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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Αποτελέσματα 1 - 5 από τα 53.
Σελίδα
... contractures Gisèle Bonneand Anne K.Lampe 15 Facioscapulohumeraldystrophy Shannon L.Venance andRabiTawil 16 Distal myopathies Bjarne Udd 17 Oculopharyngeal muscular dystrophy Bernard Brais 18 Myotonic dystrophy John Dayand CharlesA ...
... contractures Gisèle Bonneand Anne K.Lampe 15 Facioscapulohumeraldystrophy Shannon L.Venance andRabiTawil 16 Distal myopathies Bjarne Udd 17 Oculopharyngeal muscular dystrophy Bernard Brais 18 Myotonic dystrophy John Dayand CharlesA ...
Σελίδα
... contractures,torticollis, hipdislocation, and hyperextensibility ofthedistal joints. Some patients mayneverachieve ambulationwhile others willbeable to walk independently. Serumcreatinekinase levelsareusually normalormildly elevated ...
... contractures,torticollis, hipdislocation, and hyperextensibility ofthedistal joints. Some patients mayneverachieve ambulationwhile others willbeable to walk independently. Serumcreatinekinase levelsareusually normalormildly elevated ...
Σελίδα
... contractures ofmost proximal andalso distaljoints characterizethe laterphases ofthedisorder. The progressive ... contractures, elbow, knee, hip,andankle contractures also occur in most patients, inassociation with rigidity of the spine ...
... contractures ofmost proximal andalso distaljoints characterizethe laterphases ofthedisorder. The progressive ... contractures, elbow, knee, hip,andankle contractures also occur in most patients, inassociation with rigidity of the spine ...
Σελίδα
... Contractures maybepresent but severe arthrogryposis is rare.Serum CK levels arealways elevated consistent with aproblemat the interface between the musclefiber sarolemma and thebasement membrane. Whilecognitive function is usuallynormal ...
... Contractures maybepresent but severe arthrogryposis is rare.Serum CK levels arealways elevated consistent with aproblemat the interface between the musclefiber sarolemma and thebasement membrane. Whilecognitive function is usuallynormal ...
Σελίδα
... contractures atbirthwere notedinone family. Ptosis and ophthalmoplegia, facial weakness,and feedingdifficulties were present insomeof the cases. BIN1 encodes amphiphysin2, a protein withtumor suppressor features whichis downregulated ...
... contractures atbirthwere notedinone family. Ptosis and ophthalmoplegia, facial weakness,and feedingdifficulties were present insomeof the cases. BIN1 encodes amphiphysin2, a protein withtumor suppressor features whichis downregulated ...
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 | |
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