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

661 related items for PubMed ID: 11930270

  • 1. Selective muscle involvement on magnetic resonance imaging in autosomal dominant Emery-Dreifuss muscular dystrophy.
    Mercuri E, Counsell S, Allsop J, Jungbluth H, Kinali M, Bonne G, Schwartz K, Bydder G, Dubowitz V, Muntoni F.
    Neuropediatrics; 2002 Feb; 33(1):10-4. PubMed ID: 11930270
    [Abstract] [Full Text] [Related]

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

  • 3. Emery dreifuss muscular dystrophy: a clinico-pathological study.
    Gayathri N, Taly AB, Sinha S, Suresh TG, Gorai D.
    Neurol India; 2006 Jun; 54(2):197-9. PubMed ID: 16804269
    [Abstract] [Full Text] [Related]

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

  • 5.
    ; . PubMed ID:
    [No 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.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. Expression of emerin and lamins in muscle of patients with different forms of Emery-Dreifuss muscular dystrophy.
    Niebroj-Dobosz I, Fidzianska A, Hausmanowa-Petrusewicz I.
    Acta Myol; 2003 Sep; 22(2):52-7. PubMed ID: 14959564
    [Abstract] [Full Text] [Related]

  • 11. X-linked Emery-Dreifuss muscular dystrophy and vacuoles: an immunohistochemical characterization.
    Paradas C, Márquez C, Gallardo E, De Luna N, Chinchón I, Recan D, Jiménez MD, Illa I.
    Muscle Nerve; 2005 Jul; 32(1):61-5. PubMed ID: 15880484
    [Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. Early onset of X-linked Emery-Dreifuss muscular dystrophy in a boy with emerin gene deletion.
    Fujimoto S, Ishikawa T, Saito M, Wada Y, Wada I, Arahata K, Nonaka I.
    Neuropediatrics; 1999 Jun; 30(3):161-3. PubMed ID: 10480214
    [Abstract] [Full Text] [Related]

  • 14. Lamin A/C assembly defects in Emery-Dreifuss muscular dystrophy can be regulated by culture medium composition.
    Holt I, Nguyen TM, Wehnert M, Morris GE.
    Neuromuscul Disord; 2006 Jun; 16(6):368-73. PubMed ID: 16697197
    [Abstract] [Full Text] [Related]

  • 15. How does a g993t mutation in the emerin gene cause Emery-Dreifuss muscular dystrophy?
    Holt I, Clements L, Manilal S, Morris GE.
    Biochem Biophys Res Commun; 2001 Oct 12; 287(5):1129-33. PubMed ID: 11587540
    [Abstract] [Full Text] [Related]

  • 16. Deletion of the LMNA initiator codon leading to a neurogenic variant of autosomal dominant Emery-Dreifuss muscular dystrophy.
    Walter MC, Witt TN, Weigel BS, Reilich P, Richard P, Pongratz D, Bonne G, Wehnert MS, Lochmüller H.
    Neuromuscul Disord; 2005 Jan 12; 15(1):40-4. PubMed ID: 15639119
    [Abstract] [Full Text] [Related]

  • 17. Disease severity in dominant Emery Dreifuss is increased by mutations in both emerin and desmin proteins.
    Muntoni F, Bonne G, Goldfarb LG, Mercuri E, Piercy RJ, Burke M, Yaou RB, Richard P, Récan D, Shatunov A, Sewry CA, Brown SC.
    Brain; 2006 May 12; 129(Pt 5):1260-8. PubMed ID: 16585054
    [Abstract] [Full Text] [Related]

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

  • 19. Does satellite cell dysfunction contribute to disease progression in Emery-Dreifuss muscular dystrophy?
    Gnocchi VF, Ellis JA, Zammit PS.
    Biochem Soc Trans; 2008 Dec 12; 36(Pt 6):1344-9. PubMed ID: 19021553
    [Abstract] [Full Text] [Related]

  • 20. [Hauptmann-Thannhauser muscular dystrophy and differential diagnosis of myopathies associated with contractures].
    Hanisch F, Neudecker S, Wehnert M, Zierz S.
    Nervenarzt; 2002 Oct 12; 73(10):1004-11. PubMed ID: 12376891
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 34.