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Journal Abstract Search

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
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  • 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
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  • 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
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  • 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
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  • 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
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  • 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
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  • 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
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  • 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
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  • 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
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  • 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
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  • 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
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