These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

275 related articles for article (PubMed ID: 563998)

  • 21. Charcot-Marie-Tooth disease associated with "essential tremor": Report of 7 cases and a review of the literature.
    Salisachs P
    J Neurol Sci; 1976 May; 28(1):17-40. PubMed ID: 932772
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Should Charcot-Marie-Tooth disease be genetically subgrouped on motor conduction velocity.
    Salisachs P; Findley LJ; Codina M; Martinez-Lage JM
    J Neurol Neurosurg Psychiatry; 1982 Feb; 45(2):182-4. PubMed ID: 7069437
    [No Abstract]   [Full Text] [Related]  

  • 23. Mutations in the MORC2 gene cause axonal Charcot-Marie-Tooth disease.
    Sevilla T; Lupo V; Martínez-Rubio D; Sancho P; Sivera R; Chumillas MJ; García-Romero M; Pascual-Pascual SI; Muelas N; Dopazo J; Vílchez JJ; Palau F; Espinós C
    Brain; 2016 Jan; 139(Pt 1):62-72. PubMed ID: 26497905
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Axonal neuropathy with optic atrophy is caused by mutations in mitofusin 2.
    Züchner S; De Jonghe P; Jordanova A; Claeys KG; Guergueltcheva V; Cherninkova S; Hamilton SR; Van Stavern G; Krajewski KM; Stajich J; Tournev I; Verhoeven K; Langerhorst CT; de Visser M; Baas F; Bird T; Timmerman V; Shy M; Vance JM
    Ann Neurol; 2006 Feb; 59(2):276-81. PubMed ID: 16437557
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Dominantly inherited hypertrophic neuropathy.
    Mongia SK; Ghanem Q; Preston D; Lewis AJ; Atack EA
    Can J Neurol Sci; 1978 May; 5(2):239-46. PubMed ID: 667751
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Scheuermann's kyphoscoliosis associated with Charcot-Marie-Tooth syndrome.
    Kewalramani LS; Riggins RS; Fowler WM
    Arch Phys Med Rehabil; 1976 Aug; 57(8):391-7. PubMed ID: 949237
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Peroneal muscular atrophy with pyramidal features.
    Harding AE; Thomas PK
    J Neurol Neurosurg Psychiatry; 1984 Feb; 47(2):168-72. PubMed ID: 6707656
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. Naevoid basal cell carcinoma syndrome and Charcot-Marie-Tooth disease: two autosomal dominant disorders segregating in a family.
    Heimler A; Friedman E; Rosenthal AD
    J Med Genet; 1978 Aug; 15(4):288-91. PubMed ID: 712760
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. 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]  

  • 32. 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]  

  • 33. 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]  

  • 34. Clinical and electrodiagnostic features of Charcot-Marie-Tooth syndrome.
    Brust JC; Lovelace RE; Devi S
    Acta Neurol Scand Suppl; 1978; 68():1-142. PubMed ID: 212921
    [No Abstract]   [Full Text] [Related]  

  • 35. Unusual motor conduction velocity values in Charcot-Marie-Tooth disease associated with essential tremor: report of a kinship.
    Salisachs P
    Eur Neurol; 1975; 13(4):377-82. PubMed ID: 1149757
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Non-hypertrophic familial neuropathy associated with intention tremor. A variety of Charcot-Marie-Tooth disease?
    Delwaide PJ; Schoenen J
    J Neurol Sci; 1976 Jan; 27(1):59-69. PubMed ID: 175133
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Focal glomerulosclerosis associated with Charcot-Marie-Tooth disease.
    Gherardi R; Belghiti-Deprez D; Hirbec G; Bouche P; Weil B; Lagrue G
    Nephron; 1985; 40(3):357-61. PubMed ID: 4010852
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Peroneal muscular atrophy (PMA) and related disorders. I. Clinical manifestations as related to biopsy findings, nerve conduction and electromyography.
    Buchthal F; Behse F
    Brain; 1977 Mar; 100 Pt 1():41-66. PubMed ID: 861715
    [No Abstract]   [Full Text] [Related]  

  • 39. [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]  

  • 40. Charcot-Marie-Tooth disease with sensorineural hearing loss--an autosomal dominant trait.
    Kousseff BG; Hadro TA; Treiber DL; Wollner T; Morris C
    Birth Defects Orig Artic Ser; 1982; 18(3B):223-8. PubMed ID: 7139106
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 14.