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Journal Abstract Search

156 related items for PubMed ID: 6314135

  • 1. Evolution of nerve conduction abnormalities in children with dominant hypertrophic neuropathy of the Charcot-Marie-Tooth type.
    Gutmann L, Fakadej A, Riggs JE.
    Muscle Nerve; 1983 Sep; 6(7):515-9. PubMed ID: 6314135
    [Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. Electrophysiological findings in hereditary motor and sensory neuropathy type I and II--a conduction velocity study.
    Emeryk-Szajewska B, Badurska B, Kostera-Pruszczyk A.
    Electromyogr Clin Neurophysiol; 1998 Mar; 38(2):95-101. PubMed ID: 9553747
    [Abstract] [Full Text] [Related]

  • 4. 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
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  • 5. Hereditary motor and sensory neuropathy. Clinical, genetic and electrodiagnostic studies.
    Vasilescu C.
    Rom J Neurol Psychiatry; 1993 Dec; 31(3-4):207-19. PubMed ID: 8011484
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  • 6. 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]

  • 7. Neurophysiologic abnormalities in children with Charcot-Marie-Tooth disease type 1A.
    Yiu EM, Burns J, Ryan MM, Ouvrier RA.
    J Peripher Nerv Syst; 2008 Sep; 13(3):236-41. PubMed ID: 18844790
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  • 9. Charcot-Marie-Tooth type X: A novel mutation in the Cx32 gene with central conduction slowing.
    Seeman P, Mazanec R, Ctvrtecková M, Smilková D.
    Int J Mol Med; 2001 Oct; 8(4):461-8. PubMed ID: 11562788
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  • 10. [Hereditary fragility of the peripheral nerves. Clinical and neurophysiologic study of 23 cases. Review of the literature].
    Roth G, Magistris M.
    Schweiz Arch Neurol Neurochir Psychiatr; 1984 Oct; 135(2):243-64. PubMed ID: 6098008
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  • 12. [Hereditary neuropathy with liability to pressure palsies: study of six Spanish families].
    Pou Serradell A, Monells J, Téllez MJ, Fossas P, Löfgren A, Meuleman J, Timmerman V, De Jonghe P, Ceuterick C, Martin JJ.
    Rev Neurol (Paris); 2002 May; 158(5 Pt 1):579-88. PubMed ID: 12072826
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  • 13. Subclinical cranial nerve involvement in hereditary motor and sensory neuropathy: a combined conduction study with electrical and magnetic stimulation.
    Kumagai-Eto R, Kaseda Y, Tobimatsu S, Uozumi T, Tsuji S, Nakamura S.
    Clin Neurophysiol; 2004 Jul; 115(7):1689-96. PubMed ID: 15203071
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  • 14. [Comparison of electrophysiological findings between CIDP and HMSN-1].
    Hasegawa O, Matsumoto S, Iino M, Kurita R, Kubota Y.
    No To Shinkei; 1999 May; 51(5):411-4. PubMed ID: 10396746
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  • 15. The hypertrophic forms of hereditary motor and sensory neuropathy. A study of hypertrophic Charcot-Marie-Tooth disease (HMSN type I) and Dejerine-Sottas disease (HMSN type III) in childhood.
    Ouvrier RA, McLeod JG, Conchin TE.
    Brain; 1987 Feb; 110 ( Pt 1)():121-48. PubMed ID: 3467805
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  • 16. Peripheral neuropathy in Krabbe disease: effect of hematopoietic stem cell transplantation.
    Siddiqi ZA, Sanders DB, Massey JM.
    Neurology; 2006 Jul 25; 67(2):268-72. PubMed ID: 16864820
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  • 17. Acoustic nerve in peripheral neuropathy: a BAEP study. Brainstem Auditory Evoked Potentials.
    Pareyson D, Scaioli V, Berta E, Sghirlanzoni A.
    Electromyogr Clin Neurophysiol; 1995 Oct 25; 35(6):359-64. PubMed ID: 8785933
    [Abstract] [Full Text] [Related]

  • 18. The INFIR Cohort Study: assessment of sensory and motor neuropathy in leprosy at baseline.
    Van Brakel WH, Nicholls PG, Das L, Barkataki P, Maddali P, Lockwood DN, Wilder-Smith E.
    Lepr Rev; 2005 Dec 25; 76(4):277-95. PubMed ID: 16411508
    [Abstract] [Full Text] [Related]

  • 19. [Hereditary sensorimotor neuropathy in electrophysiological studies].
    Emeryk-Szajewska B, Badurska B, Kostera-Pruszczyk A.
    Neurol Neurochir Pol; 1998 Dec 25; 32(2):295-308. PubMed ID: 9760549
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