Rezultati - 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 od Duygu Selcen

    Izdano 2004
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  2. 2
    Myofibrillar myopathies

    Myofibrillar myopathies od Duygu Selcen

    Izdano 2011
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  3. 3
    Myofibrillar myopathies

    Myofibrillar myopathies od Duygu Selcen

    Izdano 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 od Teerin Liewluck, Duygu Selcen, Andrew G. Engel

    Izdano 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 od Rajat Lahoria, Duygu Selcen, Andrew G. Engel

    Izdano 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 od Duygu Selcen, Mark B. Bromberg, Steven S. Chin, Andrew G. Engel

    Izdano 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 od Xin‐Ming Shen, Duygu Selcen, Joan M. Brengman, Andrew G. Engel

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

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

    Izdano 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 od Andrew G. Engel, Xin‐Ming Shen, Duygu Selcen, Steven M. Sine

    Izdano 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 od Kinji Ohno, Bisei Ohkawara, Xin‐Ming Shen, Duygu Selcen, Andrew G. Engel

    Izdano 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 od Andrew G. Engel, Duygu Selcen, Xin‐Ming Shen, Margherita Milone, C. Michel Harper

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

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

    Izdano 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 od Duygu Selcen, Bisei Ohkawara, Xin‐Ming Shen, Kathleen M. McEvoy, Kinji Ohno, Andrew G. Engel

    Izdano 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 od Duygu Selcen, Francesco Muntoni, Barbara K. Burton, Elena Pegoraro, Caroline A. Sewry, Anna V. Bite, Andrew G. Engel

    Izdano 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 od Luc Régal, Xin‐Ming Shen, Duygu Selcen, Chantal Verhille, Sandra Meulemans, John W.M. Creemers, Andrew G. Engel

    Izdano 2014
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  16. 16
    DPAGT1 myasthenia and myopathy

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

    Izdano 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 od Marc R. Del Bigio, Albert E. Chudley, Harvey B. Sarnat, Craig Campbell, Sharan Goobie, Bernard N. Chodirker, Duygu Selcen

    Izdano 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 od Duygu Selcen, Margherita Milone, Xin‐Ming Shen, C. Michel Harper, Anthony A. Stans, Eric D. Wieben, Andrew G. Engel

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

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

    Izdano 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 od Kinji Ohno, Andrew G. Engel, Xin‐Ming Shen, Duygu Selcen, Joan M. Brengman, C. Michel Harper, Akira Tsujino, Margherita Milone

    Izdano 2002
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