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

174 related items for PubMed ID: 9674906

  • 41.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 42. The Schwartz-Jampel syndrome.
    al Gazali LI.
    Clin Dysmorphol; 1993 Jan; 2(1):47-54. PubMed ID: 8298738
    [Abstract] [Full Text] [Related]

  • 43.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 44.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 45.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 46. Congenital bowing of the long bones in two fetuses presenting features of Stüve-Wiedemann syndrome and Schwartz-Jampel syndrome type 2.
    Sigaudy S, Moncla A, Fredouille C, Bourlière B, Lambert JC, Philip N.
    Clin Dysmorphol; 1998 Oct; 7(4):257-62. PubMed ID: 9823491
    [Abstract] [Full Text] [Related]

  • 47.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 48.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 49. Spondylo-epi-metaphyseal dysplasia with myotonia. A radiographic study. (Catel-Hempel syndrome, Schwarz-Jampel syndrome, Aberfeld syndrome, chondrodystrophic myotonia).
    Kozlowski K, Wise G.
    Radiol Diagn (Berl); 1974 Oct; 15(6):817-24. PubMed ID: 4464536
    [No Abstract] [Full Text] [Related]

  • 50.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 51.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 52.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 53. Schwartz-Jampel syndrome and perlecan deficiency.
    Stum M, Davoine CS, Fontaine B, Nicole S.
    Acta Myol; 2005 Oct; 24(2):89-92. PubMed ID: 16550923
    [Abstract] [Full Text] [Related]

  • 54. Clinico-pathogenetic findings and management of chondrodystrophic myotonia (Schwartz-Jampel syndrome): a case report.
    Ho NC, Sandusky S, Madike V, Francomano CA, Dalakas MC.
    BMC Neurol; 2003 Jul 02; 3():3. PubMed ID: 12839625
    [Abstract] [Full Text] [Related]

  • 55.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 56. Stüve-Wiedemann syndrome: recurrent neonatal infections caused by impairment of JAK/STAT 3 pathway.
    Van De Maele K, Smulders C, Ecury-Goossen G, Rosina-Angelista I, Redeker E, van Haelst M.
    Clin Dysmorphol; 2019 Apr 02; 28(2):57-62. PubMed ID: 30614825
    [Abstract] [Full Text] [Related]

  • 57.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 58.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 59.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 60. Neonatal diagnosis of Schwartz-Jampel syndrome with dramatic response to carbamazepine.
    Squires LA, Prangley J.
    Pediatr Neurol; 1996 Sep 02; 15(2):172-4. PubMed ID: 8888056
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 9.