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423 related items for PubMed ID: 9553747

  • 1. 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]

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

  • 3. Hereditary motor and sensory neuropathy. Clinical, genetic and electrodiagnostic studies.
    Vasilescu C.
    Rom J Neurol Psychiatry; 1993 Mar; 31(3-4):207-19. PubMed ID: 8011484
    [Abstract] [Full Text] [Related]

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

  • 5. [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
    [Abstract] [Full Text] [Related]

  • 6. Longitudinal conduction studies in hereditary motor and sensory neuropathy type 1.
    Roy EP, Gutmann L, Riggs JE.
    Muscle Nerve; 1989 Jan; 12(1):52-5. PubMed ID: 2747736
    [Abstract] [Full Text] [Related]

  • 7. [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]

  • 8. [Central motor conduction time (CMCT) in hereditary motor sensory neuropathy type I (HMSN type I)].
    Mano Y, Nakamuro T, Ikoma K, Takayanagi T.
    Rinsho Shinkeigaku; 1990 May 19; 30(5):487-91. PubMed ID: 2401109
    [Abstract] [Full Text] [Related]

  • 9. [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 19; 158(5 Pt 1):579-88. PubMed ID: 12072826
    [Abstract] [Full Text] [Related]

  • 10. 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 19; 35(6):704-8. PubMed ID: 8210227
    [Abstract] [Full Text] [Related]

  • 11. The electrophysiologic profile of Dejerine-Sottas disease (HMSN III).
    Benstead TJ, Kuntz NL, Miller RG, Daube JR.
    Muscle Nerve; 1990 Jul 19; 13(7):586-92. PubMed ID: 2388657
    [Abstract] [Full Text] [Related]

  • 12. [Hereditary neuropathy with liability to pressure palsies (tomaculous neuropathy). Clinical, electrophysical and molecular study of two affected families].
    Eirís-Punal J, Vidal-Lijó M, Barros-Angueira F, Lopez-Fernández MJ, Pintos-Martínez E, Beiras-Iglesias A, Castro-Gago M.
    Rev Neurol; 1990 Jul 19; 31(6):506-10. PubMed ID: 11055050
    [Abstract] [Full Text] [Related]

  • 13. Hereditary motor and sensory neuropathies and hereditary spastic paraplegia: a magnetic stimulation study.
    Claus D, Waddy HM, Harding AE, Murray NM, Thomas PK.
    Ann Neurol; 1990 Jul 19; 28(1):43-9. PubMed ID: 2375632
    [Abstract] [Full Text] [Related]

  • 14. Correlation between denervation activity and compound muscle action potential amplitude in hereditary motor and sensory neuropathy I and II.
    Paraskevas GP, Panousopoulou A, Karandreas N, Piperos P, Lygidakis C, Papageorgiou C.
    Electromyogr Clin Neurophysiol; 1998 Sep 19; 38(6):343-7. PubMed ID: 9783119
    [Abstract] [Full Text] [Related]

  • 15. The application of nerve conduction and clinical studies to genetic counseling in hereditary motor and sensory neuropathy type I.
    Berciano J, Combarros O, Calleja J, Polo JM, Leno C.
    Muscle Nerve; 1989 Apr 19; 12(4):302-6. PubMed ID: 2770783
    [Abstract] [Full Text] [Related]

  • 16. [A family of X-linked motor and sensory neuropathy with a new type of connexin32 mutation].
    Ohnishi A, Yoshimura T, Takazawa A, Hashimoto T, Yamamoto T, Fukushima Y.
    Rinsho Shinkeigaku; 1995 Aug 19; 35(8):843-9. PubMed ID: 8665724
    [Abstract] [Full Text] [Related]

  • 17. 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 19; 8(4):461-8. PubMed ID: 11562788
    [Abstract] [Full Text] [Related]

  • 18. 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 19; 14(6):679-84. PubMed ID: 6651251
    [Abstract] [Full Text] [Related]

  • 19. Hereditary motor and sensory neuropathy type I: clinical and neurographical features of the 17p duplication subtype.
    Hoogendijk JE, De Visser M, Bolhuis PA, Hart AA, Ongerboer de Visser BW.
    Muscle Nerve; 1994 Jan 19; 17(1):85-90. PubMed ID: 8264707
    [Abstract] [Full Text] [Related]

  • 20. 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 19; 130(Pt 4):1062-75. PubMed ID: 17347251
    [Abstract] [Full Text] [Related]

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