Myopathies. (2014)
- Record Type:
- Book
- Title:
- Myopathies. (2014)
- Main Title:
- Myopathies.
- Other Names:
- Dimachkie, Mazen
- Contents:
- Front Cover; Myopathies; Copyright; Contributors; Contents; Neurologic Clinics; Preface; A Pattern Recognition Approach to Patients with a Suspected Myopathy; Key points; Introduction; Clinical evaluation; Which Negative and/or Positive Symptoms Do Patients Demonstrate?; What is the Temporal Evolution?; Is There a Family History of a Myopathic Disorder?; Are There Precipitating Factors That Trigger Episodic Weakness or Stiffness?; Are There Associated Systemic Symptoms or Signs?; What is the Distribution of Weakness?; Pattern recognition approach to myopathic disorders. Pattern 1: Proximal Limb-Girdle WeaknessPattern 2: Distal Weakness; Pattern 3: Proximal Arm/Distal Leg Weakness (Scapuloperoneal); Pattern 4: Distal Arm/Proximal Leg Weakness; 68-year old with slowly progressive muscle weakness; Comment; Pattern 5: Ptosis with or Without Ophthalmoparesis; 70-year old with progressive dysphagia and weakness; Comment; Pattern 6: Prominent Neck Extensor Weakness; Pattern 7: Bulbar Weakness; Pattern 8: Episodic Pain, Weakness, and Myoglobinuria; Pattern 9: Episodic Weakness Delayed or Unrelated to Exercise; Pattern 10: Stiffness and Decreased Ability to Relax. Laboratory approach in the evaluation of a suspected myopathyCK; Electrophysiologic Studies; The Muscle Biopsy; Molecular Genetic Studies; Other Tests; Summary; Web sites; References; Idiopathic Inflammatory Myopathies; Key points; Epidemiology; Clinical presentation; Dermatomyositis; Polymyositis; Necrotizing Myopathy;Front Cover; Myopathies; Copyright; Contributors; Contents; Neurologic Clinics; Preface; A Pattern Recognition Approach to Patients with a Suspected Myopathy; Key points; Introduction; Clinical evaluation; Which Negative and/or Positive Symptoms Do Patients Demonstrate?; What is the Temporal Evolution?; Is There a Family History of a Myopathic Disorder?; Are There Precipitating Factors That Trigger Episodic Weakness or Stiffness?; Are There Associated Systemic Symptoms or Signs?; What is the Distribution of Weakness?; Pattern recognition approach to myopathic disorders. Pattern 1: Proximal Limb-Girdle WeaknessPattern 2: Distal Weakness; Pattern 3: Proximal Arm/Distal Leg Weakness (Scapuloperoneal); Pattern 4: Distal Arm/Proximal Leg Weakness; 68-year old with slowly progressive muscle weakness; Comment; Pattern 5: Ptosis with or Without Ophthalmoparesis; 70-year old with progressive dysphagia and weakness; Comment; Pattern 6: Prominent Neck Extensor Weakness; Pattern 7: Bulbar Weakness; Pattern 8: Episodic Pain, Weakness, and Myoglobinuria; Pattern 9: Episodic Weakness Delayed or Unrelated to Exercise; Pattern 10: Stiffness and Decreased Ability to Relax. Laboratory approach in the evaluation of a suspected myopathyCK; Electrophysiologic Studies; The Muscle Biopsy; Molecular Genetic Studies; Other Tests; Summary; Web sites; References; Idiopathic Inflammatory Myopathies; Key points; Epidemiology; Clinical presentation; Dermatomyositis; Polymyositis; Necrotizing Myopathy; Conditions associated with dermatomyositis, polymyositis, and necrotizing myopathy; Polyarthritis; Interstitial Lung Disease; Malignancy; Autoimmune Necrotizing Myopathy; Cardiac Defects; Laboratory studies in dermatomyositis, polymyositis, and necrotizing myopathy. Cancer ScreeningPulmonary Function Testing; Biomarker Monitoring; Antibody Identification; Electrophysiology of dermatomyositis, polymyositis, and necrotizing myopathy; Muscle imaging; Muscle histopathology and pathogenesis of DM, PM, and NM; Dermatomyositis; Polymyositis; Necrotizing Myopathy; Therapy for dermatomyositis, polymyositis, and necrotizing myopathy; Corticosteroids; Methotrexate; Azathioprine; Intravenous Immunoglobulin; Treatment of Refractory Patients; IIM Associated with ILD; Promising Therapies; Physical Therapy; Prognosis; References; Inclusion Body Myositis; Key points. EpidemiologyClinical Presentation; Associated Conditions; Laboratory and Electrophysiologic Testing; Muscle Imaging; Muscle Histopathology; Pathogenesis; Diagnostic and research criteria; ENMC 2000; MRC 2010; ENMC 2011; Therapy; Ongoing Research; Prognosis; Exercise; Summary; References; Toxic Myopathies; Key points; Introduction; Pathophysiology/Pathogenesis; Necrotizing myopathy; Introduction; Statins; Clinical presentation; Laboratory features and electrophysiology; Histopathology; Pathogenesis; Treatment; Cholesterol-Lowering Drugs (Excluding Statins); Immunophilins; Clinical features. … (more)
- Publisher Details:
- Philadelphia : Elsevier
- Publication Date:
- 2014
- Extent:
- 1 online resource (305 pages)
- Subjects:
- 616.80442
Medicine
Molecular neurobiology
Nervous system -- Diseases -- Genetic aspects
Neurogenetics
HEALTH & FITNESS -- Diseases -- General
MEDICAL -- Clinical Medicine
MEDICAL -- Diseases
MEDICAL -- Evidence-Based Medicine
MEDICAL -- Internal Medicine
Medicine
Molecular neurobiology
Nervous system -- Diseases -- Genetic aspects
Neurogenetics
Electronic books - Languages:
- English
- ISBNs:
- 9780323320382
0323320384 - Related ISBNs:
- 9780323320191
0323320198 - Notes:
- Note: Print version record.
- Access Rights:
- Legal Deposit; Only available on premises controlled by the deposit library and to one user at any one time; The Legal Deposit Libraries (Non-Print Works) Regulations (UK).
- Access Usage:
- Restricted: Printing from this resource is governed by The Legal Deposit Libraries (Non-Print Works) Regulations (UK) and UK copyright law currently in force.
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library HMNTS - ELD.DS.237882
- Ingest File:
- 01_154.xml