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

188 related items for PubMed ID: 2266988

  • 1. Schwartz-Jampel syndrome with dominant inheritance.
    Pascuzzi RM, Gratianne R, Azzarelli B, Kincaid JC.
    Muscle Nerve; 1990 Dec; 13(12):1152-63. PubMed ID: 2266988
    [Abstract] [Full Text] [Related]

  • 2. Schwartz-Jampel syndrome: I. Clinical, electromyographic, and histologic studies.
    Spaans F, Theunissen P, Reekers AD, Smit L, Veldman H.
    Muscle Nerve; 1990 Jun; 13(6):516-27. PubMed ID: 2366824
    [Abstract] [Full Text] [Related]

  • 3. [Schwartz-Jampel syndrome. Clinical and histopathological study of 4 cases].
    Ben Hamida M, Miladi N, Ben Hamida C.
    Rev Neurol (Paris); 1991 Jun; 147(4):279-84. PubMed ID: 2063077
    [Abstract] [Full Text] [Related]

  • 4. A case of Schwartz-Jampel syndrome with cleft palate.
    Abdel-Aziz M, Azab NA.
    Int J Pediatr Otorhinolaryngol; 2009 Nov; 73(11):1601-3. PubMed ID: 19733405
    [Abstract] [Full Text] [Related]

  • 5. [Value of muscle studies in the early diagnosis of Schwartz-Jampel syndrome].
    Vanlieferighen P, Francannet C, Dechelotte P, Malpuech G, de Laguillaumie B, Storme B.
    J Genet Hum; 1987 Aug; 35(4):243-9. PubMed ID: 3655749
    [Abstract] [Full Text] [Related]

  • 6. Schwartz-Jampel syndrome: an atypical form?
    Figuera LE, Jimenez-Gil FJ, García-Cruz MO, Cantú JM.
    Am J Med Genet; 1993 Sep 15; 47(4):526-8. PubMed ID: 8256816
    [Abstract] [Full Text] [Related]

  • 7. Electrophysiological studies in a mouse model of Schwartz-Jampel syndrome demonstrate muscle fiber hyperactivity of peripheral nerve origin.
    Echaniz-Laguna A, Rene F, Marcel C, Bangratz M, Fontaine B, Loeffler JP, Nicole S.
    Muscle Nerve; 2009 Jul 15; 40(1):55-61. PubMed ID: 19367640
    [Abstract] [Full Text] [Related]

  • 8. [Schwartz-Jampel syndrome (osteochondromuscular dystrophy)].
    Ben Becher S, el Mabrouk J, Debbiche A, Hammou A, Ghram N, Makni S, Boudhina T.
    Arch Fr Pediatr; 1992 Nov 15; 49(9):799-802. PubMed ID: 1300968
    [Abstract] [Full Text] [Related]

  • 9. Schwartz-Jampel syndrome: clinical, electromyographic and genetic studies.
    Ishpekova B, Rasheva M, Moskov M.
    Electromyogr Clin Neurophysiol; 1996 Mar 15; 36(2):91-7. PubMed ID: 8925786
    [Abstract] [Full Text] [Related]

  • 10. Schwartz-Jampel syndrome: clinical, electromyographic and genetic studies.
    Ishpekova B, Rasheva M, Moskov M.
    Electromyogr Clin Neurophysiol; 1996 Mar 15; 36(3):151-5. PubMed ID: 8737936
    [Abstract] [Full Text] [Related]

  • 11. Schwartz Jampel syndrome in children.
    Arya R, Sharma S, Gupta N, Kumar S, Kabra M, Gulati S.
    J Clin Neurosci; 2013 Feb 15; 20(2):313-7. PubMed ID: 23219824
    [Abstract] [Full Text] [Related]

  • 12. The effect of the Schwartz-Jampel syndrome on masticatory and facial musculatures--an electromyographic analysis.
    Regalo SC, Vitti M, Semprini M, de Mattos Mda G, Hallak JE, Brandão C, Serrano KV.
    Electromyogr Clin Neurophysiol; 2005 Feb 15; 45(3):183-9. PubMed ID: 15981691
    [Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. Schwartz-Jampel syndrome: three pediatric case reports.
    Yapicioğlu H, Satar M, Yildizdaş D, Narli N, Suleymanova D, Tutak E.
    Genet Couns; 2003 Feb 15; 14(3):353-8. PubMed ID: 14577682
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 20. Genetic heterogeneity in Schwartz-Jampel syndrome: two families with neonatal Schwartz-Jampel syndrome do not map to human chromosome 1p34-p36.1.
    Brown KA, al-Gazali LI, Moynihan LM, Lench NJ, Markham AF, Mueller RF.
    J Med Genet; 1997 Aug 15; 34(8):685-7. PubMed ID: 9279765
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 10.