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 *

101 related articles for article (PubMed ID: 1027118)

  • 21. Pathogenesis of pes cavus in Charcot-Marie-Tooth disease.
    Sabir M; Lyttle D
    Clin Orthop Relat Res; 1983 May; (175):173-8. PubMed ID: 6839584
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Palmoplantar keratoderma and Charcot-Marie-Tooth disease.
    Rabbiosi G; Borroni G; Pinelli P; Cosi V
    Arch Dermatol; 1980 Jul; 116(7):789-90. PubMed ID: 6446889
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Autopsy case of Charcot-Marie-Tooth disease with optic nerve atrophy and degeneration of the spinal tract. A family with muscular atrophy, ataxia, retinal degeneration and diabetes mellitus].
    Oguchi K; Tsubaki T; Ikuta F
    Rinsho Shinkeigaku; 1977 Jan; 17(1):52-7. PubMed ID: 557401
    [No Abstract]   [Full Text] [Related]  

  • 24. 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]  

  • 25. [From gene to disease; Charcot-Marie-Tooth disease or the hereditary motor and sensory neuropathies].
    Verhamme C; Baas F
    Ned Tijdschr Geneeskd; 2005 Jul; 149(27):1505-9. PubMed ID: 16032995
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. 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]  

  • 28. [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]  

  • 29. Myasthenia gravis complicating Charcot-Marie-Tooth disease: report of a case.
    Berger JR; Ayyar DR; Kimura I; Kovacs A
    J Clin Neuroophthalmol; 1985 Jun; 5(2):76-80. PubMed ID: 2947920
    [TBL] [Abstract][Full Text] [Related]  

  • 30. A novel mutation, Thr65Ala, in the MPZ gene in a patient with Charcot-Marie-Tooth type 1B disease with focally folded myelin.
    Kochanski A; Drac H; Kabzińska D; Hausmanowa-Petrusewicz I
    Neuromuscul Disord; 2004 Mar; 14(3):229-32. PubMed ID: 15036333
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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]  

  • 32. [Ulcerative, mutilating acropathy and amyotrophy, Charcot-Marie disease: a sporadic female case with disseminated ischemic arteriopathy. Multiple sympathectomies].
    Arnott G; Krivosic I; Devambez J; Delandsheer E; Ribet M; Fortier-Berenchtein S
    Lille Med; 1980 May; 25(5):199-206. PubMed ID: 6930531
    [No Abstract]   [Full Text] [Related]  

  • 33. 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]  

  • 34. [Charcot-Marie-Tooth disease and glomerular nephropathy].
    Deniau F; Guillot M; Plus A; Leveque C; Gubler MC; Broyer M; Aicardi J; Lechevalier B
    Arch Fr Pediatr; 1986 Dec; 43(10):791-3. PubMed ID: 3827511
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Clinico-genalogic characteristics of hereditary diseases of the nervous system in the Kuibyshev region].
    Nesterov LN; Sushcheva GP; Viatkina SIa
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1978; 78(10):1506-12. PubMed ID: 152555
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [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]  

  • 37. Molecular mechanisms for Charcot-Marie-Tooth disease and related demyelinating peripheral neuropathies.
    Warner LE; Reiter LT; Murakami T; Lupski JR
    Cold Spring Harb Symp Quant Biol; 1996; 61():659-71. PubMed ID: 9246492
    [No Abstract]   [Full Text] [Related]  

  • 38. [Charcot-Marie-Tooth disease].
    Krstić S; Vidaković Z; Ignjatović M
    Neuropsihijatrija; 1976; 24(1-4):121-8. PubMed ID: 1031197
    [No Abstract]   [Full Text] [Related]  

  • 39. [Scapuloperoneal syndromes].
    Serratrice G; Pellissier JF; Pouget J; Gastaut JL; Cros D
    Rev Neurol (Paris); 1982; 138(10):691-711. PubMed ID: 7156632
    [No Abstract]   [Full Text] [Related]  

  • 40. The importance of quantitative electron microscopy in studying hypertrophic neuropathies. A comparison between a case of Déjérine Sottas disease (HMSN III) and a case of the hypertrophic form of Charcot-Marie-Tooth disease (HMSN I).
    Tredici G; Petruccioli-Pizzini MG; Gergely A; Coletti A
    Int J Tissue React; 1984; 6(3):267-74. PubMed ID: 6090332
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.