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Détail de l'auteur
Auteur C. MEIER |
Documents disponibles écrits par cet auteur (2)
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Hereditary motor sensory neuropathies in childhood / Livia N. ROSSI in Developmental Medicine & Child Neurology, 25-1 (February 1983)
[article]
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
in Developmental Medicine & Child Neurology > 25-1 (February 1983) . - p.19-31[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 Progressive neural muscular atrophy in a case of phenylketonuria / C. MEIER in Developmental Medicine & Child Neurology, 17-5 (October 1975)
[article]
Titre : Progressive neural muscular atrophy in a case of phenylketonuria Type de document : Texte imprimé et/ou numérique Auteurs : C. MEIER, Auteur ; Jürg LUTSCHG, Auteur ; F. VASELLA, Auteur ; A. BISCHOFF, Auteur Année de publication : 1975 Article en page(s) : p.625-630 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=442
in Developmental Medicine & Child Neurology > 17-5 (October 1975) . - p.625-630[article] Progressive neural muscular atrophy in a case of phenylketonuria [Texte imprimé et/ou numérique] / C. MEIER, Auteur ; Jürg LUTSCHG, Auteur ; F. VASELLA, Auteur ; A. BISCHOFF, Auteur . - 1975 . - p.625-630.
Langues : Anglais (eng)
in Developmental Medicine & Child Neurology > 17-5 (October 1975) . - p.625-630
Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=442