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Author: E. Kuhn Publisher: Springer-Verlag ISBN: 3642929206 Category : Medical Languages : de Pages : 552
Book Description
Dieses Buch, eine Zusammenstellung der Referate, Gesprache und Diskussionen des Heidelberger Symposions anlaBlich der 125. Wiederkehr des Geburtstages von WILHELM ERB, mochte diesem groBen Heidelberger Kliniker und Forscher ein ehren des und dankbares Gedenken bewahren. Dies allein rechtfertigt die Herausgabe. Wir danken den Referenten, die aus der ganzen Welt freudig unserem Ruf folgten, WILHELM ERB gebuhrend zu ehren. So konnten wir aus berufenem Munde erfahren, was wir zur Zeit auf diesem Gebiet wissen und wohin wir unseren Blick bei der weiteren Arbeit lenken sollten; nur so bekam aber au.
Author: E. Kuhn Publisher: Springer-Verlag ISBN: 3642929206 Category : Medical Languages : de Pages : 552
Book Description
Dieses Buch, eine Zusammenstellung der Referate, Gesprache und Diskussionen des Heidelberger Symposions anlaBlich der 125. Wiederkehr des Geburtstages von WILHELM ERB, mochte diesem groBen Heidelberger Kliniker und Forscher ein ehren des und dankbares Gedenken bewahren. Dies allein rechtfertigt die Herausgabe. Wir danken den Referenten, die aus der ganzen Welt freudig unserem Ruf folgten, WILHELM ERB gebuhrend zu ehren. So konnten wir aus berufenem Munde erfahren, was wir zur Zeit auf diesem Gebiet wissen und wohin wir unseren Blick bei der weiteren Arbeit lenken sollten; nur so bekam aber au.
Author: R. Heene Publisher: Springer Science & Business Media ISBN: 3642662005 Category : Medical Languages : en Pages : 104
Book Description
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 h after injection of a single dose of 300 mg/kg 2,4-0 could be distinguished from changes which developed subacutely in the course of treatment with repeated injections of one quarter to one half of the LDSO of the substance. In both con ditions white (type 2B/Am) muscle fibres were involved pre dilectively. The principal histochemical effect of acute intoxi cation observed was leakage of phosphorylase and glycogen from white muscle fibres, whereas some of the red fibres (type 2A/C) m showed an increase in primary glycogen and phosphorylase activ ity. These changes, which must be considered nonspecifi~, were established by use of a gelatin incubation technique. They occurred as typical findings in the middle and deep areas of the anterior tibial muscle. In other muscles or different layers of the same muscle, these changes varied considerably in degree. Thus the gastrocnemius and soleus muscles displayed only minor or no alterations.
Author: Jun Kimura M.D. Publisher: Oxford University Press ISBN: 0199880956 Category : Medical Languages : en Pages : 1778
Book Description
Building on the author's personal experience in working with fellows and residents in the electromyography laboratory, this volume is the definitive reference in the field. It is intended for clinicians who perform electrodiagnostic procedures as an extension of their clinical examination, and will be of value to neurologists and physiatrists who are interested in neuromuscular disorders and noninvasive electrodiagnostic methods, particularly those practicing electromyography (EMG). The book provides a comprehensive review of most peripheral nerve and muscle diseases, including specific techniques and locations for performing each test. Divided into two major sections, the first addresses the basics of electrodiagnosis, including information on anatomy and physiology, techniques for nerve conduction studies, and discussions of the blink reflex and H-reflex, etc. The second section presents each neuromuscular disorder, covering clinical aspects and extensive information on the distinctive electrophysiological findings typical of the disease. New for this edition: thorough updating of all chapters with extensive new references; entirely new sections on magnetic stimulation, human reflexes, late responses, quantitative EMG, motor unit number estimate, threshold electrotonus, and pediatric electrodiagnosis; consolidated yet comprehensive coverage of periperhal, as well as CNS studies, offering a practical approach for problem-solving; ample space allotted for clinical discussion.
Author: Thomas E. Andreoli Publisher: Springer Science & Business Media ISBN: 1468412868 Category : Medical Languages : en Pages : 283
Book Description
Clinical Disorders of Membrane Transport Processes is a softcover book containing a portion of Physiology of Membrane Disorders (Second Edition). The parent volume contains six major sections that deal with general aspects of the physiology of transport processes and specific aspects of transport processes in cells and in organized cellular systems, namely epithelia. This text contains the last section, which deals with the application of the physiology of transport processes to the understanding of clinical disorders. We hope that this smaller volume will be helpful to individuals particularly interested in clinical derangements of membrane transport processes. THOMAS E. ANDREOLI JOSEPH F. HOFFMAN DARRELL D. FANESTIL STANLEY G. SCHULTZ Vll Preface to the Second Edition The second edition of Physiology of Membrane Disorders represents an extensive revision and a considerable expansion of the fIrst edition. Yet the purpose of the second edition is identical to that of its predecessor, namely, to provide a rational analysis of membrane transport processes in individual membranes, cells, tissues, and organs, which in tum serves as a frame of reference for rationalizing disorders in which derangements of membrane transport processes playa cardinal role in the clinical expression of disease. As in the fIrst edition, this book is divided into a number of individual, but closely related, sections. Part V represents a new section where the problem of transport across epithelia is treated in some detail. Finally, Part VI, which analyzes clinical derangements, has been enlarged appreciably.
Author: Lorenzo Maggi Publisher: Frontiers Media SA ISBN: 2889664511 Category : Medical Languages : en Pages : 119
Book Description
Jean-François Desaphy is a co-inventor, with no personal financial interest, of a European patent assigned to a pharmaceutical company regarding the use of a company drug in myotonic syndromes.
Author: Michael Swash Publisher: Springer Science & Business Media ISBN: 1447138341 Category : Medical Languages : en Pages : 548
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.
Author: Ian Ramsay Publisher: Elsevier ISBN: 1483164403 Category : Medical Languages : en Pages : 193
Book Description
Thyroid Disease and Muscle Dysfunction is an attempt to clarify one of those areas in medicine where specialties overlap, namely, endocrinology and neurology, though many of the clinical problems to be considered are encountered by the general physician. Increasing attention has been drawn to the association between abnormalities of skeletal muscle and derangement of thyroid function. Thyrotoxic myopathy, previously thought to be rare, is now known to be common; muscular abnormalities are being more frequently described in patients with hypothyroidism; and the association of Myasthenia Gravis and Periodic Paralysis with hyperthyroidism is also well recognized. These associations are not surprising considering that thyroid hormone plays a major part in regulating the production of energy in the body, and indeed it is to be hoped that investigation of these diseases will throw more light on the controlling mechanisms of muscle metabolism. This text provides insights into these issues. This book is beneficial to medical students that are in need of extensive information regarding muscle disorders in thyroid disease.
Author: E. Kuhn
Author: E. Kuhn
Author: 
Author: R. Heene
Author: Jun Kimura M.D.
Author: Thomas E. Andreoli
Author: Lorenzo Maggi
Author: Michael Swash
Author: Ian Ramsay
Author: National Library of Medicine (U.S.)
Author: George G. Lunt