November 24, 2020

Download Ebook Free Klinikleitfaden Neurologie

German books in print

German books in print
Author : Anonim
Publisher : Unknown
Release Date : 2002
Category : German literature
Total pages :129
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Bibliographie Internationale Des Recensions de la Litt Érature Savante

Bibliographie Internationale Des Recensions de la Litt Érature Savante
Author : Anonim
Publisher : Unknown
Release Date : 1997
Category : Books
Total pages :129
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Verzeichnis lieferbarer Bücher

Verzeichnis lieferbarer Bücher
Author : Anonim
Publisher : Unknown
Release Date : 1999
Category :
Total pages :129
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National Library of Medicine Current Catalog

National Library of Medicine Current Catalog
Author : National Library of Medicine (U.S.)
Publisher : Unknown
Release Date : 1993
Category : Medicine
Total pages :129
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Current Catalog

Current Catalog
Author : National Library of Medicine (U.S.)
Publisher : Unknown
Release Date : 1993
Category : Medicine
Total pages :129
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First multi-year cumulation covers six years: 1965-70.

Fachpflege Intensivpflege 2.a

Fachpflege Intensivpflege 2.a
Author : Andrea Brock,Anke Kany,Eva Knipfer
Publisher : Fischer Gustav Verlag GmbH & Company KG
Release Date : 2018-05-09
Category :
Total pages :456
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Intensivpflege und Medizin - für Anfänger und Neueinsteiger! Frisch examiniert? Neu auf der Intensivstation oder einer Intermediate Care Station? Dann ist die Fachpflege Intensivpflege genau das Richtige für Sie. Hier finden Sie neben der allgemeinen und speziellen Intensivpflege auch die Grundlagen zu Hygiene, Pharmakologie sowie zu Organsystemen und ihrer wichtigsten Erkrankungen sowie deren Therapie: Aufnahme, Übergabe, Zimmercheck, Transport Schmerztherapie, Prophylaxen, Kommunikation, Positionierung, Körperpflege, Ernährung und Verdauung und natürlich Wundversorgung Beatmungsformen und Weaning Akutes Lungenversagen Sepsis, Polytrauma und Schock Neben Grundlagen der Anästhesie und der Arbeit im Aufwachraum wird auch der Reanimation ein eigenes Kapitel gewidmet. Alle Themen sind auf die Intensivpflege fokussiert, ohne die Medizin außen vor zu lassen. Dafür stehen die Herausgeberinnen und die Autoren, Pflegende und Ärzte, die allesamt aus der Praxis für die Praxis schreiben. Neu in der 2. Auflage: Krankheitsbilder Delir und Critical Illness Polyneuropathy Frühmobilisation Pflege bei Organspende Kinderanästhesie Erweiterung der Inhalte zu Anästhesie, Schutzmaßnahmen bei Isolation, Sepsis und ARDS

Fachsprache

Fachsprache
Author : Anonim
Publisher : Unknown
Release Date : 1994
Category : Language and languages
Total pages :129
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Deutsche Nationalbibliografie

Deutsche Nationalbibliografie
Author : Die deutsche Nationalbibliothek
Publisher : Unknown
Release Date : 2020
Category :
Total pages :129
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Neuromuscular Case Studies E-Book

Neuromuscular Case Studies E-Book
Author : Tulio E. Bertorini
Publisher : Elsevier Health Sciences
Release Date : 2008-05-14
Category : Medical
Total pages :632
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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.

Laboratory Assessment of Vitamin Status

Laboratory Assessment of Vitamin Status
Author : Dominic J. Harrington
Publisher : Academic Press
Release Date : 2018-11-28
Category : Medical
Total pages :340
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Laboratory Assessment of Vitamin Status provides a comprehensive understanding of the limitations of commonly used approaches used for the evaluation of vitamin status, reducing harm in the general health setting. It outlines the application of ‘Best Practice’ approaches to the evaluation of vitamin status, giving physicians and other healthcare professionals the opportunity to make evidence-based interventions. Nearly every metabolic and developmental pathway in the human body has a dependency on at least one micronutrient. Currently, the clinical utility of approaches taken by laboratories for the assessment of vitamin status is generally poorly understood, missing the opportunity to diagnosis vitamin deficiencies. This essential reference gives clinical and biomedical scientists an understanding of the limitations of commonly used approaches to the evaluation of vitamin status in the general health setting through change in practice. Nutritionists and dietitians gain an understanding of more sophisticated markers of vitamin status. Describes specialist assays in sufficient detail to enable laboratories to replicate what is being performed by expert groups Provides detailed information that supports laboratories in the setting up of methods for the evaluation of vitamin status Informs laboratories looking for third party providers of specialist investigations Provides an essential overview of reference ranges for each vitamin

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 Date : 2016-10-22
Category : Medical
Total pages :418
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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, and the growing population of young adults with primary or acquired myocardial disease, the need has arisen for a reference that offers a comprehensive approach to the understanding of basic, translational, and clinical aspects of specific muscle diseases while making the link between young adult and adult health. Reveals the link between cardiac muscle disease and skeletal muscle disease Explains how genetics and environmental factors effect muscle function of diverse origins Designates current and novel therapeutic strategies that target both cardiac and skeletal muscle systems

Veterinary Neuroanatomy and Clinical Neurology

Veterinary Neuroanatomy and Clinical Neurology
Author : Alexander DeLahunta,Eric Glass
Publisher : Elsevier Health Sciences
Release Date : 2009
Category : Medical
Total pages :540
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Covering the anatomy, physiology, and pathology of the nervous system, Veterinary Neuroanatomy and Clinical Neurology, 4th Edition helps you diagnose the location of neurologic lesions in small animals, horses, and food animals. Practical guidelines explain how to perform neurologic examinations, interpret examination results, and formulate effective treatment plans. Descriptions of neurologic disorders are accompanied by illustrations, radiographs, and clinical case examples with corresponding online video clips depicting the actual patient described in the text. Written by veterinary neuroanatomy and clinical neurology experts Alexander de Lahunta, Eric Glass, and Marc Kent, this resource is an essential tool in the diagnosis and treatment of neurologic disorders in the clinical setting. Disease content is presented as case descriptions, allowing you to learn in a manner that is similar to the challenge of diagnosing and treating neurologic disorders in the clinical setting: 1) Description of the neurologic disorder, 2) Neuroanatomic diagnosis and how it was determined, the differential diagnosis, and any ancillary data, and 3) Course of the disease, the final clinical or necropsy diagnosis, and a brief discussion of the syndrome. Over 250 high-quality radiographs and over 800 vibrant color photographs and line drawings depict anatomy, physiology, and pathology (including gross and microscopic lesions), and enhance your ability to diagnose challenging neurologic cases. A companion website hosted by Cornell University College of Veterinary Medicine features more than 380 videos that bring concepts to life and clearly demonstrate the neurologic disorders and examination techniques described in case examples throughout the text. High-quality, state-of-the-art MR images correlate with stained transverse sections of the brain, showing minute detail that the naked eye cannot see. NEW! High-quality, state-of-the-art MR images in the Neuroanatomy by Dissection chapter takes an atlas approach to presenting normal brain anatomy of the dog, filling a critical gap in the literature since Marcus Singer's The Brain of the Dog in Section. NEW Uncontrolled Involuntary Skeletal Muscle Contractions chapter provides new coverage of this movement disorder. NEW case descriptions offer additional practice in working your way through real-life scenarios to reach an accurate diagnosis and an effective treatment plan for neurologic disorders. NEW! A detailed Video Table of Contents in the front of the book makes it easier to access the videos that correlate to case examples.

Physiology of the Gastrointestinal Tract, Two Volume Set

Physiology of the Gastrointestinal Tract, Two Volume Set
Author : Hamid M. Said
Publisher : Academic Press
Release Date : 2012-05-14
Category :
Total pages :2250
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Physiology of the Gastrointestinal Tract, Fifth Edition -- winner of a 2013 Highly Commended BMA Medical Book Award for Internal Medicine -- covers the study of the mechanical, physical, and biochemical functions of the GI Tract while linking the clinical disease or disorder, bridging the gap between clinical and laboratory medicine. The gastrointestinal system is responsible for the breakdown and absorption of various foods and liquids needed to sustain life. Other diseases and disorders treated by clinicians in this area include: food allergies, constipation, chronic liver disease and cirrhosis, gallstones, gastritis, GERD, hemorrhoids, IBS, lactose intolerance, pancreatic, appendicitis, celiac disease, Crohn's disease, peptic ulcer, stomach ulcer, viral hepatitis, colorectal cancer and liver transplants. The new edition is a highly referenced and useful resource for gastroenterologists, physiologists, internists, professional researchers, and instructors teaching courses for clinical and research students. 2013 Highly Commended BMA Medical Book Award for Internal Medicine Discusses the multiple processes governing gastrointestinal function Each section edited by preeminent scientist in the field Updated, four-color illustrations

Nutrient Metabolism

Nutrient Metabolism
Author : Martin Kohlmeier
Publisher : Academic Press
Release Date : 2015-05-12
Category : Technology & Engineering
Total pages :898
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Nutrient Metabolism, Second Edition, provides a comprehensive overview of the supply and use of nutrients in the human body and how the body regulates intake. Chapters detail the principles determining digestion and absorption of food ingredients and how these compounds and their metabolites get into the brain, cross the placenta and pass through the kidneys. Each nutrient’s coverage contains a nutritional summary that describes its function, its food sources, dietary requirements, potential health risks if deficient, and impact of excessive intake. This handbook contains the latest information on the scope of structures, processes, genes and cofactors involved in maintaining a healthy balance of nutrient supplies. Of interest to a wide range of professionals because nutrient issues connect to so many audiences, the book contains a useful link to dietary supplements. Latest research findings on health and clinical effects of nutrients and of interventions affecting nutrient supply or metabolism Each nutrient covered contains a nutritional summary describing its function, food sources, dietary requirements, potential health risks if deficient, and impact of excessive intake. Nutrient information immediately accessible--from source to effect--in one volume

Pediatric Neurology Part III

Pediatric Neurology Part III
Author : Jamel Chelly,Isabelle Desguerre
Publisher : Elsevier Inc. Chapters
Release Date : 2013-04-24
Category : Medical
Total pages :732
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Infancy- or childhood-onset muscular dystrophies may be associated with profound loss of muscle function, affecting ambulation, posture, cardiac and respiratory functions, while those of late onset may be mild and associated with slight weakness or fatigability induced by effort. In addition to the distribution of muscle weakness, symptoms, and course of the disease, the diagnosis of muscular dystrophy is usually ascertained by histological findings. There is connective tissue proliferation in the perimysium and endomysium, variation in muscle fiber size, cytoarchitectural alterations of myofibers such as internal nuclei, myofibrillar whorls, and fiber splitting and lobulation, but, most of all, degeneration and regeneration of myofibers. Causes of muscular dystrophies characterized by muscle weakness and wasting are heterogeneous and include dysfunction of diverse genetic pathways and genes encoding proteins of the plasma membrane, extracellular matrix, sarcomere, and nuclear membrane components. Duchenne and Becker muscular dystrophies are prototypes illustrating advances in the field of myology. Limb-girdle muscular dystrophies (LGMDs) are clinically and genetically heterogeneous, some with autosomal dominant (LGMD1) and others with autosomal recessive (LGMD2) inheritance. Neither clinical and genetic grounds nor biopsy patterns are specific enough to distinguish them, but two common denominators are: (1) weakness and wasting predominating in pelvic and shoulder girdle muscles, with occasional involvement of the myocardium; and (2) necrosis and regeneration of myofibers. While identification of genetic causes and molecular diagnosis are increasingly improved, especially with the advent of new generation sequencing technologies, optimized care, information for the family, and prevention, including genetic counseling and prenatal diagnosis, require multidisciplinary follow-up with genetic, pediatric, and psychological involvement.