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Journal Abstract Search

130 related items for PubMed ID: 8673478

  • 1. Late-onset hereditary ataxia with global thermoanalgesia and absence of fungiform papillae on the tongue in a Japanese family.
    Fukutake T, Kita K, Sakakibara R, Takagi K, Tokumaru Y, Kojima S, Hattori T, Hirayama K.
    Brain; 1996 Jun; 119 ( Pt 3)():1011-21. PubMed ID: 8673478
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  • 4. Sensory neuropathy in infantile onset spinocerebellar ataxia (IOSCA).
    Koskinen T, Sainio K, Rapola J, Pihko H, Paetau A.
    Muscle Nerve; 1994 May; 17(5):509-15. PubMed ID: 8159181
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  • 8. A new variant of sensory ataxic neuropathy with autosomal dominant inheritance.
    van Dijk GW, Wokke JH, Oey PL, Franssen H, Ippel PF, Veldman H.
    Brain; 1995 Dec; 118 ( Pt 6)():1557-63. PubMed ID: 8595484
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  • 11. [A case of hereditary sensory autonomic neuropathy type II with late onset].
    Shimoya K, Ishimoto S, Ohnishi A, Yamamoto T.
    Rinsho Shinkeigaku; 1999 May; 39(5):551-4. PubMed ID: 10424148
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  • 12. A Japanese family with early-onset ataxia with motor and sensory neuropathy.
    Kobayashi S, Takuma H, Murayama S, Sakurai M, Kanazawa I.
    J Neurol Sci; 2007 Mar 15; 254(1-2):44-8. PubMed ID: 17258771
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  • 13. A novel TRK A (NTRK1) mutation associated with hereditary sensory and autonomic neuropathy type V.
    Houlden H, King RH, Hashemi-Nejad A, Wood NW, Mathias CJ, Reilly M, Thomas PK.
    Ann Neurol; 2001 Apr 15; 49(4):521-5. PubMed ID: 11310631
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  • 16. An hereditary sensory and autonomic neuropathy transmitted as an X-linked recessive trait.
    Jestico JV, Urry PA, Efphimiou J.
    J Neurol Neurosurg Psychiatry; 1985 Dec 15; 48(12):1259-64. PubMed ID: 3866836
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  • 17. The clinical spectrum and morphology of type II hereditary sensory neuropathy.
    Nukada H, Pollock M, Haas LF.
    Brain; 1982 Dec 15; 105 (Pt 4)():647-65. PubMed ID: 6958343
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  • 18. Hereditary sensory radicular neuropathy: defective neurogenic inflammation.
    Westerman RA, Block A, Nunn A, Delaney CA, Hahn A, Dennett X, Carr RW.
    Clin Exp Neurol; 1992 Dec 15; 29():189-209. PubMed ID: 1343862
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