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

155 related items for PubMed ID: 949237

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. A case of Charcot-Marie-Tooth disease mimicking Friedreich's ataxia: is there any association between friedreich's ataxia and Charcot-Marie-Tooth disease?
    Salisachs P, Findley LJ, Codina M, La Torre P, Martinez-Lage JM.
    Can J Neurol Sci; 1982 May; 9(2):99-103. PubMed ID: 7104897
    [Abstract] [Full Text] [Related]

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

  • 4. 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
    [Abstract] [Full Text] [Related]

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

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

  • 7. Roussy-Lévy syndrome is a phenotypic variant of Charcot-Marie-Tooth syndrome IA associated with a duplication on chromosome 17p11.2.
    Auer-Grumbach M, Strasser-Fuchs S, Wagner K, Körner E, Fazekas F.
    J Neurol Sci; 1998 Jan 21; 154(1):72-5. PubMed ID: 9543325
    [Abstract] [Full Text] [Related]

  • 8. Peroneal muscular atrophy with pyramidal features.
    Harding AE, Thomas PK.
    J Neurol Neurosurg Psychiatry; 1984 Feb 21; 47(2):168-72. PubMed ID: 6707656
    [Abstract] [Full Text] [Related]

  • 9. Evidence that Charcot-Marie-tooth disease with tremor coincides with the Roussy-Levy syndrome.
    Barbieri F, Filla A, Ragno M, Crisci C, Santoro L, Corona M, Campanella G.
    Can J Neurol Sci; 1984 Nov 21; 11(4 Suppl):534-40. PubMed ID: 6509399
    [Abstract] [Full Text] [Related]

  • 10. Ataxia and other data reviewed in Charcot-Marie-Tooth and Refsum's disease.
    Salisachs P.
    J Neurol Neurosurg Psychiatry; 1982 Dec 21; 45(12):1085-91. PubMed ID: 6186770
    [Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. Charcot-Marie-Tooth disease: study of a large kinship with an intermediate form.
    Rossi A, Paradiso C, Cioni R, Rizzuto N, Guazzi G.
    J Neurol; 1985 Dec 21; 232(2):91-8. PubMed ID: 4020397
    [Abstract] [Full Text] [Related]

  • 13. 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 21; 28(1):17-40. PubMed ID: 932772
    [Abstract] [Full Text] [Related]

  • 14. 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 21; 14(6):679-84. PubMed ID: 6651251
    [Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. Dominantly inherited hypertrophic neuropathy.
    Mongia SK, Ghanem Q, Preston D, Lewis AJ, Atack EA.
    Can J Neurol Sci; 1978 May 21; 5(2):239-46. PubMed ID: 667751
    [Abstract] [Full Text] [Related]

  • 17. Motor and sensory conduction velocity in patients with Charcot-Marie-Tooth disease exposed to carbon disulphide.
    Florescu A, Vasilescu C.
    Neurol Psychiatr (Bucur); 1976 May 21; 14(2):97-103. PubMed ID: 968423
    [No Abstract] [Full Text] [Related]

  • 18. A case of the Roussy-Levy syndrome family.
    Bartosik-Psujek H, Stelmasiak Z.
    Ann Univ Mariae Curie Sklodowska Med; 2001 May 21; 56():393-5. PubMed ID: 11977346
    [Abstract] [Full Text] [Related]

  • 19. 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 21; (184):223-35. PubMed ID: 6705352
    [Abstract] [Full Text] [Related]

  • 20. Charcot-Marie-Tooth disease associated with 'essential tremor' and normal and/or slightly diminished motor conduction velocity. Report of 7 cases.
    Salisachs P, Codina A, Gimenez-Roldan S, Zarranz JJ.
    Eur Neurol; 1979 Apr 21; 18(1):49-58. PubMed ID: 436863
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 8.