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Muscle Atrophy
  • Language: en
  • Pages: 624

Muscle Atrophy

  • Type: Book
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  • Published: 2018-11-02
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  • Publisher: Springer

The book addresses the development of muscle atrophy, which can be caused by denervation, disuse, excessive fasting, aging, and a variety of diseases including heart failure, chronic kidney diseases and cancers. Muscle atrophy reduces quality of life and increases morbidity and mortality worldwide. The book is divided into five parts, the first of which describes the general aspects of muscle atrophy including its characteristics, related economic and health burdens, and the current clinical therapy. Secondly, basic aspects of muscle atrophy including the composition, structure and function of skeletal muscle, muscle changes in response to atrophy, and experimental models are summarized. Thi...

Background and Management of Muscular Atrophy
  • Language: en
  • Pages: 190

Background and Management of Muscular Atrophy

A healthy skeletal musculature is necessary for a good quality of life and is important in sports. The loss of skeletal muscle mass leads to severe clinical complications and alters daily functioning. The aim of this book is to give an overview of skeletal muscle atrophy including pathomechanism, clinical characters, and the tools for prevention and treatment. Skeletal muscle atrophy can develop due to neurogenic or myogenic reasons, and frequently appears as an age-dependent disorder (sarcopenia). The studies of theoretical background give promising perspectives to prevent and treat muscle atrophy. The book is recommended to scientists, practitioners, students, sportsmen, and everybody who is interested in the normal and impaired function of the skeletal muscle.

Multiple System Atrophy
  • Language: en
  • Pages: 211

Multiple System Atrophy

This textbook provides a comprehensive monography on multiple system atrophy (MSA), a rare and fatal neurodegenerative disorder that presents with autonomic failure and either parkinsonism (MSA-P) or cerebellar ataxia (MSA-C).The underlying neuropathology of MSA is characterized by striatonigral degeneration (SND), olivopontocerebellar atrophy (OPCA) and unique oligodendroglial cytoplasmic alpha-synuclein inclusions. MSA is therefore classified among the alpha-synucleinopathies such as Parkinson`s disease, pure autonomic failure and dementia with Lewy bodies. Over the last decade there have been important advances in early diagnosis, pathogenesis research and clinical trial activity. The monography will cover the entire spectrum ranging from molecular and genetic work to symptomatic and interventional therapies. The book is written for movement disorder clinicians and basic neuroscientists interested in degenerative movement disorders.

Atrophy
  • Language: en

Atrophy

In 'Atrophy', an unhappily married matron named Nora Fenway hears that her one-time clandestine lover, Christopher, is severely ill; she risks her reputation by going to visit him, but is turned away by his sanctimonious sister. A heartbreaking tale which emphasises the importance of human bonds but also examines the restraints we endure at the hands of society and prejudice.

Spinal Muscular Atrophy
  • Language: en
  • Pages: 506

Spinal Muscular Atrophy

Spinal Muscular Atrophy: Disease Mechanisms and Therapy provides the latest information on a condition that is characterized by motoneuron loss and muscle atrophy, and is the leading genetic cause of infant mortality. Since the identification of the gene responsible for SMA in 1995, there have been important advances in the basic understanding of disease mechanisms, and in therapeutic development. This book provides a comprehensive accounting of recent advances in basic and clinical research that covers SMA clinical features and standards of care, multifaceted aspects of SMN protein functions and SMA disease pathology, various animal models, and biomarkers, as well as current therapeutic dev...

One Step at a Time
  • Language: en
  • Pages: 84

One Step at a Time

This book is about ataxia and multiply system atrophy, two rare conditions., that I have to live with. It was originally written for my adult kids to begin with, explaining it to them so they hopefully would understand what ataxia and MSA is and can do to someone. Then to help spread ataxia awareness, so many people have never even heard of these conditions, let a lone know anything about them.

Posterior Cortical Atrophy
  • Language: en
  • Pages: 182

Posterior Cortical Atrophy

  • Type: Book
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  • Published: 2020-01-07
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  • Publisher: Unknown

POSTERIOR CORTICAL ATROPHY"The best science in everyday language."Also called Benson's disease, posterior cortical atrophy is an Alzheimer's variant. This book provides an extensive overview, covering symptoms, stages, diagnosis, treatment, risk factors, and prevention.

Experimental Atrophy of Muscle
  • Language: en
  • Pages: 178

Experimental Atrophy of Muscle

  • Type: Book
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  • Published: 1923
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  • Publisher: Unknown

None

On Atrophy of the Stomach and on the Nervous Affections of the Digestive Organs
  • Language: en
  • Pages: 242

On Atrophy of the Stomach and on the Nervous Affections of the Digestive Organs

  • Type: Book
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  • Published: 1880
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  • Publisher: Unknown

None

Gudden's Atrophy Method: And a Summary of Its Results
  • Language: en

Gudden's Atrophy Method: And a Summary of Its Results

This medical text offers a thorough introduction to Gudden's Atrophy Method for treating mental illness. Written by one of the leading practitioners of the method, this book includes a detailed summary of the technique's results, making it a valuable resource for anyone interested in the history of psychiatry. This work has been selected by scholars as being culturally important, and is part of the knowledge base of civilization as we know it. This work is in the "public domain in the United States of America, and possibly other nations. Within the United States, you may freely copy and distribute this work, as no entity (individual or corporate) has a copyright on the body of the work. Scholars believe, and we concur, that this work is important enough to be preserved, reproduced, and made generally available to the public. We appreciate your support of the preservation process, and thank you for being an important part of keeping this knowledge alive and relevant.