Results 251 to 260 of about 1,349,150 (316)

Botulinum Toxin Treatment of Stiff Person Syndrome-A Critical Review and Update. [PDF]

open access: yesToxins (Basel)
Tohidian AG   +3 more
europepmc   +1 more source

DyABD: the abdominal muscle segmentation in dynamic MRI benchmark. [PDF]

open access: yesBMC Med Imaging
Belton N   +6 more
europepmc   +1 more source

Fibro-adipogenic progenitor cells from murine SMA muscles are intrinsically adipogenic. [PDF]

open access: yesProc Natl Acad Sci U S A
Luo YE   +5 more
europepmc   +1 more source

Axillopectoral muscle (Langer's muscle)

Clinical Anatomy, 2005
AbstractIn a routine dissection of the axillary fossa, a muscle originating from the coracoid process of the scapula and extending to the long head of triceps brachii muscle was observed. The mentioned muscle was adhering to both the triceps brachii muscle and the tendinous part of the latissimus dorsi muscle.
Peker, TUNCAY VEYSEL   +4 more
openaire   +3 more sources

Muscle Fatigue and Muscle Injury

Physical Medicine and Rehabilitation Clinics of North America, 2000
The purpose of this review is to acquaint the reader with the neurobiology of muscle fatigue. Muscle fatigue is a complex, multifactorial process. The authors have covered the chain of events bringing about skeletal muscle contraction and the manner in which fatigue may affect each step.
S A, Dugan, W R, Frontera
openaire   +2 more sources

Muscle-nerve-muscle neurotization of the orbicularis oris muscle

Journal of Cranio-Maxillofacial Surgery, 2001
A denervated half of the orbicularis oris muscle is not reinnervated spontaneously by axon sprouting from the intact contralateral side. The borderline between the facial nerve territories seems to act as a barrier. The muscle-nerve-muscle technique was advocated as a technique to reneurotize a denervated half of the orbicularis oris muscle in cases of
C, Kermer   +3 more
openaire   +2 more sources

MUSCLE CHANNELOPATHIES

Continuum, 2006
In recent years the term CHANNELOPATHY has been adopted to describe neurological disorders caused by mutations in different ion channel genes. Myopathic channelopathies include two main groups: nondystrophic myotonias and periodic paralyses. This article reviews the clinical features, diagnostic approach, molecular causes, and management of patients ...
openaire   +2 more sources

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