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229 related items for PubMed ID: 9549516

  • 1. Hereditary motor and sensory neuropathy--Lom, a novel demyelinating neuropathy associated with deafness in gypsies. Clinical, electrophysiological and nerve biopsy findings.
    Kalaydjieva L, Nikolova A, Turnev I, Petrova J, Hristova A, Ishpekova B, Petkova I, Shmarov A, Stancheva S, Middleton L, Merlini L, Trogu A, Muddle JR, King RH, Thomas PK.
    Brain; 1998 Mar; 121 ( Pt 3)():399-408. PubMed ID: 9549516
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  • 2. Hereditary motor and sensory neuropathy associated with auditory neuropathy in a Gypsy family.
    Leonardis L, Zidar J, Popovic M, Timmerman V, Löfgren A, Van Broeckhoven C, Butinar D.
    Pflugers Arch; 2000 Mar; 439(3 Suppl):R208-10. PubMed ID: 10653194
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  • 3. HMSNL in a 13-year-old Bulgarian girl.
    Baethmann M, Göhlich-Ratmann G, Schröder JM, Kalaydjieva L, Voit T.
    Neuromuscul Disord; 1998 Apr; 8(2):90-4. PubMed ID: 9608562
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  • 4. Hereditary motor and sensory neuropathy-Lom (HMSNL) in a Spanish family: clinical, electrophysiological, pathological and genetic studies.
    Colomer J, Iturriaga C, Kalaydjieva L, Angelicheva D, King RH, Thomas PK.
    Neuromuscul Disord; 2000 Dec; 10(8):578-83. PubMed ID: 11053685
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  • 6. Hereditary motor and sensory neuropathy associated with auditory neuropathy in a Gypsy family.
    Leonardis L, Zidar J, Popovič M, Timmerman V, Löfgren A, Broeckhoven CV, Butinar D.
    Pflugers Arch; 2000 Jan; 439(Suppl 1):r208-r210. PubMed ID: 28176125
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  • 9. Ultrastructural changes in peripheral nerve in hereditary motor and sensory neuropathy-Lom.
    King RH, Tournev I, Colomer J, Merlini L, Kalaydjieva L, Thomas PK.
    Neuropathol Appl Neurobiol; 1999 Aug; 25(4):306-12. PubMed ID: 10476047
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  • 10. 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
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  • 11. 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 16; 122(1):20-7. PubMed ID: 8195799
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  • 12. Sensory nerve pathology in multifocal motor neuropathy.
    Corse AM, Chaudhry V, Crawford TO, Cornblath DR, Kuncl RW, Griffin JW.
    Ann Neurol; 1996 Mar 16; 39(3):319-25. PubMed ID: 8602750
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  • 13. 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
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  • 14. 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 16; 46(5):1318-24. PubMed ID: 8628474
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  • 15. A clinicophysiologic study of central and peripheral motor conduction in hereditary demyelinating motor and sensory neuropathy.
    Mano Y, Nakamuro T, Ikoma K, Takayanagi T, Mayer RF.
    Electromyogr Clin Neurophysiol; 1993 Mar 16; 33(2):101-7. PubMed ID: 8449165
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  • 16. 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 16; 21(1):29-33. PubMed ID: 8180900
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  • 17. Hypertrophic neuropathy with complete conduction block-- hereditary motor and sensory neuropathy type III.
    Yim SY, Lee IY, Moon HW, Rah UW, Kim SH, Shim C, Joo HJ.
    Yonsei Med J; 1995 Nov 16; 36(5):466-72. PubMed ID: 8546006
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  • 18. Chronic inflammatory demyelinating polyneuropathy or hereditary motor and sensory neuropathy? Diagnostic value of morphological criteria.
    Gabreëls-Festen AA, Gabreëls FJ, Hoogendijk JE, Bolhuis PA, Jongen PJ, Vingerhoets HM.
    Acta Neuropathol; 1993 Nov 16; 86(6):630-5. PubMed ID: 8310819
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  • 19. The status of HMSN type III.
    Gabreëls-Festen AA, Gabreëls FJ, Jennekens FG, Janssen-van Kempen TW.
    Neuromuscul Disord; 1994 Jan 16; 4(1):63-9. PubMed ID: 8173353
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