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Journal Abstract Search

128 related items for PubMed ID: 8173353

  • 1.
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  • 2. Nerve and muscle biopsy in a case of hereditary motor and sensory neuropathy type III with basal lamina onion bulbs.
    Bornemann A, Hansen FJ, Schmalbruch H.
    Neuropathol Appl Neurobiol; 1996 Feb; 22(1):77-81. PubMed ID: 8866786
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  • 4. 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 Feb; 86(6):630-5. PubMed ID: 8310819
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  • 5. 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; 107(2):145-54. PubMed ID: 1564512
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  • 6. Congenital demyelinating motor and sensory neuropathy with focally folded myelin sheaths.
    Gabreëls-Festen AA, Joosten EM, Gabreëls FJ, Stegeman DF, Vos AJ, Busch HF.
    Brain; 1990 Dec; 113 ( Pt 6)():1629-43. PubMed ID: 2276038
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  • 7. 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; 122(1):20-7. PubMed ID: 8195799
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  • 8. 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; 36(5):466-72. PubMed ID: 8546006
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  • 10. 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; 42(9):1755-61. PubMed ID: 1513466
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  • 11. 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 Sep; 86(6):602-8. PubMed ID: 8310815
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  • 12. 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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  • 13. 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 16; 121 ( Pt 3)():399-408. PubMed ID: 9549516
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  • 14. The electrophysiologic profile of Dejerine-Sottas disease (HMSN III).
    Benstead TJ, Kuntz NL, Miller RG, Daube JR.
    Muscle Nerve; 1990 Jul 16; 13(7):586-92. PubMed ID: 2388657
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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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  • 18. Hereditary motor and sensory neuropathy. Clinical, genetic and electrodiagnostic studies.
    Vasilescu C.
    Rom J Neurol Psychiatry; 1993 Feb 16; 31(3-4):207-19. PubMed ID: 8011484
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  • 19. Differences between hereditary motor and sensory neuropathy type 2 and chronic idiopathic axonal neuropathy. A clinical and electrophysiological study.
    Teunissen LL, Notermans NC, Franssen H, van der Graaf Y, Oey PL, Linssen WH, van Engelen BG, Ippel PF, van Dijk GW, Gabreëls-Festen AA, Wokke JH.
    Brain; 1997 Jun 16; 120 ( Pt 6)():955-62. PubMed ID: 9217680
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  • 20. The hypertrophic forms of hereditary motor and sensory neuropathy. A study of hypertrophic Charcot-Marie-Tooth disease (HMSN type I) and Dejerine-Sottas disease (HMSN type III) in childhood.
    Ouvrier RA, McLeod JG, Conchin TE.
    Brain; 1987 Feb 16; 110 ( Pt 1)():121-48. PubMed ID: 3467805
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