Titre : | Evidence-based guideline summary: Evaluation, diagnosis, and management of congenital muscular dystrophy: Report of the Guideline Development Subcommittee of the American Academy of Neurology and the Practice Issues Review Panel of the American Association of Neuromuscular & Electrodiagnostic Medicine |
Revue : | Neurology, 85, 16 |
Auteurs : | Haliloglu G, Auteur ; Topaloglu H ; Kang PB ; Morrison L ; Iannaccone ST ; Graham RJ ; Bonnemann CG ; Rutkowski A ; Hornyak J ; Wang CH ; North K |
Type de document : | Article |
Année de publication : | 2015 |
Pages : | p 1432 |
Langues: | Anglais |
Mots-clés : | diagnostic ; dystrophie musculaire congénitale ; gène CHKB ; gène POMT1 ; gène SELENON ; lettre ; myopathie mégaconiale ; recommandation ; Turquie |
Résumé : |
Comment on:
Evidence-based guideline summary: evaluation, diagnosis, and management of congenital muscular dystrophy: Report of the Guideline Development Subcommittee of the American Academy of Neurology and the Practice Issues Review Panel of the American Association of Neuromuscular & Electrodiagnostic Medicine. [Neurology. 2015] |
Pubmed / DOI : | DOI : 10.1212/WNL.0000000000002051 / Pubmed : 26481930 |
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