Results 301 to 310 of about 1,888,139 (345)
Stroke-Related Changes in Tonic and Phasic Muscle Recruitment During Reaching Reveal Pathway-Specific Motor Deficits. [PDF]
J Cent Nerv Syst DisKorol AS, Adcock A, Gritsenko V.
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Comparison of Two Posterior Minimally Invasive Approaches for Odontoid Fractures: Midline Nuchal Ligament Approach vs. Paramedian Muscle-Splitting Approach. [PDF]
Orthop SurgQiu Y, Wang L, Wang Y, Li Y, Lu X.
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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
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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 ...
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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 ...
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Journal of Inherited Metabolic Disease, 1990
SummaryThis review describes clinical, biochemical and genetic features of the four inborn errors affecting muscle glycogen breakdown, namely deficiencies of phosphorylase, phosphorylase kinase, amylo‐1,6‐glucosidase and acid α‐glucosidase. They are characterized by a wide spectrum of clinical manifestation, affecting age of onset, clinical features ...
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SummaryThis review describes clinical, biochemical and genetic features of the four inborn errors affecting muscle glycogen breakdown, namely deficiencies of phosphorylase, phosphorylase kinase, amylo‐1,6‐glucosidase and acid α‐glucosidase. They are characterized by a wide spectrum of clinical manifestation, affecting age of onset, clinical features ...
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MUSCLE HISTOCHEMISTRY AND MUSCLE FUNCTION
Acta Paediatrica, 1980Abstract. Henriksson, K. G. (Neuromuscular Unit, Department of Neurology, Clinical Neurophysiology and Pathology I, University of Linköping, Linköping, Sweden). Muscle histochemistry and muscle function. Acta Paediatr Scand, Suppl. 283: 15, 1980.—A short review of the histochemical characteristics of the different muscle fibre types is given.
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