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Journal Abstract Search

321 related items for PubMed ID: 7231442

  • 1. 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
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  • 3. 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
    [Abstract] [Full Text] [Related]

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

  • 5. Motor nerve conduction velocity in spinal muscular atrophy of childhood.
    Moosa A, Dubowitz V.
    Arch Dis Child; 1976 Dec; 51(12):974-7. PubMed ID: 1015851
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  • 8. [Hereditary motor and sensory neuropathy. I. Principles of classification and clinical picture].
    Badurska B, Jedrzejowska H, Ryniewicz B, Drac H.
    Neurol Neurochir Pol; 1986 Dec; 20(1):24-8. PubMed ID: 3012388
    [Abstract] [Full Text] [Related]

  • 9. The peroneal muscular atrophy syndrome: clinical, genetic, electrophysiological and nerve biopsy studies. I. Clinical, genetic and electrophysiological findings and classification.
    Davis CJ, Bradley WG, Madrid R.
    J Genet Hum; 1978 Dec; 26(4):311-49. PubMed ID: 752065
    [Abstract] [Full Text] [Related]

  • 10. Recessive inheritance in a neuronal motor neuropathy form of peroneal muscular atrophy.
    Frajman M, Brilla E, Gutiérrez A, Hun L.
    Rev Invest Clin; 1983 Dec; 35(4):305-8. PubMed ID: 6672928
    [No Abstract] [Full Text] [Related]

  • 11. 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
    [Abstract] [Full Text] [Related]

  • 12. Charcot-Marie-Tooth disease.
    Martel J, Mierau D, Donat J.
    J Manipulative Physiol Ther; 1995 Sep; 18(3):168-71. PubMed ID: 7790797
    [Abstract] [Full Text] [Related]

  • 13. Deletion in the CMT1A locus on chromosome 17p11.2 in hereditary neuropathy with liability to pressure palsies.
    Verhalle D, Löfgren A, Nelis E, Dehaene I, Theys P, Lammens M, Dom R, Van Broeckhoven C, Robberecht W.
    Ann Neurol; 1994 Jun; 35(6):704-8. PubMed ID: 8210227
    [Abstract] [Full Text] [Related]

  • 14. [Hereditary motor and sensory neuropathy (Charcot-Marie-Tooth disease). Molecular-genetic aspects].
    Hertz MJ, Jensen AD, Brandt CA, Bisgård C.
    Ugeskr Laeger; 1995 Jun 19; 157(25):3613-8. PubMed ID: 7652980
    [Abstract] [Full Text] [Related]

  • 15. Electrodiagnostic findings in CMTX: a disorder of the Schwann cell and peripheral nerve myelin.
    Lewis RA, Shy ME.
    Ann N Y Acad Sci; 1999 Sep 14; 883():504-7. PubMed ID: 10586285
    [No Abstract] [Full Text] [Related]

  • 16. Study of the dispersion of motor nerve conduction in Charcot-Marie-Tooth Hoffmann disease and in the Steinert syndrome.
    Caccia MR.
    Electromyogr Clin Neurophysiol; 1972 Sep 14; 12(1):91-4. PubMed ID: 5075436
    [No Abstract] [Full Text] [Related]

  • 17. [Heterogeneity of neural muscular atrophies].
    Leblhuber F, Reisecker F, Mayr WR, Deisenhammer E.
    Nervenarzt; 1986 Jul 14; 57(7):419-21. PubMed ID: 3462518
    [Abstract] [Full Text] [Related]

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

  • 19. Dominantly inherited hypertrophic neuropathy.
    Mongia SK, Ghanem Q, Preston D, Lewis AJ, Atack EA.
    Can J Neurol Sci; 1978 May 14; 5(2):239-46. PubMed ID: 667751
    [Abstract] [Full Text] [Related]

  • 20. [Contribution of electromyography to the diagnosis of Werdnig-Hoffmann infantile spinal amyotrophy].
    Raimbault J, Laget P.
    Pathol Biol (Paris); 1972 Mar 14; 20(5):287-96. PubMed ID: 4556213
    [No Abstract] [Full Text] [Related]

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