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Journal Abstract Search

361 related items for PubMed ID: 8365058

  • 1. [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
    [Abstract] [Full Text] [Related]

  • 2. [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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  • 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. [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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  • 5. [A case of hereditary motor and sensory neuropathy with vocal cords palsy and diaphragmatic weakness].
    Fukuda H, Kitani M, Imaoka K.
    Rinsho Shinkeigaku; 1993 Feb; 33(2):175-81. PubMed ID: 8319389
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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
    [Abstract] [Full Text] [Related]

  • 7. [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
    [Abstract] [Full Text] [Related]

  • 8. [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
    [Abstract] [Full Text] [Related]

  • 9. [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
    [Abstract] [Full Text] [Related]

  • 10. [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
    [Abstract] [Full Text] [Related]

  • 11. [A patient of Charcot-Marie-tooth disease with rigid spine and respiratory failure].
    Takamure M, Nakamuro T, Sugie K, Suzumura A, Takayanagi T.
    Rinsho Shinkeigaku; 2000 May; 40(5):433-8. PubMed ID: 11002724
    [Abstract] [Full Text] [Related]

  • 12. [An autopsy case with lower motor neuron disease showing a transient-appearance of anti-GM1 antibody and an improvement of conduction block after gamma-globulin administration].
    Kikuchi H, Kawano Y, Dohura K, Kawamura T, Taniwaki T, Yamada T, Kato M, Iwaki T, Kira J.
    No To Shinkei; 1999 May; 51(5):455-64. PubMed ID: 10396755
    [Abstract] [Full Text] [Related]

  • 13. [Progressive cerebellar ataxia and distal amyotrophy of Charcot-Marie-Tooth type with hyperglutamataemia:two sibling cases].
    Tanji H, Takeda A, Tateyama M, Mochizuki H, Itoyama Y.
    Rinsho Shinkeigaku; 1995 Jul; 35(7):793-7. PubMed ID: 8777805
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  • 18. [Two siblings of distal hereditary motor neuropathy with choroideremia].
    Kawata A, Hayashi H, Yoshida H, Kanda T, Tanabe H.
    Rinsho Shinkeigaku; 1990 Sep; 30(9):1010-2. PubMed ID: 2265499
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