Facial weakness in hereditary inclusion body myopathies

被引：2

作者：

Argov, Z ^{[1
]}

Sadeh, M

Eisenberg, I

Karpati, G

Mitrani-Rosenbaum, S

机构：

[1] Hadassah Univ Hosp, Dept Neurol, IL-91120 Jerusalem, Israel

[2] Wolfson Med Ctr, Dept Neurol, Holon, Israel

[3] Hadassah Univ Hosp, Unit Dev Mol Biol & Genet Engn, IL-91120 Jerusalem, Israel

[4] McGill Univ, Montreal Neurol Inst, Dept Neurol, Montreal, PQ, Canada

来源：

NEUROLOGY | 1998年 / 50卷 / 06期

关键词：

D O I：

10.1212/WNL.50.6.1925

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

[No abstract available]

引用

页码：1925 / 1926

页数：2

共 7 条

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ANNALS OF NEUROLOGY, 1997, 41 (04) :548-551

[2]

ARGOV Z, 1998, IN PRESS ACTA MIOLOG

[3]

Askanas Valerie, 1995, Current Opinion in Rheumatology, V7, P486, DOI 10.1097/00002281-199511000-00005

[4]

EISENBERG I, 1997, P 29 M EUR SOC HUM G, P109

[5] INCLUSION-BODY MYOSITIS AND MYOPATHIES [J].

GRIGGS, RC ;

ASKANAS, V ;

DIMAURO, S ;

ENGEL, A ;

KARPATI, G ;

MENDELL, JR ;

ROWLAND, LP .

ANNALS OF NEUROLOGY, 1995, 38 (05) :705-713

[6]

MCKEE D, 1992, NEUROLOGY S, V42, pA302

[7] Hereditary inclusion body myopathy maps to chromosome 9p1-q1 [J].

MitraniRosenbaum, S ;

Argov, Z ;

Blumenfeld, A ;

Seidman, CE ;

Seidman, JG .

HUMAN MOLECULAR GENETICS, 1996, 5 (01) :159-163

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