Classification of the hereditary motor and sensory neuropathies

被引：45

作者：

Reilly, MM ^{[1
]}

机构：

[1] UCL Natl Hosp Neurol, Inst Neurol, Dept Clin Neurol, London, England

来源：

CURRENT OPINION IN NEUROLOGY | 2000年 / 13卷 / 05期

关键词：

D O I：

10.1097/00019052-200010000-00009

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：561 / 564

页数：4

共 28 条

[1] Congenital cataracts facial dysmorphism neuropathy (CCFDN) syndrome: a novel developmental disorder in Gypsies maps to 18qter [J].

Angelicheva, D ;

Turnev, I ;

Dye, D ;

Chandler, D ;

Thomas, PK ;

Kalaydjieva, L .

EUROPEAN JOURNAL OF HUMAN GENETICS, 1999, 7 (05) :560-566

[2] Identification of a new locus for autosomal recessive Charcot-Marie-Tooth disease with focally folded myelin on chromosome 11p15 [J].

Ben Othmane, K ;

Johnson, E ;

Menold, M ;

Graham, FL ;

Ben Hamida, M ;

Hasegawa, O ;

Rogala, AD ;

Ohnishi, A ;

Pericak-Vance, M ;

Hentati, F ;

Vance, JM .

GENOMICS, 1999, 62 (03) :344-349

[3] Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2 [J].

Bolino, A ;

Muglia, M ;

Conforti, FL ;

LeGuern, E ;

Salih, MAM ;

Georgiou, DM ;

Christodoulou, K ;

Hausmanowa-Petrusewicz, I ;

Mandich, P ;

Schenone, A ;

Gambardella, A ;

Bono, F ;

Quattrone, A ;

Devoto, M ;

Monaco, AP .

NATURE GENETICS, 2000, 25 (01) :17-19

[4] A locus for an axonal form of autosomal recessive Charcot-Marie-Tooth disease maps to chromosome 1q21.2q21.3 [J].

Bouhouche, A ;

Benomar, A ;

Birouk, N ;

Mularoni, A ;

Meggouh, F ;

Tassin, J ;

Grid, D ;

Vandenberghe, A ;

Yahyaoui, M ;

Chkili, T ;

Brice, A ;

LeGuern, E .

AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 65 (03) :722-727

[5] Mapping of a new locus for autosomal recessive demyelinating Charcot-Marie-Tooth disease to 19q13.1-13.3 in a large consanguineous Lebanese family:: Exclusion of MAG as a candidate gene [J].

Delague, V ;

Bareil, C ;

Tuffery, S ;

Bouvagnet, P ;

Chouery, E ;

Koussa, S ;

Maisonobe, T ;

Loiselet, J ;

Mégarbané, A ;

Claustres, M .

AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 67 (01) :236-243

[6] LOWER MOTOR AND PRIMARY SENSORY NEURON DISEASES WITH PERONEAL MUSCULAR ATROPHY .2. NEUROLOGIC GENETIC AND ELECTROPHYSIOLOGIC FINDINGS IN VARIOUS NEURONAL DEGENERATIONS [J].

DYCK, PJ ;

LAMBERT, EH .

ARCHIVES OF NEUROLOGY, 1968, 18 (06) :619-&

[7] LOWER MOTOR AND PRIMARY SENSORY NEURON DISEASES WITH PERONEAL MUSCULAR ATROPHY .I. NEUROLOGIC GENETIC AND ELECTROPHYSIOLOGIC FINDINGS IN HEREDITARY POLYNEUROPATHIES [J].

DYCK, PJ ;

LAMBERT, EH .

ARCHIVES OF NEUROLOGY, 1968, 18 (06) :603-+

[8]

Dyck PJ, 1994, PERIPHERAL NEUROPATH, P1094

[9] DE-NOVO MUTATION OF THE MYELIN P(O) GENE IN DEJERINE-SOTTAS DISEASE (HEREDITARY MOTOR AND SENSORY NEUROPATHY TYPE-III) [J].

HAYASAKA, K ;

HIMORO, M ;

SAWAISHI, Y ;

NANAO, K ;

TAKAHASHI, T ;

TAKADA, G ;

NICHOLSON, GA ;

OUVRIER, RA ;

TACHI, N .

NATURE GENETICS, 1993, 5 (03) :266-268

[10]

Ionasescu VV, 1996, MUSCLE NERVE, V19, P319, DOI 10.1002/(SICI)1097-4598(199603)19:3<319::AID-MUS6>3.3.CO

← 1 2 3 →