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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

147 related items for PubMed ID: 16198106

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  • 5. Novel truncating RAPSN mutations causing congenital myasthenic syndrome responsive to 3,4-diaminopyridine.
    Banwell BL, Ohno K, Sieb JP, Engel AG.
    Neuromuscul Disord; 2004 Mar; 14(3):202-7. PubMed ID: 15036330
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  • 9. Novel delta subunit mutation in slow-channel syndrome causes severe weakness by novel mechanisms.
    Gomez CM, Maselli RA, Vohra BP, Navedo M, Stiles JR, Charnet P, Schott K, Rojas L, Keesey J, Verity A, Wollmann RW, Lasalde-Dominicci J.
    Ann Neurol; 2002 Jan; 51(1):102-12. PubMed ID: 11782989
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  • 17. End-plate gamma- and epsilon-subunit mRNA levels in AChR deficiency syndrome due to epsilon-subunit null mutations.
    Croxen R, Young C, Slater C, Haslam S, Brydson M, Vincent A, Beeson D.
    Brain; 2001 Jul; 124(Pt 7):1362-72. PubMed ID: 11408331
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