Dépouillements

Clinics and classics in developmental medicine / Martin C. O. BAX in Developmental Medicine & Child Neurology, 29-6 (December 1987)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 29-6 (December 1987) . - p.709-710 Titre : Clinics and classics in developmental medicine Type de document : Texte imprimé et/ou numérique Auteurs : Martin C. O. BAX, Auteur Année de publication : 1987 Article en page(s) : p.709-710 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=630 [article] Clinics and classics in developmental medicine [Texte imprimé et/ou numérique] / Martin C. O. BAX, Auteur . - 1987 . - p.709-710. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 29-6 (December 1987) . - p.709-710 Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=630

Children with the fragile X chromosome at schools for the mildly mentally retarded / A. THAKE in Developmental Medicine & Child Neurology, 29-6 (December 1987)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 29-6 (December 1987) . - p.711-719 Titre : Children with the fragile X chromosome at schools for the mildly mentally retarded Type de document : Texte imprimé et/ou numérique Auteurs : A. THAKE, Auteur ; J. TODD, Auteur ; T. WEBB, Auteur ; S. BUNDLEY, Auteur Année de publication : 1987 Article en page(s) : p.711-719 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : An investigation of children in schools for the moderately mentally handicapped in Coventry demonstrated that 29 of 259 children had a significant chromosomal abnormality. 10 of 155 boys (6 per cent) and 10 of 104 girls (10 per cent) had the fragile X syndrome. The clinical features which suggested this syndrome in males were IQ in the 50 to 70 range, head circumference greater than the 50th centile and post-pubertal testicular volume greater than the 50th centile. For both males and females, large ears were a useful sign. All children with fragile X had a carrier parent. The occurrence of mental retardation among sibs was one in two for brothers and one in four sisters. Considering all the males with fragile X syndrome resident in Coventry (this and previous studies), there were twice as many in schools for the moderately mentally handicapped as there were in schools for the severely mentally handicapped. There were as many females as males in the schools for the moderately mentally handicapped. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=630 [article] Children with the fragile X chromosome at schools for the mildly mentally retarded [Texte imprimé et/ou numérique] / A. THAKE, Auteur ; J. TODD, Auteur ; T. WEBB, Auteur ; S. BUNDLEY, Auteur . - 1987 . - p.711-719. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 29-6 (December 1987) . - p.711-719 Index. décimale : PER Périodiques Résumé : An investigation of children in schools for the moderately mentally handicapped in Coventry demonstrated that 29 of 259 children had a significant chromosomal abnormality. 10 of 155 boys (6 per cent) and 10 of 104 girls (10 per cent) had the fragile X syndrome. The clinical features which suggested this syndrome in males were IQ in the 50 to 70 range, head circumference greater than the 50th centile and post-pubertal testicular volume greater than the 50th centile. For both males and females, large ears were a useful sign. All children with fragile X had a carrier parent. The occurrence of mental retardation among sibs was one in two for brothers and one in four sisters. Considering all the males with fragile X syndrome resident in Coventry (this and previous studies), there were twice as many in schools for the moderately mentally handicapped as there were in schools for the severely mentally handicapped. There were as many females as males in the schools for the moderately mentally handicapped. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=630

Kinaesthetic sensitivity of normal and clumsy children / Richard LORD in Developmental Medicine & Child Neurology, 29-6 (December 1987)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 29-6 (December 1987) . - p.720-725 Titre : Kinaesthetic sensitivity of normal and clumsy children Type de document : Texte imprimé et/ou numérique Auteurs : Richard LORD, Auteur ; Charles HULME, Auteur Année de publication : 1987 Article en page(s) : p.720-725 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Laszlo and Bairstow (1985a) stated that their Kinaesthetic Sensitivity Test (KST) was designed to be useful in researching the relationship between kinaesthesis and motor performance, and as a diagnostic tool to identify children with poor kinaesthetic function. This study examined the claim that many clumsy children perform poorly on the KST. It was found that the test failed to distinguish between the performances of clumsy children and those of an age-matched control group. Because of its psychometric shortcomings, the KST is unable to fulfil the claims of Laszlo and Bairstow, either as a research or a clinical tool. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=630 [article] Kinaesthetic sensitivity of normal and clumsy children [Texte imprimé et/ou numérique] / Richard LORD, Auteur ; Charles HULME, Auteur . - 1987 . - p.720-725. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 29-6 (December 1987) . - p.720-725 Index. décimale : PER Périodiques Résumé : Laszlo and Bairstow (1985a) stated that their Kinaesthetic Sensitivity Test (KST) was designed to be useful in researching the relationship between kinaesthesis and motor performance, and as a diagnostic tool to identify children with poor kinaesthetic function. This study examined the claim that many clumsy children perform poorly on the KST. It was found that the test failed to distinguish between the performances of clumsy children and those of an age-matched control group. Because of its psychometric shortcomings, the KST is unable to fulfil the claims of Laszlo and Bairstow, either as a research or a clinical tool. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=630

Age differences in the magnitude of associated movement / Jo-Anne C. LAZARUS in Developmental Medicine & Child Neurology, 29-6 (December 1987)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 29-6 (December 1987) . - p.726-733 Titre : Age differences in the magnitude of associated movement Type de document : Texte imprimé et/ou numérique Auteurs : Jo-Anne C. LAZARUS, Auteur ; John I. TODOR, Auteur Année de publication : 1987 Article en page(s) : p.726-733 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Using a quantitative measure of unintended mirror-movements in the contralateral limb during a unimanual task, the magnitude of associated movement across the ages from six to 16 years was determined. Male children in five age-groups (means 6.5, 8.5, 10.4, 12.4 and 16.5 years) were asked to squeeze their index finger and thumb together to various percentages of their own maximal volitional force. Results indicate that the 6.5-year-old group differ from all other age-groups, exhibiting significantly greater associated movements at all levels of force. The results are discussed in terms of the development of inhibitory control over innate neuromotor synergies. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=630 [article] Age differences in the magnitude of associated movement [Texte imprimé et/ou numérique] / Jo-Anne C. LAZARUS, Auteur ; John I. TODOR, Auteur . - 1987 . - p.726-733. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 29-6 (December 1987) . - p.726-733 Index. décimale : PER Périodiques Résumé : Using a quantitative measure of unintended mirror-movements in the contralateral limb during a unimanual task, the magnitude of associated movement across the ages from six to 16 years was determined. Male children in five age-groups (means 6.5, 8.5, 10.4, 12.4 and 16.5 years) were asked to squeeze their index finger and thumb together to various percentages of their own maximal volitional force. Results indicate that the 6.5-year-old group differ from all other age-groups, exhibiting significantly greater associated movements at all levels of force. The results are discussed in terms of the development of inhibitory control over innate neuromotor synergies. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=630

Upper airway obstruction with hypoxaemia and sleep disruption in Down syndrome / D. P. SOUTHALL in Developmental Medicine & Child Neurology, 29-6 (December 1987)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 29-6 (December 1987) . - p.734-742 Titre : Upper airway obstruction with hypoxaemia and sleep disruption in Down syndrome Type de document : Texte imprimé et/ou numérique Auteurs : D. P. SOUTHALL, Auteur ; V. A. STEBBENS, Auteur ; R. MIRZA, Auteur ; M. H. LANG, Auteur ; C. B. CROFT, Auteur ; E. A. SHINEBOURNE, Auteur Année de publication : 1987 Article en page(s) : p.734-742 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Six of 12 children with Down syndrome (DS) tested by means of long-term tape-recordings of oxygen saturation, breathing movements and expired CO2 were found to have previously undetected and severe upper airway obstruction during sleep. In five cases the obstruction occurred in the pharynx and in the sixth it was due to bilateral choanal stenosis. When compared with age-matched controls, overnight tape-recordings showed episodes of abnormal arterial hypoxaemia and an abnormally elevated end-tidal CO2. Episodes of obstruction were most marked during sleep associated with a non-regular breathing pattern. Abnormal episodes of hypoxaemia were associated with continued breathing movements. Sometimes there was no airflow (complete obstruction); at other times airflow continued normally or was reduced in amplitude (partial obstruction). During episodes of partial or complete airway obstruction the inspiratory waveform showed a characteristic shape. These results show sleep-related upper airway obstruction to be an often undetected complication of DS and all necessary measures should be taken to overcome the obstruction when it reaches the stage of producing abnormal hypoxaemia. Choanal dilatation and tracheostomy were successful in treating two of the children. Tonsillectomy and adenoidectomy were successful for one child, but only of marginal benefit for two others. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=630 [article] Upper airway obstruction with hypoxaemia and sleep disruption in Down syndrome [Texte imprimé et/ou numérique] / D. P. SOUTHALL, Auteur ; V. A. STEBBENS, Auteur ; R. MIRZA, Auteur ; M. H. LANG, Auteur ; C. B. CROFT, Auteur ; E. A. SHINEBOURNE, Auteur . - 1987 . - p.734-742. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 29-6 (December 1987) . - p.734-742 Index. décimale : PER Périodiques Résumé : Six of 12 children with Down syndrome (DS) tested by means of long-term tape-recordings of oxygen saturation, breathing movements and expired CO2 were found to have previously undetected and severe upper airway obstruction during sleep. In five cases the obstruction occurred in the pharynx and in the sixth it was due to bilateral choanal stenosis. When compared with age-matched controls, overnight tape-recordings showed episodes of abnormal arterial hypoxaemia and an abnormally elevated end-tidal CO2. Episodes of obstruction were most marked during sleep associated with a non-regular breathing pattern. Abnormal episodes of hypoxaemia were associated with continued breathing movements. Sometimes there was no airflow (complete obstruction); at other times airflow continued normally or was reduced in amplitude (partial obstruction). During episodes of partial or complete airway obstruction the inspiratory waveform showed a characteristic shape. These results show sleep-related upper airway obstruction to be an often undetected complication of DS and all necessary measures should be taken to overcome the obstruction when it reaches the stage of producing abnormal hypoxaemia. Choanal dilatation and tracheostomy were successful in treating two of the children. Tonsillectomy and adenoidectomy were successful for one child, but only of marginal benefit for two others. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=630

Visual symbol and manual sign learning by children with phonologic programming deficit syndrome / P. Steig PEARCE in Developmental Medicine & Child Neurology, 29-6 (December 1987)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 29-6 (December 1987) . - p.743-750 Titre : Visual symbol and manual sign learning by children with phonologic programming deficit syndrome Type de document : Texte imprimé et/ou numérique Auteurs : P. Steig PEARCE, Auteur ; H. Z. DARWISH, Auteur ; B. H. GAINES, Auteur Année de publication : 1987 Article en page(s) : p.743-750 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : A study was done of eight children with phonologic programming deficit syndrome (PPDS) and of eight normally developing children, to evaluate learning and recall of Blissymbols and of Signed English manual signs. The results support the view that children with this syndrome not only have motor speech deficits, but also deficits in symbolic processing. Decisions about intervention for nonverbal children should take account of their probable deficits in symbol learning. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=630 [article] Visual symbol and manual sign learning by children with phonologic programming deficit syndrome [Texte imprimé et/ou numérique] / P. Steig PEARCE, Auteur ; H. Z. DARWISH, Auteur ; B. H. GAINES, Auteur . - 1987 . - p.743-750. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 29-6 (December 1987) . - p.743-750 Index. décimale : PER Périodiques Résumé : A study was done of eight children with phonologic programming deficit syndrome (PPDS) and of eight normally developing children, to evaluate learning and recall of Blissymbols and of Signed English manual signs. The results support the view that children with this syndrome not only have motor speech deficits, but also deficits in symbolic processing. Decisions about intervention for nonverbal children should take account of their probable deficits in symbol learning. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=630

Effect of body position on later postural and functional lateralities of preterm infants / Yukuo KONISHI in Developmental Medicine & Child Neurology, 29-6 (December 1987)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 29-6 (December 1987) . - p.751-757 Titre : Effect of body position on later postural and functional lateralities of preterm infants Type de document : Texte imprimé et/ou numérique Auteurs : Yukuo KONISHI, Auteur ; Haruki MIKAWA, Auteur ; Junko SUZUKI, Auteur ; Masanori KURIYAMA, Auteur Année de publication : 1987 Article en page(s) : p.751-757 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : The effects of body position during the neonatal period on subsequent functional and postural behaviours were examined in relatively low-risk preterm infants. 44 infants were nursed in the supine position and 37 in a prone position throughout their admission period. Persistent head-turning to the right was observed more often and continued longer in the infants lying in supine. Asymmetrical postures, e.g. of skull and trunk, were more often seen in infants lying in supine than in prone. The prone position was thought to help prevent infantile scoliosis. At nine months, preference for the right hand was more marked in infants lying in supine, whereas infants lying in prone used their hands bilaterally, a tendency that persisted at 18 months. Asymmetrical gait pattern with mild gait disturbance was found more often in infants lying in supine than in prone. The prone position was thought to prevent asymmetrical posture and excessive functional asymmetries. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=630 [article] Effect of body position on later postural and functional lateralities of preterm infants [Texte imprimé et/ou numérique] / Yukuo KONISHI, Auteur ; Haruki MIKAWA, Auteur ; Junko SUZUKI, Auteur ; Masanori KURIYAMA, Auteur . - 1987 . - p.751-757. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 29-6 (December 1987) . - p.751-757 Index. décimale : PER Périodiques Résumé : The effects of body position during the neonatal period on subsequent functional and postural behaviours were examined in relatively low-risk preterm infants. 44 infants were nursed in the supine position and 37 in a prone position throughout their admission period. Persistent head-turning to the right was observed more often and continued longer in the infants lying in supine. Asymmetrical postures, e.g. of skull and trunk, were more often seen in infants lying in supine than in prone. The prone position was thought to help prevent infantile scoliosis. At nine months, preference for the right hand was more marked in infants lying in supine, whereas infants lying in prone used their hands bilaterally, a tendency that persisted at 18 months. Asymmetrical gait pattern with mild gait disturbance was found more often in infants lying in supine than in prone. The prone position was thought to prevent asymmetrical posture and excessive functional asymmetries. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=630

Development of the lateral equilibrium reaction in stance / Heidi PERHAM in Developmental Medicine & Child Neurology, 29-6 (December 1987)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 29-6 (December 1987) . - p.758-765 Titre : Development of the lateral equilibrium reaction in stance Type de document : Texte imprimé et/ou numérique Auteurs : Heidi PERHAM, Auteur ; Ann HALLUM, Auteur ; Janet E. SMICK, Auteur ; Terry NORDSTROM, Auteur Année de publication : 1987 Article en page(s) : p.758-765 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : The lateral equilibrium reaction in stance was assessed in 80 normally developing children aged from nine months to five years. A scoring system and checklist were devised to describe the character and presence of the reaction. The earliest non-functional response was seen at nine months of age, and no functional response was observed to both sides until after two years of age. A progressive increase in functional response to both directions of tilt occurred between 12 and 18 months, with an unexpected drop at 21 and 24 months. All three-year-old and five-year-old children demonstrated a functional response to both sides. The lower extremity pattern was the most consistent component observed in those with a functional response. Individual variations in movements of the trunk, upper extremities and head excluded any indication of developmental patterns for these body segments. The clinical implications of these results are discussed. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=630 [article] Development of the lateral equilibrium reaction in stance [Texte imprimé et/ou numérique] / Heidi PERHAM, Auteur ; Ann HALLUM, Auteur ; Janet E. SMICK, Auteur ; Terry NORDSTROM, Auteur . - 1987 . - p.758-765. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 29-6 (December 1987) . - p.758-765 Index. décimale : PER Périodiques Résumé : The lateral equilibrium reaction in stance was assessed in 80 normally developing children aged from nine months to five years. A scoring system and checklist were devised to describe the character and presence of the reaction. The earliest non-functional response was seen at nine months of age, and no functional response was observed to both sides until after two years of age. A progressive increase in functional response to both directions of tilt occurred between 12 and 18 months, with an unexpected drop at 21 and 24 months. All three-year-old and five-year-old children demonstrated a functional response to both sides. The lower extremity pattern was the most consistent component observed in those with a functional response. Individual variations in movements of the trunk, upper extremities and head excluded any indication of developmental patterns for these body segments. The clinical implications of these results are discussed. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=630

Periodic spasms: an unclassified type of epileptic seizure in childhood / Giuseppe GOBBI in Developmental Medicine & Child Neurology, 29-6 (December 1987)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 29-6 (December 1987) . - p.766-775 Titre : Periodic spasms: an unclassified type of epileptic seizure in childhood Type de document : Texte imprimé et/ou numérique Auteurs : Giuseppe GOBBI, Auteur ; P. GIOVANARDI ROSSI, Auteur ; Licia BRUNO, Auteur ; Antonella PINI, Auteur ; Carlo Alberto TASSINARI, Auteur Année de publication : 1987 Article en page(s) : p.766-775 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Seven boys aged between 14 months and 13 years with focal or multifocal partial epilepsy had very unusual seizures, characterized by series of periodic bilateral spasms. These consisted of a brief, complex movement of slight to severe intensity, mainly involving the axial muscles, with raising of the shoulders, adversion of the eyes and head, often with rictus-type facial grimaces and occasional stretching of the legs and emission of a guttural sound. The ictal EEG showed a pattern of periodic complexes, characterized by a slow wave with superimposed fast activity. This form of epileptic seizure is resistant to treatment and is found only in patients affected by a brain disease consisting of a fixed or progressive encephalopathy. These observations document the existence of a rare form of seizure or epileptic event, not yet included in the International Classification of epileptic seizures and clinically relevant because of its diagnostic and prognostic implications. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=631 [article] Periodic spasms: an unclassified type of epileptic seizure in childhood [Texte imprimé et/ou numérique] / Giuseppe GOBBI, Auteur ; P. GIOVANARDI ROSSI, Auteur ; Licia BRUNO, Auteur ; Antonella PINI, Auteur ; Carlo Alberto TASSINARI, Auteur . - 1987 . - p.766-775. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 29-6 (December 1987) . - p.766-775 Index. décimale : PER Périodiques Résumé : Seven boys aged between 14 months and 13 years with focal or multifocal partial epilepsy had very unusual seizures, characterized by series of periodic bilateral spasms. These consisted of a brief, complex movement of slight to severe intensity, mainly involving the axial muscles, with raising of the shoulders, adversion of the eyes and head, often with rictus-type facial grimaces and occasional stretching of the legs and emission of a guttural sound. The ictal EEG showed a pattern of periodic complexes, characterized by a slow wave with superimposed fast activity. This form of epileptic seizure is resistant to treatment and is found only in patients affected by a brain disease consisting of a fixed or progressive encephalopathy. These observations document the existence of a rare form of seizure or epileptic event, not yet included in the International Classification of epileptic seizures and clinically relevant because of its diagnostic and prognostic implications. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=631

The effect of indomethacin on cerebral blood-flow velocity in premature infants / D. H. EVANS in Developmental Medicine & Child Neurology, 29-6 (December 1987)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 29-6 (December 1987) . - p.776-782 Titre : The effect of indomethacin on cerebral blood-flow velocity in premature infants Type de document : Texte imprimé et/ou numérique Auteurs : D. H. EVANS, Auteur ; Malcolm I. LEVENE, Auteur ; L. N. J. ARCHER, Auteur Année de publication : 1987 Article en page(s) : p.776-782 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : The prostaglandin synthetase inhibitor indomethacin is known to cause significant reduction in cerebral blood-flow (CBF) in certain newborn animals. The authors studied the effect of indomethacin on the CBF velocity of small premature infants, using duplex Doppler real-time ultrasound, and made a record of blood pressure (BP) and heart rate. Indomethacin was infused intravenously in five infants. Repeated measurements were made from the anterior cerebral artery for one hour after injection. There was a significant reduction in mean blood-flow velocity of 40 per cent two minutes after the injection, and it remained 35 per cent below pre-dose levels for at least one hour. There was a simultaneous rise of 15 per cent in systemic BP by one minute after injection. It is argued that these these changes represent a significant reduction in CBF, and this may increase the likelihood of border-zone ischaemic infarction in ill premature infants with pre-existing critical cerebral perfusion. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=631 [article] The effect of indomethacin on cerebral blood-flow velocity in premature infants [Texte imprimé et/ou numérique] / D. H. EVANS, Auteur ; Malcolm I. LEVENE, Auteur ; L. N. J. ARCHER, Auteur . - 1987 . - p.776-782. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 29-6 (December 1987) . - p.776-782 Index. décimale : PER Périodiques Résumé : The prostaglandin synthetase inhibitor indomethacin is known to cause significant reduction in cerebral blood-flow (CBF) in certain newborn animals. The authors studied the effect of indomethacin on the CBF velocity of small premature infants, using duplex Doppler real-time ultrasound, and made a record of blood pressure (BP) and heart rate. Indomethacin was infused intravenously in five infants. Repeated measurements were made from the anterior cerebral artery for one hour after injection. There was a significant reduction in mean blood-flow velocity of 40 per cent two minutes after the injection, and it remained 35 per cent below pre-dose levels for at least one hour. There was a simultaneous rise of 15 per cent in systemic BP by one minute after injection. It is argued that these these changes represent a significant reduction in CBF, and this may increase the likelihood of border-zone ischaemic infarction in ill premature infants with pre-existing critical cerebral perfusion. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=631

Sonnets / Gavin EWART in Developmental Medicine & Child Neurology, 29-6 (December 1987)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 29-6 (December 1987) . - p.783 Titre : Sonnets Type de document : Texte imprimé et/ou numérique Auteurs : Gavin EWART, Auteur Année de publication : 1987 Article en page(s) : p.783 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=631 [article] Sonnets [Texte imprimé et/ou numérique] / Gavin EWART, Auteur . - 1987 . - p.783. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 29-6 (December 1987) . - p.783 Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=631

Prolonged apnoea with severe arterial hypoxaemia resulting from complex partial seizures / D. P. SOUTHALL in Developmental Medicine & Child Neurology, 29-6 (December 1987)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 29-6 (December 1987) . - p.784-789 Titre : Prolonged apnoea with severe arterial hypoxaemia resulting from complex partial seizures Type de document : Texte imprimé et/ou numérique Auteurs : D. P. SOUTHALL, Auteur ; V. A. STEBBENS, Auteur ; N. ABRAHAM, Auteur ; Louise ABRAHAM, Auteur Année de publication : 1987 Article en page(s) : p.784-789 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Multi-channel tape-recordings of the EEG, breathing movements, arterial pulsed oxygen saturation and ECG were performed on a four-year-old child with a history of cyanotic episodes. These had started at nine months of age, resulted in cardiopulmonary resuscitation on unnumerable occasions, and were refractory to anti-epileptic medication. During each episode seizure activity appeared first, followed within a few seconds by sinus tachycardia, prolonged absence of inspiratory efforts and severe arterial hypoxaemia. As the seizure activity ended, breathing movements restarted and there was a gradual improvement in oxygenation. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=631 [article] Prolonged apnoea with severe arterial hypoxaemia resulting from complex partial seizures [Texte imprimé et/ou numérique] / D. P. SOUTHALL, Auteur ; V. A. STEBBENS, Auteur ; N. ABRAHAM, Auteur ; Louise ABRAHAM, Auteur . - 1987 . - p.784-789. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 29-6 (December 1987) . - p.784-789 Index. décimale : PER Périodiques Résumé : Multi-channel tape-recordings of the EEG, breathing movements, arterial pulsed oxygen saturation and ECG were performed on a four-year-old child with a history of cyanotic episodes. These had started at nine months of age, resulted in cardiopulmonary resuscitation on unnumerable occasions, and were refractory to anti-epileptic medication. During each episode seizure activity appeared first, followed within a few seconds by sinus tachycardia, prolonged absence of inspiratory efforts and severe arterial hypoxaemia. As the seizure activity ended, breathing movements restarted and there was a gradual improvement in oxygenation. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=631

Prolonged expiratory apnoea (cyanotic 'breath-holding') in association with a medullary tumour / D. P. SOUTHALL in Developmental Medicine & Child Neurology, 29-6 (December 1987)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 29-6 (December 1987) . - p.789-793 Titre : Prolonged expiratory apnoea (cyanotic 'breath-holding') in association with a medullary tumour Type de document : Texte imprimé et/ou numérique Auteurs : D. P. SOUTHALL, Auteur ; G. M. LEWIS, Auteur ; R. BUCHANAN, Auteur ; R. O. WELLER, Auteur Année de publication : 1987 Article en page(s) : p.789-793 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : From the age of four months to his sudden, unexpected death at 2 years 11 months, a child had severe cyanotic episodes attributed to cyanotic 'breath-holding' (prolonged expiratory apnoea). At postmortem he was found to have a previously undiagnosed gangliocytoma of the medulla, which had invaded the floor of the fourth ventricle and variably affected the 7th to 12th cranial-nerve nuclei. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=631 [article] Prolonged expiratory apnoea (cyanotic 'breath-holding') in association with a medullary tumour [Texte imprimé et/ou numérique] / D. P. SOUTHALL, Auteur ; G. M. LEWIS, Auteur ; R. BUCHANAN, Auteur ; R. O. WELLER, Auteur . - 1987 . - p.789-793. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 29-6 (December 1987) . - p.789-793 Index. décimale : PER Périodiques Résumé : From the age of four months to his sudden, unexpected death at 2 years 11 months, a child had severe cyanotic episodes attributed to cyanotic 'breath-holding' (prolonged expiratory apnoea). At postmortem he was found to have a previously undiagnosed gangliocytoma of the medulla, which had invaded the floor of the fourth ventricle and variably affected the 7th to 12th cranial-nerve nuclei. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=631

Carpal tunnel syndrome in childhood / Kimmo SAINIO in Developmental Medicine & Child Neurology, 29-6 (December 1987)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 29-6 (December 1987) . - p.794-797 Titre : Carpal tunnel syndrome in childhood Type de document : Texte imprimé et/ou numérique Auteurs : Kimmo SAINIO, Auteur ; Juhani MERIKANTO, Auteur ; T. Andreo LARSEN, Auteur Année de publication : 1987 Article en page(s) : p.794-797 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Carpal tunnel syndrome is extremely rare in childhood and in almost all previously reported cases it has been secondary to some underlying condition. Three 13- to 14-year-old girls are described with idiopathic carpal tunnel syndrome, confirmed by EMG and relieved by surgical decompression. A noteworthy feature in children is short-lasting but severe attacks of pain, which may be the main symptom. Correct diagnosis is important to avoid unnecessary examinations and, if indicated, the syndrome can be cured by surgery. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=631 [article] Carpal tunnel syndrome in childhood [Texte imprimé et/ou numérique] / Kimmo SAINIO, Auteur ; Juhani MERIKANTO, Auteur ; T. Andreo LARSEN, Auteur . - 1987 . - p.794-797. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 29-6 (December 1987) . - p.794-797 Index. décimale : PER Périodiques Résumé : Carpal tunnel syndrome is extremely rare in childhood and in almost all previously reported cases it has been secondary to some underlying condition. Three 13- to 14-year-old girls are described with idiopathic carpal tunnel syndrome, confirmed by EMG and relieved by surgical decompression. A noteworthy feature in children is short-lasting but severe attacks of pain, which may be the main symptom. Correct diagnosis is important to avoid unnecessary examinations and, if indicated, the syndrome can be cured by surgery. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=631

Can head injury influence the site of demyelination in adrenoleukodystrophy? / Ian A. WILKINSON in Developmental Medicine & Child Neurology, 29-6 (December 1987)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 29-6 (December 1987) . - p.797-800 Titre : Can head injury influence the site of demyelination in adrenoleukodystrophy? Type de document : Texte imprimé et/ou numérique Auteurs : Ian A. WILKINSON, Auteur ; Ian J. HOPKINS, Auteur ; Anthony C. POLLARD, Auteur Année de publication : 1987 Article en page(s) : p.797-800 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Adrenoleukodystrophy is an inherited disorder, in which there is degeneration of white matter of the central nervous system. The disorder presents classically in males during the first decade, and although early clinical features may be asymmetrical, radiological and pathological features are essentially generalised. Two boys are reported with proven adrenoleukodystrophy, who at first had focal clinical and radiological features, with the foci in the region of local trauma. This raises the possibility that a local insult may have precipitated or hastened the degenerative process. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=631 [article] Can head injury influence the site of demyelination in adrenoleukodystrophy? [Texte imprimé et/ou numérique] / Ian A. WILKINSON, Auteur ; Ian J. HOPKINS, Auteur ; Anthony C. POLLARD, Auteur . - 1987 . - p.797-800. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 29-6 (December 1987) . - p.797-800 Index. décimale : PER Périodiques Résumé : Adrenoleukodystrophy is an inherited disorder, in which there is degeneration of white matter of the central nervous system. The disorder presents classically in males during the first decade, and although early clinical features may be asymmetrical, radiological and pathological features are essentially generalised. Two boys are reported with proven adrenoleukodystrophy, who at first had focal clinical and radiological features, with the foci in the region of local trauma. This raises the possibility that a local insult may have precipitated or hastened the degenerative process. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=631

Early fatal nemaline myopathy: case report and review / Henning SCHMALBRUCH in Developmental Medicine & Child Neurology, 29-6 (December 1987)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 29-6 (December 1987) . - p.800-804 Titre : Early fatal nemaline myopathy: case report and review Type de document : Texte imprimé et/ou numérique Auteurs : Henning SCHMALBRUCH, Auteur ; Zofia KAMIENIECKA, Auteur ; Mette ARROE, Auteur Année de publication : 1987 Article en page(s) : p.800-804 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : A newborn girl with atonia and arthrogryposis multiplex required mechanical ventilation; she died on the 14th day. Postmortem muscle histology disclosed nemaline myopathy with a lack of myofibrils. Peripheral nerves appeared to be normal. The parents are first cousins. The findings for 13 other patients who died from nemaline myopathy within the first year of life are reviewed. It is suggested that early fatal cases, in contrast to patients with the 'benign' childhood form, are homozygotic for the disease gene, and that the myopathy results from abnormal myosin synthesis. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=631 [article] Early fatal nemaline myopathy: case report and review [Texte imprimé et/ou numérique] / Henning SCHMALBRUCH, Auteur ; Zofia KAMIENIECKA, Auteur ; Mette ARROE, Auteur . - 1987 . - p.800-804. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 29-6 (December 1987) . - p.800-804 Index. décimale : PER Périodiques Résumé : A newborn girl with atonia and arthrogryposis multiplex required mechanical ventilation; she died on the 14th day. Postmortem muscle histology disclosed nemaline myopathy with a lack of myofibrils. Peripheral nerves appeared to be normal. The parents are first cousins. The findings for 13 other patients who died from nemaline myopathy within the first year of life are reviewed. It is suggested that early fatal cases, in contrast to patients with the 'benign' childhood form, are homozygotic for the disease gene, and that the myopathy results from abnormal myosin synthesis. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=631

Single-cause attribution / Alan LEVITON in Developmental Medicine & Child Neurology, 29-6 (December 1987)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 29-6 (December 1987) . - p.805-807 Titre : Single-cause attribution Type de document : Texte imprimé et/ou numérique Auteurs : Alan LEVITON, Auteur Année de publication : 1987 Article en page(s) : p.805-807 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=631 [article] Single-cause attribution [Texte imprimé et/ou numérique] / Alan LEVITON, Auteur . - 1987 . - p.805-807. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 29-6 (December 1987) . - p.805-807 Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=631

Drooling and its management in cerebral palsy / Susan R. HARRIS in Developmental Medicine & Child Neurology, 29-6 (December 1987)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 29-6 (December 1987) . - p.807-811 Titre : Drooling and its management in cerebral palsy Type de document : Texte imprimé et/ou numérique Auteurs : Susan R. HARRIS, Auteur ; Anne Holler PURDY, Auteur Année de publication : 1987 Article en page(s) : p.807-811 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=631 [article] Drooling and its management in cerebral palsy [Texte imprimé et/ou numérique] / Susan R. HARRIS, Auteur ; Anne Holler PURDY, Auteur . - 1987 . - p.807-811. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 29-6 (December 1987) . - p.807-811 Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=631

Breath-holding spells / Neil GORDON in Developmental Medicine & Child Neurology, 29-6 (December 1987)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 29-6 (December 1987) . - p.811-814 Titre : Breath-holding spells Type de document : Texte imprimé et/ou numérique Auteurs : Neil GORDON, Auteur Année de publication : 1987 Article en page(s) : p.811-814 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=632 [article] Breath-holding spells [Texte imprimé et/ou numérique] / Neil GORDON, Auteur . - 1987 . - p.811-814. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 29-6 (December 1987) . - p.811-814 Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=632

Childhood nemaline myopathy: a review of clinical presentation in relation to prognosis / B. Adelaida MARTINEZ in Developmental Medicine & Child Neurology, 29-6 (December 1987)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 29-6 (December 1987) . - p.815-820 Titre : Childhood nemaline myopathy: a review of clinical presentation in relation to prognosis Type de document : Texte imprimé et/ou numérique Auteurs : B. Adelaida MARTINEZ, Auteur ; B. D. LAKE, Auteur Année de publication : 1987 Article en page(s) : p.815-820 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=632 [article] Childhood nemaline myopathy: a review of clinical presentation in relation to prognosis [Texte imprimé et/ou numérique] / B. Adelaida MARTINEZ, Auteur ; B. D. LAKE, Auteur . - 1987 . - p.815-820. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 29-6 (December 1987) . - p.815-820 Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=632

The cerebro-hepato-renal (Zellweger) syndrome and other peroxisomal disorders / Hans ZELLWEGER in Developmental Medicine & Child Neurology, 29-6 (December 1987)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 29-6 (December 1987) . - p.821-829 Titre : The cerebro-hepato-renal (Zellweger) syndrome and other peroxisomal disorders Type de document : Texte imprimé et/ou numérique Auteurs : Hans ZELLWEGER, Auteur Année de publication : 1987 Article en page(s) : p.821-829 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=632 [article] The cerebro-hepato-renal (Zellweger) syndrome and other peroxisomal disorders [Texte imprimé et/ou numérique] / Hans ZELLWEGER, Auteur . - 1987 . - p.821-829. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 29-6 (December 1987) . - p.821-829 Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=632

Differential diagnosis of Reye's syndrome / Fiona ALLISON in Developmental Medicine & Child Neurology, 29-6 (December 1987)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 29-6 (December 1987) . - p.830 Titre : Differential diagnosis of Reye's syndrome Type de document : Texte imprimé et/ou numérique Auteurs : Fiona ALLISON, Auteur ; Michael J. BENNETT, Auteur Année de publication : 1987 Article en page(s) : p.830 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=632 [article] Differential diagnosis of Reye's syndrome [Texte imprimé et/ou numérique] / Fiona ALLISON, Auteur ; Michael J. BENNETT, Auteur . - 1987 . - p.830. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 29-6 (December 1987) . - p.830 Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=632

Intermittent therapy with clobazam for simple febrile convulsions / Massimo TONDI in Developmental Medicine & Child Neurology, 29-6 (December 1987)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 29-6 (December 1987) . - p.830-831 Titre : Intermittent therapy with clobazam for simple febrile convulsions Type de document : Texte imprimé et/ou numérique Auteurs : Massimo TONDI, Auteur ; Franca CARBONI, Auteur ; Andrea DERIU, Auteur ; Salvatore MANCA, Auteur ; Camilla MASTROPAOLO, Auteur Année de publication : 1987 Article en page(s) : p.830-831 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=632 [article] Intermittent therapy with clobazam for simple febrile convulsions [Texte imprimé et/ou numérique] / Massimo TONDI, Auteur ; Franca CARBONI, Auteur ; Andrea DERIU, Auteur ; Salvatore MANCA, Auteur ; Camilla MASTROPAOLO, Auteur . - 1987 . - p.830-831. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 29-6 (December 1987) . - p.830-831 Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=632

Treatment-generated problems associated with behavior modification in Tourette disorder / Larry BURD in Developmental Medicine & Child Neurology, 29-6 (December 1987)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 29-6 (December 1987) . - p.831-833 Titre : Treatment-generated problems associated with behavior modification in Tourette disorder Type de document : Texte imprimé et/ou numérique Auteurs : Larry BURD, Auteur ; Jacob KERBESHIAN, Auteur Année de publication : 1987 Article en page(s) : p.831-833 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=632 [article] Treatment-generated problems associated with behavior modification in Tourette disorder [Texte imprimé et/ou numérique] / Larry BURD, Auteur ; Jacob KERBESHIAN, Auteur . - 1987 . - p.831-833. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 29-6 (December 1987) . - p.831-833 Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=632

Is nocturnal myoclonus a common sleep disturbance in children with leukaemia? / Elizabeth RUIZ-PRIMO in Developmental Medicine & Child Neurology, 29-6 (December 1987)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 29-6 (December 1987) . - p.833-834 Titre : Is nocturnal myoclonus a common sleep disturbance in children with leukaemia? Type de document : Texte imprimé et/ou numérique Auteurs : Elizabeth RUIZ-PRIMO, Auteur ; Matilde VALENCIA, Auteur ; Catalina TABOADA, Auteur Année de publication : 1987 Article en page(s) : p.833-834 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=632 [article] Is nocturnal myoclonus a common sleep disturbance in children with leukaemia? [Texte imprimé et/ou numérique] / Elizabeth RUIZ-PRIMO, Auteur ; Matilde VALENCIA, Auteur ; Catalina TABOADA, Auteur . - 1987 . - p.833-834. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 29-6 (December 1987) . - p.833-834 Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=632

Developmental apraxia / Ivan LESNY in Developmental Medicine & Child Neurology, 29-6 (December 1987)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 29-6 (December 1987) . - p.834 Titre : Developmental apraxia Type de document : Texte imprimé et/ou numérique Auteurs : Ivan LESNY, Auteur Année de publication : 1987 Article en page(s) : p.834 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=632 [article] Developmental apraxia [Texte imprimé et/ou numérique] / Ivan LESNY, Auteur . - 1987 . - p.834. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 29-6 (December 1987) . - p.834 Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=632

Rett syndrome and Heller dementia / Christopher FITZPATRICK in Developmental Medicine & Child Neurology, 29-6 (December 1987)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 29-6 (December 1987) . - p.834-835 Titre : Rett syndrome and Heller dementia Type de document : Texte imprimé et/ou numérique Auteurs : Christopher FITZPATRICK, Auteur Année de publication : 1987 Article en page(s) : p.834-835 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=632 [article] Rett syndrome and Heller dementia [Texte imprimé et/ou numérique] / Christopher FITZPATRICK, Auteur . - 1987 . - p.834-835. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 29-6 (December 1987) . - p.834-835 Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=632