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Journal Abstract Search

322 related items for PubMed ID: 13328196

  • 1. [Two cases of familial congenital muscular dystrophy simulating Werdnig-Hoffman-Oppenheim disease].
    LEVESQUE J, LEPAGE F, BOESWILLWALD M, GRUNER J.
    Arch Fr Pediatr; 1956; 13(2):202-7. PubMed ID: 13328196
    [No Abstract] [Full Text] [Related]

  • 2. Heredofamilial juvenile muscular atrophy simulating muscular dystrophy.
    KUGELBERG E, WELANDER L.
    AMA Arch Neurol Psychiatry; 1956 May; 75(5):500-9. PubMed ID: 13312732
    [No Abstract] [Full Text] [Related]

  • 3. [CASE OF MYELOPATHIC MUSCULAR ATROPHY THOUGHT AT FIRST TO BE PROGRESSIVE MUSCULAR DYSTROPHY--A VIEW OF THE RELATION BETWEEN KUGELBERG-WELANDER'S MUSCULAR ATROPHY AND WERDNIG-HOFFMANN DISEASE].
    FURUKAWA S, MAMIYA S.
    Nihon Shonika Gakkai Zasshi; 1963 Nov 01; 67():745-8. PubMed ID: 14096316
    [No Abstract] [Full Text] [Related]

  • 4. [Catamnestic inquiries in conditions of hypertonia in early childhood. With a critical contribution to the differential diagnosis of infantile spinal progressive muscular atrophy (Werdnig-Hoffman disease--myatonia congenital Oppenheilm)].
    HORSTMANN W.
    Z Kinderheilkd; 1959 Nov 01; 82():649-67. PubMed ID: 13848453
    [No Abstract] [Full Text] [Related]

  • 5. Limb-girdle muscular dystrophy or spinal muscular atrophy: a source of diagnostic confusion?
    Pogue R, Jackson T, Sayli B, Curtis A, Bushby KM.
    J Med Genet; 1997 Nov 01; 34(11):958-9. PubMed ID: 9391899
    [No Abstract] [Full Text] [Related]

  • 6. [Histopathology of precocious infantile myopathy].
    LEY RA.
    Schweiz Arch Neurol Psychiatr; 1954 Nov 01; 73(1-2):490-2. PubMed ID: 13195597
    [No Abstract] [Full Text] [Related]

  • 7. Infantile progressive muscular atrophy; value of muscle biopsy in the diagnosis of and its differentiation from muscular dystrophy.
    ROSENBERG HS, McADAMS AJ.
    AMA Arch Pathol; 1954 Dec 01; 58(6):604-12. PubMed ID: 13217576
    [No Abstract] [Full Text] [Related]

  • 8. [Infantile spinal muscular atrophy. Description of 2 cases of Werdnig-Hoffmann disease].
    Priora U, Quaglia P, Vivalda M, Giachino-Amistà MT, Domeneghetti G, Sardi R.
    Minerva Pediatr; 1987 Sep 30; 39(17-18):709-14. PubMed ID: 3437861
    [No Abstract] [Full Text] [Related]

  • 9. Differentiation of Becker muscular dystrophy from limb-girdle muscular dystrophy and Kugelberg-Welander disease using a cDNA probe.
    Laing NG, Mears ME, Thomas HE, Chandler DC, Layton MG, Goldblatt J, Kakulas BA.
    Med J Aust; 1990 Mar 05; 152(5):270-1. PubMed ID: 2255288
    [Abstract] [Full Text] [Related]

  • 10. Chronic spinal muscular atrophy simulating facioscapulohumeral type and limb-girdle type of muscular dystrophy. Report of two cases.
    Kazakov VM, Kovalenko TM, Skorometz AA, Mikhailov EP.
    Eur Neurol; 1977 Mar 05; 16(1-6):90-8. PubMed ID: 615721
    [Abstract] [Full Text] [Related]

  • 11. [On the problem of spinal muscular atrophy resembling progressive muscular dystrophy (Kugelberg-Welander's juvenile muscular atrophy)].
    GOLDSZTAJN M, ZEBROWSKI S.
    Neurol Neurochir Psychiatr Pol; 1962 Mar 05; 12():669-73. PubMed ID: 13948828
    [No Abstract] [Full Text] [Related]

  • 12. Learning disabilities in neuromuscular disorders: a springboard for adult life.
    Astrea G, Battini R, Lenzi S, Frosini S, Bonetti S, Moretti E, Perazza S, Santorelli FM, Pecini C.
    Acta Myol; 2016 Oct 05; 35(2):90-95. PubMed ID: 28344438
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  • 20. Spinal muscular atrophy with respiratory distress type 1 (SMARD1).
    Kaindl AM, Guenther UP, Rudnik-Schöneborn S, Varon R, Zerres K, Schuelke M, Hübner C, von Au K.
    J Child Neurol; 2008 Feb 05; 23(2):199-204. PubMed ID: 18263757
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