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Journal Abstract Search

146 related items for PubMed ID: 9883484

  • 1. [A case of hereditary motor and sensory neuropathy (HMSN) with excessive myelin outfolding with autosomal recessive inheritance].
    Ohnishi A, Narazaki O, Hanai T.
    J UOEH; 1998 Dec 01; 20(4):345-52. PubMed ID: 9883484
    [Abstract] [Full Text] [Related]

  • 2. Dominantly inherited motor and sensory neuropathy with excessive myelin folding complex.
    Umehara F, Takenaga S, Nakagawa M, Takahashi K, Izumo S, Matsumuro K, Sakota S, Nishimura T, Yoshikawa H, Osame M.
    Acta Neuropathol; 1993 Dec 01; 86(6):602-8. PubMed ID: 8310815
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  • 3.
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  • 4. Hereditary motor and sensory neuropathy with myelin folding and juvenile onset glaucoma.
    Kiwaki T, Umehara F, Takashima H, Nakagawa M, Kamimura K, Kashio N, Sakamoto Y, Unoki K, Nobuhara Y, Michizono K, Watanabe O, Arimura H, Osame M.
    Neurology; 2000 Aug 08; 55(3):392-7. PubMed ID: 10932274
    [Abstract] [Full Text] [Related]

  • 5. Autosomal recessive hereditary neuropathy with focally folded myelin sheaths and linked to chromosome 11q23: a distinct and homogeneous entity.
    Salih MA, Maisonobe T, Kabiraj M, al Rayess M, al-Turaiki MH, Akbar M, Tahan A, Urtizberea JA, Grid D, Hamadouche T, Guilbot A, Brice A, Leguern E.
    Neuromuscul Disord; 2000 Jan 08; 10(1):10-5. PubMed ID: 10677858
    [Abstract] [Full Text] [Related]

  • 6. Autosomal recessive motor and sensory neuropathy with excessive myelin outfolding in two siblings.
    Barbieri F, Santangelo R, Capparelli G, Ciccarelli A, Crisci C.
    Can J Neurol Sci; 1994 Feb 08; 21(1):29-33. PubMed ID: 8180900
    [Abstract] [Full Text] [Related]

  • 7. Autosomal recessive motor and sensory neuropathy with excessive myelin outfolding.
    Ohnishi A, Murai Y, Ikeda M, Fujita T, Furuya H, Kuroiwa Y.
    Muscle Nerve; 1989 Jul 08; 12(7):568-75. PubMed ID: 2779605
    [Abstract] [Full Text] [Related]

  • 8. Autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths: clinical, electrophysiologic, and genetic aspects of a large family.
    Quattrone A, Gambardella A, Bono F, Aguglia U, Bolino A, Bruni AC, Montesi MP, Oliveri RL, Sabatelli M, Tamburrini O, Valentino P, Van Broeckhoven C, Zappia M.
    Neurology; 1996 May 08; 46(5):1318-24. PubMed ID: 8628474
    [Abstract] [Full Text] [Related]

  • 9. Autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths (CMT4B).
    Gambardella A, Bono F, Muglia M, Valentino P, Quattrone A.
    Ann N Y Acad Sci; 1999 Sep 14; 883():47-55. PubMed ID: 10586229
    [Abstract] [Full Text] [Related]

  • 10. Molecular analysis of three cases with hereditary motor and sensory neuropathy with myelin outfolding.
    James R, Bellone E, Nelis E, Mandich P, Schenone A, Mancardi G, Van Broeckhoven C, Abbruzzese M, Ajmar F.
    Neurosci Lett; 1995 Jul 14; 194(1-2):136-8. PubMed ID: 7478198
    [Abstract] [Full Text] [Related]

  • 11. Autosomal recessive hypermyelinating neuropathy.
    Sabatelli M, Mignogna T, Lippi G, Servidei S, Manfredi G, Ricci E, Bertini E, Lo Monaco M, Tonali P.
    Acta Neuropathol; 1994 Jul 14; 87(4):337-42. PubMed ID: 8017168
    [Abstract] [Full Text] [Related]

  • 12. Clinical syndromes associated with tomacula or myelin swellings in sural nerve biopsies.
    Sander S, Ouvrier RA, McLeod JG, Nicholson GA, Pollard JD.
    J Neurol Neurosurg Psychiatry; 2000 Apr 14; 68(4):483-8. PubMed ID: 10727485
    [Abstract] [Full Text] [Related]

  • 13. [Molecular genetics of inherited neuropathies].
    Takashima H.
    Rinsho Shinkeigaku; 2006 Jan 14; 46(1):1-18. PubMed ID: 16541790
    [Abstract] [Full Text] [Related]

  • 14. Mutations in the 5' region of the myotubularin-related protein 2 (MTMR2) gene in autosomal recessive hereditary neuropathy with focally folded myelin.
    Houlden H, King RH, Wood NW, Thomas PK, Reilly MM.
    Brain; 2001 May 14; 124(Pt 5):907-15. PubMed ID: 11335693
    [Abstract] [Full Text] [Related]

  • 15. Homozygous hypertrophic hereditary motor and sensory neuropathies.
    Sghirlanzoni A, Pareyson D, Marazzi R, Cavaletti G, Bellone E, Mandich P, Balestrini MR, Riva D.
    Ital J Neurol Sci; 1994 Feb 14; 15(1):5-14. PubMed ID: 8206746
    [Abstract] [Full Text] [Related]

  • 16. Autosomal recessive form of hereditary motor and sensory neuropathy type I.
    Gabreëls-Festen AA, Gabreëls FJ, Jennekens FG, Joosten EM, Janssen-van Kempen TW.
    Neurology; 1992 Sep 14; 42(9):1755-61. PubMed ID: 1513466
    [Abstract] [Full Text] [Related]

  • 17. Genetic heterogeneity in autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths (CMT4B).
    Gambardella A, Bolino A, Muglia M, Valentino P, Bono F, Oliveri RL, Sabatelli M, Brancolini V, Van Broeckhoven C, Romeo G, Devoto M, Quattrone A.
    Neurology; 1998 Mar 14; 50(3):799-801. PubMed ID: 9521281
    [Abstract] [Full Text] [Related]

  • 18. Early morphological features in dominantly inherited demyelinating motor and sensory neuropathy (HMSN type I).
    Gabreëls-Festen AA, Joosten EM, Gabreëls FJ, Jennekens FG, Janssen-van Kempen TW.
    J Neurol Sci; 1992 Feb 14; 107(2):145-54. PubMed ID: 1564512
    [Abstract] [Full Text] [Related]

  • 19. Demyelinating hereditary neuropathies in children: a morphometric and ultrastructural study.
    Guzzetta F, Rodríguez J, Deodato M, Guzzetta A, Ferrière G.
    Histol Histopathol; 1995 Jan 14; 10(1):91-104. PubMed ID: 7756749
    [Abstract] [Full Text] [Related]

  • 20. Hereditary motor and sensory neuropathy with deafness, mental retardation, and absence of sensory large myelinated fibers: confirmation of a new entity.
    Sabatelli M, Mignogna T, Lippi G, Servidei S, Zollino M, Padua L, Lo Monaco M, De Armas L, Mereu ML, Tonali P.
    Am J Med Genet; 1998 Jan 23; 75(3):309-13. PubMed ID: 9475604
    [Abstract] [Full Text] [Related]

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