BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

188 related articles for article (PubMed ID: 563155)

  • 1. [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]  

  • 2. Charcot-Marie-Tooth disease and schizophrenia in identical twins.
    Manyam NV; Cowell HR; Katz L
    JAMA; 1979 Jan; 241(1):54-5. PubMed ID: 569219
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Recessively inherited Charcot-Marie-Tooth syndrome in identical twins.
    Beighton PH
    Birth Defects Orig Artic Ser; 1971 Feb; 7(2):105. PubMed ID: 5173114
    [No Abstract]   [Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. [Incidence and clinical polymorphism of Charcot-Marie neural amyotrophy in the Amur region].
    Khomenko EI
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1982; 82(11):22-6. PubMed ID: 7180298
    [No Abstract]   [Full Text] [Related]  

  • 7. [A case of Charcot-Marie-Tooth muscular atrophy in monozygotic twins].
    Mrowiec W; Termińska-Mrowiec K
    Wiad Lek; 1987 Sep; 40(18):1292-5. PubMed ID: 3445607
    [No Abstract]   [Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. [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]  

  • 11. 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]  

  • 12. [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]  

  • 13. 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]  

  • 14. [Autosomal-dominant motor-sensory neuropathy type I: intrafamilial polymorphism in the Roussy-Lévy syndrome].
    Badalian LO; Temin PA; Arkhipov BA; Avakian GN; Zavedenko NN
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1988; 88(11):45-9. PubMed ID: 3223157
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Clinical and pathological phenotype of the original family with Charcot-Marie-Tooth type 1B: a 20-year study.
    Bird TD; Kraft GH; Lipe HP; Kenney KL; Sumi SM
    Ann Neurol; 1997 Apr; 41(4):463-9. PubMed ID: 9124803
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Symptomatic Charcot-Marie-Tooth? A pair of concordant monozygotic twins.
    Braathen GJ; Sand JC; Russell MB
    Acta Neurol Scand; 2006 Dec; 114(6):403-6. PubMed ID: 17083341
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Carbamazepine-sensitive neuromyotonia and Charcot-Marie-Tooth disease of the neuronal type].
    Serratrice G; Pouget J; Pellissier JF; Cros D
    Rev Neurol (Paris); 1989; 145(12):867-8. PubMed ID: 2694289
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. [Charcot-Marie-Tooth disease. Genetical, clinical and electrodiagnostic study of 2 families].
    Krstić S; Vidaković Z; Ignjatović M
    Srp Arh Celok Lek; 1975 Sep; 103(9):769-77. PubMed ID: 1228922
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 10.