检索结果 - Duygu Selcen

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

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

    出版 2004
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  2. 2
    Myofibrillar myopathies

    Myofibrillar myopathies 由 Duygu Selcen

    出版 2011
    获取全文
    Revisão
    加到收藏夹
    Saved in:
  3. 3
    Myofibrillar myopathies

    Myofibrillar myopathies 由 Duygu Selcen

    出版 2008
    获取全文
    Revisão
    加到收藏夹
    Saved in:
  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 由 Teerin Liewluck, Duygu Selcen, Andrew G. Engel

    出版 2011
    获取全文
    Artigo
    加到收藏夹
    Saved in:
  5. 5
    Microvascular alterations and the role of complement in dermatomyositis

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

    出版 2016
    获取全文
    Artigo
    加到收藏夹
    Saved in:
  6. 6
    Reducing bodies and myofibrillar myopathy features in FHL1 muscular dystrophy

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

    出版 2011
    获取全文
    Artigo
    加到收藏夹
    Saved in:
  7. 7
    Mutant SNAP25B causes myasthenia, cortical hyperexcitability, ataxia, and intellectual disability

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

    出版 2014
    获取全文
    Artigo
    加到收藏夹
    Saved in:
  8. 8
    Congenital myasthenic syndromes: pathogenesis, diagnosis, and treatment

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

    出版 2015
    获取全文
    Revisão
    加到收藏夹
    Saved in:
  9. 9
    What Have We Learned from the Congenital Myasthenic Syndromes

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

    出版 2009
    获取全文
    Revisão
    加到收藏夹
    Saved in:
  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 由 Kinji Ohno, Bisei Ohkawara, Xin‐Ming Shen, Duygu Selcen, Andrew G. Engel

    出版 2023
    获取全文 获取全文
    Revisão
    加到收藏夹
    Saved in:
  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 由 Andrew G. Engel, Duygu Selcen, Xin‐Ming Shen, Margherita Milone, C. Michel Harper

    出版 2016
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  12. 12
    Congenital myasthenic syndromes in adult neurology clinic

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

    出版 2018
    获取全文
    Artigo
    加到收藏夹
    Saved in:
  13. 13
    Impaired Synaptic Development, Maintenance, and Neuromuscular Transmission in LRP4-Related Myasthenia

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

    出版 2015
    获取全文
    Artigo
    加到收藏夹
    Saved in:
  14. 14
    Mutation in <i>BAG3</i> causes severe dominant childhood muscular dystrophy

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

    出版 2008
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  15. 15
    PREPL deficiency with or without cystinuria causes a novel myasthenic syndrome

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

    出版 2014
    获取全文
    Artigo
    加到收藏夹
    Saved in:
  16. 16
    DPAGT1 myasthenia and myopathy

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

    出版 2014
    获取全文
    Artigo
    加到收藏夹
    Saved in:
  17. 17
    Infantile muscular dystrophy in Canadian aboriginals is an αB‐crystallinopathy

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

    出版 2010
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  18. 18
    Dok‐7 myasthenia: Phenotypic and molecular genetic studies in 16 patients

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

    出版 2008
    获取全文
    Artigo
    加到收藏夹
    Saved in:
  19. 19
    Myasthenic syndrome due to defects in rapsyn

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

    出版 2009
    获取全文
    Artigo
    加到收藏夹
    Saved in:
  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 由 Kinji Ohno, Andrew G. Engel, Xin‐Ming Shen, Duygu Selcen, Joan M. Brengman, C. Michel Harper, Akira Tsujino, Margherita Milone

    出版 2002
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:

检索工具: