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Neuromuscular Disorders, ISSN 0960-8966, 05/2015, Volume 25, Issue 5, p. 403
Journal Article
Indian Journal of Pediatrics, ISSN 0019-5456, 02/2019, Volume 86, Issue 2, pp. 189 - 190
Journal Article
Clinical Neurophysiology, ISSN 1388-2457, 05/2018, Volume 129, pp. e160 - e160
Analysis of repetitive nerve stimulation in myotonic dystrophy type I (DM1). Retrospective analysis of DM1 patients in Peking Union Medical College Hospital... 
Myotonic dystrophy | Medical colleges | Analysis
Journal Article
2009, 2nd ed., Thefacts series, ISBN 9780199571970, xiii, 106
Book
BMC musculoskeletal disorders, ISSN 1471-2474, 05/2019, Volume 20, Issue 1, pp. 244 - 244
An incorrect attribution of the first study regarding the effect of exercise in DM1 mouse models needs to be revised. 
Myotonic dystrophy | Skeletal muscle | Dystrophy
Journal Article
Clinical and Experimental Dermatology, ISSN 0307-6938, 06/2019, Volume 44, Issue 4, pp. e149 - e150
Journal Article
JAMA Ophthalmology, ISSN 2168-6165, 12/2018, Volume 136, Issue 12, p. 1425
Dalvin et al express appreciation on Rosa et al and Silvestri et commentary on the association between uveal melanoma and myotonic dystrophy. Detecting an... 
Myotonic dystrophy | Melanoma | Dystrophy | Muscular dystrophy | Myogenesis
Journal Article
Journal of the neurological sciences, ISSN 0022-510X, 05/2019
Journal Article
Trends in Cardiovascular Medicine, ISSN 1050-1738, 07/2019
Journal Article
Japanese Journal of Gastroenterological Surgery, ISSN 0386-9768, 2018, Volume 51, Issue 6, pp. 400 - 405
Journal Article
Journal of Clinical Neurophysiology, ISSN 0736-0258, 01/2019, Volume 36, Issue 1, pp. 74 - 81
PURPOSE:Myotonic dystrophy type 1 is the most common muscular dystrophy in adults. Although brain involvement is well recognized, the relationship between... 
Usage | Research | Myotonic dystrophy | Magnetoencephalography | Index Medicus
Journal Article
Journal Article
by Flower, Michael and Lomeikaite, Vilija and Ciosi, Marc and Cumming, Sarah and Morales, Fernando and Lo, Kitty and Hensman Moss, Davina and Jones, Lesley and Holmans, Peter and Monckton, Darren G and Tabrizi, Sarah J and Kraus, Peter and Hoffman, Rainer and Tobin, Alan and Borowsky, Beth and Keenan, S and Whitlock, Kathryn B and Queller, Sarah and Campbell, Colin and Wang, Chiachi and Langbehn, Doug and Axelson, Eric and Johnson, Hans and Acharya, Tanka and Cash, Dave M and Frost, Chris and Jones, Rebecca and Jurgens, Caroline and ‘t Hart, Ellen P and van der Grond, Jeroen and Witjes- Ane, Marie-Noelle N and Roos, Raymund A C and Dumas, Eve M and van den Bogaard, Simon J A and Stopford, Cheryl and Craufurd, David and Callaghan, Jenny and Arran, Natalie and Rosas, Diana D and Lee, S and Monaco, W and O’Regan, Alison and Milchman, Cassie and Frajman, E and Labuschagne, Izelle and Stout, Julie and Campbell, Melissa and Andrews, Sophie C and Bechtel, Natalie and Reilmann, Ralf and Bohlen, Stefan and Kennard, Chris and Berna, Claire and Hicks, Stephen and Durr, Alexandra and Pourchot, C and Bardinet, Eric and Nigaud, Kevin and Valabre, Romain and gue, ` and Lehericy, Stephane and Marelli, Cecilia and Jauffret, Celine and Justo, Damian and Leavitt, Blair and Decolongon, Joji and Sturrock, Aaron and Coleman, Alison and Santos, Rachelle Dar and Patel, A and Gibbard, Claire and Whitehead, Daisy and Wild, Ed and Owen, Gail and Crawford, Helen and Malone, Ian and Lahiri, Nayana and Fox, Nick C and Hobbs, Nicola Z and Scahill, Rachael I and Ordidge, Roger and Pepple, Tracey and Read, Joy and Say, Miranda J and Landwehrmeyer, Bernhard and Daidj, Ferroudja and Bassez, Guillaume and Lignier, Baptiste and Couppey, Florence and Delmas, Stéphanie and Deux, Jean-François and Hankiewicz, Karolina and Dogan, Celine and Minier, Lisa and Chevalier, Pascale and Hamadouche, Amira and Catt, Michael and van Hees, Vincent and Catt, Sharon and Schwalber, Ameli and ... and OPTIMISTIC Consortium and TRACK-HD Investigators
Brain, ISSN 0006-8950, 07/2019, Volume 142, Issue 7, pp. 1876 - 1886
A genome-wide association study recently identified an MSH3/DHFR locus associated with Huntington’s disease progression. Flower, Lomeikaite et al. identify... 
myotonic dystrophy | transcriptomics | Reports | Huntington’s disease | movement disorders | association study
Journal Article
Neuromuscular Disorders, ISSN 0960-8966, 2013, Volume 23, Issue 9, pp. 833 - 833
Patients with myotonic dystrophy (DM1) have distal upper extremity weakness which initially focuses on the long finger flexors. Grip strength using a Jamar... 
Neurology | Measurement | Myotonic dystrophy
Journal Article
Neuromuscular Disorders, ISSN 0960-8966, 2013, Volume 23, Issue 9, pp. 835 - 835
Myotonic dystrophy type 1 (DM1) is an autosomal dominant disorder with multisystemic clinical features. It is the most common type of muscular dystrophy in... 
Neurology | Myotonic dystrophy
Journal Article
Neuromuscular Disorders, ISSN 0960-8966, 2013, Volume 23, Issue 9, pp. 832 - 833
Myotonic dystrophy type 1 (DM1) is one of the more common neuromuscular disorders in childhood with strongly varying prevalence in different regions. The... 
Neurology | Myotonic dystrophy
Journal Article
Muscle and Nerve, ISSN 0148-639X, 08/2011, Volume 44, Issue 2, pp. 160 - 169
Journal Article
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