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.

Produk Detail:

  • Author : Mazen Dimachkie
  • Publisher : Elsevier Health Sciences
  • Pages : 305 pages
  • ISBN : 0323320384
  • Rating : 4/5 from 21 reviews
CLICK HERE TO GET THIS BOOKMyopathies An Issue of Neurologic Clinics

Myopathies, An Issue of Neurologic Clinics,

Myopathies, An Issue of Neurologic Clinics,
  • Author : Mazen Dimachkie
  • Publisher : Elsevier Health Sciences
  • Release : 31 July 2014
GET THIS BOOKMyopathies, 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.

Polymyositis and Dermatomyositis

Polymyositis and Dermatomyositis
  • Author : Marinos C Dalakas
  • Publisher : Butterworth-Heinemann
  • Release : 22 October 2013
GET THIS BOOKPolymyositis and Dermatomyositis

Polymyositis and Dermatomyositis provides extensive information regarding Polymyositis and Dermatomyositis (PM/DM), which is described as a heterogeneous disease complex. This book is divided into four sections: Part I (Clinical Features) covers the classification of PM/DM, details of the clinical presentation, and the disease's association with the other connective tissue disorders and malignancies. Part II (Etiology and Mechanisms) covers advances in the immunopathology and viral etiology of PM/DM along with a frequently recognized entity: inclusion body myositis. Part

Cardioskeletal Myopathies in Children and Young Adults

Cardioskeletal Myopathies in Children and Young Adults
  • Author : John Lynn Jefferies,Burns Blaxall,Jeffrey Towbin,Jeffrey Robbins
  • Publisher : Academic Press
  • Release : 22 October 2016
GET THIS BOOKCardioskeletal Myopathies in Children and Young Adults

Cardioskeletal Myopathies in Children and Young Adults focuses on plaques that kill people in their 40’s-50’s and the way they start to form in young adulthood. The Annals of Family Medicine report that approximately half of young adults have at least one cardiovascular disease risk factor (Mar 2010), and an increase in cardiovascular mortality rates in young adults was substantiated in a study at Northwestern Medicine (Nov 2011). Given the increasing recognition of genetic triggers behind all types of cardiovascular disease,

The Inflammatory Myopathies

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

Evaluation and Treatment of Myopathies

Evaluation and Treatment of Myopathies
  • Author : Emma Ciafaloni,Patrick Chinnery,Robert Griggs
  • Publisher : Oxford University Press
  • Release : 26 May 2014
GET THIS BOOKEvaluation and Treatment of Myopathies

This new edition of Evaluation and Treatment of Myopathies is written for the clinician who sees patients with muscle disease, or the patient with complaints of pain or weakness of muscle. Like the original, this new edition is divided in to 3 primary sections: Approach to the Patient with Muscle Disease, Specific Myopathies, and General Strategies of Clinical Management, each section providing practical guidance to eliciting key histories and demonstrate findings upon examination. This new edition also provides guidance on the

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 BOOKMyopathies, 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 BOOKMyopathies, 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.

Experimental Myopathies and Muscular Dystrophy

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

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 BOOKMuscle 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

Myopathy: New Insights for the Healthcare Professional: 2011 Edition

Myopathy: New Insights for the Healthcare Professional: 2011 Edition
  • Author : Anonim
  • Publisher : ScholarlyEditions
  • Release : 09 January 2012
GET THIS BOOKMyopathy: New Insights for the Healthcare Professional: 2011 Edition

Myopathy: New Insights for the Healthcare Professional: 2011 Edition is a ScholarlyBrief™ that delivers timely, authoritative, comprehensive, and specialized information about Myopathy in a concise format. The editors have built Myopathy: New Insights for the Healthcare Professional: 2011 Edition on the vast information databases of ScholarlyNews.™ You can expect the information about Myopathy in this eBook to be deeper than what you can access anywhere else, as well as consistently reliable, authoritative, informed, and relevant. The content of Myopathy: New Insights for

Myopathy: New Insights for the Healthcare Professional: 2013 Edition

Myopathy: New Insights for the Healthcare Professional: 2013 Edition
  • Author : Anonim
  • Publisher : ScholarlyEditions
  • Release : 22 July 2013
GET THIS BOOKMyopathy: New Insights for the Healthcare Professional: 2013 Edition

Myopathy: New Insights for the Healthcare Professional: 2013 Edition is a ScholarlyBrief™ that delivers timely, authoritative, comprehensive, and specialized information about Additional Research in a concise format. The editors have built Myopathy: New Insights for the Healthcare Professional: 2013 Edition on the vast information databases of ScholarlyNews.™ You can expect the information about Additional Research in this book to be deeper than what you can access anywhere else, as well as consistently reliable, authoritative, informed, and relevant. The content of Myopathy: New

Myopathology

Myopathology
  • Author : Balan Louis Gaspar,Rakesh Kumar Vasishta,Bishan Dass Radotra
  • Publisher : Springer
  • Release : 24 September 2018
GET THIS BOOKMyopathology

This book covers all aspects of basic, essential, recent advances and controversies in myopathology. The major emphasis is on diagnostic myopathology of muscular dystrophies, inflammatory myopathies, mitochondrial myopathies, metabolic myopathies, congenital myopathies, myopathies of miscellaneous etiology, neurogenic and neuromuscular junction disorders, the goal being to broaden readers’ understanding of individual disease subgroups. The book also contains all the essential details needed to establish a neuromuscular lab, making it especially relevant for laboratory technical staff and research scholars.