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Journal Abstract Search

130 related items for PubMed ID: 844665

  • 21.
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  • 22. 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; 2(4):203-9. PubMed ID: 5146579
    [No Abstract] [Full Text] [Related]

  • 23. Electrophysiological findings in childhood spinal muscular atrophies.
    Hausmanowa-Petrusewicz I.
    Rev Neurol (Paris); 1988; 144(11):716-20. PubMed ID: 3231960
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  • 24. [Electroneurography or measurement of conduction velocity in peripheral nerves].
    Kaeser HE.
    Nervenarzt; 1972 Sep; 43(9):445-50. PubMed ID: 4561864
    [No Abstract] [Full Text] [Related]

  • 25. 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; 20(1):43-58. PubMed ID: 5568110
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  • 27. Abnormalities in sensory and mixed evoked potentials in ataxia-telangiectasia.
    Martínez AC, Barrio M, Gutierrez AM, López.
    J Neurol Neurosurg Psychiatry; 1977 Jan; 40(1):44-9. PubMed ID: 845606
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  • 34. [A case of Wohlfart-Kugelberg-Welander disease or hereditary familial spinal juvenile muscular atrophy].
    Manara F, Gasco P, Milani L.
    Minerva Med; 1977 Feb 04; 68(6):417-24. PubMed ID: 840437
    [No Abstract] [Full Text] [Related]

  • 35. Central vs peripheral nerve conduction. Before and after treatment of subacute combined degeneration.
    Tomoda H, Shibasaki H, Hirata I, Oda K.
    Arch Neurol; 1988 May 04; 45(5):526-9. PubMed ID: 3358705
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  • 36.
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  • 38. Abnormal nerve conduction velocity as a marker of immaturity in childhood muscle spinal atrophy.
    Krajewska G, Hausmanowa-Petrusewicz I.
    Folia Neuropathol; 2002 May 04; 40(2):67-74. PubMed ID: 12230258
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