Dépouillements

Handicap and Government / Ross G. MITCHELL in Developmental Medicine & Child Neurology, 23-2 (April 1981)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 23-2 (April 1981) . - p.145-146 Titre : Handicap and Government Type de document : Texte imprimé et/ou numérique Auteurs : Ross G. MITCHELL, Auteur Année de publication : 1981 Article en page(s) : p.145-146 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=516 [article] Handicap and Government [Texte imprimé et/ou numérique] / Ross G. MITCHELL, Auteur . - 1981 . - p.145-146. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 23-2 (April 1981) . - p.145-146 Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=516

Post-operative neuropathic fractures in patients with myelomeningocele / Denis S. DRUMMOND in Developmental Medicine & Child Neurology, 23-2 (April 1981)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 23-2 (April 1981) . - p.147-50 Titre : Post-operative neuropathic fractures in patients with myelomeningocele Type de document : Texte imprimé et/ou numérique Auteurs : Denis S. DRUMMOND, Auteur ; Marc MOREAU, Auteur ; Richard L. CRUESS, Auteur Année de publication : 1981 Article en page(s) : p.147-50 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Neuropathic fractures are common after major surgical procedures to stabilize the hip or spine in patients with myelomeningocele. Complications resulting from such fractures are frequently observed. The fractures occur particularly in the more severely involved children and are associated with prolonged immobilization after surgery. The authors advise that all necessary surgery be done within the shortest possible time, and urge that prolonged immobilization be avoided if possible. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=516 [article] Post-operative neuropathic fractures in patients with myelomeningocele [Texte imprimé et/ou numérique] / Denis S. DRUMMOND, Auteur ; Marc MOREAU, Auteur ; Richard L. CRUESS, Auteur . - 1981 . - p.147-50. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 23-2 (April 1981) . - p.147-50 Index. décimale : PER Périodiques Résumé : Neuropathic fractures are common after major surgical procedures to stabilize the hip or spine in patients with myelomeningocele. Complications resulting from such fractures are frequently observed. The fractures occur particularly in the more severely involved children and are associated with prolonged immobilization after surgery. The authors advise that all necessary surgery be done within the shortest possible time, and urge that prolonged immobilization be avoided if possible. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=516

Intergenerational factors in the etiology of anencephalus and spina bifida / Lowell E. SEVER in Developmental Medicine & Child Neurology, 23-2 (April 1981)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 23-2 (April 1981) . - p.151-154 Titre : Intergenerational factors in the etiology of anencephalus and spina bifida Type de document : Texte imprimé et/ou numérique Auteurs : Lowell E. SEVER, Auteur ; Irvin EMANUEL, Auteur Année de publication : 1981 Article en page(s) : p.151-154 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : To test the hypothesis that events and conditions early in women's lives influence their future risk of producing babies with anencephalus and spina bifida, a case-control study compared mothers of affected infants with mothers whose infants were normal. Occupational class scores of husbands and fathers of the case mothers and control mothers were also compared. While there was no difference between the scores of case and control husbands, the mean score of fathers of case mothers was significantly less than that of the fathers of control mothers. This can be an indication that case mothers grew up under less favorable conditions. These findings, in conjunction with the pattern evident from previous epidemiological studies, support the hypothesis that intergenerational factors play a rôle in the etiology of these defects. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=516 [article] Intergenerational factors in the etiology of anencephalus and spina bifida [Texte imprimé et/ou numérique] / Lowell E. SEVER, Auteur ; Irvin EMANUEL, Auteur . - 1981 . - p.151-154. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 23-2 (April 1981) . - p.151-154 Index. décimale : PER Périodiques Résumé : To test the hypothesis that events and conditions early in women's lives influence their future risk of producing babies with anencephalus and spina bifida, a case-control study compared mothers of affected infants with mothers whose infants were normal. Occupational class scores of husbands and fathers of the case mothers and control mothers were also compared. While there was no difference between the scores of case and control husbands, the mean score of fathers of case mothers was significantly less than that of the fathers of control mothers. This can be an indication that case mothers grew up under less favorable conditions. These findings, in conjunction with the pattern evident from previous epidemiological studies, support the hypothesis that intergenerational factors play a rôle in the etiology of these defects. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=516

Influence of social class on the risk of recurrence of anencephalus and spina bifida / Norman C. NEVIN in Developmental Medicine & Child Neurology, 23-2 (April 1981)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 23-2 (April 1981) . - p.155-159 Titre : Influence of social class on the risk of recurrence of anencephalus and spina bifida Type de document : Texte imprimé et/ou numérique Auteurs : Norman C. NEVIN, Auteur ; W. P. JOHNSTON, Auteur ; J. D. MERRETT, Auteur Année de publication : 1981 Article en page(s) : p.155-159 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : This study suggests that social class has an effect on the incidence of anencephalus and spina bifida, the malformations being more frequent in the lower socio-economic groups. A family study of 226 patients with a CNS malformation suggests that social class also may be important in determining the recurrence risk of such malformations: there are higher risks in social classes III, IV and V than in social classes I and II. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=516 [article] Influence of social class on the risk of recurrence of anencephalus and spina bifida [Texte imprimé et/ou numérique] / Norman C. NEVIN, Auteur ; W. P. JOHNSTON, Auteur ; J. D. MERRETT, Auteur . - 1981 . - p.155-159. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 23-2 (April 1981) . - p.155-159 Index. décimale : PER Périodiques Résumé : This study suggests that social class has an effect on the incidence of anencephalus and spina bifida, the malformations being more frequent in the lower socio-economic groups. A family study of 226 patients with a CNS malformation suggests that social class also may be important in determining the recurrence risk of such malformations: there are higher risks in social classes III, IV and V than in social classes I and II. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=516

Spina bifida: implications for 100 children at school / Gillian M. HUNT in Developmental Medicine & Child Neurology, 23-2 (April 1981)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 23-2 (April 1981) . - p.160-172 Titre : Spina bifida: implications for 100 children at school Type de document : Texte imprimé et/ou numérique Auteurs : Gillian M. HUNT, Auteur Année de publication : 1981 Article en page(s) : p.160-172 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : One hundred children with spina bifida were examined at home and reviewed at the schools they attended. The severity of the handicap had not been appreciated at the time of school entry. 27 of the 41 children who were over 10 years of age had become wheel-chair dependent; 39 of the 100 children had an IQ below 80, and incontinence remained a problem for 68 children. 64 had visual defects, including two who were totally blind, 27 had epilepsy, and 87 had suffered fractures, burns, scalds or pressure sores. Most of the children had started at an ordinary school. The teachers had to give a disproportionate amount of attention to the handicapped child, but were themselves often given inadequate information and support. Many children had learning difficulties. As they grew older their incontinence was less well tolerated. Wheelchair dependency precluded their admission to an ordinary secondary school with stairs, so the majority of older children attended special schools. Only very few will enter normal employment, and many will require a period of education and training beyond the usual school-leaving age. The education of such children should have realistic goals and aim at achieving the maximum degree of self-care. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=516 [article] Spina bifida: implications for 100 children at school [Texte imprimé et/ou numérique] / Gillian M. HUNT, Auteur . - 1981 . - p.160-172. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 23-2 (April 1981) . - p.160-172 Index. décimale : PER Périodiques Résumé : One hundred children with spina bifida were examined at home and reviewed at the schools they attended. The severity of the handicap had not been appreciated at the time of school entry. 27 of the 41 children who were over 10 years of age had become wheel-chair dependent; 39 of the 100 children had an IQ below 80, and incontinence remained a problem for 68 children. 64 had visual defects, including two who were totally blind, 27 had epilepsy, and 87 had suffered fractures, burns, scalds or pressure sores. Most of the children had started at an ordinary school. The teachers had to give a disproportionate amount of attention to the handicapped child, but were themselves often given inadequate information and support. Many children had learning difficulties. As they grew older their incontinence was less well tolerated. Wheelchair dependency precluded their admission to an ordinary secondary school with stairs, so the majority of older children attended special schools. Only very few will enter normal employment, and many will require a period of education and training beyond the usual school-leaving age. The education of such children should have realistic goals and aim at achieving the maximum degree of self-care. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=516

Parents'views of medical and social-work services for families with young cerebral-palsied children / Elizabeth C. TARRAN in Developmental Medicine & Child Neurology, 23-2 (April 1981)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 23-2 (April 1981) . - p.173-182 Titre : Parents'views of medical and social-work services for families with young cerebral-palsied children Type de document : Texte imprimé et/ou numérique Auteurs : Elizabeth C. TARRAN, Auteur Année de publication : 1981 Article en page(s) : p.173-182 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : A specialist social worker interviewed the parents of 67 cerebral-palsied children aged between three and 10 years who were attending or had recently attended for treatment at centres in Dundee and Glasgow. Data were collected on how the presence of a handicapped child affected family life, and on the parents' perceptions of the services they had received and found helpful. Although half the mothers initially were unhappy about their child being away from home for part of the day at a pre-school day placement, the majority soon found that the child's absence (especially in cases when he was receiving active therapy) made it easier to cope when he was home. Nearly half of the parents questioned were dissatisfied about the way they were first told of their child's handicap, and a majority felt they had not received enough help at this time. The requirements for a flexible and comprehensive service to meet the needs of such families are outlined. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=516 [article] Parents'views of medical and social-work services for families with young cerebral-palsied children [Texte imprimé et/ou numérique] / Elizabeth C. TARRAN, Auteur . - 1981 . - p.173-182. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 23-2 (April 1981) . - p.173-182 Index. décimale : PER Périodiques Résumé : A specialist social worker interviewed the parents of 67 cerebral-palsied children aged between three and 10 years who were attending or had recently attended for treatment at centres in Dundee and Glasgow. Data were collected on how the presence of a handicapped child affected family life, and on the parents' perceptions of the services they had received and found helpful. Although half the mothers initially were unhappy about their child being away from home for part of the day at a pre-school day placement, the majority soon found that the child's absence (especially in cases when he was receiving active therapy) made it easier to cope when he was home. Nearly half of the parents questioned were dissatisfied about the way they were first told of their child's handicap, and a majority felt they had not received enough help at this time. The requirements for a flexible and comprehensive service to meet the needs of such families are outlined. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=516

Scaphocephaly: aesthetic and psychosocial considerations / Jeanette BARRITT in Developmental Medicine & Child Neurology, 23-2 (April 1981)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 23-2 (April 1981) . - p.183-191 Titre : Scaphocephaly: aesthetic and psychosocial considerations Type de document : Texte imprimé et/ou numérique Auteurs : Jeanette BARRITT, Auteur ; Mary BROOKSBANK, Auteur ; Donald SIMPSON, Auteur Année de publication : 1981 Article en page(s) : p.183-191 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : A series of 48 children with scaphocephaly has been reviewed. 44 had synostosis of the sagittal suture alone, and four had additional involvement of other sutures. Although six children showed significant developmental delay, with eventual mental retardation in five cases, it does not appear that this is caused by mechanical constriction of the brain. In the majority of cases, scaphocephaly appears to be a benign variant in cranial development. Operation by linear craniectomy was performed for cosmetic reasons in 14 cases, and in general the results were good. Operation was not performed in the other 34 cases, including 15 seen in infancy, and review of these has shown a high incidence of anxiety among parents and children. Therefore there is an acceptable case for cosmetic correction of severe scaphocephaly in infancy. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=517 [article] Scaphocephaly: aesthetic and psychosocial considerations [Texte imprimé et/ou numérique] / Jeanette BARRITT, Auteur ; Mary BROOKSBANK, Auteur ; Donald SIMPSON, Auteur . - 1981 . - p.183-191. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 23-2 (April 1981) . - p.183-191 Index. décimale : PER Périodiques Résumé : A series of 48 children with scaphocephaly has been reviewed. 44 had synostosis of the sagittal suture alone, and four had additional involvement of other sutures. Although six children showed significant developmental delay, with eventual mental retardation in five cases, it does not appear that this is caused by mechanical constriction of the brain. In the majority of cases, scaphocephaly appears to be a benign variant in cranial development. Operation by linear craniectomy was performed for cosmetic reasons in 14 cases, and in general the results were good. Operation was not performed in the other 34 cases, including 15 seen in infancy, and review of these has shown a high incidence of anxiety among parents and children. Therefore there is an acceptable case for cosmetic correction of severe scaphocephaly in infancy. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=517

Prader-Willi syndrome and scoliosis / Vanja A. HOLM in Developmental Medicine & Child Neurology, 23-2 (April 1981)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 23-2 (April 1981) . - p.192-201 Titre : Prader-Willi syndrome and scoliosis Type de document : Texte imprimé et/ou numérique Auteurs : Vanja A. HOLM, Auteur ; Edwin L. LAURNEN, Auteur Année de publication : 1981 Article en page(s) : p.192-201 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Of 37 patients with the Prader-Willi syndrome for whom spinal x-rays were available, 32 had a structural scoliosis of 10 degrees or greater. Kyphosis was also found to be more common in older persons with this syndrome, occurring in only one of 14 adolescents but in five of 10 adults. The scoliosis was analyzed in infantile, juvenile, adolescent and adult subgroups. The results suggest that the scoliosis is present from an early age and remains stable during childhood, but progresses in 15 to 20 per cent of cases during adolescence. Scoliosis in patients with Prader-Willi syndrome has many of the clinical characteristics encountered in idiopathic scoliosis. Because it is difficult to detect in these individuals, the authors recommended that baseline spinal X-rays be obtained in all such patients who have suspicious asymmetry of the spine, followed by regular clinical examination, especially during adolescence. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=517 [article] Prader-Willi syndrome and scoliosis [Texte imprimé et/ou numérique] / Vanja A. HOLM, Auteur ; Edwin L. LAURNEN, Auteur . - 1981 . - p.192-201. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 23-2 (April 1981) . - p.192-201 Index. décimale : PER Périodiques Résumé : Of 37 patients with the Prader-Willi syndrome for whom spinal x-rays were available, 32 had a structural scoliosis of 10 degrees or greater. Kyphosis was also found to be more common in older persons with this syndrome, occurring in only one of 14 adolescents but in five of 10 adults. The scoliosis was analyzed in infantile, juvenile, adolescent and adult subgroups. The results suggest that the scoliosis is present from an early age and remains stable during childhood, but progresses in 15 to 20 per cent of cases during adolescence. Scoliosis in patients with Prader-Willi syndrome has many of the clinical characteristics encountered in idiopathic scoliosis. Because it is difficult to detect in these individuals, the authors recommended that baseline spinal X-rays be obtained in all such patients who have suspicious asymmetry of the spine, followed by regular clinical examination, especially during adolescence. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=517

Late diagnosis of congenital dislocation of the hip / D. M. DUNN in Developmental Medicine & Child Neurology, 23-2 (April 1981)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 23-2 (April 1981) . - p.202-207 Titre : Late diagnosis of congenital dislocation of the hip Type de document : Texte imprimé et/ou numérique Auteurs : D. M. DUNN, Auteur ; S. M. O'RIORDAN, Auteur Année de publication : 1981 Article en page(s) : p.202-207 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : A cohort of children presenting with clicking hips was studied in two districts. In one district any child with a clicking hip was treated as though the hip was dislocated, i.e. by splintage in abduction, but in the other district no treatment was offered. None of the 'treated' group later presented with a dislocated hip, whereas four children were found with dislocated hips among the 'untreated' group. A further four children who were not treated because their hips appeared to be normal on the second examination later presented with dislocated hips. It is suggested that the accuracy of diagnosis in all units might be improved if the examination of the newborn was carried out by a limited number of doctors to whom greater experience would accrue. Further improvements would be made if any hip which was found to click on examination was treated as an unstable hip and splinted in abduction. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=517 [article] Late diagnosis of congenital dislocation of the hip [Texte imprimé et/ou numérique] / D. M. DUNN, Auteur ; S. M. O'RIORDAN, Auteur . - 1981 . - p.202-207. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 23-2 (April 1981) . - p.202-207 Index. décimale : PER Périodiques Résumé : A cohort of children presenting with clicking hips was studied in two districts. In one district any child with a clicking hip was treated as though the hip was dislocated, i.e. by splintage in abduction, but in the other district no treatment was offered. None of the 'treated' group later presented with a dislocated hip, whereas four children were found with dislocated hips among the 'untreated' group. A further four children who were not treated because their hips appeared to be normal on the second examination later presented with dislocated hips. It is suggested that the accuracy of diagnosis in all units might be improved if the examination of the newborn was carried out by a limited number of doctors to whom greater experience would accrue. Further improvements would be made if any hip which was found to click on examination was treated as an unstable hip and splinted in abduction. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=517

A study of subacute sclerosing panencephalitis in Kenya / V. M. DIXIT in Developmental Medicine & Child Neurology, 23-2 (April 1981)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 23-2 (April 1981) . - p.208-216 Titre : A study of subacute sclerosing panencephalitis in Kenya Type de document : Texte imprimé et/ou numérique Auteurs : V. M. DIXIT, Auteur ; E. S. G. HETTIARATCHI, Auteur ; T. MUOKA, Auteur Année de publication : 1981 Article en page(s) : p.208-216 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : A retrospective study was made over a five-year period of 53 patients at the Kenyatta National Hospital, Kenya, who presented with subacute sclerosing panencephalitis. The clinical, EEG and serological findings are similar to those found in other studies. As identified by epidemiological studies elsewhere, the factors which are likely to have a bearing on the aetiology of the disease are prevalent throughout the Kenya, yet there is a strong rural distribution of cases in this study. No cases have been reported from the Masai tribe. These features are discussed with regard to the possible implications for the aetiology of the disease. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=517 [article] A study of subacute sclerosing panencephalitis in Kenya [Texte imprimé et/ou numérique] / V. M. DIXIT, Auteur ; E. S. G. HETTIARATCHI, Auteur ; T. MUOKA, Auteur . - 1981 . - p.208-216. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 23-2 (April 1981) . - p.208-216 Index. décimale : PER Périodiques Résumé : A retrospective study was made over a five-year period of 53 patients at the Kenyatta National Hospital, Kenya, who presented with subacute sclerosing panencephalitis. The clinical, EEG and serological findings are similar to those found in other studies. As identified by epidemiological studies elsewhere, the factors which are likely to have a bearing on the aetiology of the disease are prevalent throughout the Kenya, yet there is a strong rural distribution of cases in this study. No cases have been reported from the Masai tribe. These features are discussed with regard to the possible implications for the aetiology of the disease. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=517

Cognitive ability profiles in families of reading-disabled children / Sadie N. DECKER in Developmental Medicine & Child Neurology, 23-2 (April 1981)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 23-2 (April 1981) . - p.217-227 Titre : Cognitive ability profiles in families of reading-disabled children Type de document : Texte imprimé et/ou numérique Auteurs : Sadie N. DECKER, Auteur ; John C. DEFRIES, Auteur Année de publication : 1981 Article en page(s) : p.217-227 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Evidence for the heterogeneity of reading disability was sought in a family study. Psychometric test data on 125 reading-disabled children (probands) and their siblings and parents were used to identify four subtypes of reading disability, each with a distinctive cognitive ability profile. The validity of this profile analysis was then assessed by applying the same classification system to profiles of affected parents and siblings of the probands. Affected siblings of probands in subtype 3 (severely impaired reading ability but normal spatial/reasoning and coding/speed) were more likely to be of the same subtype than would be expected on the basis of chance. However, no such evidence for familial transmission of specific subtypes was found in the parental data. It is suggested that family studies may provide a strong test of the heterogeneity of reading disability, and that such studies should be used to assess the validity of alternative typologies. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=517 [article] Cognitive ability profiles in families of reading-disabled children [Texte imprimé et/ou numérique] / Sadie N. DECKER, Auteur ; John C. DEFRIES, Auteur . - 1981 . - p.217-227. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 23-2 (April 1981) . - p.217-227 Index. décimale : PER Périodiques Résumé : Evidence for the heterogeneity of reading disability was sought in a family study. Psychometric test data on 125 reading-disabled children (probands) and their siblings and parents were used to identify four subtypes of reading disability, each with a distinctive cognitive ability profile. The validity of this profile analysis was then assessed by applying the same classification system to profiles of affected parents and siblings of the probands. Affected siblings of probands in subtype 3 (severely impaired reading ability but normal spatial/reasoning and coding/speed) were more likely to be of the same subtype than would be expected on the basis of chance. However, no such evidence for familial transmission of specific subtypes was found in the parental data. It is suggested that family studies may provide a strong test of the heterogeneity of reading disability, and that such studies should be used to assess the validity of alternative typologies. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=517

CSF levels of lactate and hydroxybutyrate dehydrogenase as indicators of neurological sequelae after neonatal brain damage / Bernard DALENS in Developmental Medicine & Child Neurology, 23-2 (April 1981)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 23-2 (April 1981) . - p.228-233 Titre : CSF levels of lactate and hydroxybutyrate dehydrogenase as indicators of neurological sequelae after neonatal brain damage Type de document : Texte imprimé et/ou numérique Auteurs : Bernard DALENS, Auteur ; Jean-Louis VIALLARD, Auteur ; Elie-Jean REYNAUD, Auteur ; Bernard DASTUGE, Auteur Année de publication : 1981 Article en page(s) : p.228-233 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : A prospective study was made of levels of lactate and hydroxybutyrate dehydrogenase in the blood and cerebrospinal fluid of 57 term neonates, in relation to the time elapsed since delivery, neonatal examinations (Apgar score, neurological symptoms and EEG findings) and psychomotor outcome at one year of age. Serum determinations revealed no significant relationship with clinical assessments. CSF measurements showed significant differences near to the time of delivery between the normal and handicapped groups at age one, which supports the hypothesis of a causal link between neonatal brain damage and CSF enzyme levels. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=517 [article] CSF levels of lactate and hydroxybutyrate dehydrogenase as indicators of neurological sequelae after neonatal brain damage [Texte imprimé et/ou numérique] / Bernard DALENS, Auteur ; Jean-Louis VIALLARD, Auteur ; Elie-Jean REYNAUD, Auteur ; Bernard DASTUGE, Auteur . - 1981 . - p.228-233. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 23-2 (April 1981) . - p.228-233 Index. décimale : PER Périodiques Résumé : A prospective study was made of levels of lactate and hydroxybutyrate dehydrogenase in the blood and cerebrospinal fluid of 57 term neonates, in relation to the time elapsed since delivery, neonatal examinations (Apgar score, neurological symptoms and EEG findings) and psychomotor outcome at one year of age. Serum determinations revealed no significant relationship with clinical assessments. CSF measurements showed significant differences near to the time of delivery between the normal and handicapped groups at age one, which supports the hypothesis of a causal link between neonatal brain damage and CSF enzyme levels. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=517

Transient osteosclerosis associated with sodium valproate / Geetha JOHN in Developmental Medicine & Child Neurology, 23-2 (April 1981)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 23-2 (April 1981) . - p.234-236 Titre : Transient osteosclerosis associated with sodium valproate Type de document : Texte imprimé et/ou numérique Auteurs : Geetha JOHN, Auteur Année de publication : 1981 Article en page(s) : p.234-236 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : A 15-year-old boy on sodium valproate presented with pain in the extremities which had not responded to aspirin. X-ray of the long bones showed increased density in the metaphyses. After discontinuation of the drug his symptoms and the X-ray abnormalities disappeared. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=517 [article] Transient osteosclerosis associated with sodium valproate [Texte imprimé et/ou numérique] / Geetha JOHN, Auteur . - 1981 . - p.234-236. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 23-2 (April 1981) . - p.234-236 Index. décimale : PER Périodiques Résumé : A 15-year-old boy on sodium valproate presented with pain in the extremities which had not responded to aspirin. X-ray of the long bones showed increased density in the metaphyses. After discontinuation of the drug his symptoms and the X-ray abnormalities disappeared. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=517

Congenital myopathy with oculo-facial and skeletal abnormalities / S. David FERGUSON in Developmental Medicine & Child Neurology, 23-2 (April 1981)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 23-2 (April 1981) . - p.237-242 Titre : Congenital myopathy with oculo-facial and skeletal abnormalities Type de document : Texte imprimé et/ou numérique Auteurs : S. David FERGUSON, Auteur ; Ian D. YOUNG, Auteur ; Robert TEOH, Auteur Année de publication : 1981 Article en page(s) : p.237-242 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : A case report is presented of a boy with congenital myopathy associated with oculo-facial and skeletal abnormalities. The relationship of this case to patients with the Schwartz-Jampel and Marden-Walker syndromes is discussed. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=517 [article] Congenital myopathy with oculo-facial and skeletal abnormalities [Texte imprimé et/ou numérique] / S. David FERGUSON, Auteur ; Ian D. YOUNG, Auteur ; Robert TEOH, Auteur . - 1981 . - p.237-242. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 23-2 (April 1981) . - p.237-242 Index. décimale : PER Périodiques Résumé : A case report is presented of a boy with congenital myopathy associated with oculo-facial and skeletal abnormalities. The relationship of this case to patients with the Schwartz-Jampel and Marden-Walker syndromes is discussed. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=517

Two children with cerebral gigantism and congenital primary hypothyroidism / J. A. HULSE in Developmental Medicine & Child Neurology, 23-2 (April 1981)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 23-2 (April 1981) . - p.242-246 Titre : Two children with cerebral gigantism and congenital primary hypothyroidism Type de document : Texte imprimé et/ou numérique Auteurs : J. A. HULSE, Auteur Année de publication : 1981 Article en page(s) : p.242-246 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Two children are described in whom congenital primary hypothyroidism was associated with excessive growth during early childhood and who had typical morphological features of cerebral gigantism. One child was completely athyreotic. This association has been described previously in only one other child. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=517 [article] Two children with cerebral gigantism and congenital primary hypothyroidism [Texte imprimé et/ou numérique] / J. A. HULSE, Auteur . - 1981 . - p.242-246. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 23-2 (April 1981) . - p.242-246 Index. décimale : PER Périodiques Résumé : Two children are described in whom congenital primary hypothyroidism was associated with excessive growth during early childhood and who had typical morphological features of cerebral gigantism. One child was completely athyreotic. This association has been described previously in only one other child. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=517

Functional aspects of the chemical senses in the newborn period / Charles CROOK in Developmental Medicine & Child Neurology, 23-2 (April 1981)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 23-2 (April 1981) . - p.251-255 Titre : Functional aspects of the chemical senses in the newborn period Type de document : Texte imprimé et/ou numérique Auteurs : Charles CROOK, Auteur Année de publication : 1981 Article en page(s) : p.251-255 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=517 [article] Functional aspects of the chemical senses in the newborn period [Texte imprimé et/ou numérique] / Charles CROOK, Auteur . - 1981 . - p.251-255. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 23-2 (April 1981) . - p.251-255 Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=517

Plasticity and specificity of language localization in the developing brain / Dorothy V. M. BISHOP in Developmental Medicine & Child Neurology, 23-2 (April 1981)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 23-2 (April 1981) . - p.251-255 Titre : Plasticity and specificity of language localization in the developing brain Type de document : Texte imprimé et/ou numérique Auteurs : Dorothy V. M. BISHOP, Auteur Année de publication : 1981 Article en page(s) : p.251-255 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=518 [article] Plasticity and specificity of language localization in the developing brain [Texte imprimé et/ou numérique] / Dorothy V. M. BISHOP, Auteur . - 1981 . - p.251-255. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 23-2 (April 1981) . - p.251-255 Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=518

Tardive dyskinesia and the behavioral consequences of chronic neuroleptic treatment / C. Thomas GUALTIERI in Developmental Medicine & Child Neurology, 23-2 (April 1981)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 23-2 (April 1981) . - p.255-259 Titre : Tardive dyskinesia and the behavioral consequences of chronic neuroleptic treatment Type de document : Texte imprimé et/ou numérique Auteurs : C. Thomas GUALTIERI, Auteur ; Michelle GUIMOND, Auteur Année de publication : 1981 Article en page(s) : p.255-259 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=518 [article] Tardive dyskinesia and the behavioral consequences of chronic neuroleptic treatment [Texte imprimé et/ou numérique] / C. Thomas GUALTIERI, Auteur ; Michelle GUIMOND, Auteur . - 1981 . - p.255-259. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 23-2 (April 1981) . - p.255-259 Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=518

Long-term Prognosis after Infantile Spams / Neil GORDON in Developmental Medicine & Child Neurology, 23-2 (April 1981)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 23-2 (April 1981) . - p.260 Titre : Long-term Prognosis after Infantile Spams Type de document : Texte imprimé et/ou numérique Auteurs : Neil GORDON, Auteur Année de publication : 1981 Article en page(s) : p.260 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=518 [article] Long-term Prognosis after Infantile Spams [Texte imprimé et/ou numérique] / Neil GORDON, Auteur . - 1981 . - p.260. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 23-2 (April 1981) . - p.260 Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=518

Early intervention-fact or fiction? / Hyman R. SOBOLOFF in Developmental Medicine & Child Neurology, 23-2 (April 1981)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 23-2 (April 1981) . - p.261-266 Titre : Early intervention-fact or fiction? Type de document : Texte imprimé et/ou numérique Auteurs : Hyman R. SOBOLOFF, Auteur Année de publication : 1981 Article en page(s) : p.261-266 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : A group of 50 cerebral-palsied children seen in one clinic between 1952 and 1965 were compared with a second group of 50 seen between 1952 and 1978. The latter group had all been included in a developmental enrichment program at the clinic. The results showed that the later-treated group had had more surgical operations than the earlier group, and at younger ages; that they were able to sit and stand earlier; and that eventually they had greater ambulatory ability. Early intervention also improved family relationships, and parents and siblings became more involved in the team approach to the children's therapy. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=518 [article] Early intervention-fact or fiction? [Texte imprimé et/ou numérique] / Hyman R. SOBOLOFF, Auteur . - 1981 . - p.261-266. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 23-2 (April 1981) . - p.261-266 Index. décimale : PER Périodiques Résumé : A group of 50 cerebral-palsied children seen in one clinic between 1952 and 1965 were compared with a second group of 50 seen between 1952 and 1978. The latter group had all been included in a developmental enrichment program at the clinic. The results showed that the later-treated group had had more surgical operations than the earlier group, and at younger ages; that they were able to sit and stand earlier; and that eventually they had greater ambulatory ability. Early intervention also improved family relationships, and parents and siblings became more involved in the team approach to the children's therapy. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=518