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Journal Abstract Search

387 related items for PubMed ID: 7180679

  • 41. Juvenile spinal muscular atrophy--a new hexosaminidase deficiency phenotype.
    Johnson WG, Wigger HJ, Karp HR, Glaubiger LM, Rowland LP.
    Trans Am Neurol Assoc; 1981; 106():215-8. PubMed ID: 7348998
    [No Abstract] [Full Text] [Related]

  • 42. [Werdnig-Hoffmann spinal amyotrophy in twins].
    Mazaeva IV, Lipovetskaia NG, Balashova EG.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1973; 73(10):1491-5. PubMed ID: 4795172
    [No Abstract] [Full Text] [Related]

  • 43. The application of the nearest neighbor decision rule in the evaluation of electromyogram in spinal muscular atrophy (SMA) of childhood.
    Hausmanowa-Petrusewicz I, Jóźwik A.
    Electromyogr Clin Neurophysiol; 1986 Dec; 26(8):689-703. PubMed ID: 3830048
    [No Abstract] [Full Text] [Related]

  • 44. Electromyography in patients with lesions of the central motor neuron and the so-called parietal muscular atrophy.
    Notermans SL, Blokzijl EJ.
    Psychiatr Neurol Neurochir; 1969 Dec; 72(6):557-67. PubMed ID: 5369244
    [No Abstract] [Full Text] [Related]

  • 45. [XO-XY-sex-chromosomes-mosaicism in a child with progressive spinal muscular atrophy (author's transl)].
    Kunze J, Tolksdorf M.
    Z Kinderheilkd; 1973 Nov 19; 115(4):283-94. PubMed ID: 4778568
    [No Abstract] [Full Text] [Related]

  • 46. [Pseudomyopathical forms of spinal amyotrophy (Kugelberg-Welander disease)].
    Il'ina NA, Ivanchenko OV, Potomskaia LZ.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1971 Nov 19; 71(8):1139-44. PubMed ID: 5136816
    [No Abstract] [Full Text] [Related]

  • 47. [Mental development of children with the Duchenne type of progressive muscular dystrophy].
    Kozicka A.
    Neurol Neurochir Pol; 1971 Nov 19; 5(4):523-8. PubMed ID: 5122056
    [No Abstract] [Full Text] [Related]

  • 48. Abnormalities of the electrocardiogram in hereditary myopathies.
    Emery AE.
    J Med Genet; 1972 Mar 19; 9(1):8-12. PubMed ID: 5025488
    [No Abstract] [Full Text] [Related]

  • 49. Spinal muscular atrophy in childhood: review of 50 cases.
    Benady SG.
    Dev Med Child Neurol; 1978 Dec 19; 20(6):746-57. PubMed ID: 729928
    [Abstract] [Full Text] [Related]

  • 50. [Current views on the diagnosis, etiology and genetics of the most frequent non-metabolic congenital myopathies].
    Herrmann V.
    Padiatr Grenzgeb; 1983 Dec 19; 22(1):27-45. PubMed ID: 6866527
    [No Abstract] [Full Text] [Related]

  • 51. [Evoked potentials of the somatosensory system in patients with progressive muscular dystrophies].
    Avakian GN.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1983 Dec 19; 83(11):1628-32. PubMed ID: 6675359
    [Abstract] [Full Text] [Related]

  • 52. [Differential diagnosis of hereditary spastic spinal paralysis. Simultaneously a report on genetically independent type of recessive hereditary infantile spastic spinal paralysis].
    Malin JP.
    Nervenarzt; 1976 Nov 19; 47(11):661-8. PubMed ID: 1004664
    [No Abstract] [Full Text] [Related]

  • 53. Muscular dystrophy.
    Brown JC.
    Practitioner; 1982 Jun 19; 226(1368):1031-6. PubMed ID: 7111135
    [No Abstract] [Full Text] [Related]

  • 54. [Clinical-genetic classification of muscular dystrophies].
    López de Munain A, Andoni Urtizberea J.
    Med Clin (Barc); 1998 Sep 05; 111(6):226-35. PubMed ID: 9789230
    [No Abstract] [Full Text] [Related]

  • 55. [Haptoglobins in muscular diseases].
    Rosnowska M, Strugalska H.
    Neurol Neurochir Pol; 1970 Sep 05; 4(6):655-60. PubMed ID: 5487716
    [No Abstract] [Full Text] [Related]

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  • 58. The Kugelberg Welandar syndrome.
    Wadia RS, Hansotia PL, Irani P.
    J Assoc Physicians India; 1971 Sep 05; 19(9):667-70. PubMed ID: 5162134
    [No Abstract] [Full Text] [Related]

  • 59.
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  • 60. [Serum enzymes in muscular diseases].
    Laudahn G, Heyck H, Feustel F.
    Curr Probl Clin Biochem; 1968 Sep 05; 1():249-317. PubMed ID: 4950596
    [No Abstract] [Full Text] [Related]

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