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ﺑﺎﺯﮔﺸﺖ ﺑﻪ ﺻﻔﺤﻪ ﻗﺒﻠﯽ
خرید پکیج
تعداد آیتم قابل مشاهده باقیمانده: 4 مورد
نسخه الکترونیک
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Arthritis and other musculoskeletal manifestations of systemic lupus erythematosus
Diabetic muscle infarction
Drug-induced myopathies
Glucocorticoid-induced myopathy
Hypothyroid myopathy
Major causes of musculoskeletal chest pain in adults
Myopathies of systemic disease
Neuromuscular weakness related to critical illness
Nocturnal leg cramps
Overview of the musculoskeletal complications of diabetes mellitus
Respiratory muscle weakness due to neuromuscular disease: Clinical manifestations and evaluation
Rhabdomyolysis: Clinical manifestations and diagnosis
Rhabdomyolysis: Epidemiology and etiology
Statin muscle-related adverse events
Stiff-person syndrome
Hyperkalemic periodic paralysis
Hypokalemic periodic paralysis
Thyrotoxic periodic paralysis
Approach to the patient with muscle weakness
Diagnostic ultrasound in neuromuscular disease
Electrodiagnostic evaluation of the neuromuscular junction
Muscle enzymes in the evaluation of neuromuscular diseases
Muscle examination in the evaluation of weakness
Overview of electromyography
Overview of nerve conduction studies
Skin biopsy for the evaluation of peripheral nerve disease
Polyradiculopathy: Spinal stenosis, infectious, carcinomatous, and inflammatory nerve root syndromes
Clinical manifestations and diagnosis of inclusion body myositis
Clinical manifestations of dermatomyositis and polymyositis in adults
Diagnosis and differential diagnosis of dermatomyositis and polymyositis in adults
Initial treatment of dermatomyositis and polymyositis in adults
Interstitial lung disease in dermatomyositis and polymyositis: Clinical manifestations and diagnosis
Juvenile dermatomyositis and polymyositis: Epidemiology, pathogenesis, and clinical manifestations
Juvenile dermatomyositis and polymyositis: Treatment, complications, and prognosis
Malignancy in dermatomyositis and polymyositis
Management of inclusion body myositis
Overview of and approach to the idiopathic inflammatory myopathies
Overview of viral myositis
Pathogenesis of inflammatory myopathies
Primary pyomyositis
Statin muscle-related adverse events
Treatment of recurrent and resistant dermatomyositis and polymyositis in adults
Approach to the metabolic myopathies
Duchenne and Becker muscular dystrophy: Clinical features and diagnosis
Duchenne and Becker muscular dystrophy: Genetics and pathogenesis
Duchenne and Becker muscular dystrophy: Glucocorticoid and disease-modifying treatment
Duchenne and Becker muscular dystrophy: Management and prognosis
Emery-Dreifuss muscular dystrophy
Energy metabolism in muscle
Facioscapulohumeral muscular dystrophy
Lactate dehydrogenase deficiency
Limb-girdle muscular dystrophy
Lysosomal acid alpha-glucosidase deficiency (Pompe disease, glycogen storage disease II, acid maltase deficiency)
Lysosome-associated membrane protein 2 deficiency (glycogen storage disease IIb, Danon disease)
Metabolic myopathies caused by disorders of lipid and purine metabolism
Mitochondrial disorders: Treatment
Mitochondrial myopathies: Clinical features and diagnosis
Mitochondrial structure, function, and genetics
Myophosphorylase deficiency (glycogen storage disease V, McArdle disease)
Myotonic dystrophy: Etiology, clinical features, and diagnosis
Myotonic dystrophy: Treatment and prognosis
Oculopharyngeal, distal, and congenital muscular dystrophies
Other disorders of glycogen metabolism: GLUT2 deficiency and aldolase A deficiency
Overview of inherited disorders of glucose and glycogen metabolism
Phosphofructokinase deficiency (glycogen storage disease VII, Tarui disease)
Phosphoglycerate kinase deficiency and phosphoglycerate mutase deficiency
Acute flaccid myelitis
Clinical features of amyotrophic lateral sclerosis and other forms of motor neuron disease
Diagnosis of amyotrophic lateral sclerosis and other forms of motor neuron disease
Disease-modifying treatment of amyotrophic lateral sclerosis
Epidemiology and pathogenesis of amyotrophic lateral sclerosis
Familial amyotrophic lateral sclerosis
Hereditary spastic paraplegia
Patient perspective: Amyotrophic lateral sclerosis (ALS)
Poliomyelitis and post-polio syndrome
Symptom-based management of amyotrophic lateral sclerosis
Chronic immunotherapy for myasthenia gravis
Clinical manifestations of myasthenia gravis
Diagnosis of myasthenia gravis
Differential diagnosis of myasthenia gravis
Lambert-Eaton myasthenic syndrome: Clinical features and diagnosis
Lambert-Eaton myasthenic syndrome: Treatment and prognosis
Management of myasthenia gravis in pregnancy
Myasthenic crisis
Ocular myasthenia gravis
Overview of neuromuscular junction toxins
Overview of the treatment of myasthenia gravis
Pathogenesis of myasthenia gravis
Role of thymectomy in patients with myasthenia gravis
Differential diagnosis of peripheral nerve and muscle disease
Foot drop: Etiology, diagnosis, and treatment
Guillain-Barré syndrome in adults: Pathogenesis, clinical features, and diagnosis
Guillain-Barré syndrome in adults: Treatment and prognosis
Neuromuscular weakness related to critical illness
Polyradiculopathy: Spinal stenosis, infectious, carcinomatous, and inflammatory nerve root syndromes

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