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Pediatrics, ISSN 0031-4005, 10/2018, Volume 142, Issue Suppl 2, pp. S17 - S33
Steadily improving management of Duchenne muscular dystrophy (DMD) continues to lead to improved physical and functional status, allowing increasingly... 
Activities of daily living | Deformation | Glucocorticoids | Decision making | Medical treatment | Management | Disease control | Muscular dystrophy | Life span | Technology | Duchenne's muscular dystrophy | Adults | Rehabilitation | Dystrophy | Children
Journal Article
Pediatrics, ISSN 0031-4005, 10/2018, Volume 142, Issue Suppl 2, pp. S82 - S89
Orthopedic care is an important aspect of the overall management of patients with Duchenne muscular dystrophy (DMD). In addition to progressive muscle weakness... 
Medical personnel | Pediatrics | Glucocorticoids | Complications | Physicians | Muscles | Management | Disease control | Patients | Muscular dystrophy | Osteoporosis | Side effects | Biomedical materials | Fractures | Life span | Scoliosis | Orthopedics | Surgery | Duchenne's muscular dystrophy | Surgeons | Biocompatibility | Dystrophy | Rehabilitation | Bone strength
Journal Article
Pediatrics, ISSN 0031-4005, 10/2018, Volume 142, Issue Suppl 2, pp. S90 - S98
Primary care providers (PCPs) are usually the first point of contact with the health care system for patients with Duchenne muscular dystrophy (DMD), and... 
Health care | Medical personnel | Immunization | Nutrition | Knowledge acquisition | Complications | Physicians | Medical services | Emergency management | Emergency medical care | Primary care | Patients | Muscular dystrophy | Domains | Medicine | Duchenne's muscular dystrophy | Dystrophy | Emergency preparedness | Emergency medical services
Journal Article
Muscle & Nerve, ISSN 0148-639X, 05/2017, Volume 55, Issue 5, pp. 626 - 634
Journal Article
PM&R, ISSN 1934-1482, 09/2017, Volume 9, Issue 9, pp. S285 - S286
Journal Article
Journal Article
Journal of pediatric rehabilitation medicine, ISSN 1874-5393, 2014, Volume 7, Issue 2, pp. 133 - 142
Journal Article
The Lancet Neurology, ISSN 1474-4422, 03/2018, Volume 17, Issue 3, pp. 251 - 267
Journal Article
The Lancet Neurology, ISSN 1474-4422, 05/2018, Volume 17, Issue 5, pp. 445 - 455
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
Surgical Neurology International, ISSN 2229-5097, 01/2016, Volume 7, Issue 1, pp. 105 - 105
Complications of intrathecal baclofen (ITB) pump implantation for treatment of pediatric patients with spasticity and dystonia associated with cerebral palsy... 
cerebral palsy | CSF leak | spasticity | hydrocephalus | Arrested hydrocephalus | intrathecal baclofen pump | Cerebral palsy | Pediatrics | Nuclear magnetic resonance--NMR | Breakdowns | Patients | Drug dosages | Quality of life
Journal Article
Pediatric Radiology, ISSN 0301-0449, 3/2018, Volume 48, Issue 3, pp. 392 - 397
Journal Article