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Journal Abstract Search

137 related items for PubMed ID: 10932274

  • 1. 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
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  • 2. 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
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  • 4. [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
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  • 5. 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 01; 124(Pt 5):907-15. PubMed ID: 11335693
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  • 6. 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
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  • 7. 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 Mar 01; 86(6):602-8. PubMed ID: 8310815
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  • 10. 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
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  • 11. A novel MPZ gene mutation in dominantly inherited neuropathy with focally folded myelin sheaths.
    Nakagawa M, Suehara M, Saito A, Takashima H, Umehara F, Saito M, Kanzato N, Matsuzaki T, Takenaga S, Sakoda S, Izumo S, Osame M.
    Neurology; 1999 Apr 12; 52(6):1271-5. PubMed ID: 10214757
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  • 12. 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 Apr 12; 87(4):337-42. PubMed ID: 8017168
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  • 14. Recessive inheritance of a new point mutation of the PMP22 gene in Dejerine-Sottas disease.
    Parman Y, Planté-Bordeneuve V, Guiochon-Mantel A, Eraksoy M, Said G.
    Ann Neurol; 1999 Apr 12; 45(4):518-22. PubMed ID: 10211478
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  • 17. [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 12; 35(8):843-9. PubMed ID: 8665724
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  • 18. Hereditary motor and sensory neuropathy with congenital glaucoma. Report on a family.
    Arruda WO, Comerlato EA, Scola RH, Silvado CE, Werneck LC.
    Arq Neuropsiquiatr; 1999 Jun 12; 57(2A):190-4. PubMed ID: 10412516
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