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Volumn 883, Issue , 1999, Pages 439-442

Distal hereditary motor neuronopathy of the Jerash type

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CHILD; CHROMOSOME 9; CHROMOSOME MAP; FEMALE; GENETIC LINKAGE; GENETICS; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; JORDAN; MALE; MIDDLE AGED; ONSET AGE; PATHOPHYSIOLOGY; PEDIGREE;

EID: 0033554323     PISSN: 00778923     EISSN: None     Source Type: Book Series    
DOI: 10.1111/j.1749-6632.1999.tb08604.x     Document Type: Article
Times cited : (10)

References (12)
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    • Dyck, P.J.1    Lambert, E.H.2
  • 2
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    • HARDING, A.E. 1993. In Peripheral Neuropathy. P.J. Dyck, P.K. Thomas, et al., Eds.: 2: 1051-1064. W.B. Saunders, Harcourt Brace Jovanovich. Pennsylvania.
    • (1993) Peripheral Neuropathy , vol.2 , pp. 1051-1064
    • Harding, A.E.1
  • 3
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    • Hereditary motor neuronopathies, clinical, neurophysiological and genetic aspects
    • KYRIAKIDES, T., et al. 1998. Hereditary motor neuronopathies, clinical, neurophysiological and genetic aspects. Acta Myolog. 2: 55-58.
    • (1998) Acta Myolog. , vol.2 , pp. 55-58
    • Kyriakides, T.1
  • 4
    • 0018120729 scopus 로고
    • Pathological involvement of primary sensory neurons in Werdnig-Hoffman disease
    • CARPENTER, S., et al. 1978. Pathological involvement of primary sensory neurons in Werdnig-Hoffman disease. Acta Neuropathol. (Berlin) 42: 91-97.
    • (1978) Acta Neuropathol. (Berlin) , vol.42 , pp. 91-97
    • Carpenter, S.1
  • 5
    • 0026354610 scopus 로고
    • Sensory axonopathy in hereditary distal spinal muscular atrophy
    • FREQUIN, S.T.F.M., et al. 1991. Sensory axonopathy in hereditary distal spinal muscular atrophy. Clin. Neurol. Ncurosurg. 19 (4): 323-326.
    • (1991) Clin. Neurol. Ncurosurg. , vol.19 , Issue.4 , pp. 323-326
    • Frequin, S.T.F.M.1
  • 6
    • 0020457362 scopus 로고
    • X-linked recessive bulbospinal neuronopathy: A report of ten cases
    • HARDING, A.E., et al. 1982. X-linked recessive bulbospinal neuronopathy: a report of ten cases. J. Neurol. Neurosurg. Psychol. 45: 1012-1019.
    • (1982) J. Neurol. Neurosurg. Psychol. , vol.45 , pp. 1012-1019
    • Harding, A.E.1
  • 7
    • 0029145426 scopus 로고
    • Mapping of a distal form of spinal muscular atrophy with upper limb predominance to chromosome 7p
    • CHRISTODOULOU, K., et al. 1995. Mapping of a distal form of spinal muscular atrophy with upper limb predominance to chromosome 7p. Hum. Mol. Gen. 4(9): 1629-1632.
    • (1995) Hum. Mol. Gen. , vol.4 , Issue.9 , pp. 1629-1632
    • Christodoulou, K.1
  • 8
    • 0029831478 scopus 로고    scopus 로고
    • Autosomal dominant Charcot-Marie-Tooth axonal neuropathy mapped on chromosome 7p (CMT2D)
    • IONASESCU, V., et al. 1996 Autosomal dominant Charcot-Marie-Tooth axonal neuropathy mapped on chromosome 7p (CMT2D). Hum. Mol. Genet. 5: 1373-1375.
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    • Ionasescu, V.1
  • 9
    • 0032569930 scopus 로고    scopus 로고
    • Autosomal dominant distal spinal muscular atrophy type V (dSMA-V) and Charcot-Marie-Tooth disease type 2D (CMT2D) segregate within single large kindred and map to a refined region on chromosome 7p15
    • SAMBUUGHIN, N., et al. 1998. Autosomal dominant distal spinal muscular atrophy type V (dSMA-V) and Charcot-Marie-Tooth disease type 2D (CMT2D) segregate within single large kindred and map to a refined region on chromosome 7p15. J. Neurol. Sci. 161: 23-28,
    • (1998) J. Neurol. Sci. , vol.161 , pp. 23-28
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  • 10
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    • TTMMERMAN, V., et al. 1996. Distal hereditary motor neuropathy type II (distal HMN II): mapping of a locus to chromosome 12q24. Hum. Mol. Gen. 5 (7): 1065-1069.
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  • 11
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    • A novel form of hereditary motor neuronopathy maps to chromosome 9p21.1-p12
    • in press
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  • 12
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    • Christodoulou, K.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.