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Journal Abstract Search

135 related items for PubMed ID: 8546006

  • 1. 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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  • 3. The status of HMSN type III.
    Gabreëls-Festen AA, Gabreëls FJ, Jennekens FG, Janssen-van Kempen TW.
    Neuromuscul Disord; 1994 Jan; 4(1):63-9. PubMed ID: 8173353
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  • 4. The electrophysiologic profile of Dejerine-Sottas disease (HMSN III).
    Benstead TJ, Kuntz NL, Miller RG, Daube JR.
    Muscle Nerve; 1990 Jul; 13(7):586-92. PubMed ID: 2388657
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  • 5. 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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  • 6. [Acute idiopathic sensory neuropathy: a case report].
    Werneck LC, Correa Neto Y, Scola RH.
    Arq Neuropsiquiatr; 1993 Sep; 51(3):389-94. PubMed ID: 8297247
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  • 9. [Hereditary motor and sensory neuropathy].
    Guo YP.
    Zhonghua Shen Jing Jing Shen Ke Za Zhi; 1992 Oct; 25(5):261-3, 315. PubMed ID: 1291244
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  • 10. [A juvenile case of chronic inflammatory demyelinating polyradiculoneuropathy with severe onion bulb-like change mimicking hereditary neuropathy].
    Oda M, Udaka F, Kubori T, Oka N, Kameyama M.
    No To Shinkei; 1999 Dec; 51(12):1075-9. PubMed ID: 10654306
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  • 11. [A case of sporadic polyneuropathy with tomacula demonstrating marked nerve conduction delay].
    Hashimoto K, Kawai M, Sakuta M.
    Rinsho Shinkeigaku; 1988 Sep; 28(9):1023-9. PubMed ID: 3246103
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  • 12. 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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  • 13. Hereditary motor and sensory neuropathy. Clinical, genetic and electrodiagnostic studies.
    Vasilescu C.
    Rom J Neurol Psychiatry; 1993 Sep; 31(3-4):207-19. PubMed ID: 8011484
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  • 14. Electrophysiological findings in hereditary motor and sensory neuropathy type I and II--a conduction velocity study.
    Emeryk-Szajewska B, Badurska B, Kostera-Pruszczyk A.
    Electromyogr Clin Neurophysiol; 1998 Mar; 38(2):95-101. PubMed ID: 9553747
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  • 16. 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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  • 18. 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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  • 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; 110 ( Pt 1)():121-48. PubMed ID: 3467805
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