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Journal Abstract Search

101 related items for PubMed ID: 5487716

  • 1. [Haptoglobins in muscular diseases].
    Rosnowska M, Strugalska H.
    Neurol Neurochir Pol; 1970; 4(6):655-60. PubMed ID: 5487716
    [No Abstract] [Full Text] [Related]

  • 2. [A genetic questionnaire. The genetic aspects of a case of benign spinal muscular dystrophy].
    Klein D.
    J Genet Hum; 1970 Dec; 18(4):421-2. PubMed ID: 5524821
    [No Abstract] [Full Text] [Related]

  • 3. [Mental development of children with the Duchenne type of progressive muscular dystrophy].
    Kozicka A.
    Neurol Neurochir Pol; 1971 Dec; 5(4):523-8. PubMed ID: 5122056
    [No Abstract] [Full Text] [Related]

  • 4. An unusual inheritane pattern for spinal muscular atrophy.
    White NR, Blaw ME.
    Dev Med Child Neurol; 1971 Oct; 13(5):621-4. PubMed ID: 5119919
    [No Abstract] [Full Text] [Related]

  • 5. [Serum aldolase activity in patients with myopathies and in their close reltives].
    Dzhuraev A.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1971 Oct; 71(8):1159-63. PubMed ID: 5136820
    [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 Oct; 72(10):1445-9. PubMed ID: 4660417
    [No Abstract] [Full Text] [Related]

  • 7. Spinal muscular atrophy type II. A separate genetic and clinical entity from type I (Werdnig-Hoffmann disease) and type 3 (Kugelberg-Welander disease).
    Fried K, Emery AE.
    Clin Genet; 1971 Oct; 2(4):203-9. PubMed ID: 5146579
    [No Abstract] [Full Text] [Related]

  • 8. Reontgenologic evaluation of disorders of muscle.
    Gay BB, Weens HS.
    Semin Roentgenol; 1973 Jan; 8(1):25-36. PubMed ID: 4682800
    [No Abstract] [Full Text] [Related]

  • 9. [Clinical study of muscular atrophy].
    Shinoda M.
    Hokkaido Igaku Zasshi; 1974 Jan; 49(1):23-31. PubMed ID: 4376121
    [No Abstract] [Full Text] [Related]

  • 10. [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 Jan; 28(7):38-44. PubMed ID: 4786657
    [No Abstract] [Full Text] [Related]

  • 11. A new genetic variant of the spinal muscular atrophies in infancy.
    Zellweger H, Hanhart E, Schneider HJ.
    J Med Genet; 1972 Dec; 9(4):401-7. PubMed ID: 4646546
    [No Abstract] [Full Text] [Related]

  • 12. Editorial: Diagnosis of childhood spinal muscular atrophy.
    Br Med J; 1973 Oct 06; 4(5883):2-3. PubMed ID: 4755211
    [No Abstract] [Full Text] [Related]

  • 13. Diseases of the anterior horn cell.
    Wadia RS, Karandikar R, Pallod S, Grant KB, Sardesai HV.
    J Assoc Physicians India; 1972 Jun 06; 20(6):415-22. PubMed ID: 4655115
    [No Abstract] [Full Text] [Related]

  • 14. [Neurogenic muscular atrophy in children].
    Hainaut H, Chapelle P, Hariga J.
    Acta Paediatr Belg; 1969 Jun 06; 23(5):261-74. PubMed ID: 5398928
    [No Abstract] [Full Text] [Related]

  • 15. [Carbohydrate metabolism disorders in hereditary forms of neuromuscular diseases].
    Golubeva VV.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1971 Jun 06; 71(8):1153-9. PubMed ID: 5136819
    [No Abstract] [Full Text] [Related]

  • 16. [Serum enzymes in muscular diseases].
    Laudahn G, Heyck H, Feustel F.
    Curr Probl Clin Biochem; 1968 Jun 06; 1():249-317. PubMed ID: 4950596
    [No Abstract] [Full Text] [Related]

  • 17. Spinal muscular atrophy.
    McLeod JG, Williams IM.
    Minn Med; 1971 Jun 06; 54(6):457-61. PubMed ID: 5559368
    [No Abstract] [Full Text] [Related]

  • 18. Juvenile motor neuron diseases--the sex influence in benign juvenile pseudodystrophic spinal muscular atrophy.
    Hausmanowa-Petrusewicz I, Borkowska J, Zaremba J.
    Adv Neurol; 1982 Jun 06; 36():131-7. PubMed ID: 7180679
    [No Abstract] [Full Text] [Related]

  • 19. [Infantile progressive spinal muscular atrophy. Werdnig-Hoffmann disease].
    Mohr W, Olischläger A, Carl H.
    Med Welt; 1971 Aug 28; 35():1317-9. PubMed ID: 5564452
    [No Abstract] [Full Text] [Related]

  • 20. [Malate dehydrogenase activity in patients with different forms of progressive muscular dystrophy].
    Gil'manov VKh.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1970 Aug 28; 70(9):1309-12. PubMed ID: 5511109
    [No Abstract] [Full Text] [Related]

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