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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

356 related items for PubMed ID: 6965173

  • 1. Charcot-Marie-Tooth's disease with severe trophic and sensory disorders. Study of a case following along a half a century with anatomical studies.
    Barraquer-Bordas L, Navarro C, Salisachs P.
    Acta Neurol Latinoam; 1981; 27(3-4):177-89. PubMed ID: 6965173
    [Abstract] [Full Text] [Related]

  • 2. Hypertrophic motor and sensory neuropathy type I (Charcot-Marie-Tooth disease): ultrastructural study of sural nerve biopsy in members of a family.
    Calore EE, Alonso Neto JL, Cavaliere MJ, Perez NM, Russo DH, Wakamatsu A, Maeda MY, Kitamura C.
    Pathologica; 1994 Jun; 86(3):279-83. PubMed ID: 7808799
    [Abstract] [Full Text] [Related]

  • 3. [Charcot-Marie-Tooth: a family case report].
    García de la Rocha ML, Moreno Martínez JM, Martín Araguz A.
    An Med Interna; 1990 May; 7(5):255-7. PubMed ID: 2102722
    [Abstract] [Full Text] [Related]

  • 4. [Hereditary sensory motor neuropathy: degenerative disease or a disease with an immune-mediated pathogenesis?].
    Cadoni A, Zicca A, Mancardi GL, De Martini I, Schenone A, Zaccheo D.
    Boll Soc Ital Biol Sper; 1989 May; 65(5):399-404. PubMed ID: 2775546
    [Abstract] [Full Text] [Related]

  • 5. 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]

  • 6. 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
    [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 Apr; 12():23-5. PubMed ID: 1215391
    [Abstract] [Full Text] [Related]

  • 8. [Nephropathy and Charcot-Marie-Tooth disease. A case report].
    Fillod I, Cochat P, Colon S, Wright C, David L.
    Pediatrie; 1990 Apr; 45(5):319-22. PubMed ID: 2165244
    [Abstract] [Full Text] [Related]

  • 9. Phenotypic spectrum of disorders associated with glycyl-tRNA synthetase mutations.
    Sivakumar K, Kyriakides T, Puls I, Nicholson GA, Funalot B, Antonellis A, Sambuughin N, Christodoulou K, Beggs JL, Zamba-Papanicolaou E, Ionasescu V, Dalakas MC, Green ED, Fischbeck KH, Goldfarb LG.
    Brain; 2005 Oct; 128(Pt 10):2304-14. PubMed ID: 16014653
    [Abstract] [Full Text] [Related]

  • 10. [Charcot-Marie-Tooth disease. Peroneal muscular atrophy].
    Hagen T, Jensen D, Dietrichson P, Heiberg A.
    Tidsskr Nor Laegeforen; 1990 Oct 10; 110(24):3110-5. PubMed ID: 2237866
    [Abstract] [Full Text] [Related]

  • 11. Modafinil reduces fatigue in Charcot-Marie-Tooth disease type 1A: a case series.
    Carter GT, Han JJ, Mayadev A, Weiss MD.
    Am J Hosp Palliat Care; 2006 Oct 10; 23(5):412-6. PubMed ID: 17060310
    [Abstract] [Full Text] [Related]

  • 12. 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 09; 119(5):455-8. PubMed ID: 688147
    [Abstract] [Full Text] [Related]

  • 13. A patient with both Charcot-Marie-Tooth disease (CMT 1A) and mild spinal muscular atrophy (SMA 3).
    Jedrzejowska M, Ryniewicz B, Kabzińska D, Drac H, Hausmanowa-Petrusewicz I, Kochański A.
    Neuromuscul Disord; 2008 Apr 09; 18(4):339-41. PubMed ID: 18337101
    [Abstract] [Full Text] [Related]

  • 14. Pathogenesis of pes cavus in Charcot-Marie-Tooth disease.
    Sabir M, Lyttle D.
    Clin Orthop Relat Res; 1983 May 09; (175):173-8. PubMed ID: 6839584
    [Abstract] [Full Text] [Related]

  • 15. Audiologic evaluation in Charcot-Marie-Tooth disease.
    Pérez H, Vílchez J, Sevilla T, Martínez L.
    Scand Audiol Suppl; 1988 May 09; 30():211-3. PubMed ID: 3227273
    [Abstract] [Full Text] [Related]

  • 16. [Charcot-Marie-Tooth disease associated with dilated cardiomyopathy: an autopsy case report].
    Yoshida H, Inagaki M, Shukuya M, Ono S, Shimizu N, Doba N, Shimizu N, Sugano I, Nagao K.
    Kokyu To Junkan; 1991 Mar 09; 39(3):295-8. PubMed ID: 2047612
    [Abstract] [Full Text] [Related]

  • 17. Autosomal recessive axonal Charcot-Marie-Tooth disease (ARCMT2): phenotype-genotype correlations in 13 Moroccan families.
    Bouhouche A, Birouk N, Azzedine H, Benomar A, Durosier G, Ente D, Muriel MP, Ruberg M, Slassi I, Yahyaoui M, Dubourg O, Ouazzani R, LeGuern E.
    Brain; 2007 Apr 09; 130(Pt 4):1062-75. PubMed ID: 17347251
    [Abstract] [Full Text] [Related]

  • 18. Erythrocyte insulin binding in a family with hereditary motor sensory neuropathy (Charcot-Marie-Tooth) with superimposed insulin-dependent type I diabetes mellitus.
    Ivarsson SA, Bjerre I.
    Diabetes Res; 1989 Jan 09; 10(1):49-51. PubMed ID: 2667841
    [Abstract] [Full Text] [Related]

  • 19. Clinical, electrophysiological and morphological findings of Charcot-Marie-Tooth neuropathy with vocal cord palsy and mutations in the GDAP1 gene.
    Sevilla T, Cuesta A, Chumillas MJ, Mayordomo F, Pedrola L, Palau F, Vílchez JJ.
    Brain; 2003 Sep 09; 126(Pt 9):2023-33. PubMed ID: 12821518
    [Abstract] [Full Text] [Related]

  • 20. 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 09; 41(3):306-13. PubMed ID: 10962051
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 18.