Results 161 to 170 of about 7,022 (221)

Clinical Trial Readiness in Limb Girdle Muscular Dystrophy R1 (LGMDR1): A GRASP Consortium Study. [PDF]

Ann Clin Transl Neurol
Hunn SM, Alfano LN, Jones A, Butler A, Lowes LP, Iammarino MA, Reash NF, Pietruszewski L, Sasidharan S, Currence M, Statland JM, Strahler T, Will R, Wicklund M, Dixon S, Augsburger R, Mozaffar T, Laubscher KM, Mockler SRH, Mathews KD, Stinson N, Leung DG, Stark MM, Horton RA, Kang PB, James MK, Clause A, Weihl CC, Johnson NE, GRASP‐LGMD Consortium.   +29 more
europepmc   +1 more source

Dysferlin and the Regulation of Ca²⁺ Release in Skeletal Muscle. [PDF]

Cells
Bloch RJ, Muriel J, Lukyanenko V.
europepmc   +1 more source

A Scale-Invariant Looming Detector for UAV Return Missions in Power Line Scenarios. [PDF]

Biomimetics (Basel)
Zhao J, Zhao Q, Wu C, Li Z, Shuang F.
europepmc   +1 more source

Pain Experiences and Prescription Pain Medications Among People With Selected Muscular Dystrophies in the Muscular Dystrophy Surveillance, Tracking, and Research Network. [PDF]

Muscle Nerve
Suhl J, Conway KM, Thomas S, Rasmussen SA, Howard JF, Johnson NE, Romitti PA, Mathews KD, Muscular Dystrophy Surveillance, Tracking and Research Network (MD STARnet).   +9 more
europepmc   +1 more source

Comparison of whole-body muscle imaging findings between GNE myopathy and other young adult-onset hereditary myopathies. [PDF]

PLoS One
Boonsri P, Yamutai S, Tanutit P, Sattayapornpipat J, Charalsawadi C, Koonalintip P, Sathirapanya P, Setthawatcharawanich S, Leelawattana R, Korathanakhun P.   +9 more
europepmc   +1 more source

Investigating genotype-phenotype correlation of limb-girdle muscular dystrophy R8: association of clinical severity, protein biological function and protein oligomerization. [PDF]

Acta Neuropathol Commun
Liang X, Si J, Xie H, Guan Y, Lin W, Lin Z, Zheng G, Wei X, Xiong X, Zhuang Z, Shang X.   +10 more
europepmc   +1 more source

コンチュウ シカクケイ ノ ケイサン ゲンリ ニ マナンダ ショウトツ カイヒ ノ タメ ノ タンガン ロボットビジョン [PDF]

Okuno, Hirotugu, オクノ, ヒロツグ, 奥野, 弘嗣   +2 more
core  

Uncovering compound heterozygous <i>DYSF</i> variants in a Chinese family affected by limb-girdle muscular dystrophy type 2B. [PDF]

Front Genet
Li J, Zhou J, Ji C, Ma S, Zhu J, Yang T, Dong D, Ping Y.   +7 more
europepmc   +1 more source

Myxovirus Resistance A Protein Expression in Idiopathic Inflammatory Myopathies and Hereditary Muscle Diseases with Inflammatory Cell Infiltration: A North African Study. [PDF]

Int J Mol Sci
Farhat E, Zamali I, Younes TB, Klaa H, Stenzel W, Samoud S, Ben Rhouma H, Galai Y, Ben Youssef-Turki I, Kraoua I, Ben Ahmed M, Ben Hmid A.   +11 more
europepmc   +1 more source