Dépouillements

Keeping Up-to-Date / Martin C. O. BAX in Developmental Medicine & Child Neurology, 25-1 (February 1983)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 25-1 (February 1983) . - p.1-2 Titre : Keeping Up-to-Date Type de document : Texte imprimé et/ou numérique Auteurs : Martin C. O. BAX, Auteur Année de publication : 1983 Article en page(s) : p.1-2 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=559 [article] Keeping Up-to-Date [Texte imprimé et/ou numérique] / Martin C. O. BAX, Auteur . - 1983 . - p.1-2. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 25-1 (February 1983) . - p.1-2 Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=559

The nosology of genetic peripheral neuropathies in Swedish children / Bengt HAGBERG in Developmental Medicine & Child Neurology, 25-1 (February 1983)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 25-1 (February 1983) . - p.3-18 Titre : The nosology of genetic peripheral neuropathies in Swedish children Type de document : Texte imprimé et/ou numérique Auteurs : Bengt HAGBERG, Auteur ; Barbro WESTERBERG, Auteur Année de publication : 1983 Article en page(s) : p.3-18 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : 103 consecutive childhood cases of genetic peripheral neuropathies of heredodegenerative background were collected from Gothenburg from 1973 to 1980. From this series, 63 hereditary motor and sensory neuropathies (HMSN) were distinguished: 31 cases of demyelinating and remyelinating HMSN (HMSN I), 21 (18 families) with an autosomal dominant and 10 with sporadic mode of inheritance and unaffected parents; and 32 cases of neuronal-axonal types (HMSN II), 27 of whom (25 families) had at least one affected, if asymptomatic, parent. In one family, both parents were neurologically and neurophysiologically completely normal. Three cases of uncharacteristic HSN were diagnosed. Among 37 cases with a combined degenerative encephalopathy/myelopathy and a peripheral neuropathy, nine had hereditary spastic paraplegia, six had heredoataxias (three of the Friedreich type), nine had lysosomal storage diseases (five of the Krabbe type), seven had other known inborn metabolic errors and six had biochemically undefined disorders. Progressive neuropathies are important manifestations of a large variety of genetically determined heredodegenerative neurological disorders of infancy and childhood. For classification of HMSN, clinical and neurophysiological examinations are necessary for the index case and for both parents as well. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=559 [article] The nosology of genetic peripheral neuropathies in Swedish children [Texte imprimé et/ou numérique] / Bengt HAGBERG, Auteur ; Barbro WESTERBERG, Auteur . - 1983 . - p.3-18. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 25-1 (February 1983) . - p.3-18 Index. décimale : PER Périodiques Résumé : 103 consecutive childhood cases of genetic peripheral neuropathies of heredodegenerative background were collected from Gothenburg from 1973 to 1980. From this series, 63 hereditary motor and sensory neuropathies (HMSN) were distinguished: 31 cases of demyelinating and remyelinating HMSN (HMSN I), 21 (18 families) with an autosomal dominant and 10 with sporadic mode of inheritance and unaffected parents; and 32 cases of neuronal-axonal types (HMSN II), 27 of whom (25 families) had at least one affected, if asymptomatic, parent. In one family, both parents were neurologically and neurophysiologically completely normal. Three cases of uncharacteristic HSN were diagnosed. Among 37 cases with a combined degenerative encephalopathy/myelopathy and a peripheral neuropathy, nine had hereditary spastic paraplegia, six had heredoataxias (three of the Friedreich type), nine had lysosomal storage diseases (five of the Krabbe type), seven had other known inborn metabolic errors and six had biochemically undefined disorders. Progressive neuropathies are important manifestations of a large variety of genetically determined heredodegenerative neurological disorders of infancy and childhood. For classification of HMSN, clinical and neurophysiological examinations are necessary for the index case and for both parents as well. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=559

Hereditary motor sensory neuropathies in childhood / Livia N. ROSSI in Developmental Medicine & Child Neurology, 25-1 (February 1983)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 25-1 (February 1983) . - p.19-31 Titre : Hereditary motor sensory neuropathies in childhood Type de document : Texte imprimé et/ou numérique Auteurs : Livia N. ROSSI, Auteur ; C. MEIER, Auteur ; Jürg LUTSCHG, Auteur ; Franco VASSELLA, Auteur Année de publication : 1983 Article en page(s) : p.19-31 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Clinical data on 24 patients with hereditary motor sensory neuropathies, with onset in the paediatric period, and of their relatives, is reported. Electrophysiological studies were done in all patients and in 15 relatives. The patients were divided into two groups (Types I and II) and their hereditary trait was determined. In 11 patients a sural nerve biopsy was performed and revealed different patterns of histological alterations. The nerve biopsy always confirmed the value of conduction velocity in distinguishing between Types I and II. A genetic discordance was observed, both in regard to the phenotype and the conduction velocity, and there was increased slowing of the conduction velocity as individuals grew older. Thus the classification of these disorders in childhood can be particularly difficult. The rôle of sural nerve biopsy is discussed. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=559 [article] Hereditary motor sensory neuropathies in childhood [Texte imprimé et/ou numérique] / Livia N. ROSSI, Auteur ; C. MEIER, Auteur ; Jürg LUTSCHG, Auteur ; Franco VASSELLA, Auteur . - 1983 . - p.19-31. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 25-1 (February 1983) . - p.19-31 Index. décimale : PER Périodiques Résumé : Clinical data on 24 patients with hereditary motor sensory neuropathies, with onset in the paediatric period, and of their relatives, is reported. Electrophysiological studies were done in all patients and in 15 relatives. The patients were divided into two groups (Types I and II) and their hereditary trait was determined. In 11 patients a sural nerve biopsy was performed and revealed different patterns of histological alterations. The nerve biopsy always confirmed the value of conduction velocity in distinguishing between Types I and II. A genetic discordance was observed, both in regard to the phenotype and the conduction velocity, and there was increased slowing of the conduction velocity as individuals grew older. Thus the classification of these disorders in childhood can be particularly difficult. The rôle of sural nerve biopsy is discussed. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=559

Involvement of the central nervous system in congenital muscular dystrophies / Jos EGGER in Developmental Medicine & Child Neurology, 25-1 (February 1983)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 25-1 (February 1983) . - p.32-42 Titre : Involvement of the central nervous system in congenital muscular dystrophies Type de document : Texte imprimé et/ou numérique Auteurs : Jos EGGER, Auteur ; Magda ERDOHAZI, Auteur ; Brian E. KENDALL, Auteur ; B. D. LAKE, Auteur ; J. WILSON, Auteur ; E. M. BRETT, Auteur Année de publication : 1983 Article en page(s) : p.32-42 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Three children, two siblings and one unrelated child, with congenital muscular dystrophy with central nervous system (CNS) involvement are discussed. The siblings appeared to suffer from a relatively mild myopathy with progressive brain disease, of which brain biopsy in one showed astrocytic proliferation in the white matter. In the patient with severe muscle disease, autopsy showed widespread patchy demyelination in the white matter and developmental abnormalities in the cerebral and cerebellar cortex. These patients differ from the Japanese (Fukuyama) cases of CMD in the severity of the changes in the cerebral white matter, and from Santavuori's cases in the absence of ocular abnormalities and hydrocephalus. Their unique nosology is discussed. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=559 [article] Involvement of the central nervous system in congenital muscular dystrophies [Texte imprimé et/ou numérique] / Jos EGGER, Auteur ; Magda ERDOHAZI, Auteur ; Brian E. KENDALL, Auteur ; B. D. LAKE, Auteur ; J. WILSON, Auteur ; E. M. BRETT, Auteur . - 1983 . - p.32-42. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 25-1 (February 1983) . - p.32-42 Index. décimale : PER Périodiques Résumé : Three children, two siblings and one unrelated child, with congenital muscular dystrophy with central nervous system (CNS) involvement are discussed. The siblings appeared to suffer from a relatively mild myopathy with progressive brain disease, of which brain biopsy in one showed astrocytic proliferation in the white matter. In the patient with severe muscle disease, autopsy showed widespread patchy demyelination in the white matter and developmental abnormalities in the cerebral and cerebellar cortex. These patients differ from the Japanese (Fukuyama) cases of CMD in the severity of the changes in the cerebral white matter, and from Santavuori's cases in the absence of ocular abnormalities and hydrocephalus. Their unique nosology is discussed. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=559

Severe autosomal recessive muscular dystrophy in an extended Sudanese kindred / Mustafa A. M. SALIH in Developmental Medicine & Child Neurology, 25-1 (February 1983)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 25-1 (February 1983) . - p.43-52 Titre : Severe autosomal recessive muscular dystrophy in an extended Sudanese kindred Type de document : Texte imprimé et/ou numérique Auteurs : Mustafa A. M. SALIH, Auteur ; Mohamed Ibrahim A. OMER, Auteur ; Riad A. BAYOUMI, Auteur ; Omer KARRAR, Auteur ; M. JOHNSON, Auteur Année de publication : 1983 Article en page(s) : p.43-52 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : The clinical manifestations, biochemical, electrocardiographic, histological and histochemical features of a severe autosomal recessive muscular dystrophy (MD)--as seen in 15 members of a large Sudanese kindred, both male and female--are reported and discussed. The age of onset ranged from three to five years, the pattern of muscular weakness was similar to that of Duchenne MD and pseudohypertrophy was a remarkable feature. Both sexes became completely dependent by 16 years, and died at or before 20 years of age. The clinical picture in this family and the histological features are compared with those of Duchenne MD and with cases reported from Tunisia, Qatar and Libya. Certain clinical and histological features distinguish all of these types from each other and from the milder autosomal recessive MD of childhood which is more usual in the United Kingdom, Europe, Australia and North America. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=559 [article] Severe autosomal recessive muscular dystrophy in an extended Sudanese kindred [Texte imprimé et/ou numérique] / Mustafa A. M. SALIH, Auteur ; Mohamed Ibrahim A. OMER, Auteur ; Riad A. BAYOUMI, Auteur ; Omer KARRAR, Auteur ; M. JOHNSON, Auteur . - 1983 . - p.43-52. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 25-1 (February 1983) . - p.43-52 Index. décimale : PER Périodiques Résumé : The clinical manifestations, biochemical, electrocardiographic, histological and histochemical features of a severe autosomal recessive muscular dystrophy (MD)--as seen in 15 members of a large Sudanese kindred, both male and female--are reported and discussed. The age of onset ranged from three to five years, the pattern of muscular weakness was similar to that of Duchenne MD and pseudohypertrophy was a remarkable feature. Both sexes became completely dependent by 16 years, and died at or before 20 years of age. The clinical picture in this family and the histological features are compared with those of Duchenne MD and with cases reported from Tunisia, Qatar and Libya. Certain clinical and histological features distinguish all of these types from each other and from the milder autosomal recessive MD of childhood which is more usual in the United Kingdom, Europe, Australia and North America. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=559

Dermatoglyphic and palmar-crease alterations as indicators of early intra-uterine insult in mental retardation / Hannah DAR in Developmental Medicine & Child Neurology, 25-1 (February 1983)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 25-1 (February 1983) . - p.53-59 Titre : Dermatoglyphic and palmar-crease alterations as indicators of early intra-uterine insult in mental retardation Type de document : Texte imprimé et/ou numérique Auteurs : Hannah DAR, Auteur ; Michael JAFFE, Auteur Année de publication : 1983 Article en page(s) : p.53-59 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : A comparative study of unusual dermatoglyphic and palmar patterns revealed significant differences between the frequencies of certain patterns among 200 congenitally affected mentally retarded children and 500 normal controls. A scoring method demonstrating the significance of eight unusual patterns as non-specific indicators of early intra-uterine fetal insult was devised. 10 per cent of the children previously classified as idiopathically mentally retarded were shown to have been exposed to early intra-uterine insult. Dermatoglyphic and palmar-crease analysis should be included as a routine investigation for children with mental retardation of unknown cause. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=559 [article] Dermatoglyphic and palmar-crease alterations as indicators of early intra-uterine insult in mental retardation [Texte imprimé et/ou numérique] / Hannah DAR, Auteur ; Michael JAFFE, Auteur . - 1983 . - p.53-59. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 25-1 (February 1983) . - p.53-59 Index. décimale : PER Périodiques Résumé : A comparative study of unusual dermatoglyphic and palmar patterns revealed significant differences between the frequencies of certain patterns among 200 congenitally affected mentally retarded children and 500 normal controls. A scoring method demonstrating the significance of eight unusual patterns as non-specific indicators of early intra-uterine fetal insult was devised. 10 per cent of the children previously classified as idiopathically mentally retarded were shown to have been exposed to early intra-uterine insult. Dermatoglyphic and palmar-crease analysis should be included as a routine investigation for children with mental retardation of unknown cause. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=559

Biomechanical measurement of spastic plantarflexors / James C. OTIS in Developmental Medicine & Child Neurology, 25-1 (February 1983)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 25-1 (February 1983) . - p.60-66 Titre : Biomechanical measurement of spastic plantarflexors Type de document : Texte imprimé et/ou numérique Auteurs : James C. OTIS, Auteur ; Leon ROOT, Auteur ; Jeanne R. PAMILLA, Auteur ; Michael A. KROLL, Auteur Année de publication : 1983 Article en page(s) : p.60-66 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : A study was conducted to determine the feasibility of quantifying spasticity in plantarflexors by measuring the resistance to passive dorsiflexion of the ankle joint at several constant angular speeds. Repeated testing was conducted on normal subjects and spastic patients. Good repeatability was found for both groups and both groups were found to differ significantly from each other with respect to the measurement variable. The method will provide a useful tool for quantifying alterations in plantarflexor spasticity which result from various surgical and non-surgical treatments. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=559 [article] Biomechanical measurement of spastic plantarflexors [Texte imprimé et/ou numérique] / James C. OTIS, Auteur ; Leon ROOT, Auteur ; Jeanne R. PAMILLA, Auteur ; Michael A. KROLL, Auteur . - 1983 . - p.60-66. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 25-1 (February 1983) . - p.60-66 Index. décimale : PER Périodiques Résumé : A study was conducted to determine the feasibility of quantifying spasticity in plantarflexors by measuring the resistance to passive dorsiflexion of the ankle joint at several constant angular speeds. Repeated testing was conducted on normal subjects and spastic patients. Good repeatability was found for both groups and both groups were found to differ significantly from each other with respect to the measurement variable. The method will provide a useful tool for quantifying alterations in plantarflexor spasticity which result from various surgical and non-surgical treatments. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=559

Childhood nocturnal enuresis: factors associated with outcome of treatment with an enuresis alarm / Sylvia DISCHE in Developmental Medicine & Child Neurology, 25-1 (February 1983)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 25-1 (February 1983) . - p.67-80 Titre : Childhood nocturnal enuresis: factors associated with outcome of treatment with an enuresis alarm Type de document : Texte imprimé et/ou numérique Auteurs : Sylvia DISCHE, Auteur ; William YULE, Auteur ; John CORBETT, Auteur ; David HAND, Auteur Année de publication : 1983 Article en page(s) : p.67-80 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : A study was carried out to assess the factors that may affect the outcome of a single course of treatment for childhood nocturnal enuresis by use of an enuresis alarm. 113 children were treated and followed up; those showing failure of initial arrest of wetting, relapse and longterm successful outcome were analysed separately. Emphasis is placed on the need for the adoption of clear criteria regarding the definition of these three groups, and for an adequate follow-up of treated cases. Unsatisfactory housing conditions and circumstances giving rise to family difficulties were significantly associated with a less favourable rate of initial arrest. In the long term, family difficulties again were found to be significantly related to poor outcome. Behavioural deviance, as revealed by a teacher's behavioural questionnaire also adversely affected long-term success, although less significantly so. Family difficulties emerged as the most important predictor for outcome of treatment and adversely influenced the rate of initial arrest of wetting, the relapse rate and the long-term success rate. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=559 [article] Childhood nocturnal enuresis: factors associated with outcome of treatment with an enuresis alarm [Texte imprimé et/ou numérique] / Sylvia DISCHE, Auteur ; William YULE, Auteur ; John CORBETT, Auteur ; David HAND, Auteur . - 1983 . - p.67-80. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 25-1 (February 1983) . - p.67-80 Index. décimale : PER Périodiques Résumé : A study was carried out to assess the factors that may affect the outcome of a single course of treatment for childhood nocturnal enuresis by use of an enuresis alarm. 113 children were treated and followed up; those showing failure of initial arrest of wetting, relapse and longterm successful outcome were analysed separately. Emphasis is placed on the need for the adoption of clear criteria regarding the definition of these three groups, and for an adequate follow-up of treated cases. Unsatisfactory housing conditions and circumstances giving rise to family difficulties were significantly associated with a less favourable rate of initial arrest. In the long term, family difficulties again were found to be significantly related to poor outcome. Behavioural deviance, as revealed by a teacher's behavioural questionnaire also adversely affected long-term success, although less significantly so. Family difficulties emerged as the most important predictor for outcome of treatment and adversely influenced the rate of initial arrest of wetting, the relapse rate and the long-term success rate. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=559

The analysis of acquired dysarthria in childhood / E. BAK in Developmental Medicine & Child Neurology, 25-1 (February 1983)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 25-1 (February 1983) . - p.81-87 Titre : The analysis of acquired dysarthria in childhood Type de document : Texte imprimé et/ou numérique Auteurs : E. BAK, Auteur ; Hugo R. VAN DONGEN, Auteur ; W. F. M. ARTS, Auteur Année de publication : 1983 Article en page(s) : p.81-87 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : A rare case of acquired dysarthria caused by a brain-stem infarct in a six-year-old boy is reported. Applying the analysis of Darley et al. (1969, 1975), 14 'dimensions' of dysarthria were recognised. The course of this dysarthria is described, by comparing samples of spontaneous speech, repetition and singing. The dysarthria is mainly characterised by imprecise consonants, distorted vowels, hypernasality and a breathy voice. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=560 [article] The analysis of acquired dysarthria in childhood [Texte imprimé et/ou numérique] / E. BAK, Auteur ; Hugo R. VAN DONGEN, Auteur ; W. F. M. ARTS, Auteur . - 1983 . - p.81-87. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 25-1 (February 1983) . - p.81-87 Index. décimale : PER Périodiques Résumé : A rare case of acquired dysarthria caused by a brain-stem infarct in a six-year-old boy is reported. Applying the analysis of Darley et al. (1969, 1975), 14 'dimensions' of dysarthria were recognised. The course of this dysarthria is described, by comparing samples of spontaneous speech, repetition and singing. The dysarthria is mainly characterised by imprecise consonants, distorted vowels, hypernasality and a breathy voice. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=560

The neuropathology of propionic acidemia / Lawrence STEINMAN in Developmental Medicine & Child Neurology, 25-1 (February 1983)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 25-1 (February 1983) . - p.87-94 Titre : The neuropathology of propionic acidemia Type de document : Texte imprimé et/ou numérique Auteurs : Lawrence STEINMAN, Auteur ; Henry URICH, Auteur ; Robert R. CLANCY, Auteur ; Howard CANN, Auteur Année de publication : 1983 Article en page(s) : p.87-94 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : The neuropathology in two biochemically documented cases of propionic acidemia is presented. While spongiform changes in white matter were seen in the infant who died at 12 days, no such changes were evident in an older patient who died at age 23 months. These findings are compared with other aminoacidemias. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=560 [article] The neuropathology of propionic acidemia [Texte imprimé et/ou numérique] / Lawrence STEINMAN, Auteur ; Henry URICH, Auteur ; Robert R. CLANCY, Auteur ; Howard CANN, Auteur . - 1983 . - p.87-94. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 25-1 (February 1983) . - p.87-94 Index. décimale : PER Périodiques Résumé : The neuropathology in two biochemically documented cases of propionic acidemia is presented. While spongiform changes in white matter were seen in the infant who died at 12 days, no such changes were evident in an older patient who died at age 23 months. These findings are compared with other aminoacidemias. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=560

Is the academic pediatric neurologist an endangered species? / Richard S. K. YOUNG in Developmental Medicine & Child Neurology, 25-1 (February 1983)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 25-1 (February 1983) . - p.95-97 Titre : Is the academic pediatric neurologist an endangered species? Type de document : Texte imprimé et/ou numérique Auteurs : Richard S. K. YOUNG, Auteur ; Susan K. YAGEL, Auteur ; Arthur L. PRENSKY, Auteur Année de publication : 1983 Article en page(s) : p.95-97 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Some argue that the physician-researcher is an endangered specie and that the 'bedside connection' is severely strained. Our survey of recent graduates of pediatric neurology training programs does not substantiate this. Almost one-half of graduating pediatric neurology residents are embarking on full-time, university-based careers. Laboratory experience seems to play a decisive role in career orientation, confirming the intention of those interested in an academic career, and dissuading those who ultimately decide on private practice. Finally, a large number of young pediatric neurology trainees have taken additional years of fellowship training, although primarily in clinical neurology. This survey indicates that even more people would be inclined toward fellowship training if stipends were somewhat higher. In summary, despite considerable uncertainties about grant support and low salaries, a substantial number of graduates of pediatric neurology training programs are planning careers as physician-researchers. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=560 [article] Is the academic pediatric neurologist an endangered species? [Texte imprimé et/ou numérique] / Richard S. K. YOUNG, Auteur ; Susan K. YAGEL, Auteur ; Arthur L. PRENSKY, Auteur . - 1983 . - p.95-97. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 25-1 (February 1983) . - p.95-97 Index. décimale : PER Périodiques Résumé : Some argue that the physician-researcher is an endangered specie and that the 'bedside connection' is severely strained. Our survey of recent graduates of pediatric neurology training programs does not substantiate this. Almost one-half of graduating pediatric neurology residents are embarking on full-time, university-based careers. Laboratory experience seems to play a decisive role in career orientation, confirming the intention of those interested in an academic career, and dissuading those who ultimately decide on private practice. Finally, a large number of young pediatric neurology trainees have taken additional years of fellowship training, although primarily in clinical neurology. This survey indicates that even more people would be inclined toward fellowship training if stipends were somewhat higher. In summary, despite considerable uncertainties about grant support and low salaries, a substantial number of graduates of pediatric neurology training programs are planning careers as physician-researchers. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=560

Treatment of congenital dislocation of the hip / Tudor L. THOMAS in Developmental Medicine & Child Neurology, 25-1 (February 1983)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 25-1 (February 1983) . - p.97-99 Titre : Treatment of congenital dislocation of the hip Type de document : Texte imprimé et/ou numérique Auteurs : Tudor L. THOMAS, Auteur Année de publication : 1983 Article en page(s) : p.97-99 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=560 [article] Treatment of congenital dislocation of the hip [Texte imprimé et/ou numérique] / Tudor L. THOMAS, Auteur . - 1983 . - p.97-99. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 25-1 (February 1983) . - p.97-99 Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=560

Neonatal spinal-cord dysfunction / Jean AICARDI in Developmental Medicine & Child Neurology, 25-1 (February 1983)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 25-1 (February 1983) . - p.100 Titre : Neonatal spinal-cord dysfunction Type de document : Texte imprimé et/ou numérique Auteurs : Jean AICARDI, Auteur Année de publication : 1983 Article en page(s) : p.100 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=560 [article] Neonatal spinal-cord dysfunction [Texte imprimé et/ou numérique] / Jean AICARDI, Auteur . - 1983 . - p.100. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 25-1 (February 1983) . - p.100 Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=560

Achondroplasia / S. J. ILET in Developmental Medicine & Child Neurology, 25-1 (February 1983)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 25-1 (February 1983) . - 100-101 Titre : Achondroplasia Type de document : Texte imprimé et/ou numérique Auteurs : S. J. ILET, Auteur Année de publication : 1983 Article en page(s) : 100-101 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=560 [article] Achondroplasia [Texte imprimé et/ou numérique] / S. J. ILET, Auteur . - 1983 . - 100-101. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 25-1 (February 1983) . - 100-101 Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=560

Annual meeting of the American Academy for Cerebral Palsy and Developmental Medicine, 1982 / Sue JENKINS in Developmental Medicine & Child Neurology, 25-1 (February 1983)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 25-1 (February 1983) . - p.102-117 Titre : Annual meeting of the American Academy for Cerebral Palsy and Developmental Medicine, 1982 Type de document : Texte imprimé et/ou numérique Auteurs : Sue JENKINS, Auteur Année de publication : 1983 Article en page(s) : p.102-117 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=560 [article] Annual meeting of the American Academy for Cerebral Palsy and Developmental Medicine, 1982 [Texte imprimé et/ou numérique] / Sue JENKINS, Auteur . - 1983 . - p.102-117. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 25-1 (February 1983) . - p.102-117 Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=560