716 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : The number of perinatal deaths and of children with cerebral palsy among 23,039 total births between 1973 and 1978 in one Swedish county were examined by comparing two populations which differed by the presence or absence of a neonatal ward (special care baby unit) in the maternity hospital for the district. No support was found for the assumption that lower perinatal mortality in the region without a neonatal ward would be at the cost of an increased number with cerebral palsy. Between the two three-year periods there was a highly significant decrease in perinatal mortality in the sample without a neonatal ward. When perinatal deaths and cerebral palsy were considered together the decline remained highly significant. The corresponding change in the sample with a neonatal ward was smaller and non-significant. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=584
in Developmental Medicine & Child Neurology > 26-6 (December 1994) . - p.709-716[article] Cerebral palsy and perinatal deaths in geographically defined populations with different perinatal services [Texte imprimé et/ou numérique] / Jan ARVIDSSON, Auteur ; Roland EKSMYR, Auteur . - 1984 . - p.709-716.
Langues : Anglais (eng)
in Developmental Medicine & Child Neurology > 26-6 (December 1994) . - p.709-716
Index. décimale : PER Périodiques Résumé : The number of perinatal deaths and of children with cerebral palsy among 23,039 total births between 1973 and 1978 in one Swedish county were examined by comparing two populations which differed by the presence or absence of a neonatal ward (special care baby unit) in the maternity hospital for the district. No support was found for the assumption that lower perinatal mortality in the region without a neonatal ward would be at the cost of an increased number with cerebral palsy. Between the two three-year periods there was a highly significant decrease in perinatal mortality in the sample without a neonatal ward. When perinatal deaths and cerebral palsy were considered together the decline remained highly significant. The corresponding change in the sample with a neonatal ward was smaller and non-significant. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=584 Myasthenia gravis in Chinese children / W. Y. CHAN-LUI in Developmental Medicine & Child Neurology, 26-6 (December 1994)
[article]
Titre : Myasthenia gravis in Chinese children Type de document : Texte imprimé et/ou numérique Auteurs : W. Y. CHAN-LUI, Auteur ; N. K. LEUNG, Auteur ; T. T. Y. LAU, Auteur Année de publication : 1984 Article en page(s) : p.717-724 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : A clinical study of 50 Southern Chinese myasthenic children observed for periods of two to 18 years (six years on average) revealed manifestations different from those of caucasian patients. Onset was early, at an average of 4.8 years. 82 per cent had ocular myasthenia. Ophthalmoplegia followed ptosis between three months and 10 years later. Additional facial and isolated limb-muscle fatigability developed in only 6 per cent within three months to 3 1/2 years. Only 12 per cent developed generalized myasthenia. Although extension from ocular to the generalized form did not occur later than 20 months after onset, a deterioration in ocular symptoms, without extension into generalized myasthenia, occurred in nine of 18 children during adolescence. Ptosis and generalized myasthenia responded better to anticholinesterase and/or prednisone. Ophthalmoplegia was difficult to treat. The natural clinical course was benign. Spontaneous remission occurred in 62 per cent of cases, but 54.8 per cent of these relapsed, all confined to ocular muscles. Although there was no familial occurrence of myasthenia gravis, an association was found between myasthenia and thyroid disorders in some patients and their relatives. The association with HLA BW46 antigen was striking. Acetylcholine receptor antibodies were absent in the majority, but mildly elevated titres were found in three of five patients whose ocular symptoms deteriorated during adolescence, without extension into generalized myasthenia. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=584
in Developmental Medicine & Child Neurology > 26-6 (December 1994) . - p.717-724[article] Myasthenia gravis in Chinese children [Texte imprimé et/ou numérique] / W. Y. CHAN-LUI, Auteur ; N. K. LEUNG, Auteur ; T. T. Y. LAU, Auteur . - 1984 . - p.717-724.
Langues : Anglais (eng)
in Developmental Medicine & Child Neurology > 26-6 (December 1994) . - p.717-724
Index. décimale : PER Périodiques Résumé : A clinical study of 50 Southern Chinese myasthenic children observed for periods of two to 18 years (six years on average) revealed manifestations different from those of caucasian patients. Onset was early, at an average of 4.8 years. 82 per cent had ocular myasthenia. Ophthalmoplegia followed ptosis between three months and 10 years later. Additional facial and isolated limb-muscle fatigability developed in only 6 per cent within three months to 3 1/2 years. Only 12 per cent developed generalized myasthenia. Although extension from ocular to the generalized form did not occur later than 20 months after onset, a deterioration in ocular symptoms, without extension into generalized myasthenia, occurred in nine of 18 children during adolescence. Ptosis and generalized myasthenia responded better to anticholinesterase and/or prednisone. Ophthalmoplegia was difficult to treat. The natural clinical course was benign. Spontaneous remission occurred in 62 per cent of cases, but 54.8 per cent of these relapsed, all confined to ocular muscles. Although there was no familial occurrence of myasthenia gravis, an association was found between myasthenia and thyroid disorders in some patients and their relatives. The association with HLA BW46 antigen was striking. Acetylcholine receptor antibodies were absent in the majority, but mildly elevated titres were found in three of five patients whose ocular symptoms deteriorated during adolescence, without extension into generalized myasthenia. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=584 Progressive ventriculomegaly following minor intracranial hemorrhage in premature infants / Marvin A. FISHMAN in Developmental Medicine & Child Neurology, 26-6 (December 1994)
[article]
Titre : Progressive ventriculomegaly following minor intracranial hemorrhage in premature infants Type de document : Texte imprimé et/ou numérique Auteurs : Marvin A. FISHMAN, Auteur ; Robert V. DUTTON, Auteur ; Sada OKUMURA, Auteur Année de publication : 1984 Article en page(s) : p.725-731 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Progressive hydrocephalus following subependymal-intraventricular hemorrhages (SEH-IVH) in premature infants has been noted after moderate to severe degrees of hemorrhage. The ventricular dilatation often has been noted to resolve spontaneously, or not continue to progress after four weeks of age. 11 premature infants with moderate to marked degrees of ventricular enlargement following minor degrees of SEH-IVH have been identified over an 18-month period, and in six of these infants the dilatation continued to progress after one month of age. This sequence of events has not been well documented, and it emphasizes the need to closely follow all infants who have sustained any degree of intracranial hemorrhage. The authors recommend routine real-time ultrasound brain-scans at one month of age for all infants with SEH-IVH, and continued close observation with serial head-measurements of those with enlarged ventricular systems at that time. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=584
in Developmental Medicine & Child Neurology > 26-6 (December 1994) . - p.725-731[article] Progressive ventriculomegaly following minor intracranial hemorrhage in premature infants [Texte imprimé et/ou numérique] / Marvin A. FISHMAN, Auteur ; Robert V. DUTTON, Auteur ; Sada OKUMURA, Auteur . - 1984 . - p.725-731.
Langues : Anglais (eng)
in Developmental Medicine & Child Neurology > 26-6 (December 1994) . - p.725-731
Index. décimale : PER Périodiques Résumé : Progressive hydrocephalus following subependymal-intraventricular hemorrhages (SEH-IVH) in premature infants has been noted after moderate to severe degrees of hemorrhage. The ventricular dilatation often has been noted to resolve spontaneously, or not continue to progress after four weeks of age. 11 premature infants with moderate to marked degrees of ventricular enlargement following minor degrees of SEH-IVH have been identified over an 18-month period, and in six of these infants the dilatation continued to progress after one month of age. This sequence of events has not been well documented, and it emphasizes the need to closely follow all infants who have sustained any degree of intracranial hemorrhage. The authors recommend routine real-time ultrasound brain-scans at one month of age for all infants with SEH-IVH, and continued close observation with serial head-measurements of those with enlarged ventricular systems at that time. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=584 A simple method of assessing intracranial pressure in hydrocephalic patients with shunts / Godfrey A. LAFERLA in Developmental Medicine & Child Neurology, 26-6 (December 1994)
[article]
Titre : A simple method of assessing intracranial pressure in hydrocephalic patients with shunts Type de document : Texte imprimé et/ou numérique Auteurs : Godfrey A. LAFERLA, Auteur ; Alasdair H. B. FYFE, Auteur ; Ian K. DRAINER, Auteur Année de publication : 1984 Article en page(s) : p.732-736 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : A simple method is described for assessing intracranial pressure in patients with Holter valves when the function is questionable. The method entails measuring intravalvular pressure by puncturing the valve belly with a fine needle connected to a manometer. High pressure suggests a distal occlusion; very low pressure coupled with difficulty in aspirating CSF suggests a proximal occlusion. All pressures have to be corrected by the addition of a factor equal to half the pressure specification of the valve. The results of a pilot study support these conclusions. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=584
in Developmental Medicine & Child Neurology > 26-6 (December 1994) . - p.732-736[article] A simple method of assessing intracranial pressure in hydrocephalic patients with shunts [Texte imprimé et/ou numérique] / Godfrey A. LAFERLA, Auteur ; Alasdair H. B. FYFE, Auteur ; Ian K. DRAINER, Auteur . - 1984 . - p.732-736.
Langues : Anglais (eng)
in Developmental Medicine & Child Neurology > 26-6 (December 1994) . - p.732-736
Index. décimale : PER Périodiques Résumé : A simple method is described for assessing intracranial pressure in patients with Holter valves when the function is questionable. The method entails measuring intravalvular pressure by puncturing the valve belly with a fine needle connected to a manometer. High pressure suggests a distal occlusion; very low pressure coupled with difficulty in aspirating CSF suggests a proximal occlusion. All pressures have to be corrected by the addition of a factor equal to half the pressure specification of the valve. The results of a pilot study support these conclusions. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=584 Propanolol ('Inderal') in the treatment of childhood migraine / W. I. FORSYTHE in Developmental Medicine & Child Neurology, 26-6 (December 1994)
[article]
Titre : Propanolol ('Inderal') in the treatment of childhood migraine Type de document : Texte imprimé et/ou numérique Auteurs : W. I. FORSYTHE, Auteur ; D. GILLIES, Auteur ; M. A. SILLS, Auteur Année de publication : 1984 Article en page(s) : p.737-741 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : In a double-blind crossover study of 39 children with established migraine, there was no difference between treatment with propanolol and placebo as regards frequency, severity or average duration of migraine attacks. There was some evidence that propanolol increased the average length of headaches. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=584
in Developmental Medicine & Child Neurology > 26-6 (December 1994) . - p.737-741[article] Propanolol ('Inderal') in the treatment of childhood migraine [Texte imprimé et/ou numérique] / W. I. FORSYTHE, Auteur ; D. GILLIES, Auteur ; M. A. SILLS, Auteur . - 1984 . - p.737-741.
Langues : Anglais (eng)
in Developmental Medicine & Child Neurology > 26-6 (December 1994) . - p.737-741
Index. décimale : PER Périodiques Résumé : In a double-blind crossover study of 39 children with established migraine, there was no difference between treatment with propanolol and placebo as regards frequency, severity or average duration of migraine attacks. There was some evidence that propanolol increased the average length of headaches. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=584 One drug for childhood grand mal: medical audit for three-year remissions / W. I. FORSYTHE in Developmental Medicine & Child Neurology, 26-6 (December 1994)
[article]
Titre : One drug for childhood grand mal: medical audit for three-year remissions Type de document : Texte imprimé et/ou numérique Auteurs : W. I. FORSYTHE, Auteur ; M. A. SILLS, Auteur Année de publication : 1984 Article en page(s) : p.742-748 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : A comparative study was made of monotherapy for grand mal seizures among four groups of children between three and 14 years of age. The first-choice anticonvulsants were phenobarbitone (N = 159), phenytoin (N = 185), carbamazepine (N = 178) and sodium valproate (N = 63). The proportions in each group with a three-year remission of seizures were, respectively, 22, 34, 40 and 16 per cent. The results were better for children with primary grand mal (25, 39, 45 and 21 per cent) and were worse for those with secondary grand mal (3, 21, 25 and 4 per cent), respectively. 119 of the children obtained no reduction in seizure frequency, and for them there is an urgent need for new and more effective anticonvulsants. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=584
in Developmental Medicine & Child Neurology > 26-6 (December 1994) . - p.742-748[article] One drug for childhood grand mal: medical audit for three-year remissions [Texte imprimé et/ou numérique] / W. I. FORSYTHE, Auteur ; M. A. SILLS, Auteur . - 1984 . - p.742-748.
Langues : Anglais (eng)
in Developmental Medicine & Child Neurology > 26-6 (December 1994) . - p.742-748
Index. décimale : PER Périodiques Résumé : A comparative study was made of monotherapy for grand mal seizures among four groups of children between three and 14 years of age. The first-choice anticonvulsants were phenobarbitone (N = 159), phenytoin (N = 185), carbamazepine (N = 178) and sodium valproate (N = 63). The proportions in each group with a three-year remission of seizures were, respectively, 22, 34, 40 and 16 per cent. The results were better for children with primary grand mal (25, 39, 45 and 21 per cent) and were worse for those with secondary grand mal (3, 21, 25 and 4 per cent), respectively. 119 of the children obtained no reduction in seizure frequency, and for them there is an urgent need for new and more effective anticonvulsants. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=584 Altered ratio of carbamazepine-10,11-epoxide/carbamazepine in plasma of children: evidence of anticonvulsant drug / Johan F. SCHOEMAN in Developmental Medicine & Child Neurology, 26-6 (December 1994)
[article]
Titre : Altered ratio of carbamazepine-10,11-epoxide/carbamazepine in plasma of children: evidence of anticonvulsant drug Type de document : Texte imprimé et/ou numérique Auteurs : Johan F. SCHOEMAN, Auteur ; E. M. BRETT, Auteur ; A. A. ELYAS, Auteur ; P. T. LASCELLES, Auteur Année de publication : 1984 Article en page(s) : p.749-755 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : A method of measuring carbamazepine-10,11-epoxide (CBZ-10,11-EPOX) has been developed and used to monitor plasma concentrations in children suffering from various forms of epilepsy. Children stabilised on standard doses of CBZ alone showed a ratio of CBZ-10,11-EPOX/CBZ of 18.92 +/- 8.08, expressed as a percentage of the CBZ concentration, while those on multiple-drug therapy (with the exception of benzodiazepines and phenobarbitone) showed both increased values of CBZ-10,11-EPOX/CBZ ratio and increased absolute concentrations of CBZ-10,11-EPOX in plasma. These changes correlated with clinical side-effects which could not be attributed to CBZ itself or to the other drugs administered concurrently. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=584
in Developmental Medicine & Child Neurology > 26-6 (December 1994) . - p.749-755[article] Altered ratio of carbamazepine-10,11-epoxide/carbamazepine in plasma of children: evidence of anticonvulsant drug [Texte imprimé et/ou numérique] / Johan F. SCHOEMAN, Auteur ; E. M. BRETT, Auteur ; A. A. ELYAS, Auteur ; P. T. LASCELLES, Auteur . - 1984 . - p.749-755.
Langues : Anglais (eng)
in Developmental Medicine & Child Neurology > 26-6 (December 1994) . - p.749-755
Index. décimale : PER Périodiques Résumé : A method of measuring carbamazepine-10,11-epoxide (CBZ-10,11-EPOX) has been developed and used to monitor plasma concentrations in children suffering from various forms of epilepsy. Children stabilised on standard doses of CBZ alone showed a ratio of CBZ-10,11-EPOX/CBZ of 18.92 +/- 8.08, expressed as a percentage of the CBZ concentration, while those on multiple-drug therapy (with the exception of benzodiazepines and phenobarbitone) showed both increased values of CBZ-10,11-EPOX/CBZ ratio and increased absolute concentrations of CBZ-10,11-EPOX in plasma. These changes correlated with clinical side-effects which could not be attributed to CBZ itself or to the other drugs administered concurrently. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=584 Correlation between plasma carbamazepine-10,11-epoxide concentration and drug side-effects in children with epilepsy / Johan F. SCHOEMAN in Developmental Medicine & Child Neurology, 26-6 (December 1994)
[article]
Titre : Correlation between plasma carbamazepine-10,11-epoxide concentration and drug side-effects in children with epilepsy Type de document : Texte imprimé et/ou numérique Auteurs : Johan F. SCHOEMAN, Auteur ; E. M. BRETT, Auteur ; A. A. ELYAS, Auteur ; P. T. LASCELLES, Auteur Année de publication : 1984 Article en page(s) : p.756-764 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Ninety children with epilepsy were treated with carbamazepine (CBZ) alone or with other anticonvulsant drugs. Side-effects were noted in 14 patients. When 25 patients treated with CBZ alone (group 1) were compared with 27 on CBZ and sodium valproate (group 2) and with 38 on CBZ and one or more other anticonvulsants (group 3), the incidence of side-effects was two in group 1 (of whom one patient had a toxic plasma level of CBZ), but 12 in groups 2 and 3 combined. In all but three of the 14 patients with side-effects, plasma levels of CBZ were within the 'therapeutic range'. A significant difference was found between the carbamazepine-10,11-epoxide (CBZ-10,11-EPOX) levels in plasma and CBZ-10,11-EPOX/CBZ ratio in patients with and without side-effects. For five patients on CBZ and other drugs, changes in treatment resulted in changes in side-effects, and also in CBZ-10,11-EPOX levels. Three of these patients showed an interaction between CBZ and sodium valproate, with a correlation between plasma CBZ-10,11-EPOX and side-effects when either drug was introduced or withdrawn, the plasma levels of CBZ itself and of sodium valproate being within the 'therapeutic range'. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=584
in Developmental Medicine & Child Neurology > 26-6 (December 1994) . - p.756-764[article] Correlation between plasma carbamazepine-10,11-epoxide concentration and drug side-effects in children with epilepsy [Texte imprimé et/ou numérique] / Johan F. SCHOEMAN, Auteur ; E. M. BRETT, Auteur ; A. A. ELYAS, Auteur ; P. T. LASCELLES, Auteur . - 1984 . - p.756-764.
Langues : Anglais (eng)
in Developmental Medicine & Child Neurology > 26-6 (December 1994) . - p.756-764
Index. décimale : PER Périodiques Résumé : Ninety children with epilepsy were treated with carbamazepine (CBZ) alone or with other anticonvulsant drugs. Side-effects were noted in 14 patients. When 25 patients treated with CBZ alone (group 1) were compared with 27 on CBZ and sodium valproate (group 2) and with 38 on CBZ and one or more other anticonvulsants (group 3), the incidence of side-effects was two in group 1 (of whom one patient had a toxic plasma level of CBZ), but 12 in groups 2 and 3 combined. In all but three of the 14 patients with side-effects, plasma levels of CBZ were within the 'therapeutic range'. A significant difference was found between the carbamazepine-10,11-epoxide (CBZ-10,11-EPOX) levels in plasma and CBZ-10,11-EPOX/CBZ ratio in patients with and without side-effects. For five patients on CBZ and other drugs, changes in treatment resulted in changes in side-effects, and also in CBZ-10,11-EPOX levels. Three of these patients showed an interaction between CBZ and sodium valproate, with a correlation between plasma CBZ-10,11-EPOX and side-effects when either drug was introduced or withdrawn, the plasma levels of CBZ itself and of sodium valproate being within the 'therapeutic range'. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=584 Neurological and neuropsychological deficiencies in a group of older adolescents with dyslexia / Roger BYRING in Developmental Medicine & Child Neurology, 26-6 (December 1994)
[article]
Titre : Neurological and neuropsychological deficiencies in a group of older adolescents with dyslexia Type de document : Texte imprimé et/ou numérique Auteurs : Roger BYRING, Auteur ; Veijo PULLIAINEN, Auteur Année de publication : 1984 Article en page(s) : p.765-773 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : A group of 34 male adolescents with poor results on a spelling test and 34 controls were examined neurologically and neuropsychologically. The index group was inferior to the controls mainly in tasks involving fine motor control of the left hand, but also in auditory non-verbal sequential information processing and phoneme manipulation tasks. The manual sequencing disorder and the verbal and non-verbal auditory problems could be interpreted in terms of deficient information-processing in the left hemisphere, but the reason for the psychomotor disorder of co-ordination, mainly in the left hand, remains unclear. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=584
in Developmental Medicine & Child Neurology > 26-6 (December 1994) . - p.765-773[article] Neurological and neuropsychological deficiencies in a group of older adolescents with dyslexia [Texte imprimé et/ou numérique] / Roger BYRING, Auteur ; Veijo PULLIAINEN, Auteur . - 1984 . - p.765-773.
Langues : Anglais (eng)
in Developmental Medicine & Child Neurology > 26-6 (December 1994) . - p.765-773
Index. décimale : PER Périodiques Résumé : A group of 34 male adolescents with poor results on a spelling test and 34 controls were examined neurologically and neuropsychologically. The index group was inferior to the controls mainly in tasks involving fine motor control of the left hand, but also in auditory non-verbal sequential information processing and phoneme manipulation tasks. The manual sequencing disorder and the verbal and non-verbal auditory problems could be interpreted in terms of deficient information-processing in the left hemisphere, but the reason for the psychomotor disorder of co-ordination, mainly in the left hand, remains unclear. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=584 Changes in popliteal angle measurement in infants up to one year of age / Elaine READE in Developmental Medicine & Child Neurology, 26-6 (December 1994)
[article]
Titre : Changes in popliteal angle measurement in infants up to one year of age Type de document : Texte imprimé et/ou numérique Auteurs : Elaine READE, Auteur ; Ann HALLUM, Auteur ; Leslie HOM, Auteur ; Rosalie LOPOPOLO, Auteur Année de publication : 1984 Article en page(s) : p.774-780 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : The purpose of this study was to determine trends in the changes of the popliteal angle in 130 normal infants between one day and 12 months of age, for use in assessing infants with possible neuromuscular pathology. Using a 360 degree goniometer, the popliteal angle was measured with the hip held at 90 degree flexion, to indicate hamstring-muscle tightness. Limitation of knee extension was also measured with the hip extended (HEKE angle) to indicate capsular tightness. Both the popliteal and HEKE angle measurements showed greatest limitation of knee extension at birth, which decreased until eight months of age, when most infants showed no limitation. A highly significant negative correlation was found between age and mean popliteal and HEKE angles. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=584
in Developmental Medicine & Child Neurology > 26-6 (December 1994) . - p.774-780[article] Changes in popliteal angle measurement in infants up to one year of age [Texte imprimé et/ou numérique] / Elaine READE, Auteur ; Ann HALLUM, Auteur ; Leslie HOM, Auteur ; Rosalie LOPOPOLO, Auteur . - 1984 . - p.774-780.
Langues : Anglais (eng)
in Developmental Medicine & Child Neurology > 26-6 (December 1994) . - p.774-780
Index. décimale : PER Périodiques Résumé : The purpose of this study was to determine trends in the changes of the popliteal angle in 130 normal infants between one day and 12 months of age, for use in assessing infants with possible neuromuscular pathology. Using a 360 degree goniometer, the popliteal angle was measured with the hip held at 90 degree flexion, to indicate hamstring-muscle tightness. Limitation of knee extension was also measured with the hip extended (HEKE angle) to indicate capsular tightness. Both the popliteal and HEKE angle measurements showed greatest limitation of knee extension at birth, which decreased until eight months of age, when most infants showed no limitation. A highly significant negative correlation was found between age and mean popliteal and HEKE angles. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=584 Behavior and bladder disturbance of enuretic children: a rational classification of a common disorder / David SHAFFER in Developmental Medicine & Child Neurology, 26-6 (December 1994)
[article]
Titre : Behavior and bladder disturbance of enuretic children: a rational classification of a common disorder Type de document : Texte imprimé et/ou numérique Auteurs : David SHAFFER, Auteur ; Barbara HEDGE, Auteur ; Andrew GARDNER, Auteur Année de publication : 1984 Article en page(s) : p.781-792 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : A group of 126 enuretic children were evaluated as to their psychiatric and neurological states, functional bladder volume and environmental circumstances. Few differences were found when the children were grouped according to presence or absence of social disadvantage, the presence of a family history of enuresis, or the nature of onset of enuresis. No classification differentially predicted response to treatment. However, children with an associated psychiatric disorder had significantly lower bladder volumes and had more developmental delays. It is concluded that the classifications of primary or secondary enuresis, or familial or non-familial, etc., are of little practical value. When psychiatric disorder is found, it is probably related to other constitutional abnormalities. Rather than there being two separate groups of enuretic children with behavior disorder and low functional bladder volume, these two abnormalities are found in conjunction. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=585
in Developmental Medicine & Child Neurology > 26-6 (December 1994) . - p.781-792[article] Behavior and bladder disturbance of enuretic children: a rational classification of a common disorder [Texte imprimé et/ou numérique] / David SHAFFER, Auteur ; Barbara HEDGE, Auteur ; Andrew GARDNER, Auteur . - 1984 . - p.781-792.
Langues : Anglais (eng)
in Developmental Medicine & Child Neurology > 26-6 (December 1994) . - p.781-792
Index. décimale : PER Périodiques Résumé : A group of 126 enuretic children were evaluated as to their psychiatric and neurological states, functional bladder volume and environmental circumstances. Few differences were found when the children were grouped according to presence or absence of social disadvantage, the presence of a family history of enuresis, or the nature of onset of enuresis. No classification differentially predicted response to treatment. However, children with an associated psychiatric disorder had significantly lower bladder volumes and had more developmental delays. It is concluded that the classifications of primary or secondary enuresis, or familial or non-familial, etc., are of little practical value. When psychiatric disorder is found, it is probably related to other constitutional abnormalities. Rather than there being two separate groups of enuretic children with behavior disorder and low functional bladder volume, these two abnormalities are found in conjunction. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=585 Roentgenographic cranial-base and calvarial measurements of Jamaican children between one month and five years / Sunit SINGHI in Developmental Medicine & Child Neurology, 26-6 (December 1994)
[article]
Titre : Roentgenographic cranial-base and calvarial measurements of Jamaican children between one month and five years Type de document : Texte imprimé et/ou numérique Auteurs : Sunit SINGHI, Auteur ; Pratibha SINGHI, Auteur ; Francis FERNANDEZ, Auteur ; N. MOULE, Auteur Année de publication : 1984 Article en page(s) : p.793-798 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Three-hundred-and-thirty lateral skull-films obtained from apparently healthy normocephalic Jamaican children between the age of one month and five years were studied, using bony reference points nasion (N), tuberculum sellae (Ts), internal occipital prominence (IOP), inion (I), bregma (B) and lambda (L). Cranial-base length was measured between N-Ts, Ts-IOP and N-I. Calvarial height was measured between Ts-B (anterior calvarium) and Ts-L (posterior calvarium). All the measurements showed an increase with age and were higher in boys. Significant correlations were seen between N-Ts and Ts-IOP, N-Ts and N-I, N-Ts and Ts-B, N-Ts and Ts-L and N-I and Ts-L at all the ages and in both sexes. Ratios between lengths of anterior and posterior cranial-base, as well as between cranial-base lengths and anterior cranial heights, were nearly constant at all the ages and in both sexes. These observations support the view that there is definite proportionality between the growth of anterior and posterior cranial-base lengths, and between anterior calvarial height and cranial-base lengths. On the other hand, a significant increase with age was seen in the ratios N-Ts/Ts-L, N-I/Ts/L and Ts/B/Ts-L, suggesting a progressive decrease in growth of posterior calvarial height. A comparison of the data with previously published figures for Indian and Norwegian populations suggests a racial difference in the various cranial-base and calvarial ratios. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=585
in Developmental Medicine & Child Neurology > 26-6 (December 1994) . - p.793-798[article] Roentgenographic cranial-base and calvarial measurements of Jamaican children between one month and five years [Texte imprimé et/ou numérique] / Sunit SINGHI, Auteur ; Pratibha SINGHI, Auteur ; Francis FERNANDEZ, Auteur ; N. MOULE, Auteur . - 1984 . - p.793-798.
Langues : Anglais (eng)
in Developmental Medicine & Child Neurology > 26-6 (December 1994) . - p.793-798
Index. décimale : PER Périodiques Résumé : Three-hundred-and-thirty lateral skull-films obtained from apparently healthy normocephalic Jamaican children between the age of one month and five years were studied, using bony reference points nasion (N), tuberculum sellae (Ts), internal occipital prominence (IOP), inion (I), bregma (B) and lambda (L). Cranial-base length was measured between N-Ts, Ts-IOP and N-I. Calvarial height was measured between Ts-B (anterior calvarium) and Ts-L (posterior calvarium). All the measurements showed an increase with age and were higher in boys. Significant correlations were seen between N-Ts and Ts-IOP, N-Ts and N-I, N-Ts and Ts-B, N-Ts and Ts-L and N-I and Ts-L at all the ages and in both sexes. Ratios between lengths of anterior and posterior cranial-base, as well as between cranial-base lengths and anterior cranial heights, were nearly constant at all the ages and in both sexes. These observations support the view that there is definite proportionality between the growth of anterior and posterior cranial-base lengths, and between anterior calvarial height and cranial-base lengths. On the other hand, a significant increase with age was seen in the ratios N-Ts/Ts-L, N-I/Ts/L and Ts/B/Ts-L, suggesting a progressive decrease in growth of posterior calvarial height. A comparison of the data with previously published figures for Indian and Norwegian populations suggests a racial difference in the various cranial-base and calvarial ratios. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=585 Perinatal risk factors in the aetiology of hearing loss in preschool children / Klara THIRINGER in Developmental Medicine & Child Neurology, 26-6 (December 1994)
[article]
Titre : Perinatal risk factors in the aetiology of hearing loss in preschool children Type de document : Texte imprimé et/ou numérique Auteurs : Klara THIRINGER, Auteur ; Aira KANKKUNEN, Auteur ; Gunnar LIDEN, Auteur ; Aimon NIKALSSON, Auteur Année de publication : 1984 Article en page(s) : p.799-807 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : In order to assess the importance of pertinent perinatal risk factors in causing hearing loss (HI), a retrospective evaluation was made of the records of 146 affected children born in the city of Göteborg between 1970 and 1979. The incidence among six-year-olds born between 1970 and 1974 was 3.8 per 1000 newborns. If only HI of more severe degree was taken into account (above 40dB in the best ear), the remaining incidence was 1.4/1000. Sensorineural HI (SNHI) accounted for 87 per cent of the cases. A positive hereditary tendency for HI was found in 55 per cent. In 61 per cent the origin of the HI was presumably prenatal, either positive heredity alone or in the form of facio-auricular anomalies, syndromes and toxic influences (infection and alcohol) during early pregnancy. Postnatal infections (meningitis, parotitis and secretory otitis media) could be ascertained as causes in about 20 per cent of the cases. For 12 per cent no aetiology could be determined. Perinatal aetiology was probable or possible in about 10 per cent of the children. The frequency of SNHI was found to be increased among survivors of neonatal intensive care, VLBW, LBW and SFD infants. Caesarean section, ventouse and breech delivery were not associated with increased rates, nor were hyperbilirubinaemia, exchange transfusion or birth asphyxia. No cases could be traced to aminoglycoside treatment. Neonatal sepsis/meningitis may have been the cause in two of the 146 cases. Hypoxia as a consequence of apnoea and respiratory distress syndrome necessitating mechanical ventilation appeared to be the major risk-factor in the neonatal period. However, in comparison with genetic predisposition, potentially damaging perinatal factors appeared to be of minor importance. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=585
in Developmental Medicine & Child Neurology > 26-6 (December 1994) . - p.799-807[article] Perinatal risk factors in the aetiology of hearing loss in preschool children [Texte imprimé et/ou numérique] / Klara THIRINGER, Auteur ; Aira KANKKUNEN, Auteur ; Gunnar LIDEN, Auteur ; Aimon NIKALSSON, Auteur . - 1984 . - p.799-807.
Langues : Anglais (eng)
in Developmental Medicine & Child Neurology > 26-6 (December 1994) . - p.799-807
Index. décimale : PER Périodiques Résumé : In order to assess the importance of pertinent perinatal risk factors in causing hearing loss (HI), a retrospective evaluation was made of the records of 146 affected children born in the city of Göteborg between 1970 and 1979. The incidence among six-year-olds born between 1970 and 1974 was 3.8 per 1000 newborns. If only HI of more severe degree was taken into account (above 40dB in the best ear), the remaining incidence was 1.4/1000. Sensorineural HI (SNHI) accounted for 87 per cent of the cases. A positive hereditary tendency for HI was found in 55 per cent. In 61 per cent the origin of the HI was presumably prenatal, either positive heredity alone or in the form of facio-auricular anomalies, syndromes and toxic influences (infection and alcohol) during early pregnancy. Postnatal infections (meningitis, parotitis and secretory otitis media) could be ascertained as causes in about 20 per cent of the cases. For 12 per cent no aetiology could be determined. Perinatal aetiology was probable or possible in about 10 per cent of the children. The frequency of SNHI was found to be increased among survivors of neonatal intensive care, VLBW, LBW and SFD infants. Caesarean section, ventouse and breech delivery were not associated with increased rates, nor were hyperbilirubinaemia, exchange transfusion or birth asphyxia. No cases could be traced to aminoglycoside treatment. Neonatal sepsis/meningitis may have been the cause in two of the 146 cases. Hypoxia as a consequence of apnoea and respiratory distress syndrome necessitating mechanical ventilation appeared to be the major risk-factor in the neonatal period. However, in comparison with genetic predisposition, potentially damaging perinatal factors appeared to be of minor importance. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=585 A new spinal brace for use in Duchenne muscular dystrophy / Archie YOUNG in Developmental Medicine & Child Neurology, 26-6 (December 1994)
[article]
Titre : A new spinal brace for use in Duchenne muscular dystrophy Type de document : Texte imprimé et/ou numérique Auteurs : Archie YOUNG, Auteur ; Diana JOHNSON, Auteur ; Elizabeth O'GORMON, Auteur ; Terry MACMILLAN, Auteur ; Andrew P. CHASE, Auteur Année de publication : 1984 Article en page(s) : p.808-813 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Nine boys with Duchenne muscular dystrophy, chairbound but without scoliosis, were fitted with a recently developed brace of metal and moulded medium-density polyethylene, the modified Calot brace. Each was also fitted with a wrap-around, moulded leather jacket. Each brace held the relaxed lumbar spine in an angle of lordosis similar to that achieved by a brief active effort to sit erect without a brace. Over-all, they proved equally acceptable to patients and carers. The modified Calot brace caused substantially less restriction of pulmonary function and so may be preferable to the moulded leather jacket. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=585
in Developmental Medicine & Child Neurology > 26-6 (December 1994) . - p.808-813[article] A new spinal brace for use in Duchenne muscular dystrophy [Texte imprimé et/ou numérique] / Archie YOUNG, Auteur ; Diana JOHNSON, Auteur ; Elizabeth O'GORMON, Auteur ; Terry MACMILLAN, Auteur ; Andrew P. CHASE, Auteur . - 1984 . - p.808-813.
Langues : Anglais (eng)
in Developmental Medicine & Child Neurology > 26-6 (December 1994) . - p.808-813
Index. décimale : PER Périodiques Résumé : Nine boys with Duchenne muscular dystrophy, chairbound but without scoliosis, were fitted with a recently developed brace of metal and moulded medium-density polyethylene, the modified Calot brace. Each was also fitted with a wrap-around, moulded leather jacket. Each brace held the relaxed lumbar spine in an angle of lordosis similar to that achieved by a brief active effort to sit erect without a brace. Over-all, they proved equally acceptable to patients and carers. The modified Calot brace caused substantially less restriction of pulmonary function and so may be preferable to the moulded leather jacket. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=585 Acute hemiplegia in Kawasaki disease and infantile polyarteritis nodosa / Ronald M. LAXER in Developmental Medicine & Child Neurology, 26-6 (December 1994)
[article]
Titre : Acute hemiplegia in Kawasaki disease and infantile polyarteritis nodosa Type de document : Texte imprimé et/ou numérique Auteurs : Ronald M. LAXER, Auteur ; Henry G. DUNN, Auteur ; Olof FLODMARK, Auteur Année de publication : 1984 Article en page(s) : p.814-818 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Although aseptic meningitis, lethargy and irritability occur frequently in Kawasaki disease and infantile polyarteritis nodosa, other neurological manifestations are rare. The authors report one case of Kawasaki disease and one of infantile polyarteritis nodosa, both associated with acute hemiplegia. Both patients had received courses of oral corticosteroids for their underlying disease prior to the onset of the hemiplegia. Pathological studies, as well as the four previously reported cases, are reviewed. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=585
in Developmental Medicine & Child Neurology > 26-6 (December 1994) . - p.814-818[article] Acute hemiplegia in Kawasaki disease and infantile polyarteritis nodosa [Texte imprimé et/ou numérique] / Ronald M. LAXER, Auteur ; Henry G. DUNN, Auteur ; Olof FLODMARK, Auteur . - 1984 . - p.814-818.
Langues : Anglais (eng)
in Developmental Medicine & Child Neurology > 26-6 (December 1994) . - p.814-818
Index. décimale : PER Périodiques Résumé : Although aseptic meningitis, lethargy and irritability occur frequently in Kawasaki disease and infantile polyarteritis nodosa, other neurological manifestations are rare. The authors report one case of Kawasaki disease and one of infantile polyarteritis nodosa, both associated with acute hemiplegia. Both patients had received courses of oral corticosteroids for their underlying disease prior to the onset of the hemiplegia. Pathological studies, as well as the four previously reported cases, are reviewed. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=585 An unusual case of recovery from infantile spasms / Raili RIIKONEN in Developmental Medicine & Child Neurology, 26-6 (December 1994)
[article]
Titre : An unusual case of recovery from infantile spasms Type de document : Texte imprimé et/ou numérique Auteurs : Raili RIIKONEN, Auteur Année de publication : 1984 Article en page(s) : p.818-821 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : A six-month-old boy with an uneventful early history and normal development was admitted for treatment of infantile spasms and hypsarrhythmia lasting for a week. Sagittal craniosynostosis was corrected surgically, in preference to a course of ACTH. Large doses of short-acting barbiturates were given during anaesthesia. The child recovered promptly after the operation: there have been no relapses and development was normal when he was seen two years later. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=585
in Developmental Medicine & Child Neurology > 26-6 (December 1994) . - p.818-821[article] An unusual case of recovery from infantile spasms [Texte imprimé et/ou numérique] / Raili RIIKONEN, Auteur . - 1984 . - p.818-821.
Langues : Anglais (eng)
in Developmental Medicine & Child Neurology > 26-6 (December 1994) . - p.818-821
Index. décimale : PER Périodiques Résumé : A six-month-old boy with an uneventful early history and normal development was admitted for treatment of infantile spasms and hypsarrhythmia lasting for a week. Sagittal craniosynostosis was corrected surgically, in preference to a course of ACTH. Large doses of short-acting barbiturates were given during anaesthesia. The child recovered promptly after the operation: there have been no relapses and development was normal when he was seen two years later. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=585 When not to treat epilepsy with drugs / David C. TAYLOR in Developmental Medicine & Child Neurology, 26-6 (December 1994)
[article]
Titre : When not to treat epilepsy with drugs Type de document : Texte imprimé et/ou numérique Auteurs : David C. TAYLOR, Auteur ; Ian MCKINLAY, Auteur Année de publication : 1984 Article en page(s) : p.822-827 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=585
in Developmental Medicine & Child Neurology > 26-6 (December 1994) . - p.822-827[article] When not to treat epilepsy with drugs [Texte imprimé et/ou numérique] / David C. TAYLOR, Auteur ; Ian MCKINLAY, Auteur . - 1984 . - p.822-827.
Langues : Anglais (eng)
in Developmental Medicine & Child Neurology > 26-6 (December 1994) . - p.822-827
Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=585 Fetal neurosurgery--a new challenge on the horizon / Carys M. BANNISTER in Developmental Medicine & Child Neurology, 26-6 (December 1994)
[article]
Titre : Fetal neurosurgery--a new challenge on the horizon Type de document : Texte imprimé et/ou numérique Auteurs : Carys M. BANNISTER, Auteur Année de publication : 1984 Article en page(s) : p.827-830 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=585
in Developmental Medicine & Child Neurology > 26-6 (December 1994) . - p.827-830[article] Fetal neurosurgery--a new challenge on the horizon [Texte imprimé et/ou numérique] / Carys M. BANNISTER, Auteur . - 1984 . - p.827-830.
Langues : Anglais (eng)
in Developmental Medicine & Child Neurology > 26-6 (December 1994) . - p.827-830
Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=585 Treatment of multiple tics and the Tourette syndrome / D. GILLIES in Developmental Medicine & Child Neurology, 26-6 (December 1994)
[article]
Titre : Treatment of multiple tics and the Tourette syndrome Type de document : Texte imprimé et/ou numérique Auteurs : D. GILLIES, Auteur ; W. I. FORSYTHE, Auteur Année de publication : 1984 Article en page(s) : p.830-833 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=585
in Developmental Medicine & Child Neurology > 26-6 (December 1994) . - p.830-833[article] Treatment of multiple tics and the Tourette syndrome [Texte imprimé et/ou numérique] / D. GILLIES, Auteur ; W. I. FORSYTHE, Auteur . - 1984 . - p.830-833.
Langues : Anglais (eng)
in Developmental Medicine & Child Neurology > 26-6 (December 1994) . - p.830-833
Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=585