Search Results - Duygu Selcen

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  1. 1
    Myofibrillar myopathy: clinical, morphological and genetic studies in 63 patients

    Myofibrillar myopathy: clinical, morphological and genetic studies in 63 patients by Duygu Selcen

    Published 2004
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  2. 2
    Myofibrillar myopathies

    Myofibrillar myopathies by Duygu Selcen

    Published 2011
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  3. 3
    Myofibrillar myopathies

    Myofibrillar myopathies by Duygu Selcen

    Published 2008
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  4. 4
    Beneficial effects of albuterol in congenital endplate acetylcholinesterase deficiency and Dok‐7 myasthenia

    Beneficial effects of albuterol in congenital endplate acetylcholinesterase deficiency and Dok‐7 myasthenia by Teerin Liewluck, Duygu Selcen, Andrew G. Engel

    Published 2011
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  5. 5
    Microvascular alterations and the role of complement in dermatomyositis

    Microvascular alterations and the role of complement in dermatomyositis by Rajat Lahoria, Duygu Selcen, Andrew G. Engel

    Published 2016
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  6. 6
    Reducing bodies and myofibrillar myopathy features in FHL1 muscular dystrophy

    Reducing bodies and myofibrillar myopathy features in FHL1 muscular dystrophy by Duygu Selcen, Mark B. Bromberg, Steven S. Chin, Andrew G. Engel

    Published 2011
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  7. 7
    Mutant SNAP25B causes myasthenia, cortical hyperexcitability, ataxia, and intellectual disability

    Mutant SNAP25B causes myasthenia, cortical hyperexcitability, ataxia, and intellectual disability by Xin‐Ming Shen, Duygu Selcen, Joan M. Brengman, Andrew G. Engel

    Published 2014
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  8. 8
    Congenital myasthenic syndromes: pathogenesis, diagnosis, and treatment

    Congenital myasthenic syndromes: pathogenesis, diagnosis, and treatment by Andrew G. Engel, Xin‐Ming Shen, Duygu Selcen, Steven M. Sine

    Published 2015
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  9. 9
    What Have We Learned from the Congenital Myasthenic Syndromes

    What Have We Learned from the Congenital Myasthenic Syndromes by Andrew G. Engel, Xin‐Ming Shen, Duygu Selcen, Steven M. Sine

    Published 2009
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  10. 10
    Clinical and Pathologic Features of Congenital Myasthenic Syndromes Caused by 35 Genes—A Comprehensive Review

    Clinical and Pathologic Features of Congenital Myasthenic Syndromes Caused by 35 Genes—A Comprehensive Review by Kinji Ohno, Bisei Ohkawara, Xin‐Ming Shen, Duygu Selcen, Andrew G. Engel

    Published 2023
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  11. 11
    Loss of MUNC13-1 function causes microcephaly, cortical hyperexcitability, and fatal myasthenia

    Loss of MUNC13-1 function causes microcephaly, cortical hyperexcitability, and fatal myasthenia by Andrew G. Engel, Duygu Selcen, Xin‐Ming Shen, Margherita Milone, C. Michel Harper

    Published 2016
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  12. 12
    Congenital myasthenic syndromes in adult neurology clinic

    Congenital myasthenic syndromes in adult neurology clinic by Justin Kao, Margherita Milone, Duygu Selcen, Xin‐Ming Shen, Andrew G. Engel, Teerin Liewluck

    Published 2018
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  13. 13
    Impaired Synaptic Development, Maintenance, and Neuromuscular Transmission in LRP4-Related Myasthenia

    Impaired Synaptic Development, Maintenance, and Neuromuscular Transmission in LRP4-Related Myasthenia by Duygu Selcen, Bisei Ohkawara, Xin‐Ming Shen, Kathleen M. McEvoy, Kinji Ohno, Andrew G. Engel

    Published 2015
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  14. 14
    Mutation in <i>BAG3</i> causes severe dominant childhood muscular dystrophy

    Mutation in <i>BAG3</i> causes severe dominant childhood muscular dystrophy by Duygu Selcen, Francesco Muntoni, Barbara K. Burton, Elena Pegoraro, Caroline A. Sewry, Anna V. Bite, Andrew G. Engel

    Published 2008
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  15. 15
    PREPL deficiency with or without cystinuria causes a novel myasthenic syndrome

    PREPL deficiency with or without cystinuria causes a novel myasthenic syndrome by Luc Régal, Xin‐Ming Shen, Duygu Selcen, Chantal Verhille, Sandra Meulemans, John W.M. Creemers, Andrew G. Engel

    Published 2014
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  16. 16
    DPAGT1 myasthenia and myopathy

    DPAGT1 myasthenia and myopathy by Duygu Selcen, Xin‐Ming Shen, Joan M. Brengman, Ying Li, Anthony A. Stans, Eric D. Wieben, Andrew G. Engel

    Published 2014
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  17. 17
    Infantile muscular dystrophy in Canadian aboriginals is an αB‐crystallinopathy

    Infantile muscular dystrophy in Canadian aboriginals is an αB‐crystallinopathy by Marc R. Del Bigio, Albert E. Chudley, Harvey B. Sarnat, Craig Campbell, Sharan Goobie, Bernard N. Chodirker, Duygu Selcen

    Published 2010
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  18. 18
    Dok‐7 myasthenia: Phenotypic and molecular genetic studies in 16 patients

    Dok‐7 myasthenia: Phenotypic and molecular genetic studies in 16 patients by Duygu Selcen, Margherita Milone, Xin‐Ming Shen, C. Michel Harper, Anthony A. Stans, Eric D. Wieben, Andrew G. Engel

    Published 2008
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  19. 19
    Myasthenic syndrome due to defects in rapsyn

    Myasthenic syndrome due to defects in rapsyn by Margherita Milone, Xin‐Ming Shen, Duygu Selcen, Kinji Ohno, Joan M. Brengman, Susan T. Iannaccone, Charles M. Harper, Andrew G. Engel

    Published 2009
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  20. 20
    Rapsyn Mutations in Humans Cause Endplate Acetylcholine-Receptor Deficiency and Myasthenic Syndrome

    Rapsyn Mutations in Humans Cause Endplate Acetylcholine-Receptor Deficiency and Myasthenic Syndrome by Kinji Ohno, Andrew G. Engel, Xin‐Ming Shen, Duygu Selcen, Joan M. Brengman, C. Michel Harper, Akira Tsujino, Margherita Milone

    Published 2002
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