
- <Centre d'Information et de documentation du CRA Rhône-Alpes
- CRA
- Informations pratiques
-
Adresse
Centre d'information et de documentation
Horaires
du CRA Rhône-Alpes
Centre Hospitalier le Vinatier
bât 211
95, Bd Pinel
69678 Bron CedexLundi au Vendredi
Contact
9h00-12h00 13h30-16h00Tél: +33(0)4 37 91 54 65
Mail
Fax: +33(0)4 37 91 54 37
-
Adresse
Détail de l'auteur
Auteur Francis M. BRINNER |
Documents disponibles écrits par cet auteur (1)



Fingerprint body myopathy: a report of twins / Richard G. CURLESS in Developmental Medicine & Child Neurology, 20-6 (December 1978)
[article]
Titre : Fingerprint body myopathy: a report of twins Type de document : Texte imprimé et/ou numérique Auteurs : Richard G. CURLESS, Auteur ; Claire M. PAYNE, Auteur ; Francis M. BRINNER, Auteur Année de publication : 1978 Article en page(s) : p.793-798 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Ultramicroscopic changes of subsarcolemmal fingerprints in the muscle of children with infantile hypotonia and weakness may represent a specific congenital entity. Four children have been reported so far. The two children reported in the present paper are the first full siblings to be described and, in addition, are identical twins. Four of these six children also had mental retardation, which suggests that this disorder may carry with it a significant risk of central nervous system abnormality. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=486
in Developmental Medicine & Child Neurology > 20-6 (December 1978) . - p.793-798[article] Fingerprint body myopathy: a report of twins [Texte imprimé et/ou numérique] / Richard G. CURLESS, Auteur ; Claire M. PAYNE, Auteur ; Francis M. BRINNER, Auteur . - 1978 . - p.793-798.
Langues : Anglais (eng)
in Developmental Medicine & Child Neurology > 20-6 (December 1978) . - p.793-798
Index. décimale : PER Périodiques Résumé : Ultramicroscopic changes of subsarcolemmal fingerprints in the muscle of children with infantile hypotonia and weakness may represent a specific congenital entity. Four children have been reported so far. The two children reported in the present paper are the first full siblings to be described and, in addition, are identical twins. Four of these six children also had mental retardation, which suggests that this disorder may carry with it a significant risk of central nervous system abnormality. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=486