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Journal Abstract Search

146 related items for PubMed ID: 9883484

  • 21. 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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  • 22. Hereditary motor and sensory neuropathy. Clinical, genetic and electrodiagnostic studies.
    Vasilescu C.
    Rom J Neurol Psychiatry; 1993 Apr 12; 31(3-4):207-19. PubMed ID: 8011484
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  • 25. 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 12; 25(4):306-12. PubMed ID: 10476047
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  • 26. 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 12; 50(4):452-7. PubMed ID: 11601496
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  • 28. 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 12; 22(1):77-81. PubMed ID: 8866786
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  • 29. Decreased axon caliber and neurofilaments in hereditary motor and sensory neuropathy, type I.
    Nukada H, Dyck PJ.
    Ann Neurol; 1984 Aug 12; 16(2):238-41. PubMed ID: 6541018
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  • 30. 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 12; 46(9):973-7. PubMed ID: 2775013
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  • 32. Hereditary motor and sensory neuropathy: HMSN type II (neuronal type) and X-linked HMSN.
    Hahn AF.
    Brain Pathol; 1993 Apr 12; 3(2):147-55. PubMed ID: 8293176
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  • 33. Hereditary motor and sensory neuropathy with absence of large myelinated fibers due to absence of large neurons in dorsal root ganglia and anterior horns, clinically associated with deafness, mental retardation, and epilepsy (HMSN-ADM).
    Müller HD, Mugler M, Ramaekers VT, Schröder JM.
    J Peripher Nerv Syst; 2000 Sep 12; 5(3):147-57. PubMed ID: 11442171
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  • 34. 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 12; 62(4):385-7. PubMed ID: 9120454
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  • 35. A novel type of hereditary motor and sensory neuropathy characterized by a mild phenotype.
    De Jonghe P, Timmerman V, Nelis E, De Vriendt E, Löfgren A, Ceuterick C, Martin JJ, Van Broeckhoven C.
    Arch Neurol; 1999 Oct 12; 56(10):1283-8. PubMed ID: 10520946
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  • 36. Occurrence of active demyelinating lesions in children with hereditary motor and sensory neuropathy (HMSN) type I.
    Vital A, Vital C, Julien J, Fontan D.
    Acta Neuropathol; 1992 Oct 12; 84(4):433-6. PubMed ID: 1441924
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  • 37. 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 12; 38(2):95-101. PubMed ID: 9553747
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