Results 151 to 160 of about 110,072 (307)

Graphic Medicine Reflective Learning Activity on Chronic Pain Beliefs Among Dentistry Students

Journal of Dental Education, EarlyView.
Susan M Tupper, Amrinderbir Singh, Erin Beckwell, Barbara Fornssler   +3 more
wiley   +1 more source

Reachable Workspace as a Clinical Outcome for Upper Extremity Function: A Narrative Review

Muscle &Nerve, EarlyView.
ABSTRACT Motion sensing technology can be utilized to capture detailed upper extremity (UE) motion to reconstruct an individual's three‐dimensional (3D) reachable workspace (RWS). The RWS can be quantified as relative surface area (RSA), providing an innovative surrogate measure to assess UE mobility and function.
Jay J. Han, Lawrence J. Hayward, Christina Adams, Juan Perez‐Ibarra   +3 more
wiley   +1 more source

A panoramic view of the expression and function of the Doublesex/DMRT gene family in <i>C. elegans</i>. [PDF]

Sci Adv
Wang 王琛 C, Salzberg Y, Oren-Suissa M, Hobert O.   +3 more
europepmc   +1 more source

DMD & BMD – CLINICAL: P.51 DMD Hub: demonstrating impact for DMD trials

, 2020
Heslop, E., Guglieri, M., Irvin, A., Turner, C., Crow, B., George, E., Johnson, A., Crossley, E., Muntoni, F., Straub, V.   +9 more
openaire   +1 more source

BMP antagonists enhance myogenic differentiation and ameliorate the dystrophic phenotype in a DMD mouse model

, 2010
Songting Shi, Willem M.H. Hoogaars, David J. J. de Gorter, Sandra H. van Heiningen, Herbert Y. Lin, Charles C. Hong, Dwi U. Kemaladewi, Annemieke Aartsma‐Rus, Peter ten Dijke, Peter A.C. ’t Hoen   +9 more
openalex   +2 more sources

Asynchrony Related to Mechanical Ventilation Exacerbates Diaphragm Dysfunction in a Mouse Model of Duchenne Muscular Dystrophy

Muscle &Nerve, EarlyView.
ABSTRACT Introduction/Aims In dystrophic mice (mdx, a genetic homolog of Duchenne muscular dystrophy: DMD), previous studies showed that mechanical ventilation (MV) induces ventilator‐induced diaphragmatic dysfunction (VIDD). However, susceptibility to mechanical stress caused by asynchrony remains unknown.
Mohamad Yehya, Haikel Dridi, Eric Estève, Johan Moreau, Steven Reiken, Andrew R. Marks, Alain Lacampagne, Stefan Matecki   +7 more
wiley   +1 more source

Dmd mdx mice have defective oligodendrogenesis, delayed myelin compaction and persistent hypomyelination [PDF]

Andrea J. Arreguin, Zijian Shao, Holly Colognato   +2 more
openalex   +1 more source

DMD treatment in pigs [PDF]

, 2020
Ellen P. Neff
openalex   +1 more source

With Regard to the Expression Status of Sarcolemmal Aquaporin 4 in Human Muscular Dystrophies

Neurology and Clinical Neuroscience, EarlyView.
ABSTRACT Human muscular dystrophies are inherited muscle‐wasting diseases caused by the various kinds of gene mutations. Among them, Duchenne muscular dystrophy (DMD) is a representative type. Before the discovery of the causative dystrophin gene of DMD, the fragile myofiber plasma membrane was thought to be the trigger of myofiber necrosis in DMD ...
Yoshihiro Wakayama, Takahiro Jimi
wiley   +1 more source

Estimating health-state utility values for family-caregivers of patients with Duchenne muscular dystrophy using time trade-off valuation. [PDF]

J Patient Rep Outcomes
Borecka O, Llewellyn S, Woollacott I, Richardson L, Fellows A, Lawrence J, Bottomley C, Biggane AM.   +7 more
europepmc   +1 more source