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Journal Abstract Search

149 related items for PubMed ID: 8017168

  • 1. 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; 87(4):337-42. PubMed ID: 8017168
    [Abstract] [Full Text] [Related]

  • 2. [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]

  • 3. Hereditary motor and sensory neuropathy with myelin outfolding: clinical, genetic and neuropathological study of three cases.
    Schenone A, Abbruzzese M, Uccelli A, Mandich P, James R, Bellone E, Giunchedi M, Rolando S, Capello E, Mandich R [corrected to Mandich P].
    J Neurol Sci; 1994 Mar 01; 122(1):20-7. PubMed ID: 8195799
    [Abstract] [Full Text] [Related]

  • 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 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]

  • 6. 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]

  • 7. 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 08; 124(Pt 5):907-15. PubMed ID: 11335693
    [Abstract] [Full Text] [Related]

  • 8. 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 May 08; 86(6):602-8. PubMed ID: 8310815
    [Abstract] [Full Text] [Related]

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  • 10. Demyelinating hereditary neuropathies in children: a morphometric and ultrastructural study.
    Guzzetta F, Rodríguez J, Deodato M, Guzzetta A, Ferrière G.
    Histol Histopathol; 1995 Jan 08; 10(1):91-104. PubMed ID: 7756749
    [Abstract] [Full Text] [Related]

  • 11. Hereditary motor and sensory neuropathy-russe: new autosomal recessive neuropathy in Balkan Gypsies.
    Thomas PK, Kalaydjieva L, Youl B, Rogers T, Angelicheva D, King RH, Guergueltcheva V, Colomer J, Lupu C, Corches A, Popa G, Merlini L, Shmarov A, Muddle JR, Nourallah M, Tournev I.
    Ann Neurol; 2001 Oct 08; 50(4):452-7. PubMed ID: 11601496
    [Abstract] [Full Text] [Related]

  • 12. 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]

  • 13. Autosomal recessive inheritance of hereditary motor and sensory neuropathy with optic atrophy.
    Chalmers RM, Riordan-Eva P, Wood NW.
    J Neurol Neurosurg Psychiatry; 1997 Apr 08; 62(4):385-7. PubMed ID: 9120454
    [Abstract] [Full Text] [Related]

  • 14. [Hereditary motor and sensory neuropathy type III. Case report and review of the literature].
    Haverkamp F, Behring B.
    Klin Padiatr; 1995 Apr 08; 207(1):24-7. PubMed ID: 7885014
    [Abstract] [Full Text] [Related]

  • 15. Hereditary motor and sensory neuropathy with optic atrophy. Ultrastructural and morphometric observations on nerve fibers, mitochondria, and dense-cored vesicles.
    Sommer C, Schröder JM.
    Arch Neurol; 1989 Sep 08; 46(9):973-7. PubMed ID: 2775013
    [Abstract] [Full Text] [Related]

  • 16. Four novel cases of periaxin-related neuropathy and review of the literature.
    Marchesi C, Milani M, Morbin M, Cesani M, Lauria G, Scaioli V, Piccolo G, Fabrizi GM, Cavallaro T, Taroni F, Pareyson D.
    Neurology; 2010 Nov 16; 75(20):1830-8. PubMed ID: 21079185
    [Abstract] [Full Text] [Related]

  • 17. 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 16; 107(2):145-54. PubMed ID: 1564512
    [Abstract] [Full Text] [Related]

  • 18. Hereditary demyelinating motor and sensory neuropathy.
    Gabreëls-Festen A, Gabreëls F.
    Brain Pathol; 1993 Apr 16; 3(2):135-46. PubMed ID: 8293175
    [Abstract] [Full Text] [Related]

  • 19. 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 16; 15(1):5-14. PubMed ID: 8206746
    [Abstract] [Full Text] [Related]

  • 20. Hereditary motor and sensory neuropathy: HMSN type II (neuronal type) and X-linked HMSN.
    Hahn AF.
    Brain Pathol; 1993 Apr 16; 3(2):147-55. PubMed ID: 8293176
    [Abstract] [Full Text] [Related]

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