Disorders of Voluntary MuscleCambridge University Press, 21 Ιαν 2010 - 1069 σελίδες This major new edition fulfils the need for a single-volume, up-to-date information resource on the etiology, pathogenesis, diagnosis and treatment of diseases of skeletal muscles, including the muscular dystrophies, mitochondrial myopathies, metabolic myopathies, ion channel disorders, and dysimmune myopathies. As background to the clinical coverage, relevant information on advances in molecular and developmental biology, immunopathology, mitochondrial biology, ion-channel dynamics, cell membrane and signal transduction science, and imaging technology is summarized. Combining essential new knowledge with the fundamentals of history-taking and clinical examination, this extensively illustrated book will continue to be the mainstay for practising physicians and biomedical scientists concerned with muscle disease. Regular updates on the clinical and basic science aspects of muscle disease - written mainly by rising stars of myology - will be published on an accompanying website. |
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... muscle weakness and atrophy; Miyoshimyopathy (MM), whichincontrast affectspredominantlythe distalmuscles, inparticular the posterior compartment (calfmuscle beingthemost severely affected);and a distal anterior compartment myopathy ...
... muscle weakness and atrophy; Miyoshimyopathy (MM), whichincontrast affectspredominantlythe distalmuscles, inparticular the posterior compartment (calfmuscle beingthemost severely affected);and a distal anterior compartment myopathy ...
Σελίδα
... muscular dystrophy withlossof sarcolemmal integrityanda preserved dystrophinassociated protein complex.These models ... distal myopathy, anda persistently highCK(hyperCKemia). Thus there isarangeof skeletal muscle involvement, ranging ...
... muscular dystrophy withlossof sarcolemmal integrityanda preserved dystrophinassociated protein complex.These models ... distal myopathy, anda persistently highCK(hyperCKemia). Thus there isarangeof skeletal muscle involvement, ranging ...
Σελίδα
... distal muscles.Ptosis andlimitation ofeye movementsare common features.In ... myopathy [140]. Theage of onset ranged from birth to childhood, the ... myopathy families localize to the N terminus,the BAR, or to the SH3 domain. Analysis of ...
... distal muscles.Ptosis andlimitation ofeye movementsare common features.In ... myopathy [140]. Theage of onset ranged from birth to childhood, the ... myopathy families localize to the N terminus,the BAR, or to the SH3 domain. Analysis of ...
Σελίδα
... myopathy, the reason why nuclei are displaced to the center of the fiber is ... myopathy in whichcardiomyopathy is not afeature. However, it should be noted ... distal involvement mayalsobe present. Presentation is usually in childhood ...
... myopathy, the reason why nuclei are displaced to the center of the fiber is ... myopathy in whichcardiomyopathy is not afeature. However, it should be noted ... distal involvement mayalsobe present. Presentation is usually in childhood ...
Σελίδα
... myopathy, distal arthrogryposis, cap disease,actin myopathy, congenital fibertype disproportion, rodcore myopathy, intranuclearrodmyopathy, anddistal myopathy; with nemaline myopathythe most common[157]. Cofilin2 isinvolved in the ...
... myopathy, distal arthrogryposis, cap disease,actin myopathy, congenital fibertype disproportion, rodcore myopathy, intranuclearrodmyopathy, anddistal myopathy; with nemaline myopathythe most common[157]. Cofilin2 isinvolved in the ...
Περιεχόμενα
Dystrophic myopathies of early childhood onset | |
Investigation of muscle disease 4 Electrophysiological evaluation of suspected myopathy | |
Eugenio MercuriandMarianne deVisser Section 3A Descriptionofmuscledisease general aspects 8 The clinical assessmentanda guide to classification o... | |
The congenitalmyopathies Carina WallgrenPettersson and NigelG Laing 14 Muscle diseases with prominent muscle contractures | |
Defects ofcarbohydrate andlipid | |
Muscular dystrophies presenting with proximal muscle | |
Muscle ionchannelopathies and related disorders | |
Other myopathies Giovanni Meolaand Michael Swash | |
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Συχνά εμφανιζόμενοι όροι και φράσεις
abnormalities actin activity andthe antibodies associated associatedwith atrophy autosomal dominant Biol Brain canbe cardiac cardiomyopathy caused caveolin3 chromosome clinical CMAP collagen complex congenital muscular dystrophy congenital myopathies contractures defects deficiency dehydrogenase deletions denervation dermatomyositis diagnosis disorders distal myopathy Duchenne muscular dystrophy dysferlin dystroglycan encoding enzyme etal exon expression facioscapulohumeral facioscapulohumeral muscular dystrophy Figure filaments FSHD function gene Genet glycogen glycosylation identified inclusion body myositis inflammatory myopathies involvement isoforms Karpati lamina LGMD LGMD2I limbgirdle muscular dystrophy membrane metabolic mice missense mitochondrial molecular motor unit mtDNA muscle biopsy muscle disease muscle fibers Muscle Nerve muscle weakness musclefibers mutationsin myoblasts myofiber myofibrillar myosin myotilin myotonia myotonic dystrophy nemaline myopathy Neurol Neurology neuromuscular normal nuclear nuclei ofmuscle ofthe onset pathology patients patientswith phenotype protein receptor recessive regeneration respiratory RYR1 sarcoglycan sarcolemma sarcomere satellite cells skeletal muscle staining syndrome therapy tissue utrophin vacuoles Xlinked