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 contracted in the stretch reflex [1]. He postulated that each step was produced by the allornone action of a single motor neuron upon the muscle fibers it innervated.Sherrington's concept of the motor unit assumed that each muscle ...
... muscle contracted in the stretch reflex [1]. He postulated that each step was produced by the allornone action of a single motor neuron upon the muscle fibers it innervated.Sherrington's concept of the motor unit assumed that each muscle ...
Σελίδα
... fibers). Gamma,or fusimotor, neuronsare considerably smaller [11]and exclusively innervate oneormore ofthe threetypesof specialized muscle fibers within the muscle spindle – stretch receptor organs that are present in virtually all ...
... fibers). Gamma,or fusimotor, neuronsare considerably smaller [11]and exclusively innervate oneormore ofthe threetypesof specialized muscle fibers within the muscle spindle – stretch receptor organs that are present in virtually all ...
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... muscle fiber is more than tenfold greater than the volume of cytoplasm in the motor neuron plus its axon. Contributed ... muscle fibers are essentially the same as those of alpha motor neurons [16]. For this reason, alpha and beta motor ...
... muscle fiber is more than tenfold greater than the volume of cytoplasm in the motor neuron plus its axon. Contributed ... muscle fibers are essentially the same as those of alpha motor neurons [16]. For this reason, alpha and beta motor ...
Σελίδα
... muscle fiber [23],but exceptions are found in some cranial muscles, such as the laryngeal [24] andextraocular muscles [25]. On a given muscle ... fibers Theskeletal musclefiberis a cylindrical,multinucleated cellthatis formedbythe fusionof ...
... muscle fiber [23],but exceptions are found in some cranial muscles, such as the laryngeal [24] andextraocular muscles [25]. On a given muscle ... fibers Theskeletal musclefiberis a cylindrical,multinucleated cellthatis formedbythe fusionof ...
Σελίδα
... fibers and their neuromuscular junctions scattered alongthelengthofthemuscle belly in irregular arrays. Forces produced by individual fibers are transmitted to the tendons of origin and ... muscle fibers, called fascicles, are bound.
... fibers and their neuromuscular junctions scattered alongthelengthofthemuscle belly in irregular arrays. Forces produced by individual fibers are transmitted to the tendons of origin and ... muscle fibers, called fascicles, are bound.
Περιεχόμενα
Dedication Section scientific basis | |
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 | |
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