Author:
Marques W.,Freitas M. R.,Nascimento O. J. M.,Oliveira A. B.,Calia L.,Melo A.,Lucena R.,Rocha V.,Barreira A. A.
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical),Neurology
Reference55 articles.
1. Aiyesimoju AB, Osuntokun BO,
Bademosi O, Adeuja AO (1984) Hereditary
neurodegenerative disorders in
Nigerian Africans. Neurology 34:361–362
2. Auer-Grumbach M, Wagner K,
Strasser-Fuchs S, Loscher WN, Fazekas
F, Millner M, Hartung HP (2000) Clinical
predominance of proximal upper
limb weakness in CMT1A syndrome.
Muscle Nerve 23:1243–1249
3. Baker RS, Upton AR (1979) Variation
of phenotype in Charcot-Marie-Tooth
disease. Neuropédiatrie 10:290–295
4. Bellone E, Mandich P, Mancardi GL,
Schenone A, Uccelli A, Abbruzzese M,
Sghirlanzoni A, Pareyson D, Ajmar F
(1992) Charcot-Marie-Tooth (CMT) 1a
duplication at 17p11.2 in Italian families.
J Med Genet 29:492–493
5. Birouk N, Gouider R, Le Guern E,
Gugenheim M, Tardieu S, Maisonobe T,
Le Forestier N, Agid Y, Brice A, Bouche
P (1997) Charcot-Marie-Tooth disease
type 1A with 17p11.2 duplication.
Clinical and electrophysiological phenotype
study and factors influencing
disease severity in 119 cases. Brain
120(Pt 5):813–823
Cited by
46 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献