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Journal Abstract Search

145 related items for PubMed ID: 1301335

  • 1. [A case of chronic multifocal myositis].
    Maruyama T, Kondo K, Tabata K, Yanagisawa N.
    Rinsho Shinkeigaku; 1992 Nov; 32(11):1294-8. PubMed ID: 1301335
    [Abstract] [Full Text] [Related]

  • 2. [A 54-year-old man with progressive proximal muscle atrophy and gynecomastia].
    Anno M, Gotoh K, Hirasawa E, Mori H, Nakajima Y, Mizuno Y.
    No To Shinkei; 1995 Jan; 47(1):87-96. PubMed ID: 7669408
    [Abstract] [Full Text] [Related]

  • 3. [Polymyositis with rimmed vacuoles in a case of chronic thyroiditis].
    Taniguchi A, Niwa A, Nakayama S, Hamaguchi Y, Kuzuhara S.
    Rinsho Shinkeigaku; 1995 Apr; 35(4):403-7. PubMed ID: 7614767
    [Abstract] [Full Text] [Related]

  • 4. [A manifesting carrier of Duchenne muscular dystrophy presenting mosaic distribution of dystrophin negative and positive muscle fibers].
    Kikumoto O, Yoshinaga J, Sasaki T, Ideshita H, Hikiji A, Arahata K.
    Rinsho Shinkeigaku; 1990 Jan; 30(1):107-9. PubMed ID: 2184962
    [Abstract] [Full Text] [Related]

  • 5. [Distal myopathy with rimmed vacuoles and sudden death--report of two siblings].
    Kimpara T, Imamura T, Tsuda T, Sato K, Tsuburaya K.
    Rinsho Shinkeigaku; 1993 Aug; 33(8):886-90. PubMed ID: 8261702
    [Abstract] [Full Text] [Related]

  • 6. [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]

  • 7. [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; 31(4):433-8. PubMed ID: 1914330
    [Abstract] [Full Text] [Related]

  • 8. [Two cases of post-poliomyelitis muscular atrophy].
    Kohara N, Kuzuhara S, Kaneko T, Yamanouchi H, Toyokura Y.
    Rinsho Shinkeigaku; 1989 Jul; 29(7):919-23. PubMed ID: 2805516
    [Abstract] [Full Text] [Related]

  • 9. [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]

  • 10. [A patient of late-onset nemaline myopathy with mononuclear cell infiltration].
    Miura H, Kannari K, Kashiwamura H, Nonaka I.
    Rinsho Shinkeigaku; 1994 Oct; 34(10):1061-3. PubMed ID: 7834955
    [Abstract] [Full Text] [Related]

  • 11. [Two cases of neuralgic amyotrophy].
    Mihori A, Ohno S, Nakayama M, Ono S, Shimizu N.
    Rinsho Shinkeigaku; 1998 Jul; 38(7):669-72. PubMed ID: 9868314
    [Abstract] [Full Text] [Related]

  • 12. [A 34-year-old woman with delayed motor milestones, high arched palate, and proximal muscle weakness].
    Yamamoto T, Kitada T, Hirasawa E, Mori H, Mizuno Y.
    No To Shinkei; 1996 Jul; 48(7):677-84. PubMed ID: 8753005
    [Abstract] [Full Text] [Related]

  • 13. [A 54-year-old man with generalized muscle atrophy and oculomotor paresis].
    Komiya T, Shike T, Mori H, Santo ML, Suda K, Kondo T, Mizuno Y.
    No To Shinkei; 1994 Sep; 46(9):895-904. PubMed ID: 7999450
    [Abstract] [Full Text] [Related]

  • 14. [A case of deletion of the short arm of chromosome 18 associated with chronic polymyositis].
    Matsunaga K, Kubo M, Tsuji S, Ohnishi A, Murai Y.
    Rinsho Shinkeigaku; 1993 Sep; 33(9):980-4. PubMed ID: 8299280
    [Abstract] [Full Text] [Related]

  • 15. [A case of myotonic dystrophy showing proximal dominant muscle involvement but not myotonia].
    Mihori A, Miyauchi H, Kaneda K, Nakayama M, Ono S, Shimizu N.
    Rinsho Shinkeigaku; 1999 Apr; 39(4):461-4. PubMed ID: 10391974
    [Abstract] [Full Text] [Related]

  • 16. [A 22-year-old man with long-standing weakness and atrophy predominantly in the lower extremities].
    Mori H, Sato K, Hirasawa E, Kondo T, Mizuno Y.
    No To Shinkei; 1996 Aug; 48(8):763-71. PubMed ID: 8797213
    [Abstract] [Full Text] [Related]

  • 17. [Complete deficiency of adhalin (50 kDa DAG) in skeletal muscle of malignant limb-girdle muscular dystrophy].
    Kawai H, Inui T, Mitsui T, Campbell KP, Shimizu T, Matsumura K.
    Rinsho Shinkeigaku; 1995 Feb; 35(2):184-9. PubMed ID: 7781237
    [Abstract] [Full Text] [Related]

  • 18. [A 21-year-old man with distal dominant progressive muscle atrophy].
    Hattori Y, Nohara C, Hirasawa E, Mori H, Imai H, Mizuno Y.
    No To Shinkei; 1995 May; 47(5):509-18. PubMed ID: 7786629
    [Abstract] [Full Text] [Related]

  • 19. [Neurological CPC.57. An 80-year-old woman with four years history of muscle atrophy involving lower extremities predominantly on the right side].
    Miwa H, Mori H, Sumino S, Matsuoka S, Shirai T, Imai H, Mizuno Y.
    No To Shinkei; 1997 Sep; 49(9):857-65. PubMed ID: 9311007
    [Abstract] [Full Text] [Related]

  • 20. [A case of X-linked recessive bulbospinal muscular atrophy with demyelinating neuropathy and hypertrophy of the calves].
    Saito T, Matsuoka M, Masaki K, Torii J, Kowa H.
    Rinsho Shinkeigaku; 1993 May; 33(5):514-8. PubMed ID: 8365057
    [Abstract] [Full Text] [Related]

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