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Volumn 24, Issue 135, 1996, Pages 1382-1384

Nosología actual de las polineuropatiás en la infancia

Author keywords

Charcot Marie Tooth disease; D jerine Sottas disease; Hereditary polineuropathy

Indexed keywords

MYELIN PROTEIN;

EID: 0030293380     PISSN: 02100010     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (1)

References (10)
  • 1
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    • Localization of a gene (CMT2A) for autosomal dominant Charcot-Marie-Tooth disease type 2 to chromosome 1p and evidence of genetic heterogeneity
    • Ben Othmane K, Middelton LT, Loprets W, et al. Localization of a gene (CMT2A) for autosomal dominant Charcot-Marie-Tooth disease type 2 to chromosome 1p and evidence of genetic heterogeneity Genomics 1993; 17: 370 375.
    • (1993) Genomics , vol.17 , pp. 370375
    • Ben Othmane, K.1    Middelton, L.T.2    Loprets, W.3
  • 2
    • 0027491703 scopus 로고
    • Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8q
    • Ben Othmane K, Hentafi F, Lennon F, et al. Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8q. Hum Mol Genet 1993; 2: 1625-1628.
    • (1993) Hum Mol Genet , vol.2 , pp. 1625-1628
    • Ben Othmane, K.1    Hentafi, F.2    Lennon, F.3
  • 3
    • 0020817785 scopus 로고
    • Neuropatias hereditarias en la infancia. Estudio de 31 pacientes
    • Colomer J, Fabregues I, Fernández-Álvarez E. Neuropatias hereditarias en la infancia. Estudio de 31 pacientes. An Esp Pediatr 1983; 19: 193-203.
    • (1983) An Esp Pediatr , vol.19 , pp. 193-203
    • Colomer, J.1    Fabregues, I.2    Fernández-Álvarez, E.3
  • 4
    • 84957371233 scopus 로고
    • Over families met hereditaire dispositie tot het optreden van neuritiden gecorrellered met migraine
    • De Jong JGY. Over families met hereditaire dispositie tot het optreden van neuritiden gecorrellered met migraine. Psychiat Neurol Bull (Amst) 1947; 50: 60-76.
    • (1947) Psychiat Neurol Bull (Amst) , vol.50 , pp. 60-76
    • De Jong, J.G.Y.1
  • 6
    • 0001768884 scopus 로고
    • Dyck PJ, Thomas PK, Lambert EH, eds. New York: WB Saunders Co.
    • Dyck PJ. Peripheral neuropathy.En Dyck PJ, Thomas PK, Lambert EH, eds. New York: WB Saunders Co., 1975; 791-824.
    • (1975) Peripheral Neuropathy , pp. 791-824
    • Dyck, P.J.1
  • 7
    • 0018962193 scopus 로고
    • Sex-linked recessive inheritance in Charcot-Marie-Tooth disease with partial manifestations, in female carriers
    • Fryns JP, Van der Berghe H. Sex-linked recessive inheritance in Charcot-Marie-Tooth disease with partial manifestations, in female carriers. Human Genetics 1980; 55: 415-415.
    • (1980) Human Genetics , vol.55 , pp. 415-415
    • Fryns, J.P.1    Van Der Berghe, H.2
  • 8
    • 0026761768 scopus 로고
    • Autosomal recessive form of motorand sensory neuropathy type I
    • Gabreels-Festen M, Gabreels FJM, Jennekens FGI. Autosomal recessive form of motorand sensory neuropathy type I. Neurology 1992; 42: 1755-1761.
    • (1992) Neurology , vol.42 , pp. 1755-1761
    • Gabreels-Festen, M.1    Gabreels, F.J.M.2    Jennekens, F.G.I.3
  • 9
    • 0019351028 scopus 로고
    • Pooled European series of hereditary peripheral neuropathies in infancy and childhood. A correspondence workshop report of the European Federation of Child Neurology Societies (EFCNS)
    • Hagberg B, Lyon G. Pooled European series of hereditary peripheral neuropathies in infancy and childhood. A correspondence workshop report of the European Federation of Child Neurology Societies (EFCNS). Neuropediatrics 1981; 12: 517.
    • (1981) Neuropediatrics , vol.12 , pp. 517
    • Hagberg, B.1    Lyon, G.2
  • 10
    • 0020622008 scopus 로고
    • Hereditary motor and sensory neurophaties in Swedish children
    • Hagberg B, Westenberg B. Hereditary motor and sensory neurophaties in Swedish children. Acta Ped Scand 1983; 72: 379-383.
    • (1983) Acta Ped Scand , vol.72 , pp. 379-383
    • Hagberg, B.1    Westenberg, B.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.