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There are 25975 results for: content related to: Evidence-based path to newborn screening for duchenne muscular dystrophy

  1. Parental attitudes toward newborn screening for Duchenne/Becker muscular dystrophy and spinal muscular atrophy

    Muscle & Nerve

    Volume 49, Issue 6, June 2014, Pages: 822–828, Molly F. Wood, Sarah C. Hughes, Lauren P. Hache, Edwin W. Naylor, Hoda Z. Abdel-Hamid, M. Michael Barmada, Steven F. Dobrowolski, David E. Stickler and Paula R. Clemens

    Version of Record online : 17 MAY 2014, DOI: 10.1002/mus.24100

  2. Cystic fibrosis newborn screening: A model for neuromuscular disease screening?

    Annals of Neurology

    Volume 77, Issue 2, February 2015, Pages: 189–197, Michele A. Scully, Philip M. Farrell, Emma Ciafaloni, Robert C. Griggs and Jennifer M. Kwon

    Version of Record online : 13 DEC 2014, DOI: 10.1002/ana.24316

  3. Report of MDA muscle disease symposium on newborn screening for Duchenne muscular dystrophy

    Muscle & Nerve

    Volume 48, Issue 1, July 2013, Pages: 21–26, Jerry R. Mendell and Michele Lloyd-Puryear

    Version of Record online : 28 MAY 2013, DOI: 10.1002/mus.23810

  4. Screening for conditions that do not meet the Wilson and Jungner criteria: The case of Duchenne muscular dystrophy

    American Journal of Medical Genetics Part A

    Volume 140A, Issue 8, 15 April 2006, Pages: 914–922, Lainie Friedman Ross

    Version of Record online : 9 MAR 2006, DOI: 10.1002/ajmg.a.31165

  5. Twenty-year follow-up of newborn screening for patients with muscular dystrophy

    Muscle & Nerve

    Volume 53, Issue 4, April 2016, Pages: 570–578, Jeffrey Chung, Andrea L. Smith, Sarah C. Hughes, Gabriela Niizawa, Hoda Z. Abdel-Hamid, Edwin W. Naylor, Timothy Hughes and Paula R. Clemens

    Version of Record online : 10 SEP 2015, DOI: 10.1002/mus.24880

  6. Screening for duchenne muscular dystrophy: An improved screening test for creatine kinase and its application in an infant screening program

    Muscle & Nerve

    Volume 9, Issue 1, January 1986, Pages: 11–23, Dr. Günter Scheuerbrandt, Mr. Arne Lundin, Dr. Timo Lövgren and Dr. Wilhelm Mortier

    Version of Record online : 13 OCT 2004, DOI: 10.1002/mus.880090103

  7. Newborn screening for mucopolysaccharidoses: opinions of patients and their families

    Clinical Genetics

    Volume 71, Issue 5, May 2007, Pages: 446–450, IM Hayes, V Collins, M Sahhar, JE Wraith and MB Delatycki

    Version of Record online : 28 MAR 2007, DOI: 10.1111/j.1399-0004.2007.00783.x

  8. Attitudes of genetic counselors towards expanding newborn screening and offering predictive genetic testing to children

    American Journal of Medical Genetics Part A

    Volume 140A, Issue 21, 1 November 2006, Pages: 2312–2319, Susan Hiraki, Kelly E. Ormond, Katherine Kim and Lainie Friedman Ross

    Version of Record online : 11 OCT 2006, DOI: 10.1002/ajmg.a.31485

  9. Molecular Diagnosis of Duchenne Muscular Dystrophy

    Unit

    Current Protocols in Human Genetics

    9:9.25.1–9.25.29

    Babi Ramesh Reddy Nallamilli, Arunkanth Ankala and Madhuri Hegde

    Published Online : 1 OCT 2014, DOI: 10.1002/0471142905.hg0925s83

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    An improved algorithm for the shallow water equations model reduction: Dynamic Mode Decomposition vs POD

    International Journal for Numerical Methods in Fluids

    Volume 78, Issue 9, 30 July 2015, Pages: 552–580, D. A. Bistrian and I. M. Navon

    Version of Record online : 15 APR 2015, DOI: 10.1002/fld.4029

  11. Nanotherapy for Duchenne muscular dystrophy

    Wiley Interdisciplinary Reviews: Nanomedicine and Nanobiotechnology

    Michael E. Nance, Chady H. Hakim, N. Nora Yang and Dongsheng Duan

    Version of Record online : 11 APR 2017, DOI: 10.1002/wnan.1472

  12. You have full text access to this OnlineOpen article
    The TREAT-NMD DMD Global Database: Analysis of More than 7,000 Duchenne Muscular Dystrophy Mutations

    Human Mutation

    Volume 36, Issue 4, April 2015, Pages: 395–402, Catherine L. Bladen, David Salgado, Soledad Monges, Maria E. Foncuberta, Kyriaki Kekou, Konstantina Kosma, Hugh Dawkins, Leanne Lamont, Anna J. Roy, Teodora Chamova, Velina Guergueltcheva, Sophelia Chan, Lawrence Korngut, Craig Campbell, Yi Dai, Jen Wang, Nina Barišić, Petr Brabec, Jaana Lahdetie, Maggie C. Walter, Olivia Schreiber-Katz, Veronika Karcagi, Marta Garami, Venkatarman Viswanathan, Farhad Bayat, Filippo Buccella, En Kimura, Zaïda Koeks, Janneke C. van den Bergen, Miriam Rodrigues, Richard Roxburgh, Anna Lusakowska, Anna Kostera-Pruszczyk, Janusz Zimowski, Rosário Santos, Elena Neagu, Svetlana Artemieva, Vedrana Milic Rasic, Dina Vojinovic, Manuel Posada, Clemens Bloetzer, Pierre-Yves Jeannet, Franziska Joncourt, Jordi Díaz-Manera, Eduard Gallardo, A. Ayşe Karaduman, Haluk Topaloğlu, Rasha El Sherif, Angela Stringer, Andriy V. Shatillo, Ann S. Martin, Holly L. Peay, Matthew I. Bellgard, Jan Kirschner, Kevin M. Flanigan, Volker Straub, Kate Bushby, Jan Verschuuren, Annemieke Aartsma-Rus, Christophe Béroud and Hanns Lochmüller

    Version of Record online : 17 MAR 2015, DOI: 10.1002/humu.22758

  13. The TREAT-NMD Duchenne Muscular Dystrophy Registries: Conception, Design, and Utilization by Industry and Academia

    Human Mutation

    Volume 34, Issue 11, November 2013, Pages: 1449–1457, Catherine L. Bladen, Karen Rafferty, Volker Straub, Soledad Monges, Angélica Moresco, Hugh Dawkins, Anna Roy, Teodora Chamova, Velina Guergueltcheva, Lawrence Korngut, Craig Campbell, Yi Dai, Nina Barišić, Tea Kos, Petr Brabec, Jes Rahbek, Jaana Lahdetie, Sylvie Tuffery-Giraud, Mireille Claustres, France Leturcq, Rabah Ben Yaou, Maggie C. Walter, Olivia Schreiber, Veronika Karcagi, Agnes Herczegfalvi, Venkatarman Viswanathan, Farhad Bayat, Isis de la caridad Guerrero Sarmiento, Anna Ambrosini, Francesca Ceradini, En Kimura, Janneke C. van den Bergen, Miriam Rodrigues, Richard Roxburgh, Anna Lusakowska, Jorge Oliveira, Rosário Santos, Elena Neagu, Niculina Butoianu, Svetlana Artemieva, Vedrana Milic Rasic, Manuel Posada, Francesc Palau, Björn Lindvall, Clemens Bloetzer, Ayşe Karaduman, Haluk Topaloğlu, Serap Inal, Piraye Oflazer, Angela Stringer, Andriy V. Shatillo, Ann S. Martin, Holly Peay, Kevin M. Flanigan, David Salgado, Brigitta von Rekowski, Stephen Lynn, Emma Heslop, Sabina Gainotti, Domenica Taruscio, Jan Kirschner, Jan Verschuuren, Kate Bushby, Christophe Béroud and Hanns Lochmüller

    Version of Record online : 26 AUG 2013, DOI: 10.1002/humu.22390

  14. Dried blood spots: Concepts, present status, and future perspectives in bioanalysis

    Drug Testing and Analysis

    Volume 6, Issue 5, May 2014, Pages: 399–414, Abhisheak Sharma, Swati Jaiswal, Mahendra Shukla and Jawahar Lal

    Version of Record online : 1 APR 2014, DOI: 10.1002/dta.1646

  15. MLPA Application in Clinical Diagnosis of DMD/BMD in Shanghai

    Journal of Clinical Laboratory Analysis

    Volume 29, Issue 5, September 2015, Pages: 405–411, Xing Ji, Jingmin Zhang, Yan Xu, Fei Long, Wei Sun, Xiaoqin Liu, Yingwei Chen and Wenting Jiang

    Version of Record online : 17 AUG 2014, DOI: 10.1002/jcla.21787

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    Muscle and joint elastic properties during elbow flexion in Duchenne muscular dystrophy

    The Journal of Physiology

    Volume 533, Issue 2, June 2001, Pages: 605–616, Christophe Cornu, Francis Goubel and Michel Fardeau

    Version of Record online : 5 AUG 2004, DOI: 10.1111/j.1469-7793.2001.0605a.x

  17. Preimplantation genetic diagnosis (PGD) for Duchenne muscular dystrophy (DMD) by triplex-nested PCR

    Prenatal Diagnosis

    Volume 25, Issue 13, 30 December 2005, Pages: 1200–1205, Mira Malcov, Dalit Ben-Yosef, Tamar Schwartz, Nava Mey-Raz, Foad Azem, Joseph B. Lessing, Ami Amit and Yuval Yaron

    Version of Record online : 14 DEC 2005, DOI: 10.1002/pd.1317

  18. Rapid identification of female carriers of DMD/BMD by quantitative real-time PCR

    Human Mutation

    Volume 23, Issue 4, April 2004, Pages: 385–391, Franziska Joncourt, Barbara Neuhaus, Kristin Jostarndt-Foegen, Stephanie Kleinle, Bernhard Steiner and Sabina Gallati

    Version of Record online : 4 MAR 2004, DOI: 10.1002/humu.20007

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    Lunar regional dark mantle deposits: Geologic, multispectral, and modeling studies

    Journal of Geophysical Research: Planets (1991–2012)

    Volume 103, Issue E10, 25 September 1998, Pages: 22725–22759, Catherine M. Weitz, James W. Head III, Carle M. Pieters

    Version of Record online : 1 SEP 1998, DOI: 10.1029/98JE02027

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    Duchenne and Becker Muscular Dystrophy: From Gene Diagnosis to Molecular Therapy

    IUBMB Life

    Volume 53, Issue 3, March 2002, Pages: 147–152, Masafumi Matsuo

    Version of Record online : 3 JAN 2008, DOI: 10.1080/15216540212333