Spinocerebellar Degenerations Advances in Research and Treatment 2012 Edition

Spinocerebellar Degenerations   Advances in Research and Treatment  2012 Edition
Author: Anonim
Publsiher: ScholarlyEditions
Total Pages: 24
Release: 2012-12-26
ISBN 10: 1481631446
ISBN 13: 9781481631440
Language: EN, FR, DE, ES & NL

Spinocerebellar Degenerations Advances in Research and Treatment 2012 Edition Book Review:

Spinocerebellar Degenerations—Advances in Research and Treatment: 2012 Edition is a ScholarlyPaper™ that delivers timely, authoritative, and intensively focused information about Spinocerebellar Degenerations in a compact format. The editors have built Spinocerebellar Degenerations—Advances in Research and Treatment: 2012 Edition on the vast information databases of ScholarlyNews.™ You can expect the information about Spinocerebellar Degenerations 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 Spinocerebellar Degenerations—Advances in Research and Treatment: 2012 Edition has been produced by the world’s leading scientists, engineers, analysts, research institutions, and companies. All of the content is from peer-reviewed sources, and all of it is written, assembled, and edited by the editors at ScholarlyEditions™ and available exclusively from us. You now have a source you can cite with authority, confidence, and credibility. More information is available at http://www.ScholarlyEditions.com/.

Spinocerebellar Degenerations Advances in Research and Treatment 2011 Edition

Spinocerebellar Degenerations  Advances in Research and Treatment  2011 Edition
Author: Anonim
Publsiher: ScholarlyEditions
Total Pages: 14
Release: 2012-02-14
ISBN 10: 1464969639
ISBN 13: 9781464969638
Language: EN, FR, DE, ES & NL

Spinocerebellar Degenerations Advances in Research and Treatment 2011 Edition Book Review:

Spinocerebellar Degenerations: Advances in Research and Treatment: 2011 Edition is a ScholarlyPaper™ that delivers timely, authoritative, and intensively focused information about Spinocerebellar Degenerations in a compact format. The editors have built Spinocerebellar Degenerations: Advances in Research and Treatment: 2011 Edition on the vast information databases of ScholarlyNews.™ You can expect the information about Spinocerebellar Degenerations 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 Spinocerebellar Degenerations: Advances in Research and Treatment: 2011 Edition has been produced by the world’s leading scientists, engineers, analysts, research institutions, and companies. All of the content is from peer-reviewed sources, and all of it is written, assembled, and edited by the editors at ScholarlyEditions™ and available exclusively from us. You now have a source you can cite with authority, confidence, and credibility. More information is available at http://www.ScholarlyEditions.com/.

TRH and Spinocerebellar Degeneration

TRH and Spinocerebellar Degeneration
Author: Itsurō Sobue
Publsiher: Elsevier Science Limited
Total Pages: 268
Release: 1986
ISBN 10:
ISBN 13: UOM:39015010157199
Language: EN, FR, DE, ES & NL

TRH and Spinocerebellar Degeneration Book Review:

Index Medicus

Index Medicus
Author: Anonim
Publsiher: Anonim
Total Pages: 329
Release: 2003
ISBN 10:
ISBN 13: OSU:32436011091699
Language: EN, FR, DE, ES & NL

Index Medicus Book Review:

Cerebellar Degenerations Clinical Neurobiology

Cerebellar Degenerations  Clinical Neurobiology
Author: Andreas Plaitakis
Publsiher: Springer Science & Business Media
Total Pages: 507
Release: 2012-12-06
ISBN 10: 1461535107
ISBN 13: 9781461535102
Language: EN, FR, DE, ES & NL

Cerebellar Degenerations Clinical Neurobiology Book Review:

This book encompasses basic and clinical reports on the cerebellum and its primary atrophic disorders, the cerebellar degenerations. Rapid progress has been made in undestanding the organization and function of the cerebellum at the neuronal, synaptic, and molecular level. Of particular importance has been the identification of the chemical transmitters utilized by the cer ebellar cellular systems. More than any other brain region, the cerebellum utilizes amino acids as its main excitatory and inhibitory neurotransmitters. Excitatory amino acid transmitters, in addition to serving neuronal com munication, may also mediate trophic and toxic effects, and as such, they may playa role in neurodegenerative processes. The cerebellar degenerations were among the first human disorders with primary system atrophy to be studied clinically and pathologically. This field of clinical cerebellar sciences, no longer confined to the previously known descriptive level, is now advancing rapidly, propelled by rapid advances in neuroimaging, immunology, and molecular biology. The advent of CT, MRI, and PET has in recent years permitted the study of central nervous system alterations in living patients, thus contributing substantially to the accuracy of the diagnosis and the classification of these disorders. The nosology of cerebellar degenerations, which has been the subject of much debate for over a century, is presently a dynamic field, with new entities being recognized and old "classic ataxias" being redefined in the light of new genetic evidence.

The Olivopontocerebellar Atrophies

The Olivopontocerebellar Atrophies
Author: Roger C. Duvoisin,Andreas Plaitakis
Publsiher: Anonim
Total Pages: 286
Release: 1984
ISBN 10:
ISBN 13: UOM:39015006697927
Language: EN, FR, DE, ES & NL

The Olivopontocerebellar Atrophies Book Review:

Robbins and Cotran Pathologic Basis of Disease Professional Edition E Book

Robbins and Cotran Pathologic Basis of Disease  Professional Edition E Book
Author: Vinay Kumar,Abul K. Abbas,Nelson Fausto,Jon C. Aster
Publsiher: Elsevier Health Sciences
Total Pages: 1464
Release: 2009-06-10
ISBN 10: 1437721826
ISBN 13: 9781437721829
Language: EN, FR, DE, ES & NL

Robbins and Cotran Pathologic Basis of Disease Professional Edition E Book Book Review:

One of the best-selling medical textbooks of all time, Robbins and Cotran Pathologic Basis of Disease is the one book you likely purchased as a medical student that still provides answers now that you're in practice. The new PROFESSIONAL EDITION is the same "who's who" of pathology experts that delivers the most dependable, current, and complete coverage of today's essential pathology knowledge, now enhanced with PERKS DESIGNED SPECIALLY FOR YOU AS A PRACTITIONER. Masterful editing and a practical organization make learning or reinforcing every concept remarkably easy. The result remains the ideal source for an optimal understanding of pathology at its core. Offers the most authoritative and comprehensive, yet readable coverage available in any pathology textbook, making it ideal for USMLE or specialty board preparation as well as for course work

Neuromuscular Case Studies E Book

Neuromuscular Case Studies E Book
Author: Tulio E. Bertorini
Publsiher: Elsevier Health Sciences
Total Pages: 632
Release: 2008-05-14
ISBN 10: 0702038695
ISBN 13: 9780702038693
Language: EN, FR, DE, ES & NL

Neuromuscular Case Studies E Book Book Review:

In this unique book, Dr. Bertorini guides you through more than 100 cases that demonstrate the diagnosis and management of a wide range of common and rare neuromuscular disorders. No other reference boasts such a large array of clinical studies devoted to all areas of this broad topic! Each case study reviews the etiologies, pathogenesis, differential diagnosis, and management of a particular disorder, helping you not only recognize its presentation, but also determine a diagnosis and the best treatment plans for your patients. You’ll also find expert guidance on the basic mechanisms of neuromuscular disorders, clinical examination, and diagnostic tests—including EMG, muscle biopsy, genetic testing, and more. More than 100 detailed case studies explore both common and rare neuromuscular disorders and the treatment protocols for each, equipping you with the knowledge you need to confidently manage any challenge. Each case includes a summary of important points or highlights of the study. Case studies are arranged either by complaint or by diagnosis so that you can successfully manage your patients with or without an initial diagnosis. Comprehensive coverage of EMGs and nerve conduction studies and other diagnostic tests, including muscle and nerve biopsies and genetic testing, helps you accurately diagnose nerve, muscle, and neuromuscular transmission disorders. Detailed discussions of treatment plans and commonly used drugs enhance your management of autoimmune disorders, painful neuropathy, dysautonomia, and other neuromuscular disorders. A reader-friendly format takes you step by step through the diagnosis and treatment of neuromuscular disorders, from the basic anatomy and physiology of the nerve and muscle through to clinical evaluation, diagnostic testing, and therapy. More than 350 high-quality illustrations, including full-color patient photographs, biopsies, and EMG tracings, make complex concepts easier to understand and apply.

Ultimate Review for the Neurology Boards Second Edition

Ultimate Review for the Neurology Boards  Second Edition
Author: Stephan Eisenchenk, MD,Michael S. Okun, MD
Publsiher: Demos Medical Publishing
Total Pages: 550
Release: 2009-08-14
ISBN 10: 1935281852
ISBN 13: 9781935281856
Language: EN, FR, DE, ES & NL

Ultimate Review for the Neurology Boards Second Edition Book Review:

Preparing for the Neurology Boards, recertification, or the AAN's RITE® Residency In-Service Training Exam can be daunting, years of study, training, and volumes of material to be processed, organized, and distilled for ready recall when the moment arrives. It may seem impossible to retain so much information. However, the completely revised and expanded Second Edition of this unique, easy-to-use bestselling review guide gives you all the tools you need to tie it all together no additional texts needed. And with Ultimate Review for the Neurology Boards you have free web support including: access to online cases, flashcards, and a medications data bank. Free access when you register with the password included in the book. The book breaks down the field of neurology into 24 chapters covering all subjects on the neurology boards including child and adult psychiatry, neuropsychiatry, and neurophysiology. Using an expanded outline format and innovative heading hierarchy for in-depth or rapid review, the topics are arranged so that you will read the easiest-to-remember first and the most-likely-to-be-forgotten last. Every chapter has been brought up-to-date to reflect current science and practice and includes information on: pivotal trials, new medications and treatments, diagnostic criteria, genetic disorders, and AAN guidelines. Complete your study on the web with the hundreds of cases, flashcards, and images. The Expanded Second Edition Features: 24 thoroughly updated chapters covering all subjects on the neurology boards A new Mini-Atlas of EEG tracings to hone proficiency in interpretation More NB (nota bene) items throughout flag must-know high-yield information More diagrams, illustrations, and tables to solidify concepts, streamline dense material, and enhance learning Additional Notes page the end of each chapter for personal annotations Are You Really Ready? - completely new practice test with questions, answers, and explanations to gauge preparedness Free access to enhanced web features and new case modules to extend and reinforce the material in the book Ultimate Review for the Neurology Boards is a must-have for residents preparing for boards or studying for the RITE exam, and for neurologists preparing for recertification. The Second Edition continues to deliver the Ultimate in high-yield board review, in print and on the web.

Medical Subject Headings

Medical Subject Headings
Author: Anonim
Publsiher: Anonim
Total Pages: 329
Release: 2004
ISBN 10:
ISBN 13: MINN:31951D02403102O
Language: EN, FR, DE, ES & NL

Medical Subject Headings Book Review:

Medical Neurology

Medical Neurology
Author: John Gilroy,John Stirling Meyer
Publsiher: MacMillan Publishing Company
Total Pages: 787
Release: 1979
ISBN 10:
ISBN 13: UOM:39015000848526
Language: EN, FR, DE, ES & NL

Medical Neurology Book Review:

Current Neurology

Current Neurology
Author: Anonim
Publsiher: Anonim
Total Pages: 329
Release: 1993
ISBN 10:
ISBN 13: UCSD:31822015587892
Language: EN, FR, DE, ES & NL

Current Neurology Book Review:

Neurogenetics

Neurogenetics
Author: Roger N. Rosenberg
Publsiher: Lippincott Williams & Wilkins
Total Pages: 324
Release: 1986
ISBN 10:
ISBN 13: UOM:39015009581185
Language: EN, FR, DE, ES & NL

Neurogenetics Book Review:

Movement Disorders

Movement Disorders
Author: Hubert H. Fernandez, MD,Marcelo Merello, MD
Publsiher: Demos Medical Publishing
Total Pages: 344
Release: 2012-07-18
ISBN 10: 161705058X
ISBN 13: 9781617050589
Language: EN, FR, DE, ES & NL

Movement Disorders Book Review:

Clinical case studies have long been recognized as a useful adjunct to problem-based learning and continuing professional development. Movement Disorders collects over 90 of the most memorable and challenging movement disorder cases from the worldís leading authorities in this specialty. Compelling vignettes covering the entire phenomenology of movement disorders are presented succinctly but descriptively to walk the reader through the diagnostic processómuch like being in the examining room with a master clinician. Each case follows a set format consisting of four sections: The Case; The Approach; The Lesson; Reference and Suggested Readings. Imaging findings and other illustrations amplify the discussion where pertinent. Movement Disorders features: Collection of over 90 compelling cases covering standard movement disorders phenomenology Cases are vividly described, well-illustrated, and authoritatively written with a section on ìlessons learnedî at the end of each vignette Captures the ìhuman elementî in medicineófirst-person narratives simulate the experience of sitting at the elbow of a master clinician interviewing and examining the patient Designed to help hone diagnostic skills and inform treatment decisions for the full spectrum of movement disorders Vignette titles serve as a reference index for clinicians to easily search similar cases they may have encountered (i.e. An Elderly Man with Dystonia; Chorea in a Young Athlete)

Medical Subject Headings

Medical Subject Headings
Author: National Library of Medicine (U.S.)
Publsiher: Anonim
Total Pages: 329
Release: 2003
ISBN 10:
ISBN 13: UOM:39015057847777
Language: EN, FR, DE, ES & NL

Medical Subject Headings Book Review:

Cecil Loeb Textbook of Medicine

Cecil Loeb Textbook of Medicine
Author: Russell La Fayette Cecil,Robert Frederick Loeb
Publsiher: Anonim
Total Pages: 1923
Release: 1971
ISBN 10: 9780721616575
ISBN 13: 0721616577
Language: EN, FR, DE, ES & NL

Cecil Loeb Textbook of Medicine Book Review:

Neuromuscular Diseases

Neuromuscular Diseases
Author: Michael Swash,Martin S. Schwartz
Publsiher: Springer Science & Business Media
Total Pages: 541
Release: 2013-03-14
ISBN 10: 1447138341
ISBN 13: 9781447138341
Language: EN, FR, DE, ES & NL

Neuromuscular Diseases Book Review:

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.

Lyme Neuroborreliosis

Lyme Neuroborreliosis
Author: Klaus Hansen
Publsiher: Anonim
Total Pages: 44
Release: 1994
ISBN 10:
ISBN 13: UCSD:31822018404210
Language: EN, FR, DE, ES & NL

Lyme Neuroborreliosis Book Review:

Clinical Neurology

Clinical Neurology
Author: Bernard Jacob Alpers,Elliott L. Mancall
Publsiher: Anonim
Total Pages: 1072
Release: 1971
ISBN 10:
ISBN 13: UOM:39015003789818
Language: EN, FR, DE, ES & NL

Clinical Neurology Book Review:

250 Cases in Clinical Medicine E Book

250 Cases in Clinical Medicine E Book
Author: Ragavendra R. Baliga
Publsiher: Elsevier Health Sciences
Total Pages: 928
Release: 2012-01-27
ISBN 10: 0702050261
ISBN 13: 9780702050268
Language: EN, FR, DE, ES & NL

250 Cases in Clinical Medicine E Book Book Review:

A new, fully updated edition of Baliga's very popular collection of short cases arranged by clinical area, emphasising the key diagnostic features of clinical conditions as commonly presented in the short-case part of the Final MB and MRCP examinations. Also included are likely instructions or commands expected from the examiner for each condition, and the key points which the candidate must tell the examiner. A must-have for the final-year undergraduate and trainee doctor. From customer reviews of the previous edition: 'This book is the most useful guide that money can buy for the final exams in the current MBChB undergraduate course. It covers important areas of clinical medicine in a question based format and highlights classical scenarios. The questions raised are classical of examiners in the long and short case examinations. This is a must buy for any undergraduate medical student!!!' 'The book is a must during the period that the young doctor or student is on the wards. It allows one to focus on the important physical findings and the relavant clinical pearls associated with the different medical conditions met... It discusses important physical findings and their diagnostic importance. I have found it useful in preparing for attending ward rounds and also for sharpening my clinical skills. The discussion section is well organised such that undergraduates as well as postgraduates can benefit and the material is up to date with good references for further reading.' 'Excellent preparation for finals as well the MRCP ...MUST HAVE before MRCP PACES.' Features Ideal for use in the ward. Each of the 250 cases presents a disease or topic which is covered consistently to address:● salient features ● history ● examination ● diagnosis ● questions covering investigations and differentiations ● advanced-level questions ● management. New to this edition: Over 350 new images Enhanced advanced-level questions Many more tables