Results 251 to 260 of about 1,349,150 (316)
Botulinum Toxin Treatment of Stiff Person Syndrome-A Critical Review and Update. [PDF]
Tohidian AG +3 more
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Temperature and pH-dependent potassium currents of muscles of the stomatogastric nervous system of the crab, <i>Cancer borealis</i>. [PDF]
Jacquerie K +3 more
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DyABD: the abdominal muscle segmentation in dynamic MRI benchmark. [PDF]
Belton N +6 more
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Fibro-adipogenic progenitor cells from murine SMA muscles are intrinsically adipogenic. [PDF]
Luo YE +5 more
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Axillopectoral muscle (Langer's muscle)
Clinical Anatomy, 2005AbstractIn 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, 2000The 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
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Muscle-nerve-muscle neurotization of the orbicularis oris muscle
Journal of Cranio-Maxillofacial Surgery, 2001A 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
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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
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

