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Journal Abstract Search

103 related items for PubMed ID: 1332322

  • 1. [Infantile facioscapulohumeral muscular dystrophy].
    Badalian LO, Temin PA, Mukhin KIu, Bulaeva NV, Zavadenko NN, Nikanorova MIu, Shnaĭdman RV, Lysov VL.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1992; 92(3):28-30. PubMed ID: 1332322
    [Abstract] [Full Text] [Related]

  • 2. [Rapidly progressing facio-scapulo-humero-femoro-peroneal muscular dystrophy with sensorineural deafness].
    Badalian LO, Temin PA, Mukhin KIu, Nikanorova MIu, Bulaeva NV, Kret LA, Lysov VL.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1991; 91(9):5-8. PubMed ID: 1664615
    [Abstract] [Full Text] [Related]

  • 3. [Variant of the facial-scapular-humeral-gluteal-femoral form of primary myopathy in children].
    Grinio LP.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1979; 79(10):1338-41. PubMed ID: 494906
    [Abstract] [Full Text] [Related]

  • 4. [Spinal facioscapulo-peroneal (or facioscapulo-crural) muscular atrophy and facioscapulo-peroneal muscular dystrophy].
    Kazakov VM, Skoromets AA, Mikhaĭlov EP, Barantsevich ER.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1986; 86(5):662-7. PubMed ID: 3739474
    [Abstract] [Full Text] [Related]

  • 5. [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]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. Infantile facioscapulohumeral muscular dystrophy: new observations.
    Bailey RO, Marzulo DC, Hans MB.
    Acta Neurol Scand; 1986 Jul; 74(1):51-8. PubMed ID: 3766116
    [Abstract] [Full Text] [Related]

  • 8. Poikiloderma atrophicans vasculare associated with muscular dystrophy.
    Woolfson H, McQueen A.
    Arch Dermatol; 1973 Jan; 107(1):115-7. PubMed ID: 4682534
    [No Abstract] [Full Text] [Related]

  • 9. Scapuloperoneal myopathy.
    Todman DH, Cooke RA.
    Clin Exp Neurol; 1984 Jan; 20():169-74. PubMed ID: 6568938
    [Abstract] [Full Text] [Related]

  • 10. Facioscapulohumeral dystrophy presenting in infancy with facial diplegia and sensorineural deafness.
    Korf BR, Bresnan MJ, Shapiro F, Sotrel A, Abroms IF.
    Ann Neurol; 1985 May; 17(5):513-6. PubMed ID: 4004175
    [Abstract] [Full Text] [Related]

  • 11. Facioscapulohumeral muscular dystrophy with congenital absence of sternocleidomastoid muscles.
    Penchaszadeh V.
    Birth Defects Orig Artic Ser; 1971 Feb; 7(2):116-7. PubMed ID: 5173120
    [No Abstract] [Full Text] [Related]

  • 12. [Articulation disorder as the initial manifestation of facioscapulohumeral muscular dystrophy in childhood].
    Lischka A, Grisold W, Weninger M, Toifl K, Tatzer E.
    Klin Padiatr; 1986 Feb; 198(2):119-21. PubMed ID: 3702273
    [Abstract] [Full Text] [Related]

  • 13. 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; 7(2):72-81. PubMed ID: 5173129
    [Abstract] [Full Text] [Related]

  • 14. [Ocular myopathy. A familial case of oculo-pharyngeal and skeletal muscular dystrophy with late onset].
    Manigand G, Lucsko M, Deparis M.
    Sem Hop; 1969 Nov 08; 45(45):2803-8. PubMed ID: 4312491
    [No Abstract] [Full Text] [Related]

  • 15. [Facial-scapular-humeral myodystrophy (genetic and clinical features)].
    Bogorodinskiĭ DK, Znoĭko ZV, Kazakov VM, Skoromets AA.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1973 Nov 08; 73(6):801-9. PubMed ID: 4753589
    [No Abstract] [Full Text] [Related]

  • 16. Early muscular dystrophy: differential patterns of weakness in duchenne, limb-girdle and facioscapulohumeral types.
    Chyatte SB, Vignos PJ, Watkins M.
    Arch Phys Med Rehabil; 1966 Aug 08; 47(8):499-503. PubMed ID: 5914825
    [No Abstract] [Full Text] [Related]

  • 17. [Pseudohypertrophic proximal progressive muscular dystrophy with a malignant course manifesting itself in adolescence].
    Badalian LO, Temin PA, Saidbegov DG, Nikitin MV, Arkhipov BA.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1989 Aug 08; 89(3):113-20. PubMed ID: 2728733
    [Abstract] [Full Text] [Related]

  • 18. New type of X-linked progressive muscular dystrophy involving shoulder girdle and back.
    Ji XW, Tan J, Chen XY, Yi SX, Liang H.
    Am J Med Genet; 1990 Oct 08; 37(2):209-12. PubMed ID: 2248287
    [Abstract] [Full Text] [Related]

  • 19. [Quadriceps myopathy: a type of late focal dystrophy in a case].
    Cartier L, Hernández JE, Stuardo A, González J, Villagra R.
    Rev Med Chil; 1995 Jan 08; 123(1):81-4. PubMed ID: 7569450
    [Abstract] [Full Text] [Related]

  • 20. Limb-girdle muscular dystrophy: clinical manifestations and detection of preclinical disease.
    Jackson CE, Strehler DA.
    Pediatrics; 1968 Feb 08; 41(2):495-502. PubMed ID: 5637795
    [No Abstract] [Full Text] [Related]

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