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Journal Abstract Search

151 related items for PubMed ID: 6530365

  • 1. Clinical study of proximal spinal muscular atrophy. Report on 89 cases.
    Tonali P, Servidei S, Uncini A, Restuccia D, Galluzzi G.
    Ital J Neurol Sci; 1984 Dec; 5(4):423-32. PubMed ID: 6530365
    [Abstract] [Full Text] [Related]

  • 2. The nosology of the spinal muscular atrophies.
    Emery AE.
    J Med Genet; 1971 Dec; 8(4):481-95. PubMed ID: 4948374
    [No Abstract] [Full Text] [Related]

  • 3. A clinical and genetic study of spinal muscular atrophy of adult onset: the autosomal recessive form as a discrete disease entity.
    Pearn JH, Hudgson P, Walton JN.
    Brain; 1978 Dec; 101(4):591-606. PubMed ID: 737522
    [Abstract] [Full Text] [Related]

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

  • 5. Late-onset X-linked recessive spinal and bulbar muscular atrophy.
    Ringel SP, Lava NS, Treihaft MM, Lubs ML, Lubs HA.
    Muscle Nerve; 1978 Jun; 1(4):297-307. PubMed ID: 571530
    [Abstract] [Full Text] [Related]

  • 6. [Pseudomyopathic spinal diseases].
    Heyck H.
    Beitr Orthop Traumatol; 1975 Jan; 22(1):15-25. PubMed ID: 1122229
    [No Abstract] [Full Text] [Related]

  • 7. Progressive proximal spinal and bulbar muscular atrophy of late onset. A sex-linked recessive trait.
    Kennedy WR, Alter M, Sung JH.
    Neurology; 1968 Jul; 18(7):671-80. PubMed ID: 4233749
    [No Abstract] [Full Text] [Related]

  • 8. Genetic counseling in families with spinal muscular atrophy type Kugelberg-Welander.
    Zerres K, Grimm T.
    Hum Genet; 1983 Jul; 65(1):74-5. PubMed ID: 6642509
    [No Abstract] [Full Text] [Related]

  • 9. Autosomal dominant spinal muscular atrophy: a clinical and genetic study.
    Pearn J.
    J Neurol Sci; 1978 Sep; 38(2):263-75. PubMed ID: 712386
    [Abstract] [Full Text] [Related]

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

  • 11. [Proximal spinal muscular atrophy--a contribution to the question of intrafamiliar variability and the genetics of the disease (author's transl)].
    Kollmann D, Murken JD, Förster C.
    Monatsschr Kinderheilkd (1902); 1974 Jun; 122(6):327-30. PubMed ID: 4849530
    [No Abstract] [Full Text] [Related]

  • 12. Spinal muscular atrophy (a report of 44 cases).
    Mondkar VP, George R.
    J Postgrad Med; 1983 Oct; 29(4):242-50. PubMed ID: 6672183
    [No Abstract] [Full Text] [Related]

  • 13. 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]

  • 14. Fasciculation of the eyelids: an additional clue to clinical diagnosis in spinal muscular atrophy.
    Skouteli H, Dubowitz V.
    Neuropediatrics; 1984 Aug; 15(3):145-6. PubMed ID: 6483112
    [Abstract] [Full Text] [Related]

  • 15. Spinal muscular atrophy in childhood: review of 50 cases.
    Benady SG.
    Dev Med Child Neurol; 1978 Dec; 20(6):746-57. PubMed ID: 729928
    [Abstract] [Full Text] [Related]

  • 16. [Hereditary proximal neurogenic muscular atrophy (Wohlfart-Kugelberg-Welander disease). Electromyographic, anatomo-pathologic and clinical study in 3 brothers].
    De Freitas MR, Nascimento OJ.
    Arq Neuropsiquiatr; 1976 Mar; 34(1):81-8. PubMed ID: 1259636
    [Abstract] [Full Text] [Related]

  • 17. Infantile and juvenile spinal muscular atrophy.
    Hausmanowa-Petrusewicz I, Askanas W, Badurska B, Emeryk B, Fidziańska A, Garbalińska W, Hetnarska L, Kamieniecka Z, Prot J, Niebrój-Dobosz I, Jedrzejowska H, Sawicka E.
    J Neurol Sci; 1968 Mar; 6(2):269-87. PubMed ID: 5707429
    [No Abstract] [Full Text] [Related]

  • 18. [Type II proximal spinal muscular atrophy. Clinical, electrophysiological, histopathological and histochemical studies].
    Tangheroni W, Cao A, Cianchetti C, Calisti L.
    Minerva Pediatr; 1974 Jun 23; 26(22):1125-45. PubMed ID: 4276719
    [No Abstract] [Full Text] [Related]

  • 19. Werdnig-Hoffmann-Wohlfart-Kugelberg-Welander disease. Nosological unity and clinical variability in intrafamilial cases.
    Ghetti B, Amati A, Turra MV, Pacini A, Del Vecchio M, Guazzi GC.
    Acta Genet Med Gemellol (Roma); 1971 Jan 23; 20(1):43-58. PubMed ID: 5568110
    [No Abstract] [Full Text] [Related]

  • 20. Classification of spinal muscular atrophies.
    Pearn J.
    Lancet; 1980 Apr 26; 1(8174):919-22. PubMed ID: 6103267
    [Abstract] [Full Text] [Related]

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