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PUBMED FOR HANDHELDS

Journal Abstract Search


109 related items for PubMed ID: 477132

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. [A case of subacute spinal muscular atrophy of facio-bulbo-scapulo-humeral type associated with unconjugated hyperbilirubinemia (author's transl)].
    Shinoda K, Konishi S, Masui T, Takenaka M, Mozai T.
    Rinsho Shinkeigaku; 1980 Sep; 20(9):697-703. PubMed ID: 7460431
    [No Abstract] [Full Text] [Related]

  • 3. [Atypical facioscapulohumeral muscular dystrophy associated with congenital facial diplegia noted during infancy].
    Miyazaki M, Tawara S, Terao A, Araki S, Shirabe T.
    Rinsho Shinkeigaku; 1976 Jan; 16(1):32-8. PubMed ID: 943262
    [No Abstract] [Full Text] [Related]

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  • 5. [Some views of the actual possibilities in the treatment of facial palsy (author's transl)].
    Meyer R, Botta Y, Failat AS.
    Schweiz Rundsch Med Prax; 1979 Nov 27; 68(48):1586-99. PubMed ID: 395533
    [No Abstract] [Full Text] [Related]

  • 6. [Muscle innervation in Werdnig-Hoffmann spinal amyotrophy and several other atrophies in children].
    Olenev SN, Savel'eva-Vasil'eva, Zav'ialova NS.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1972 Nov 27; 72(10):1445-9. PubMed ID: 4660417
    [No Abstract] [Full Text] [Related]

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  • 8. Diseases of the anterior horn cell.
    Wadia RS, Karandikar R, Pallod S, Grant KB, Sardesai HV.
    J Assoc Physicians India; 1972 Jun 27; 20(6):415-22. PubMed ID: 4655115
    [No Abstract] [Full Text] [Related]

  • 9. [Serum aldolase activity in patients with myopathies and in their close reltives].
    Dzhuraev A.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1971 Jun 27; 71(8):1159-63. PubMed ID: 5136820
    [No Abstract] [Full Text] [Related]

  • 10.
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  • 11. [Congenital facioscapulohumeral muscular dystrophy associated with tongue atrophy and sensorineural hearing disturbance].
    Shimizu T, Miyamoto K, Hayashi H, Nagashima T, Hirose K, Tanabe H.
    Rinsho Shinkeigaku; 1991 Apr 27; 31(4):433-8. PubMed ID: 1914330
    [Abstract] [Full Text] [Related]

  • 12. Characteristic clinical findings in some neurogenic myopathies and in some myogenic myopathies causing muscular weakness, hypotonia and atrophy in infancy and early childhood.
    Gamstorp I.
    Birth Defects Orig Artic Ser; 1971 Feb 27; 7(2):72-81. PubMed ID: 5173129
    [Abstract] [Full Text] [Related]

  • 13. [A case of facioscapulohumeral muscular atrophy presenting unusual squatting gait, associated with tongue atrophy and sensorineural hearing loss].
    Goto K, Sugihara R.
    Rinsho Shinkeigaku; 1994 Nov 27; 34(11):1157-61. PubMed ID: 7729099
    [Abstract] [Full Text] [Related]

  • 14.
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  • 15. Facioscapulohumeral type spinal muscular atrophy: report of a case.
    Hsu SC, Wang PJ, Chen CF, Shen YZ.
    Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi; 1989 Nov 27; 30(1):40-5. PubMed ID: 2637583
    [Abstract] [Full Text] [Related]

  • 16. [Werdnig-Hoffmann spinal amyotrophy in twins].
    Mazaeva IV, Lipovetskaia NG, Balashova EG.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1973 Nov 27; 73(10):1491-5. PubMed ID: 4795172
    [No Abstract] [Full Text] [Related]

  • 17. [Identification of primary and secondary forms of progressive muscular dystrophy, from data of clinico-genetic and biochemical studies].
    Bondarenko ES, Tamarkina AD, Zakoshchikova LV.
    Vestn Akad Med Nauk SSSR; 1973 Nov 27; 28(7):38-44. PubMed ID: 4786657
    [No Abstract] [Full Text] [Related]

  • 18. [The muscular atrophies following facial nerve paralysis. Biochemical and electromyographical data].
    Silvestrini Biavati M, Viti M.
    Riv Ital Stomatol; 1969 Oct 27; 24(10):967-76. PubMed ID: 5266397
    [No Abstract] [Full Text] [Related]

  • 19. [Congenital facial paralysis in dizygotic twins].
    Masaki S.
    Jibiinkoka; 1970 Jul 27; 42(7):517-22. PubMed ID: 5466251
    [No Abstract] [Full Text] [Related]

  • 20. [Moebius' syndrome and amyotrophies of the extremities (5 cases)].
    Tridon P, André JM, André M, Brichet B, Arnould G.
    Rev Neurol (Paris); 1971 May 27; 124(5):367-78. PubMed ID: 5126782
    [No Abstract] [Full Text] [Related]


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