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PUBMED FOR HANDHELDS

Journal Abstract Search

481 related items for PubMed ID: 8665724

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  • 3. [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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  • 4. [A family of hereditary motor and sensory neuropathy type I with a mutation (Arg98-->His) in myelin Po--report on a second Japanese family].
    Ohnishi A, Kashiwada E, Hashimoto T, Yamamoto T, Murai Y, Ohashi H, Ikegami T, Hayasaka K, Sudo K, Yamamori S.
    J UOEH; 1996 Mar 01; 18(1):19-29. PubMed ID: 8851708
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  • 6. [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 01; 38(12):1037-41. PubMed ID: 10349345
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  • 8. [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 01; 30(4):448-51. PubMed ID: 2387117
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  • 9. [Clinical, pathologic and molecular genetic studies of patients with hereditary motor and sensory neuropathy (HMSN)].
    Ohnishi A.
    Rinsho Shinkeigaku; 1995 Dec 01; 35(12):1438-40. PubMed ID: 8752423
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  • 10. [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 01; 33(5):519-24. PubMed ID: 8365058
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  • 11. [A familial Charcot-Marie-Tooth disease type 1B (CMTD1B) manifesting a new mutation of myelin P0 gene].
    Mitsui Y, Matsui T, Nakamura Y, Takahashi M, Yoshikawa H, Hayasaka K.
    Rinsho Shinkeigaku; 1994 Nov 01; 34(11):1162-7. PubMed ID: 7537189
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  • 12. [Clinical report of hereditary motor and sensory neuropathy with proximal dominance in Shiga prefecture].
    Takahashi M, Mitsui Y, Yorifuji S, Nakamura Y, Tsukamoto Y, Nishimoto K.
    Rinsho Shinkeigaku; 2007 Sep 01; 47(9):571-6. PubMed ID: 18018614
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  • 13. [A family with autosomal dominant temporal lobe epilepsy accompanied by motor and sensory neuropathy].
    Matsuoka T, Furuya H, Ikezoe K, Murai H, Ohyagi Y, Yoshiura T, Sasaki M, Tobimatsu S, Kira J.
    Rinsho Shinkeigaku; 2004 Jan 01; 44(1):43-9. PubMed ID: 15199738
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  • 14. [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 01; 35(8):878-83. PubMed ID: 8665730
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  • 15. [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 01; 33(9):957-60. PubMed ID: 8299275
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  • 16. [A case of chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) with bilateral recurrent nerve palsy and primary alveolar hypoventilation--comparative studies of the histological findings of the two sural nerve biopsies with 9 years interval].
    Yamamoto T, Ohnishi A, Miyoshi T, Hashimoto T, Murai Y.
    Rinsho Shinkeigaku; 1994 Jul 01; 34(7):712-6. PubMed ID: 7955730
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  • 17. Genotype/phenotype correlations in X-linked dominant Charcot-Marie-Tooth disease.
    Hahn AF, Bolton CF, White CM, Brown WF, Tuuha SE, Tan CC, Ainsworth PJ.
    Ann N Y Acad Sci; 1999 Sep 14; 883():366-82. PubMed ID: 10586261
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  • 18. [Hereditary neuropathy with liability to pressure palsies: study of six Spanish families].
    Pou Serradell A, Monells J, Téllez MJ, Fossas P, Löfgren A, Meuleman J, Timmerman V, De Jonghe P, Ceuterick C, Martin JJ.
    Rev Neurol (Paris); 2002 May 14; 158(5 Pt 1):579-88. PubMed ID: 12072826
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  • 19. A family with X-linked dominant Charcot-Marie-Tooth caused by a connexin32 mutation.
    Verhelst HE, Lofgren A, Van Coster RN.
    Eur J Paediatr Neurol; 2000 May 14; 4(5):235-8. PubMed ID: 11030070
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  • 20. [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 14; 29(10):1272-7. PubMed ID: 2691166
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