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Mention de date : October 1985
Paru le : 01/10/1985 |
[n° ou bulletin]
[n° ou bulletin]
27-5 - October 1985 [Texte imprimé et/ou numérique] . - 1985. Langues : Anglais (eng)
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Code-barres | Cote | Support | Localisation | Section | Disponibilité |
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PER0000262 | PER DMC | Périodique | Centre d'Information et de Documentation du CRA Rhône-Alpes | PER - Périodiques | Exclu du prêt |
Dépouillements


The doctor and the rare disease / Martin C. O. BAX in Developmental Medicine & Child Neurology, 27-5 (October 1985)
[article]
Titre : The doctor and the rare disease Type de document : Texte imprimé et/ou numérique Auteurs : Martin C. O. BAX, Auteur Année de publication : 1985 Article en page(s) : p.561-562 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=595
in Developmental Medicine & Child Neurology > 27-5 (October 1985) . - p.561-562[article] The doctor and the rare disease [Texte imprimé et/ou numérique] / Martin C. O. BAX, Auteur . - 1985 . - p.561-562.
Langues : Anglais (eng)
in Developmental Medicine & Child Neurology > 27-5 (October 1985) . - p.561-562
Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=595 Developmental abnormalities in infants and children with acquired immune deficiency syndrome (AIDS) and AIDS-related complex / Monica H. ULTMANN in Developmental Medicine & Child Neurology, 27-5 (October 1985)
[article]
Titre : Developmental abnormalities in infants and children with acquired immune deficiency syndrome (AIDS) and AIDS-related complex Type de document : Texte imprimé et/ou numérique Auteurs : Monica H. ULTMANN, Auteur ; Holly RUFF, Auteur ; Anita L. BELMAN, Auteur ; Brian E. NOVICK, Auteur ; Barbara CONE-WESSON, Auteur ; Herbert J. COHEN, Auteur ; Arye RUBINSTEIN, Auteur Année de publication : 1985 Article en page(s) : p.563-571 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Children with acquired immune deficiency syndrome (AIDS) display two types of clinical picture: a full-blown AIDS characterized by the presence of opportunistic infections and/or Kaposi's sarcoma and a prodromal stage now identified as AIDS-related complex (ARC). Neurological complications have been identified in infants and children with the disease. This paper discusses the developmental abnormalities in 16 pediatric patients, seven with AIDS and nine with ARC, ranging in age from six months to six years. In all cases, the mothers of these children either had ARC, AIDS and/or used intravenous drugs. Developmental histories showed delayed acquisition of milestones in most children following the diagnosis of AIDS or ARC, with delayed motor milestones consistently noted in both groups. Several children with AIDS actually lost milestones as their illness progressed; this has not occurred in the ARC group. Psychometric testing revealed more severe cognitive dysfunction in the group with AIDS. Involvement of the central nervous system was documented clinically, radiologically, and/or electrophysiologically in all patients with AIDS. In the ARC group the course of the illness has shown greater variability. Medical and social factors that may contribute to the developmental abnormalities are discussed. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=595
in Developmental Medicine & Child Neurology > 27-5 (October 1985) . - p.563-571[article] Developmental abnormalities in infants and children with acquired immune deficiency syndrome (AIDS) and AIDS-related complex [Texte imprimé et/ou numérique] / Monica H. ULTMANN, Auteur ; Holly RUFF, Auteur ; Anita L. BELMAN, Auteur ; Brian E. NOVICK, Auteur ; Barbara CONE-WESSON, Auteur ; Herbert J. COHEN, Auteur ; Arye RUBINSTEIN, Auteur . - 1985 . - p.563-571.
Langues : Anglais (eng)
in Developmental Medicine & Child Neurology > 27-5 (October 1985) . - p.563-571
Index. décimale : PER Périodiques Résumé : Children with acquired immune deficiency syndrome (AIDS) display two types of clinical picture: a full-blown AIDS characterized by the presence of opportunistic infections and/or Kaposi's sarcoma and a prodromal stage now identified as AIDS-related complex (ARC). Neurological complications have been identified in infants and children with the disease. This paper discusses the developmental abnormalities in 16 pediatric patients, seven with AIDS and nine with ARC, ranging in age from six months to six years. In all cases, the mothers of these children either had ARC, AIDS and/or used intravenous drugs. Developmental histories showed delayed acquisition of milestones in most children following the diagnosis of AIDS or ARC, with delayed motor milestones consistently noted in both groups. Several children with AIDS actually lost milestones as their illness progressed; this has not occurred in the ARC group. Psychometric testing revealed more severe cognitive dysfunction in the group with AIDS. Involvement of the central nervous system was documented clinically, radiologically, and/or electrophysiologically in all patients with AIDS. In the ARC group the course of the illness has shown greater variability. Medical and social factors that may contribute to the developmental abnormalities are discussed. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=595 Cavitary periventricular leukomalacia: incidence and short-term outcome in infants weighing less than or equal to 1200 grams at birth / M. E. A. BOZYNSKI in Developmental Medicine & Child Neurology, 27-5 (October 1985)
[article]
Titre : Cavitary periventricular leukomalacia: incidence and short-term outcome in infants weighing less than or equal to 1200 grams at birth Type de document : Texte imprimé et/ou numérique Auteurs : M. E. A. BOZYNSKI, Auteur ; M. N. NELSON, Auteur ; T. A. S. MATALON, Auteur ; D. R. GENAZE, Auteur ; C. ROSATI-SKERTICH, Auteur ; P. M. NAUGHTON, Auteur ; W. A. MEIER, Auteur Année de publication : 1985 Article en page(s) : p.572-577 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : One hundred surviving infants with birthweights less than or equal to 1200 g were examined longitudinally, using real-time ultrasonography of the brain. Five infants were diagnosed as having cavitary periventricular leukomalacia (PVL). One infant expired within a month following discharge; the remaining four entered a follow-up program and received developmental assessments. Three infants had moderate-severe spastic diplegia and the fourth had spastic quadriplegia. Cavitary PVL can be diagnosed in vivo and predicts future motor delay or cerebral palsy. Since the typical site of PVL involves the optic radiations, and the incidence of visual-perceptual disturbances is high in premature infants, further research is needed to explore the possible relationship between these two abnormalities. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=595
in Developmental Medicine & Child Neurology > 27-5 (October 1985) . - p.572-577[article] Cavitary periventricular leukomalacia: incidence and short-term outcome in infants weighing less than or equal to 1200 grams at birth [Texte imprimé et/ou numérique] / M. E. A. BOZYNSKI, Auteur ; M. N. NELSON, Auteur ; T. A. S. MATALON, Auteur ; D. R. GENAZE, Auteur ; C. ROSATI-SKERTICH, Auteur ; P. M. NAUGHTON, Auteur ; W. A. MEIER, Auteur . - 1985 . - p.572-577.
Langues : Anglais (eng)
in Developmental Medicine & Child Neurology > 27-5 (October 1985) . - p.572-577
Index. décimale : PER Périodiques Résumé : One hundred surviving infants with birthweights less than or equal to 1200 g were examined longitudinally, using real-time ultrasonography of the brain. Five infants were diagnosed as having cavitary periventricular leukomalacia (PVL). One infant expired within a month following discharge; the remaining four entered a follow-up program and received developmental assessments. Three infants had moderate-severe spastic diplegia and the fourth had spastic quadriplegia. Cavitary PVL can be diagnosed in vivo and predicts future motor delay or cerebral palsy. Since the typical site of PVL involves the optic radiations, and the incidence of visual-perceptual disturbances is high in premature infants, further research is needed to explore the possible relationship between these two abnormalities. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=595 The contribution of fetal-newborn complications to motor and cognitive deficits / J. A. LOW in Developmental Medicine & Child Neurology, 27-5 (October 1985)
[article]
Titre : The contribution of fetal-newborn complications to motor and cognitive deficits Type de document : Texte imprimé et/ou numérique Auteurs : J. A. LOW, Auteur ; R. S. GALBRAITH, Auteur ; D. W. MUIR, Auteur ; L. H. BROEKHOVEN, Auteur ; J. W. WILKINSON, Auteur ; E. J. KARCHMAR, Auteur Année de publication : 1985 Article en page(s) : p.578-587 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : A total of 364 selected high-risk premature and mature infants were studied prospectively to assess the relationship between fetal-newborn complications and motor and cognitive deficits identified during the first year of life. Deficits occurred in 24 per cent of the children: 14 per cent had one or more major deficit and the other 10 per cent had one or more minor deficit. Prematurity was one of the fetal-newborn complications not associated with deficits at one year. Complications that were associated with deficits included fetal hypoxia, respiratory difficulties, infection and newborn encephalopathy. There was also a significant association between fetal hypoxia, newborn respiratory complications, infection and newborn encephalopathy, which is in keeping with the concept that the first three may be mechanisms in CNS injury and subsequent deficits, while newborn encephalopathy reflects the injury and is an important predictor of such deficits. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=595
in Developmental Medicine & Child Neurology > 27-5 (October 1985) . - p.578-587[article] The contribution of fetal-newborn complications to motor and cognitive deficits [Texte imprimé et/ou numérique] / J. A. LOW, Auteur ; R. S. GALBRAITH, Auteur ; D. W. MUIR, Auteur ; L. H. BROEKHOVEN, Auteur ; J. W. WILKINSON, Auteur ; E. J. KARCHMAR, Auteur . - 1985 . - p.578-587.
Langues : Anglais (eng)
in Developmental Medicine & Child Neurology > 27-5 (October 1985) . - p.578-587
Index. décimale : PER Périodiques Résumé : A total of 364 selected high-risk premature and mature infants were studied prospectively to assess the relationship between fetal-newborn complications and motor and cognitive deficits identified during the first year of life. Deficits occurred in 24 per cent of the children: 14 per cent had one or more major deficit and the other 10 per cent had one or more minor deficit. Prematurity was one of the fetal-newborn complications not associated with deficits at one year. Complications that were associated with deficits included fetal hypoxia, respiratory difficulties, infection and newborn encephalopathy. There was also a significant association between fetal hypoxia, newborn respiratory complications, infection and newborn encephalopathy, which is in keeping with the concept that the first three may be mechanisms in CNS injury and subsequent deficits, while newborn encephalopathy reflects the injury and is an important predictor of such deficits. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=595 Predictors for survival and normal neurodevelopmental outcome of infants weighing less than 1001 grams at birth / Helen N. SKOUTELI in Developmental Medicine & Child Neurology, 27-5 (October 1985)
[article]
Titre : Predictors for survival and normal neurodevelopmental outcome of infants weighing less than 1001 grams at birth Type de document : Texte imprimé et/ou numérique Auteurs : Helen N. SKOUTELI, Auteur ; Lilly M. S. DUBOWITZ, Auteur ; Malcolm I. LEVENE, Auteur ; Geoffrey MILLER, Auteur Année de publication : 1985 Article en page(s) : p.588-595 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Between 1979 and 1981, 67 infants weighing 1000 g or less at birth were admitted to the Hammersmith Hospital Neonatal Intensive Care Unit. 29 survived the neonatal period. Low acidosis score, without a metabolic component, was the most powerful predictor of survival. Other factors were gestational age, five-minute Apgar score, the need for ventilatory support, hypoxia, hypercapnia, pneumothorax, hypotension and the presence of a larger PVH. Of the 24 survivors followed up to three years of age, 11 were optimal, nine had some neurodevelopmental deficits and three had moderate functional handicap. Only one child has cerebral palsy and global mental retardation. Five-minute Apgar score and the presence of PDA correlated with normal outcome. None of the 20 obstetrical factors examined appeared to influence either survival or neurological outcome. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=596
in Developmental Medicine & Child Neurology > 27-5 (October 1985) . - p.588-595[article] Predictors for survival and normal neurodevelopmental outcome of infants weighing less than 1001 grams at birth [Texte imprimé et/ou numérique] / Helen N. SKOUTELI, Auteur ; Lilly M. S. DUBOWITZ, Auteur ; Malcolm I. LEVENE, Auteur ; Geoffrey MILLER, Auteur . - 1985 . - p.588-595.
Langues : Anglais (eng)
in Developmental Medicine & Child Neurology > 27-5 (October 1985) . - p.588-595
Index. décimale : PER Périodiques Résumé : Between 1979 and 1981, 67 infants weighing 1000 g or less at birth were admitted to the Hammersmith Hospital Neonatal Intensive Care Unit. 29 survived the neonatal period. Low acidosis score, without a metabolic component, was the most powerful predictor of survival. Other factors were gestational age, five-minute Apgar score, the need for ventilatory support, hypoxia, hypercapnia, pneumothorax, hypotension and the presence of a larger PVH. Of the 24 survivors followed up to three years of age, 11 were optimal, nine had some neurodevelopmental deficits and three had moderate functional handicap. Only one child has cerebral palsy and global mental retardation. Five-minute Apgar score and the presence of PDA correlated with normal outcome. None of the 20 obstetrical factors examined appeared to influence either survival or neurological outcome. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=596 Effect of gestational age on neurological functioning of the very low-birthweight infant at 40 weeks / Martha C. PIPER in Developmental Medicine & Child Neurology, 27-5 (October 1985)
[article]
Titre : Effect of gestational age on neurological functioning of the very low-birthweight infant at 40 weeks Type de document : Texte imprimé et/ou numérique Auteurs : Martha C. PIPER, Auteur ; Ildiko KUNOS, Auteur ; Diane M. WILLIS, Auteur ; Barbara MAZER, Auteur Année de publication : 1985 Article en page(s) : p.596-605 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : A cohort of 97 very low-birthweight infants who had had prolonged care in two neonatal units was identified prospectively and subdivided into three groups according to gestational age at birth (23 to 27, 28 to 31 and 32 to 36 weeks). The neurological status of the three groups was compared at 40 weeks gestational age. The effects of various medical complications also were analyzed by comparing the neurological performances at term of nine 'at-risk' fullterm infants with 'complicated' preterm infants, and 15 'normal' fullterm infants with 'healthy' preterm infants. After controlling for medical complications, no significant difference in neurological scores was found between the three preterm groups, nor between the preterm groups and the 'at-risk' fullterm group. However, 'healthy' preterm infants had significantly lower scores than fullterm 'normal' infants. Item analyses also showed significant differences between the three preterm groups: those with gestations between 23 and 27 weeks were more likely to exhibit tremors than the other two groups; and those with gestations of 32 to 36 weeks were more likely to have opisthotonic postures, overshooting movements, hypertonus and exaggerated responses. While preterm infants in general do not differ in neurological functioning from 'at-risk' fullterm infants, they do differ significantly from 'normal' fullterm babies. Similarly, some groups of infants born too soon exhibit specific neurological features which differentiate them from their preterm counterparts. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=596
in Developmental Medicine & Child Neurology > 27-5 (October 1985) . - p.596-605[article] Effect of gestational age on neurological functioning of the very low-birthweight infant at 40 weeks [Texte imprimé et/ou numérique] / Martha C. PIPER, Auteur ; Ildiko KUNOS, Auteur ; Diane M. WILLIS, Auteur ; Barbara MAZER, Auteur . - 1985 . - p.596-605.
Langues : Anglais (eng)
in Developmental Medicine & Child Neurology > 27-5 (October 1985) . - p.596-605
Index. décimale : PER Périodiques Résumé : A cohort of 97 very low-birthweight infants who had had prolonged care in two neonatal units was identified prospectively and subdivided into three groups according to gestational age at birth (23 to 27, 28 to 31 and 32 to 36 weeks). The neurological status of the three groups was compared at 40 weeks gestational age. The effects of various medical complications also were analyzed by comparing the neurological performances at term of nine 'at-risk' fullterm infants with 'complicated' preterm infants, and 15 'normal' fullterm infants with 'healthy' preterm infants. After controlling for medical complications, no significant difference in neurological scores was found between the three preterm groups, nor between the preterm groups and the 'at-risk' fullterm group. However, 'healthy' preterm infants had significantly lower scores than fullterm 'normal' infants. Item analyses also showed significant differences between the three preterm groups: those with gestations between 23 and 27 weeks were more likely to exhibit tremors than the other two groups; and those with gestations of 32 to 36 weeks were more likely to have opisthotonic postures, overshooting movements, hypertonus and exaggerated responses. While preterm infants in general do not differ in neurological functioning from 'at-risk' fullterm infants, they do differ significantly from 'normal' fullterm babies. Similarly, some groups of infants born too soon exhibit specific neurological features which differentiate them from their preterm counterparts. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=596 The results of a selective surgical policy on the cognitive abilities of children with spina bifida / Brian TEW in Developmental Medicine & Child Neurology, 27-5 (October 1985)
[article]
Titre : The results of a selective surgical policy on the cognitive abilities of children with spina bifida Type de document : Texte imprimé et/ou numérique Auteurs : Brian TEW, Auteur ; Margaret THOMAS, Auteur ; Ralph EVANS, Auteur ; Janice FORD, Auteur Année de publication : 1985 Article en page(s) : p.606-614 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : A cohort of spina-bifida children born between 1973 and 1978 and subjected to selection for surgery was divided into those who met specific physical criteria at birth and were offered immediate treatment, and those who had delayed treatment because of adverse criteria. There was a significantly higher level of intelligence among children treated immediately but a fifth of those given delayed treatment had normal levels of intelligence. There were negligible differences in intelligence between the children given delayed treatment and an unselectively treated series of children born between 1964 and 1966, suggesting that postponing surgery for a period does not necessarily have a disastrous effect upon ability. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=596
in Developmental Medicine & Child Neurology > 27-5 (October 1985) . - p.606-614[article] The results of a selective surgical policy on the cognitive abilities of children with spina bifida [Texte imprimé et/ou numérique] / Brian TEW, Auteur ; Margaret THOMAS, Auteur ; Ralph EVANS, Auteur ; Janice FORD, Auteur . - 1985 . - p.606-614.
Langues : Anglais (eng)
in Developmental Medicine & Child Neurology > 27-5 (October 1985) . - p.606-614
Index. décimale : PER Périodiques Résumé : A cohort of spina-bifida children born between 1973 and 1978 and subjected to selection for surgery was divided into those who met specific physical criteria at birth and were offered immediate treatment, and those who had delayed treatment because of adverse criteria. There was a significantly higher level of intelligence among children treated immediately but a fifth of those given delayed treatment had normal levels of intelligence. There were negligible differences in intelligence between the children given delayed treatment and an unselectively treated series of children born between 1964 and 1966, suggesting that postponing surgery for a period does not necessarily have a disastrous effect upon ability. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=596 Interobserver agreement in the classification of cerebral palsy / Eve BLAIR in Developmental Medicine & Child Neurology, 27-5 (October 1985)
[article]
Titre : Interobserver agreement in the classification of cerebral palsy Type de document : Texte imprimé et/ou numérique Auteurs : Eve BLAIR, Auteur ; Fiona J. STANLEY, Auteur Année de publication : 1985 Article en page(s) : p.615-622 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Interobserver variation in diagnosis is thought to be an important source of bias in studies of cerebral palsy. Kappa (kappa) statistics were used as a measure of interobserver diagnostic agreement for two case series of 20 children attending an institution for the motor handicapped. kappa increased threefold after standardisation of diagnostic terms. Sources of diagnostic variation are discussed and possibilities and benefits of its further reduction explored. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=596
in Developmental Medicine & Child Neurology > 27-5 (October 1985) . - p.615-622[article] Interobserver agreement in the classification of cerebral palsy [Texte imprimé et/ou numérique] / Eve BLAIR, Auteur ; Fiona J. STANLEY, Auteur . - 1985 . - p.615-622.
Langues : Anglais (eng)
in Developmental Medicine & Child Neurology > 27-5 (October 1985) . - p.615-622
Index. décimale : PER Périodiques Résumé : Interobserver variation in diagnosis is thought to be an important source of bias in studies of cerebral palsy. Kappa (kappa) statistics were used as a measure of interobserver diagnostic agreement for two case series of 20 children attending an institution for the motor handicapped. kappa increased threefold after standardisation of diagnostic terms. Sources of diagnostic variation are discussed and possibilities and benefits of its further reduction explored. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=596 Triple arthrodesis for children with spastic cerebral palsy / M. lloyd IRELAND in Developmental Medicine & Child Neurology, 27-5 (October 1985)
[article]
Titre : Triple arthrodesis for children with spastic cerebral palsy Type de document : Texte imprimé et/ou numérique Auteurs : M. lloyd IRELAND, Auteur ; Mark HOFFER, Auteur Année de publication : 1985 Article en page(s) : p.623-627 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : A retrospective review was done of 20 children with spastic cerebral palsy who had had a total of 25 triple arthrodeses at Rancho Los Amigos Hospital. The average age at the time of surgery was 15.5 years and average follow-up was 4.5 years. Indications for surgery were progressive deformity (15) and relief of pain (five). The deformities was planovalgus (12), equinovalgus (six), equinovarus (six) and calcaneovalgus (one). All 13 patients with braces had problems in wearing them. Two patients were non-ambulatory preoperatively and remained so after fusion. Of the 18 who were ambulatory preoperatively, 15 remained so and there was no change in the type of ambulation: the other three stopped ambulating. Three children were made independent of braces. It is concluded that triple arthrodesis is an excellent procedure for children with spastic cerebral palsy, to correct deformity and relieve pain, but it should be done while the children are still walking for the best chances of continued ambulation. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=596
in Developmental Medicine & Child Neurology > 27-5 (October 1985) . - p.623-627[article] Triple arthrodesis for children with spastic cerebral palsy [Texte imprimé et/ou numérique] / M. lloyd IRELAND, Auteur ; Mark HOFFER, Auteur . - 1985 . - p.623-627.
Langues : Anglais (eng)
in Developmental Medicine & Child Neurology > 27-5 (October 1985) . - p.623-627
Index. décimale : PER Périodiques Résumé : A retrospective review was done of 20 children with spastic cerebral palsy who had had a total of 25 triple arthrodeses at Rancho Los Amigos Hospital. The average age at the time of surgery was 15.5 years and average follow-up was 4.5 years. Indications for surgery were progressive deformity (15) and relief of pain (five). The deformities was planovalgus (12), equinovalgus (six), equinovarus (six) and calcaneovalgus (one). All 13 patients with braces had problems in wearing them. Two patients were non-ambulatory preoperatively and remained so after fusion. Of the 18 who were ambulatory preoperatively, 15 remained so and there was no change in the type of ambulation: the other three stopped ambulating. Three children were made independent of braces. It is concluded that triple arthrodesis is an excellent procedure for children with spastic cerebral palsy, to correct deformity and relieve pain, but it should be done while the children are still walking for the best chances of continued ambulation. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=596 The effects of sex, birth order and admission to a special care baby unit on the fear of strangers reaction of infants / D. H. GARROW in Developmental Medicine & Child Neurology, 27-5 (October 1985)
[article]
Titre : The effects of sex, birth order and admission to a special care baby unit on the fear of strangers reaction of infants Type de document : Texte imprimé et/ou numérique Auteurs : D. H. GARROW, Auteur ; D. R. CROCKER, Auteur Année de publication : 1985 Article en page(s) : p.628-634 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : The fear-of-stranger reaction was studied in 65 babies at seven, eight and nine months of age. It was more marked in first-born babies and in girls, and developed earlier in girls than boys. The type of response was independent of the sex of the stranger. Babies who had been in the Special Care Baby Unit (SCBU) tended to show less fear of strangers than controls, especially at seven months, and whereas later-born control girls were significantly more fearful of strangers than later-born control boys, this difference was not apparent in the group who had been in the SCBU. It is suggested that the difference is due to later-born girls who had been admitted to SCBU receiving relatively more social stimulation from their mothers. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=596
in Developmental Medicine & Child Neurology > 27-5 (October 1985) . - p.628-634[article] The effects of sex, birth order and admission to a special care baby unit on the fear of strangers reaction of infants [Texte imprimé et/ou numérique] / D. H. GARROW, Auteur ; D. R. CROCKER, Auteur . - 1985 . - p.628-634.
Langues : Anglais (eng)
in Developmental Medicine & Child Neurology > 27-5 (October 1985) . - p.628-634
Index. décimale : PER Périodiques Résumé : The fear-of-stranger reaction was studied in 65 babies at seven, eight and nine months of age. It was more marked in first-born babies and in girls, and developed earlier in girls than boys. The type of response was independent of the sex of the stranger. Babies who had been in the Special Care Baby Unit (SCBU) tended to show less fear of strangers than controls, especially at seven months, and whereas later-born control girls were significantly more fearful of strangers than later-born control boys, this difference was not apparent in the group who had been in the SCBU. It is suggested that the difference is due to later-born girls who had been admitted to SCBU receiving relatively more social stimulation from their mothers. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=596 Normal gross motor development: the influences of race, sex and socio-economic status / Arnold J. CAPUTE in Developmental Medicine & Child Neurology, 27-5 (October 1985)
[article]
Titre : Normal gross motor development: the influences of race, sex and socio-economic status Type de document : Texte imprimé et/ou numérique Auteurs : Arnold J. CAPUTE, Auteur ; Bruce K. SHAPIRO, Auteur ; Renee C. WACHTEL, Auteur ; Frederick B. PALMER, Auteur ; Alan ROSS, Auteur Année de publication : 1985 Article en page(s) : p.635-643 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : The ages at attainment of 12 gross motor milestones were obtained prospectively during well-baby visits in the first two years of life for 381 children. All had been born at term and were judged to be normal at one year. A longitudinal analysis, using an index summarizing each child's progress for eight selected milestones, is reported for the 284 children for whom data were complete. A high percentage of parents were able to report the age at attaining milestones with an acceptable degree of variability. The children attained milestones at earlier ages than traditionally reported. There were only minor sex differences in age at attainment, but black children attained milestones earlier than white children. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=596
in Developmental Medicine & Child Neurology > 27-5 (October 1985) . - p.635-643[article] Normal gross motor development: the influences of race, sex and socio-economic status [Texte imprimé et/ou numérique] / Arnold J. CAPUTE, Auteur ; Bruce K. SHAPIRO, Auteur ; Renee C. WACHTEL, Auteur ; Frederick B. PALMER, Auteur ; Alan ROSS, Auteur . - 1985 . - p.635-643.
Langues : Anglais (eng)
in Developmental Medicine & Child Neurology > 27-5 (October 1985) . - p.635-643
Index. décimale : PER Périodiques Résumé : The ages at attainment of 12 gross motor milestones were obtained prospectively during well-baby visits in the first two years of life for 381 children. All had been born at term and were judged to be normal at one year. A longitudinal analysis, using an index summarizing each child's progress for eight selected milestones, is reported for the 284 children for whom data were complete. A high percentage of parents were able to report the age at attaining milestones with an acceptable degree of variability. The children attained milestones at earlier ages than traditionally reported. There were only minor sex differences in age at attainment, but black children attained milestones earlier than white children. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=596 Intracranial pressure monitoring in tuberculous meningitis: clinical and computerized tomographic correlation / Johan F. SCHOEMAN in Developmental Medicine & Child Neurology, 27-5 (October 1985)
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Titre : Intracranial pressure monitoring in tuberculous meningitis: clinical and computerized tomographic correlation Type de document : Texte imprimé et/ou numérique Auteurs : Johan F. SCHOEMAN, Auteur ; Deon LE ROUX, Auteur ; Piet B. BEZUIDENHOUT, Auteur ; Peter R. DONALD, Auteur Année de publication : 1985 Article en page(s) : p.644-654 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Cerebrospinal fluid (CSF) pressure was monitored in 24 children with acute tuberculous meningitis. 19 had raised intracranial pressure (ICP) as reflected by increased baseline pressure, pressure waves (e.g. B-waves) and increased amplitude of the pulse wave. Correlation between clinical signs of raised ICP and monitored CSF pressure showed that clinical diagnosis of the presence and degree of raised ICP is unreliable, especially in children with a closed anterior fontanelle. Computerized tomographic (CT) scans showed that hydrocephalus was present in all children with raised CSF pressure. No direct correlation was found between the degree of hydrocephalus and the degree of raised ICP. The rôle of ICP monitoring in the diagnosis and management of raised ICP in children with tuberculous meningitis is discussed. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=596
in Developmental Medicine & Child Neurology > 27-5 (October 1985) . - p.644-654[article] Intracranial pressure monitoring in tuberculous meningitis: clinical and computerized tomographic correlation [Texte imprimé et/ou numérique] / Johan F. SCHOEMAN, Auteur ; Deon LE ROUX, Auteur ; Piet B. BEZUIDENHOUT, Auteur ; Peter R. DONALD, Auteur . - 1985 . - p.644-654.
Langues : Anglais (eng)
in Developmental Medicine & Child Neurology > 27-5 (October 1985) . - p.644-654
Index. décimale : PER Périodiques Résumé : Cerebrospinal fluid (CSF) pressure was monitored in 24 children with acute tuberculous meningitis. 19 had raised intracranial pressure (ICP) as reflected by increased baseline pressure, pressure waves (e.g. B-waves) and increased amplitude of the pulse wave. Correlation between clinical signs of raised ICP and monitored CSF pressure showed that clinical diagnosis of the presence and degree of raised ICP is unreliable, especially in children with a closed anterior fontanelle. Computerized tomographic (CT) scans showed that hydrocephalus was present in all children with raised CSF pressure. No direct correlation was found between the degree of hydrocephalus and the degree of raised ICP. The rôle of ICP monitoring in the diagnosis and management of raised ICP in children with tuberculous meningitis is discussed. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=596 Prognosis for low-birthweight infants up to the age of 14: a population study / Paula RANTAKALLIO in Developmental Medicine & Child Neurology, 27-5 (October 1985)
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Titre : Prognosis for low-birthweight infants up to the age of 14: a population study Type de document : Texte imprimé et/ou numérique Auteurs : Paula RANTAKALLIO, Auteur ; Lennart VON WENDT, Auteur Année de publication : 1985 Article en page(s) : p.655-663 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : A birth cohort of 12,058 infants was followed up to 14 years of age. Cerebral palsy, epilepsy, severe hearing defects, mental retardation and educational subnormality all had a higher incidence among the 411 children with a low birthweight (less than 2500 g). 6 per cent of the total cohort had educational problems with or without some other neurological handicap, and there was a higher prevalence among low-birthweight infants. 1.5 per cent had a handicap but normal school performance. Children with birthweight 1500 to 2499 g had a significantly higher percentage of handicaps than those of heavier birthweight. All the neurological handicaps were more common among boys than girls, but only in mental subnormality was there a marked difference. Height at 14 years was significantly less among low-birthweight children. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=596
in Developmental Medicine & Child Neurology > 27-5 (October 1985) . - p.655-663[article] Prognosis for low-birthweight infants up to the age of 14: a population study [Texte imprimé et/ou numérique] / Paula RANTAKALLIO, Auteur ; Lennart VON WENDT, Auteur . - 1985 . - p.655-663.
Langues : Anglais (eng)
in Developmental Medicine & Child Neurology > 27-5 (October 1985) . - p.655-663
Index. décimale : PER Périodiques Résumé : A birth cohort of 12,058 infants was followed up to 14 years of age. Cerebral palsy, epilepsy, severe hearing defects, mental retardation and educational subnormality all had a higher incidence among the 411 children with a low birthweight (less than 2500 g). 6 per cent of the total cohort had educational problems with or without some other neurological handicap, and there was a higher prevalence among low-birthweight infants. 1.5 per cent had a handicap but normal school performance. Children with birthweight 1500 to 2499 g had a significantly higher percentage of handicaps than those of heavier birthweight. All the neurological handicaps were more common among boys than girls, but only in mental subnormality was there a marked difference. Height at 14 years was significantly less among low-birthweight children. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=596 Brain dysfunction in an adolescent with the neuromuscular form of hexosaminidase deficiency / John F. MANTOVANI in Developmental Medicine & Child Neurology, 27-5 (October 1985)
[article]
Titre : Brain dysfunction in an adolescent with the neuromuscular form of hexosaminidase deficiency Type de document : Texte imprimé et/ou numérique Auteurs : John F. MANTOVANI, Auteur ; Jaclyn VIDGOFF, Auteur ; Mary CASS, Auteur Année de publication : 1985 Article en page(s) : p.664-667 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : A 14-year-old girl of Ashkenazi Jewish background is described who has severe deficiency of hexosaminidase A. She presented with slowly progressive motor neuron degeneration and was found to have subtle deficiencies on neuropsychological testing, abnormal cortical evoked potentials and structural abnormalities of the cerebellum on CT scan. This patient extends the reported clinical findings for adolescents and suggests the possibility of similar abnormalities in others with neuromuscular deterioration. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=596
in Developmental Medicine & Child Neurology > 27-5 (October 1985) . - p.664-667[article] Brain dysfunction in an adolescent with the neuromuscular form of hexosaminidase deficiency [Texte imprimé et/ou numérique] / John F. MANTOVANI, Auteur ; Jaclyn VIDGOFF, Auteur ; Mary CASS, Auteur . - 1985 . - p.664-667.
Langues : Anglais (eng)
in Developmental Medicine & Child Neurology > 27-5 (October 1985) . - p.664-667
Index. décimale : PER Périodiques Résumé : A 14-year-old girl of Ashkenazi Jewish background is described who has severe deficiency of hexosaminidase A. She presented with slowly progressive motor neuron degeneration and was found to have subtle deficiencies on neuropsychological testing, abnormal cortical evoked potentials and structural abnormalities of the cerebellum on CT scan. This patient extends the reported clinical findings for adolescents and suggests the possibility of similar abnormalities in others with neuromuscular deterioration. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=596 Vertebro-basilar thrombosis and involuntary movements / Neil GORDON in Developmental Medicine & Child Neurology, 27-5 (October 1985)
[article]
Titre : Vertebro-basilar thrombosis and involuntary movements Type de document : Texte imprimé et/ou numérique Auteurs : Neil GORDON, Auteur ; M. LENDON, Auteur Année de publication : 1985 Article en page(s) : p.667-670 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : There are a number of causes of thrombosis in the vertebro-basilar system, and among these are trauma and abnormal movements. This is particularly likely to occur if there are anomalies or abnormalities of the spine or arteries. A case is reported which suggests that involuntary movements should be included in the possible aetiologies. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=597
in Developmental Medicine & Child Neurology > 27-5 (October 1985) . - p.667-670[article] Vertebro-basilar thrombosis and involuntary movements [Texte imprimé et/ou numérique] / Neil GORDON, Auteur ; M. LENDON, Auteur . - 1985 . - p.667-670.
Langues : Anglais (eng)
in Developmental Medicine & Child Neurology > 27-5 (October 1985) . - p.667-670
Index. décimale : PER Périodiques Résumé : There are a number of causes of thrombosis in the vertebro-basilar system, and among these are trauma and abnormal movements. This is particularly likely to occur if there are anomalies or abnormalities of the spine or arteries. A case is reported which suggests that involuntary movements should be included in the possible aetiologies. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=597 Congenital trypanosomiasis in a child born in London / S. LINGAM in Developmental Medicine & Child Neurology, 27-5 (October 1985)
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Titre : Congenital trypanosomiasis in a child born in London Type de document : Texte imprimé et/ou numérique Auteurs : S. LINGAM, Auteur ; J. WILSON, Auteur ; W. C. MARSHALL, Auteur ; J. M. GOULD, Auteur ; M. C. REINHARDT, Auteur ; D. A. EVANS, Auteur Année de publication : 1985 Article en page(s) : 670-674 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : A female infant of 22 months was referred to the Hospital for Sick Children, London, because of delayed psychomotor development. Extensive investigations revealed no cause, but eventually trypanosomiasis was diagnosed. The infant had not been outside the UK, but her mother came from Zaire, where the disease is endemic, but had lived in Kinshasa, where there is no sleeping sickness. It is thought, that the mother may have been asymptomatically infected by a fresh-blood transfusion four years earlier, since no other source of infection was apparent. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=597
in Developmental Medicine & Child Neurology > 27-5 (October 1985) . - 670-674[article] Congenital trypanosomiasis in a child born in London [Texte imprimé et/ou numérique] / S. LINGAM, Auteur ; J. WILSON, Auteur ; W. C. MARSHALL, Auteur ; J. M. GOULD, Auteur ; M. C. REINHARDT, Auteur ; D. A. EVANS, Auteur . - 1985 . - 670-674.
Langues : Anglais (eng)
in Developmental Medicine & Child Neurology > 27-5 (October 1985) . - 670-674
Index. décimale : PER Périodiques Résumé : A female infant of 22 months was referred to the Hospital for Sick Children, London, because of delayed psychomotor development. Extensive investigations revealed no cause, but eventually trypanosomiasis was diagnosed. The infant had not been outside the UK, but her mother came from Zaire, where the disease is endemic, but had lived in Kinshasa, where there is no sleeping sickness. It is thought, that the mother may have been asymptomatically infected by a fresh-blood transfusion four years earlier, since no other source of infection was apparent. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=597 Pitfalls in muscle biopsies of hypotonic children / Charlotte E. THOMPSON in Developmental Medicine & Child Neurology, 27-5 (October 1985)
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Titre : Pitfalls in muscle biopsies of hypotonic children Type de document : Texte imprimé et/ou numérique Auteurs : Charlotte E. THOMPSON, Auteur Année de publication : 1985 Article en page(s) : p.675-677 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=597
in Developmental Medicine & Child Neurology > 27-5 (October 1985) . - p.675-677[article] Pitfalls in muscle biopsies of hypotonic children [Texte imprimé et/ou numérique] / Charlotte E. THOMPSON, Auteur . - 1985 . - p.675-677.
Langues : Anglais (eng)
in Developmental Medicine & Child Neurology > 27-5 (October 1985) . - p.675-677
Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=597 Do chronically ill and handicapped children become depressed? / Gordana MILAVIC in Developmental Medicine & Child Neurology, 27-5 (October 1985)
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Titre : Do chronically ill and handicapped children become depressed? Type de document : Texte imprimé et/ou numérique Auteurs : Gordana MILAVIC, Auteur Année de publication : 1985 Article en page(s) : p.677-682 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=597
in Developmental Medicine & Child Neurology > 27-5 (October 1985) . - p.677-682[article] Do chronically ill and handicapped children become depressed? [Texte imprimé et/ou numérique] / Gordana MILAVIC, Auteur . - 1985 . - p.677-682.
Langues : Anglais (eng)
in Developmental Medicine & Child Neurology > 27-5 (October 1985) . - p.677-682
Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=597 Motor control in infants with Down syndrome / Mechthild M. RAST in Developmental Medicine & Child Neurology, 27-5 (October 1985)
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Titre : Motor control in infants with Down syndrome Type de document : Texte imprimé et/ou numérique Auteurs : Mechthild M. RAST, Auteur ; Susan R. HARRIS, Auteur Année de publication : 1985 Article en page(s) : p.682-685 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=597
in Developmental Medicine & Child Neurology > 27-5 (October 1985) . - p.682-685[article] Motor control in infants with Down syndrome [Texte imprimé et/ou numérique] / Mechthild M. RAST, Auteur ; Susan R. HARRIS, Auteur . - 1985 . - p.682-685.
Langues : Anglais (eng)
in Developmental Medicine & Child Neurology > 27-5 (October 1985) . - p.682-685
Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=597 Congenital hypothyroidism / Peter PHAROAH in Developmental Medicine & Child Neurology, 27-5 (October 1985)
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Titre : Congenital hypothyroidism Type de document : Texte imprimé et/ou numérique Auteurs : Peter PHAROAH, Auteur ; Kevin CONNOLLY, Auteur Année de publication : 1985 Article en page(s) : p.686-687 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=597
in Developmental Medicine & Child Neurology > 27-5 (October 1985) . - p.686-687[article] Congenital hypothyroidism [Texte imprimé et/ou numérique] / Peter PHAROAH, Auteur ; Kevin CONNOLLY, Auteur . - 1985 . - p.686-687.
Langues : Anglais (eng)
in Developmental Medicine & Child Neurology > 27-5 (October 1985) . - p.686-687
Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=597
[article]
Titre : Are AFOs beneficial? Type de document : Texte imprimé et/ou numérique Auteurs : Joanne BURT, Auteur Année de publication : 1985 Article en page(s) : p.687 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=597
in Developmental Medicine & Child Neurology > 27-5 (October 1985) . - p.687[article] Are AFOs beneficial? [Texte imprimé et/ou numérique] / Joanne BURT, Auteur . - 1985 . - p.687.
Langues : Anglais (eng)
in Developmental Medicine & Child Neurology > 27-5 (October 1985) . - p.687
Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=597