Results 171 to 180 of about 362,296 (275)

Task-based effective connectivity finds alterations in frontoparietal network in Duchenne muscular dystrophy. [PDF]

Brain Commun
Thangarajh M, Ridder M, Karra H, Javalkar S, Zuniga E, Harper A, Mukhopadhyay ND, Cadrain R, Moeller FG, Bjork JM, Ma L.   +10 more
europepmc   +1 more source

Longitudinal Changes of Motor Function in Becker Muscular Dystrophy. [PDF]

Neurol Genet
Bello L, Riguzzi P, Capece G, Penzo M, Petrosino A, Sogus E, Mastellaro S, Caroli M, Villa M, Sabbatini D, Gorgoglione D, Vianello S, Sorarù G, Pegoraro E.   +13 more
europepmc   +1 more source

NAD+ repletion improves muscle function in muscular dystrophy and counters global PARylation

Science Translational Medicine, 2016
D. Ryu, Hongbo Zhang, E. Ropelle, Vincenzo Sorrentino, D. Mázala, L. Mouchiroud, Philip L. Marshall, M. D. Campbell, Amir S. Ali, Gary M. Knowels, Stéphanie Bellemin, S. Iyer, Xu Wang, K. Gariani, A. Sauve, C. Cantó, K. Conley, Ludivine Walter, R. Lovering, E. Chin, B. Jasmin, D. Marcinek, Keir J. Menzies, J. Auwerx   +23 more
semanticscholar   +1 more source

Impaired myogenesis in limb girdle muscular dystrophy type 2B. [PDF]

Sci Rep
Souza LS, Ishiba R, Ribeiro-Junior AF, Zogbi IA, Bouragba D, Bigot A, Mouly V, Vainzof M.   +7 more
europepmc   +1 more source

Case of Muscular Dystrophy [PDF]

Proceedings of the Royal Society of Medicine, 1916
openaire   +2 more sources

Linker proteins restore basement membrane and correct LAMA2-related muscular dystrophy in mice

Science Translational Medicine, 2017
J. Reinhard, Shuo Lin, K. McKee, S. Meinen, S. Crosson, M. Sury, S. Hobbs, G. Maier, P. Yurchenco, M. Rüegg   +9 more
semanticscholar   +1 more source

Perioperative Considerations in a Patient With Oculopharyngeal Muscular Dystrophy: A Case Report. [PDF]

Cureus
Bajaj P, Overholt D, Chura M.
europepmc   +1 more source

Estrogen-Related Receptor Alpha Promotes Skeletal Muscle Regeneration and Mitigates Muscular Dystrophy. [PDF]

FASEB J
Nguyen TTH, Huang YX, Poliakova S, Citu C, Mann E, Sopariwala DH, Zhao Z, Kumar A, Narkar VA.   +8 more
europepmc   +1 more source

A heterozygous 21-bp deletion in CAPN3 causes dominantly inherited limb girdle muscular dystrophy.

Brain : a journal of neurology, 2016
J. Vissing, R. Barresi, N. Witting, M. Van Ghelue, Lise Gammelgaard, L. Bindoff, V. Straub, Hanns Lochmüller, J. Hudson, C. Wahl, S. Arnardóttir, K. Dahlbom, C. Jonsrud, M. Duno   +13 more
semanticscholar   +1 more source