These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

229 related items for PubMed ID: 13897523

  • 1. [On the morphology, nosological position and pathogenesis of Oppenheim's myotonia congenita and Werdnig-Hoffmann's infantile spinal progressive muscular atrophy].
    GEILER G, GEILER G.
    Virchows Arch Pathol Anat Physiol Klin Med; 1962; 335():654-67. PubMed ID: 13897523
    [No Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3. [A newborn child with Werdnig-Hoffmann's disease (infantile spinal muscular atrophy)].
    WILLEMSE J.
    Ned Tijdschr Geneeskd; 1961 Feb 04; 105():243-5. PubMed ID: 13785363
    [No Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5. [Two cases of a proximal spinal muscular atrophy (Werdnig-Hoffmann's disease) in one family].
    Nurbekova UA.
    Zh Nevrol Psikhiatr Im S S Korsakova; 2014 Feb 04; 114(10):106-7. PubMed ID: 25591528
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. [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]

  • 10. Infantile spinal muscular atrophy (morbus Werdnig-Hoffmann) causing neonatal asphyxia.
    Kyllerman M.
    Neuropadiatrie; 1977 Feb 30; 8(1):53-6. PubMed ID: 576732
    [Abstract] [Full Text] [Related]

  • 11. [Familial case of myotonia with muscular hypertrophy, weakness corrected by effort and atrophy of type II fibers].
    Pépin B, Haguenau M, Mikol J.
    Rev Neurol (Paris); 1975 Apr 30; 131(4):285-92. PubMed ID: 1224112
    [Abstract] [Full Text] [Related]

  • 12. Amyotonia congenita (Oppenheim's disease).
    CUNNINGHAM JA.
    South Med J; 1946 Mar 30; 39():222-9. PubMed ID: 21014949
    [No Abstract] [Full Text] [Related]

  • 13. [Myatonia congenita Oppenheim, with special reference to its relation to Werdnig-Hoffmann disease].
    FUKUYAMA Y.
    Sogo Igaku; 1961 Oct 30; 18():671-82. PubMed ID: 13895848
    [No Abstract] [Full Text] [Related]

  • 14. [Infantile spinal amyotrophy with myotonia. Electromyographic study].
    Renault F.
    Neurophysiol Clin; 1989 May 30; 19(2):155-61. PubMed ID: 2725454
    [Abstract] [Full Text] [Related]

  • 15. Hereditary factors in infantile progressive muscular atrophy; study of 112 cases in 70 families.
    BRANDT S.
    Am J Dis Child (1911); 1949 Aug 30; 78(2):226-36. PubMed ID: 18135521
    [No Abstract] [Full Text] [Related]

  • 16. [Clinical picture, pathogenesis and geneology of hereditary progressive spinal muscular atrophies].
    Nesterov LN, Sushcheva GP, Viatkina SIa, Novikova NP.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1984 Aug 30; 84(3):321-30. PubMed ID: 6326437
    [Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. [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 Aug 30; 12():669-73. PubMed ID: 13948828
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 12.