BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

272 related articles for article (PubMed ID: 829740)

  • 1. Peroneal musclar atrophy (of Charcot-Marie-Tooth) in two African brothers.
    Billinghurst JR
    Afr J Med Med Sci; 1976 Dec; 5(4):269-72. PubMed ID: 829740
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Homozygous expression of a dominant gene for Charcot-Marie-Tooth neuropathy.
    Killian JM; Kloepfer HW
    Ann Neurol; 1979 Jun; 5(6):515-22. PubMed ID: 475348
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Dominantly inherited peroneal muscular atrophy (hereditary motor and sensory neuropathy type I) in infancy and childhood.
    Vanasse M; Dubowitz V
    Muscle Nerve; 1981; 4(1):26-30. PubMed ID: 7231442
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Recessive inheritance in a neuronal motor neuropathy form of peroneal muscular atrophy.
    Frajman M; Brilla E; Gutiérrez A; Hun L
    Rev Invest Clin; 1983; 35(4):305-8. PubMed ID: 6672928
    [No Abstract]   [Full Text] [Related]  

  • 5. [Charcot-Marie-Tooth disease. Report of a family (author's transl)].
    Alonso ME; Figueroa HH; Zermeño F; Escobar A; Flores T
    Rev Invest Clin; 1981; 33(3):303-7. PubMed ID: 7330503
    [No Abstract]   [Full Text] [Related]  

  • 6. Neurophysiology and molecular genetics of Charcot-Marie-Tooth type 1 neuropathy in Croatian children: follow-up study.
    Barisić N; Mihatov I
    Croat Med J; 2000 Sep; 41(3):306-13. PubMed ID: 10962051
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A family with Charcot-Marie-Tooth disease and Leber's optic atrophy.
    McLeod JG; Low PA; Morgan JA
    Proc Aust Assoc Neurol; 1975; 12():23-5. PubMed ID: 1215391
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genetic linkage evidence for heterogeneity in Charcot-Marie-Tooth neuropathy (HMSN type I).
    Bird TD; Ott J; Giblett ER; Chance PF; Sumi SM; Kraft GH
    Ann Neurol; 1983 Dec; 14(6):679-84. PubMed ID: 6651251
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Variation of phenotype in Charcot-Marie-Tooth disease.
    Baker RS; Upton AR
    Neuropadiatrie; 1979 Aug; 10(3):290-5. PubMed ID: 583067
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Peroneal muscular atrophy with autosomal dominant inheritance.
    McLeod JG; Low PA
    Clin Exp Neurol; 1977; 14():142-53. PubMed ID: 616594
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Heterogeneity of neural muscular atrophies].
    Leblhuber F; Reisecker F; Mayr WR; Deisenhammer E
    Nervenarzt; 1986 Jul; 57(7):419-21. PubMed ID: 3462518
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Neuromyotonia in the spinal form of Charcot-Marie-Tooth disease.
    Lance JW; Durke D; Pollard J
    Clin Exp Neurol; 1979; 16():49-56. PubMed ID: 550956
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Clinical and electrophysiological characteristics of autosomal recessive axonal Charcot-Marie-Tooth disease (ARCMT2B) that maps to chromosome 19q13.3.
    Berghoff C; Berghoff M; Leal A; Morera B; Barrantes R; Reis A; Neundörfer B; Rautenstrauss B; Del Valle G; Heuss D
    Neuromuscul Disord; 2004 May; 14(5):301-6. PubMed ID: 15099588
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Pathogenesis of Charcot-Marie-Tooth disease. Gait analysis and electrophysiologic, genetic, histopathologic, and enzyme studies in a kinship.
    Sabir M; Lyttle D
    Clin Orthop Relat Res; 1984 Apr; (184):223-35. PubMed ID: 6705352
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Charcot-Marie-Tooth disease. Peroneal muscular atrophy].
    Hagen T; Jensen D; Dietrichson P; Heiberg A
    Tidsskr Nor Laegeforen; 1990 Oct; 110(24):3110-5. PubMed ID: 2237866
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Variability in nerve biopsy findings in a kinship with dominantly inherited Charcot-Marie-Tooth disease.
    Van Weerden TW; Houthoff HJ; Sie O; Minderhoud JM
    Muscle Nerve; 1982 Mar; 5(3):185-96. PubMed ID: 7088015
    [No Abstract]   [Full Text] [Related]  

  • 17. Leber's optic neuropathy and Charcot-Marie-Tooth disease. Report of a case.
    McCluskey DJ; O'Connor PS; Sheehy JT
    J Clin Neuroophthalmol; 1986 Jun; 6(2):76-81. PubMed ID: 2942573
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Hereditary angioneurotic edema and Charcot-Marie-Tooth disease in the same family.
    Fernandez PG; Day JH; Simpson NE; Zachariah PK
    Can Med Assoc J; 1978 Sep; 119(5):455-8. PubMed ID: 688147
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Polymorphism of Charcot-Marie-Tooth neural amyotrophy in uniovular twins].
    Popov'ian MD; Dubinskaia EE; Ageeva TS
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1977; 77(10):1446-8. PubMed ID: 563155
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Charcot-Marie-Tooth disease with Leber optic atrophy.
    McLeod JG; Low PA; Morgan JA
    Neurology; 1978 Feb; 28(2):179-84. PubMed ID: 563998
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.