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Journal Abstract Search

372 related items for PubMed ID: 10349345

  • 1. [A case of hereditary motor and sensory neuropathy with pyramidal tract sign, optic nerve atrophy and mental retardation].
    Adachi T, Imaoka K, Shirasawa A, Yamaguchi S, Kobayashi S.
    Rinsho Shinkeigaku; 1998 Dec; 38(12):1037-41. PubMed ID: 10349345
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  • 2. [A case of hereditary motor and sensory neuropathy type I with optic atrophy, neural deafness and pyramidal tract signs].
    Saito T, Nishioka M, Ogino M, Endo K, Kowa H.
    Rinsho Shinkeigaku; 1993 May; 33(5):519-24. PubMed ID: 8365058
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  • 3. [A case of hereditary motor and sensory neuropathy of neuronal type with retardation of motor development].
    Nakano S, Ohnishi A, Yamamoto T, Oishi T, Murai Y.
    Rinsho Shinkeigaku; 1990 Apr; 30(4):448-51. PubMed ID: 2387117
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  • 4. [A family of X-linked motor and sensory neuropathy with a new type of connexin32 mutation].
    Ohnishi A, Yoshimura T, Takazawa A, Hashimoto T, Yamamoto T, Fukushima Y.
    Rinsho Shinkeigaku; 1995 Aug; 35(8):843-9. PubMed ID: 8665724
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  • 5. [A case of hereditary motor and sensory neuropathy (HMSN type 2) with bilateral recurrent nerve palsy].
    Kamei H, Nishimaru K, Abe H, Irie M, Ohnishi A.
    Rinsho Shinkeigaku; 1993 Sep; 33(9):957-60. PubMed ID: 8299275
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  • 6. [An unusual case of peroneal muscular atrophy with rigidity, polyneuropathy, mental retardation, and diabetes mellitus developed in familial Parkinson's disease].
    Saito T, Hosoda M, Aoto K, Hasegawa H, Kowa H.
    Rinsho Shinkeigaku; 1995 Aug; 35(8):878-83. PubMed ID: 8665730
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  • 7. [A family of hereditary motor and sensory neuropathy with spastic paraplegia (HMSN type V)].
    Murayama T, Nagamatsu M, Sugimura K, Matsuoka Y, Takahashi A.
    Rinsho Shinkeigaku; 1989 Oct; 29(10):1272-7. PubMed ID: 2691166
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  • 10. Hereditary motor and sensory neuropathy type I and motor neuron disease. An unusual association.
    La Pia S, Valiani R, Vitolo S, Galdiero S, Rossi V, Santangelo R, Barbieri F.
    Acta Neurol (Napoli); 1989 Aug; 11(4):226-32. PubMed ID: 2801256
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  • 11. [A family of hereditary motor and sensory neuropathy with spastic paraplegia (HMSN type V) presenting with phenotypic uniformity including onset in early childhood].
    Yamashita M, Yamamoto T, Oka N.
    No To Shinkei; 1999 Nov; 51(11):975-9. PubMed ID: 10586415
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  • 12. [An autopsy case of neuronal type Charcot-Marie-Tooth disease (HMSN type II) with nerve deafness and psychiatric symptoms].
    Yoshimura I, Yoshimura N, Hanazono T, Usutani S, Muramoto Y, Fukushima Y.
    No To Shinkei; 1992 Jun; 44(6):571-8. PubMed ID: 1389565
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  • 13. [A case of hereditary motor and sensory neuropathy type I with a new type of peripheral myelin protein (PMP)-22 mutation].
    Ohnishi A, Yoshimura T, Kanehisa Y, Fukushima Y.
    Rinsho Shinkeigaku; 1995 Jul; 35(7):788-92. PubMed ID: 8777804
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  • 14. [A family of hereditary motor and sensory neuropathy type I with a new type of myelin P0 mutation].
    Ohnishi A, Ohnari K, Hashimoto T, Hayasaka K, Yoshimura T, Fukushima Y.
    Rinsho Shinkeigaku; 1994 Jun; 34(6):546-51. PubMed ID: 7525134
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  • 15. Hereditary motor and sensory neuropathy. Clinical, genetic and electrodiagnostic studies.
    Vasilescu C.
    Rom J Neurol Psychiatry; 1993 Jun; 31(3-4):207-19. PubMed ID: 8011484
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  • 19. [Familial idiopathic vitamin E deficiency associated with cerebellar atrophy].
    Aoki K, Washimi Y, Fujimori N, Maruyama K, Yanagisawa N.
    Rinsho Shinkeigaku; 1990 Sep; 30(9):966-71. PubMed ID: 2265507
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  • 20. [A case of mitochondrial myopathy with external ophthalmoplegia and ataxic neuropathy].
    Mano A, Kikukawa H, Tsuchiya T, Tanaka K, Tanaka M.
    Rinsho Shinkeigaku; 2003 Sep; 43(9):564-7. PubMed ID: 14727565
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