Muscle Diseases
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Muscle Diseases
A Guide to Differential Diagnosis, Investigation and Management
Brady, Stefen; Merrison, Andria
Taylor & Francis Ltd
02/2025
212
Dura
9781138368330
Pré-lançamento - envio 15 a 20 dias após a sua edição
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History, Muscle Examination, Serological Tests, Muscle Antibodies, Neurophysiology, Muscle Pathology/ Muscle Biopsy, Muscle Imaging, Genetic investigations in neuromuscular diseases, Management, treatment and therapy for Neuromuscular conditions, Becker muscular dystrophy, Duchenne muscular dystrophy, Facioscapulohumeral muscular dystrophy, Recessive limb girdle muscular dystrophy R1 (calpainopathy), Recessive limb girdle muscular dystrophy R12 (ANO5), Dominant limb girdle muscular dystrophy (Emery-Dreifuss muscular dystrophy 2), Collagen VI myopathy, Nemaline myopathy, Emery-Dreifuss muscular dystrophy, GNE myopathy, Ryanodine receptor 1 (RyR1) congenital myopathy, BAG3 myofibrillar myopathy, Distal myopathy, Oculopharyngeal muscular dystrophy, Tubular aggregate myopathy, Myotonic dystrophy type 1, Myotonic dystrophy type 2, Myotonia congenita, Inclusion body myositis (IBM), Dermatomyositis, ASS, Sarcoid myopathy, Statin-related myopathy, Critical illness myopathy, Thyroid myopathy, Asymptomatic hyperCKaemia, Neck extensor myopathy, McArdle disease, Acid maltase deficiency (Pompe disease), Fatty acid oxidation disorders, Adult-onset ryanodine receptor 1 (RYR1) related myopathy, Progressive external ophthalmoplegia, Mitochondrial encephalopathy, lactic acidosis & stroke-like episodes (MELAS), Limb-girdle congenital myasthenia syndrome, Spinal muscular atrophy, Kennedy's disease
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Myopathy;Muscle diagnosis;Neuromuscular disease;Muscular dystrophy;Muscle biopsy
History, Muscle Examination, Serological Tests, Muscle Antibodies, Neurophysiology, Muscle Pathology/ Muscle Biopsy, Muscle Imaging, Genetic investigations in neuromuscular diseases, Management, treatment and therapy for Neuromuscular conditions, Becker muscular dystrophy, Duchenne muscular dystrophy, Facioscapulohumeral muscular dystrophy, Recessive limb girdle muscular dystrophy R1 (calpainopathy), Recessive limb girdle muscular dystrophy R12 (ANO5), Dominant limb girdle muscular dystrophy (Emery-Dreifuss muscular dystrophy 2), Collagen VI myopathy, Nemaline myopathy, Emery-Dreifuss muscular dystrophy, GNE myopathy, Ryanodine receptor 1 (RyR1) congenital myopathy, BAG3 myofibrillar myopathy, Distal myopathy, Oculopharyngeal muscular dystrophy, Tubular aggregate myopathy, Myotonic dystrophy type 1, Myotonic dystrophy type 2, Myotonia congenita, Inclusion body myositis (IBM), Dermatomyositis, ASS, Sarcoid myopathy, Statin-related myopathy, Critical illness myopathy, Thyroid myopathy, Asymptomatic hyperCKaemia, Neck extensor myopathy, McArdle disease, Acid maltase deficiency (Pompe disease), Fatty acid oxidation disorders, Adult-onset ryanodine receptor 1 (RYR1) related myopathy, Progressive external ophthalmoplegia, Mitochondrial encephalopathy, lactic acidosis & stroke-like episodes (MELAS), Limb-girdle congenital myasthenia syndrome, Spinal muscular atrophy, Kennedy's disease
Este título pertence ao(s) assunto(s) indicados(s). Para ver outros títulos clique no assunto desejado.
