Atlas of the Ultrastructure of Diseased Human Muscle PDF Download
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Author: William George Parker Mair
Publisher: Williams & Wilkins
ISBN:
Category : Medical
Languages : en
Pages : 268
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Book Description
Atlas of the Ultrastructure of Diseased Human Muscle ...
Author: William George Parker Mair
Publisher: Williams & Wilkins
ISBN:
Category : Medical
Languages : en
Pages : 268
Get Book Here
Book Description
Atlas of the Ultrastructure of Diseased Human Muscle ...
Author: William George Parker Mair
Publisher:
ISBN:
Category :
Languages : fr
Pages : 249
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Book Description
![Atlas of the Ultrastructure of Diseased Human Muscle [by] W.G.P. Mair [and] F.M.S. Tomé PDF](https://books.google.com/books/content/images/frontcover/Bi2XswEACAAJ?fife=w80-h100)
Author: William George Parker Mair
Publisher:
ISBN:
Category : Histology, Pathological
Languages : en
Pages : 249
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Book Description
Author: W. P. G. Mair
Publisher:
ISBN:
Category :
Languages : en
Pages : 0
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Book Description
![Atlas of the Ultrastructure of Diseased Human Muscle ; Mair, W[illiam] G[eorge] P[arker], F.M.S. Tomé PDF](https://books.google.com/books/content/images/frontcover/aCSXMwAACAAJ?fife=w80-h100)
Author: William George Parker Mair
Publisher:
ISBN:
Category :
Languages : en
Pages : 249
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Book Description
Author: W G P Mair
Publisher: Elsevier
ISBN: 1483280993
Category : Science
Languages : en
Pages : 260
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Book Description
Atlas of the Ultrastructure of Diseased Human Muscle provides a general view of the ultrastructure of normal and diseased human muscle. This book contains five chapters that illustrate the changes that take place in common pathological conditions and outline the patterns of change, which occur in particular diseases. Chapter 1 describes the ultrastructure of normal striated muscle and the extra-ocular and cardiac muscle. This chapter also deals with skeletal and cardiac muscle of the human fetus. Chapter 2 examines the changes in the ultrastructure of muscle fibers, including changes in myofibrils, mitochondria, lipid bodies, plasma, and basement membranes. Chapters 3 and 4 evaluate the changes in blood capillaries, interstitial tissue of muscle, nerves, motor end plates, and muscle spindles. Chapter 5 discusses the ultrastructural changes in various muscle diseases, such as denervation atrophy of muscle, muscular dystrophies, polymyositis, and congenital myopathies.
Author: Fred Hossler
Publisher: John Wiley & Sons
ISBN: 1118284534
Category : Science
Languages : en
Pages : 966
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Book Description
Ultrastructure Atlas of Human Tissues presents a variety of scanning and transmission electron microscope images of the major systems of the human body. Photography with the electron microscope records views of the intricate substructures and microdesigns of objects and tissues, and reveals details within them inaccessible to the naked eye or light microscope. Many of these views have significance in understanding normal structure and function, as well as disease processes. This book offers a unique and comprehensive look at the structure and function of tissues at the subcellular and molecular level, an important perspective in understanding and combating diseases. • Presents the major systems of the human body through scanning and transmission electron microscope images • Has images prepared almost exclusively from human tissues • Includes electron micrographs of common pathologies such as fibrotic and emphysemic lung, kidney stones, sickle cell anemia, and skin parasites • Contains sets of 3D images in most chapters
Author: William George Parker Mair
Publisher:
ISBN:
Category :
Languages : en
Pages : 249
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Book Description
Author: National Library of Medicine (U.S.)
Publisher:
ISBN:
Category : Medicine
Languages : en
Pages :
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Book Description
First multi-year cumulation covers six years: 1965-70.
Author: Michael Swash
Publisher: Springer Science & Business Media
ISBN: 1447138341
Category : Medical
Languages : en
Pages : 548
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Book Description
Nine years have elapsed since the second edition of this book was published. In this time the principal advances in neuromuscular diseases have been in the application of molecular genetics to understanding the aetiology and pathogenesis of this group of disorders. As a result many previously unrecognised disorders have been charac terised. Some clinical syndromes, such as the limb girdle dystrophies, have become better defined. In many such instances the new genetic information has led to major advances in knowledge of the biology of cell structures, for example, the membrane structural and channel proteins. The clinical syndromes themselves, and their patho logical and electrophysiological characteristics, however, remain as important as ever, since they constitute the clinical problem itself and, indeed, the database from which all other concepts emerge. Knowledge of the pathogenesis, genetics, and molecular biology of neuromuscular disorders is essential both in developing and applying new therapies and preventive measures, and in formulating genetic and prognostic advice. However, this informa tion does not necessarily always define clinically useful syndromes. Myotonia, for example, is an electrophysiological finding in some syndromes in which it is un detectable by clinical examination, although the phenomenon itself was originally defined as a clinical entity. The limb girdle muscular dystrophy syndromes can be defined by severity, distribution of weakness, age of onset, sex distribution and other characteristics and many of these can be better understood by study of the under lying defect in cell structural proteins.
