Evaluation and Treatment of Myopathies

Produk Detail:
  • Author : Robert Griggs
  • Publisher : Contemporary Neurology
  • Pages : 364 pages
  • ISBN : 0199873933
  • Rating : /5 from reviews
CLICK HERE TO GET THIS BOOK >>>Evaluation and Treatment of Myopathies

Download or Read online Evaluation and Treatment of Myopathies full in PDF, ePub and kindle. this book written by Robert Griggs and published by Contemporary Neurology which was released on 03 December 2021 with total page 364 pages. We cannot guarantee that Evaluation and Treatment of Myopathies book is available in the library, click Get Book button and read full online book in your kindle, tablet, IPAD, PC or mobile whenever and wherever You Like. Preceded by Evaluation and treatment of myopathies / Robert C. Griggs, Jerry R. Mendell, Robert G. Miller. c1995.

Muscle Aging Inclusion Body Myositis and Myopathies

Muscle Aging  Inclusion Body Myositis and Myopathies
  • Author : Valerie Askanas,W. King Engel
  • Publisher : John Wiley & Sons
  • Release : 27 February 2012
GET THIS BOOK Muscle Aging Inclusion Body Myositis and Myopathies

Muscle weakness with ageing is almost inevitable, generally beginning to manifest beyond the age of 40, and is usually unstoppable. It can lead to reduced mobility, increased risk of falling, injury, and even death. But ?you?re just getting old? is not a sufficient diagnosis. Specific causes of neuromuscular symptoms may explain progressive muscle weakness, and should be investigated for potential treatment. Muscle Ageing, Inclusion-Body Myositis and Myopathies explores the clinical and pathological expression of muscle weakness in aging persons. Case

Experimental Myopathies and Muscular Dystrophy

Experimental Myopathies and Muscular Dystrophy
  • Author : R. Heene
  • Publisher : Springer Science & Business Media
  • Release : 06 December 2012
GET THIS BOOK Experimental Myopathies and Muscular Dystrophy

Experimental Myopathies and Muscular Dystrophy. A Study of the Formal Pathogenesis of Primary Myopathies as Exemplified in the Myopathy of 2,4-Dichlorophenoxyacetic Acid The histochemical types of muscle fibres are described and a report presented of the histological and histochemical altera tions in skeletal muscles (tibialis anterior, gastrocnemius and soleus muscles) of rats given intraperitoneal injections of the herbicide, 2,4-dichlorophenoxyacetic acid (2,4-0). The liver and myocardium of the experimental animals were also examined. In skeletal muscle, alterations occurring acutely within 1 to 1. 5

Myopathies an Issue of Neurologic Clinics

Myopathies  an Issue of Neurologic Clinics
  • Author : Mazen Dimachkie
  • Publisher : Elsevier Health Sciences
  • Release : 23 July 2014
GET THIS BOOK Myopathies an Issue of Neurologic Clinics

Congential myopathies, Muscular dystropies, Glycogen storage diseases of muscle, and Idiopathic and Inflammatory myopathies are presented in this volume of Neurologic Clinics. Topics include: Muscle channelopathies; Pompe disease; Congenital myopathies and muscular dystrophies; Duchenne and Becker muscular dystrophies; Distal myopathies; Limb-girdle muscular dystrophy; Fascioscapulomuneral muscular dystrophy; Myotonic dystrophy; Metabolic and mitochondrial myopathies; Sporadic inclusion body myositis; Toxic myopathies; Idiopathic Inflammatory myopathies; Approach to muscle disease.

Myopathies An Issue of Rheumatic Disease Clinics E Book

Myopathies  An Issue of Rheumatic Disease Clinics   E Book
  • Author : Robert L. Wortmann
  • Publisher : Elsevier Health Sciences
  • Release : 12 May 2011
GET THIS BOOK Myopathies An Issue of Rheumatic Disease Clinics E Book

This issue of Rheumatic Disease Clinics provides important updates in myopathies. The following essential topics are covered. Clinical features, pathophysiology, and treatment of polymyositis and dermatomyositis; inclusion body myositis; metabolic myopathies; drug-induced myopathies; muscular dystrophies and neurologic diseases; laboratory testing and imaging; electrophysiological studies; metabolic and genetic testing; and pathology.

Pediatric Neurology Part III

Pediatric Neurology Part III
  • Author : Norma Beatriz Romero,Nigel F. Clarke
  • Publisher : Elsevier Inc. Chapters
  • Release : 24 April 2013
GET THIS BOOK Pediatric Neurology Part III

Congenital myopathies are a heterogeneous group of inherited muscle disorders, characterized by the predominance of particular histopathological features on muscle biopsy, such as cores (central core disease) or rods (nemaline myopathy). Clinically, early onset of the disease, stable or slowly progressive muscle weakness, hypotonia and delayed motor development are common in most forms. As a result, the diagnosis of a subtype of congenital myopathy is largely based on the presence of specific structural abnormalities in the skeletal muscle detected by

Hereditary myopathies

Hereditary myopathies
  • Author : Sics Editore
  • Publisher : SICS Editore
  • Release : 01 October 2014
GET THIS BOOK Hereditary myopathies

The majority of patients with myopathies have an inherited disease. Symptoms alone are not usually enough to diagnose myopathy, but they warrant further neurological examinations that are performed in larger hospitals and in special outpatient clinics for neuromuscular disorders.

The Inflammatory Myopathies

The Inflammatory Myopathies
  • Author : Lawrence J. Kagen
  • Publisher : Springer Science & Business Media
  • Release : 10 June 2009
GET THIS BOOK The Inflammatory Myopathies

This book presents a comprehensive review of the inflammatory myopathies, including dermatomyositis, polymyositis, and inclusion body myositis. Representing the most up-to-date knowledge on this family of diseases, this book is the gold-standard in its field.

Idiopathic Inflammatory Myopathies

Idiopathic Inflammatory Myopathies
  • Author : Jan Tore Gran
  • Publisher : BoD – Books on Demand
  • Release : 15 September 2011
GET THIS BOOK Idiopathic Inflammatory Myopathies

The term "myositis" covers a variety of disorders often designated "idiopathic inflammatory myopathies". Although they are rather rare compared to other rheumatic diseases, they often cause severe disability and not infrequently increased mortality. The additional involvement of important internal organs such as the heart and lungs, is not uncommon. Thus, there is a great need for a better understanding of the etiopathogenesis of myositis, which may lead to improved treatment and care for these patients. Major advances regarding research and

Pediatric Neurology Part III

Pediatric Neurology Part III
  • Author : Adele D'amico,Enrico Bertini
  • Publisher : Elsevier Inc. Chapters
  • Release : 24 April 2013
GET THIS BOOK Pediatric Neurology Part III

Inborn errors of metabolism may impact on muscle and peripheral nerve. Abnormalities involve mitochondria and other subcellular organelles such as peroxisomes and lysosomes related to the turnover and recycling of cellular compartments. Treatable causes are β-oxidation defects producing progressive neuropathy; pyruvate dehydrogenase deficiency, porphyria, or vitamin B12 deficiency causing recurrent episodes of neuropathy or acute motor deficit mimicking Guillain–Barré syndrome. On the other hand, lysosomal (mucopolysaccharidosis, Gaucher and Fabry diseases), mitochondriopathic (mitochondrial or nuclear mutations or mDNA depletion), peroxisomal (

Pediatric Neurology Part III

Pediatric Neurology Part III
  • Author : Kristl G. Claeys,Michel Fardeau
  • Publisher : Elsevier Inc. Chapters
  • Release : 24 April 2013
GET THIS BOOK Pediatric Neurology Part III

Myofibrillar myopathies (MFMs) are rare, inherited or sporadic, progressive neuromuscular disorders with considerable clinical and genetic heterogeneity. MFMs are defined morphologically by foci of myofibril dissolution that begins at the Z-disk, accumulation of myofibrillar degradation products, and ectopic expression of a large number of proteins including desmin. To date, mutations in six genes are known to cause MFMs, accounting for approximately half of the MFM patients identified. The causative genes encode mainly sarcomeric Z-disk(-related) proteins: desmin, αB-crystallin, myotilin, Z-band

Hereditary Myopathies

Hereditary Myopathies
  • Author : Arlek Marion González-Jamett
  • Publisher : Unknown
  • Release : 03 December 2021
GET THIS BOOK Hereditary Myopathies

Hereditary myopathies are inherited disorders primarily affecting the skeletal muscle tissue. These are caused by mutations in different genes-encoding proteins that play important roles in muscle structure and function. Skeletal muscle weakness and hypotonia are typical clinical manifestations in most of hereditary myopathies. Histological features such as fiber type disproportion, myofibrillar disorganization, and structural abnormalities are usually observed in muscle biopsies of non-dystrophic myopathies, while fibrosis, fiber regeneration, wasting, and atrophy are characteristic of dystrophic myopathies. However, similar histopathological features

Metabolic Myopathies

Metabolic Myopathies
  • Author : David Hilton-Jones
  • Publisher : W B Saunders Company
  • Release : 03 December 1995
GET THIS BOOK Metabolic Myopathies

This is a comprehensive resource giving practical guidance on assessment and diagnosis of metabolic myopathies, plus state-of-the-art data on their biochemical foundation. It reviews all current knowledge on the myopathies of metabolic origin, including information on genetic factors.