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Developmental Medicine & Child Neurology, ISSN 0012-1622, 07/2016, Volume 58, Issue 7, pp. 652 - 652
This commentary is on the original article by Johnson et al. on pages 698–705 of this issue. 
PEDIATRICS | CLINICAL NEUROLOGY | Humans | Myotonic Dystrophy
Journal Article
Neuropediatrics, ISSN 0174-304X, 08/2014, Volume 45, Issue 4, pp. 265 - 265
Journal Article
Neuropediatrics, ISSN 0174-304X, 06/2014, Volume 45, Issue 3, pp. 200 - 200
Journal Article
European Journal of Paediatric Neurology, ISSN 1090-3798, 09/2017, Volume 21, Issue 5, pp. 697 - 698
Journal Article
Lancet, The, ISSN 0140-6736, 2015, Volume 385, Issue 9979, pp. 1748 - 1757
Journal Article
InFo Neurologie & Psychiatrie, ISSN 1437-062X, 08/2018, Volume 20, Issue 7-8, pp. 12 - 13
Journal Article
Journal Article
Neuropediatrics, ISSN 0174-304X, 08/2018, Volume 49, Issue 4, pp. 299 - 300
Journal Article
by McDonald, Craig M and Campbell, Craig and Torricelli, Ricardo Erazo and Finkel, Richard S and Flanigan, Kevin M and Goemans, Nathalie and Heydemann, Peter and Kaminska, Anna and Kirschner, Janbernd and Muntoni, Francesco and Osorio, Andrés Nascimento and Schara, Ulrike and Sejersen, Thomas and Shieh, Perry B and Sweeney, H Lee and Topaloglu, Haluk and Tulinius, Már and Vilchez, Juan J and Voit, Thomas and Wong, Brenda and Elfring, Gary and Kroger, Hans and Luo, Xiaohui and McIntosh, Joseph and Ong, Tuyen and Riebling, Peter and Souza, Marcio and Spiegel, Robert J and Peltz, Stuart W and Mercuri, Eugenio and Alfano, Lindsay N and Eagle, Michelle and James, Meredith K and Lowes, Linda and Mayhew, Anna and Mazzone, Elena S and Nelson, Leslie and Rose, Kristy J and Abdel-Hamid, Hoda Z and Apkon, Susan D and Barohn, Richard J and Bertini, Enrico and Bloetzer, Clemens and de Vaud, Lausanne Canton and Butterfield, Russell J and Chabrol, Brigitte and Chae, Jong-Hee and Jongno-gu, Daehak-ro and Comi, Giacomi Pietro and Darras, Basil T and Dastgir, Jahannaz and Desguerre, Isabelle and Escobar, Raul G and Finanger, Erika and Guglieri, Michela and Hughes, Imelda and Iannaccone, Susan T and Jones, Kristi J and Karachunski, Peter and Kudr, Martin and Lotze, Timothy and Mah, Jean K and Mathews, Katherine and Nevo, Yoram and Parsons, Julie and Péréon, Yann and de Queiroz Campos Araujo, Alexandra Prufer and Renfroe, J Ben and de Resende, Maria Bernadete Dutra and Ryan, Monique and Selby, Kathryn and Tennekoon, Gihan and Vita, Giuseppe and Clinical Evaluator Training Grp and ACT DMD Study Grp and Clinical Evaluator Training Group and ACT DMD Study Group
The Lancet, ISSN 0140-6736, 09/2017, Volume 390, Issue 10101, pp. 1489 - 1498
Duchenne muscular dystrophy (DMD) is a severe, progressive, and rare neuromuscular, X-linked recessive disease. Dystrophin deficiency is the underlying cause... 
MEDICINE, GENERAL & INTERNAL | END-POINTS | RELIABILITY | STAR AMBULATORY ASSESSMENT | 6-MINUTE WALK TEST | VALIDITY | Clinical trials | Care and treatment | Genetic aspects | Dystrophin | Duchenne muscular dystrophy | Analysis | Muscular dystrophy | Proteins | Neuromuscular diseases | Nonsense mutation | Duchenne's muscular dystrophy | Dystrophy | Mutation | Drug therapy | Patients
Journal Article
Padiatrische Praxis, ISSN 0030-9346, 05/2013, Volume 80, Issue 3, pp. 447 - 460
Journal Article
Aktuelle Neurologie, ISSN 0302-4350, 05/2018, Volume 45, Issue 4, pp. 283 - 287
Journal Article
2015, ISBN 9783662442395
Angeborene Muskelerkrankungen gehören zu den „Orphan Diseases“, die von der Pädiatrie zunehmend in die Erwachsenenmedizin hinein reichen -  darunter die... 
Medicine | Neurology | Pediatrics | Internal medicine | Orthopedics | Family medicine
Web Resource
Neuropediatrics, 08/2018, Volume 49, Issue 4, p. 299
Journal Article
Neuropediatrics, ISSN 0174-304X, 2013, Volume 44, Issue 4, p. 179
Journal Article
Journal Article
PloS one, ISSN 1932-6203, 2017, Volume 12, Issue 4, p. e0175611
[This corrects the article DOI: 10.1371/journal.pone.0173144.]. 
Journal Article
Archives of Disease in Childhood, ISSN 0003-9888, 06/2019, Volume 104, Issue Suppl 3, p. A124
AimFetal acetylcholine receptor inactivation syndrome (FARIS) occurs in offspring of mothers affected by myasthenia gravis (MG), from in-utero exposure to... 
Journal Article
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