메뉴 건너뛰기




Volumn 50, Issue 4, 2001, Pages 452-457

Hereditary motor and sensory neuropathy-Russe: New autosomal recessive neuropathy in Balkan gypsies

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CHROMOSOME 10Q; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; FEMALE; FOOT MALFORMATION; GENE MUTATION; GIPSY; HAND MALFORMATION; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; LEG; MALE; MOTOR NERVE CONDUCTION; MUSCLE WEAKNESS; MYELINATED NERVE; NERVE POTENTIAL; NERVE REGENERATION; NEUROPATHIC JOINT DISEASE; PRIORITY JOURNAL; SCHOOL CHILD; SENSORY DYSFUNCTION; SENSORY NERVE; SURAL NERVE;

EID: 0034790977     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/ana.1137     Document Type: Article
Times cited : (49)

References (27)
  • 2
    • 0031882018 scopus 로고    scopus 로고
    • Hereditary motor and sensory neuropathy-Lom (HMSNL), a novel demyelinating neuropathy associated with deafness in Gypsies: Clinical, electrophysiological and nerve biopsy findings
    • (1998) Brain , vol.121 , pp. 399-408
    • Kalaydjieva, L.1    Nikolova, A.2    Turnev, I.3
  • 4
    • 0033015804 scopus 로고    scopus 로고
    • Congenital cataracts facial dysmorphism neuropathy syndrome, a novel complex genetic disease in Balkan Gypsies: Clinical and electrophysiological observations
    • (1999) Ann Neurol , vol.45 , pp. 742-750
    • Tournev, I.1    Kalaydjieva, L.2    Youl, B.3
  • 10
  • 12
    • 0014301249 scopus 로고
    • Lower motor and sensory neuron diseases with peroneal muscular atrophy. I. Neurologic, genetic and electrophysiologic findings in hereditary polyneuropathies
    • (1968) Arch Neurol , vol.18 , pp. 603-618
    • Dyck, P.J.1    Lambert, E.H.2
  • 13
    • 0014301112 scopus 로고
    • Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. II. Neurologic, genetic and electrophysiologic findings in various neuronal degenerations
    • (1968) Arch Neurol , vol.18 , pp. 619-625
    • Dyck, P.J.1    Lambert, E.H.2
  • 18
    • 0030015647 scopus 로고    scopus 로고
    • Localization of a gene responsible for autosomal recessive demyelinating neuropathy with focally folded myelin sheaths to chromosome 11q23 by homozygosity mapping and haplotype sharing
    • (1996) Hum Mol Genet , vol.5 , pp. 1051-1054
    • Bolino, A.1    Brancolini, V.2    Bono, F.3
  • 22
    • 0030900182 scopus 로고    scopus 로고
    • A clinical, electro-physiologic, neuropathologic, and genetic study of two large Algerian families with an autosomal recessive demyelinating form of Charcot-Marie-Tooth disease
    • (1997) Neurology , vol.48 , pp. 867-873
    • Kessali, M.1    Zemmouri, R.2    Guilbot, A.3
  • 23
    • 0033924959 scopus 로고    scopus 로고
    • 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
    • (2000) Am J Hum Genet , vol.67 , pp. 236-243
    • Delague, V.1    Bareil, C.2    Tuffery, S.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.