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Détail de l'auteur
Auteur B. D. LAKE |
Documents disponibles écrits par cet auteur (2)
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Childhood nemaline myopathy: a review of clinical presentation in relation to prognosis / B. Adelaida MARTINEZ in Developmental Medicine & Child Neurology, 29-6 (December 1987)
[article]
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
in Developmental Medicine & Child Neurology > 29-6 (December 1987) . - p.815-820[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 Involvement of the central nervous system in congenital muscular dystrophies / Jos EGGER in Developmental Medicine & Child Neurology, 25-1 (February 1983)
[article]
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
in Developmental Medicine & Child Neurology > 25-1 (February 1983) . - p.32-42[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