Are you looking for read ebook online? Search for your book and save it on your Kindle device, PC, phones or tablets. Download Fast Facts: Cold Agglutinin Disease PDF full book. Access full book title Fast Facts: Cold Agglutinin Disease by Wilma Barcellini. Download full books in PDF and EPUB format.
Author: Wilma Barcellini Publisher: Karger Medical and Scientific Publishers ISBN: 3318072338 Category : Medical Languages : en Pages : 70
Book Description
Cold agglutinin disease (CAD) is a rare, autoimmune hemolytic anemia in which cold-reacting autoantibodies (cold agglutinins) bind to normal antigens on the surface of red blood cells during passage through the cooler peripheral circulation. These antibodies cause agglutination of red blood cells, leading to an immune response and premature destruction of the healthy red blood cells. The authors have written this resource to give clinicians the information they need to successfully diagnose and manage CAD in adult patients.
Author: Wilma Barcellini Publisher: Karger Medical and Scientific Publishers ISBN: 3318072338 Category : Medical Languages : en Pages : 70
Book Description
Cold agglutinin disease (CAD) is a rare, autoimmune hemolytic anemia in which cold-reacting autoantibodies (cold agglutinins) bind to normal antigens on the surface of red blood cells during passage through the cooler peripheral circulation. These antibodies cause agglutination of red blood cells, leading to an immune response and premature destruction of the healthy red blood cells. The authors have written this resource to give clinicians the information they need to successfully diagnose and manage CAD in adult patients.
Author: C. Buske Publisher: Karger Medical and Scientific Publishers ISBN: 3318071951 Category : Medical Languages : en Pages : 76
Book Description
Waldenström macroglobulinemia (WM) is a rare lymphoplasmacytic lymphoma characterized by the presence of an immunoglobulin M (IgM) monoclonal protein. WM is a chronic, indolent disease, which can remain undiagnosed for years. A better understanding of the role of signaling pathways in the development of the disease and the identification of clinical and genetic markers have driven the development of targeted therapeutic strategies, improving overall survival.
Author: Bertil Glader Publisher: Karger Medical and Scientific Publishers ISBN: 191079788X Category : Medical Languages : en Pages : 66
Book Description
You may be unfamiliar with pyruvate kinase (PK) deficiency. It is a rare inherited enzyme disorder that affects the glycolytic pathway used by red blood cells to generate energy, manifesting as hemolytic anemia. The symptoms vary greatly between individuals, making diagnosis difficult, and management primarily comprises supportive treatments. Written by experts in the field, 'Fast Facts: Pyruvate Kinase Deficiency' provides a comprehensive introduction to the condition, including details of: • the underlying defect • its mode of inheritance, and the relationship between genotype and phenotype • how the condition manifests • the fundamentals of diagnosis and how to differentiate it from a heterogeneous group of hemolytic disorders • monitoring and managing the complications that may arise. 'Fast Facts: Pyruvate Kinase Deficiency' will be of interest to primary care providers, hematologists, oncologists, pediatricians, internal medicine specialists, hematology nurses and medical students; indeed, anyone who wishes to learn more about this rare genetic blood disorder. Contents: • Overview • Epidemiology and etiology • Differential diagnosis • Diagnosis of pyruvate kinase deficiency • Complications and monitoring • Supportive treatment
Author: Shirley D'Sa Publisher: Karger Medical and Scientific Publishers ISBN: 3318070181 Category : Medical Languages : en Pages : 51
Book Description
Waldenström macroglobulinemia (shortened to WM) is a rare blood cancer. WM usually progresses slowly; some people do not show symptoms for several years after diagnosis. A person who does not have symptoms usually does not need treatment, but active monitoring is essential so that treatment can be started as soon as it is needed. Although there is no cure for WM, different treatment options can keep the disease under control for many years in a lot of people. Eventually, the treatments tend to lose their effect. New therapies are being tested in clinical trials across the world, with promising results. Table of Contents: • What is Waldenström macroglobulinemia? How will WM affect me? Who is in my care team? What tests will I need to have? Common feelings when diagnosed • Helping yourself • Active monitoring • Starting treatment • Types of treatment • What are supportive treatments? How do I know if treatment has worked? Follow-up after treatment • When WM comes back • Research and new treatments • Understanding WM
Author: Fred F. Ferri Publisher: Elsevier Health Sciences ISBN: 0323078591 Category : Medical Languages : en Pages : 441
Book Description
Expert clinical know-how that fits inside a breast pocket! Authored by Fred Ferri, MD, the author of the best-selling Practical Guide to the Care of the Medical Patient, 6th Edition, this new resource presents "need-to-know" information on nearly 400 diseases and disorders. Its concise, user-friendly format delivers just the information practitioners need, just the way they need it, at the point of care! Offers content expanded from the Practical Guide to the Care of the Medical Patient, 6th Edition, a well-established source of focused clinical guidance. Covers nearly 400 diseases and disorders, including 200 important new topics not found in the Practical Guide. Organizes disorders alphabetically for speedy reference. Summarizes each condition's definition, diagnosis, etiology, treatment, and clinical pearls at a glance. Embodies the expertise of world-respected author Fred Ferri, MD, FACP, for information readers can depend on.
Author: Fred F. Ferri Publisher: Elsevier Health Sciences ISBN: 1437708471 Category : Medical Languages : en Pages : 454
Book Description
Written by renowned author Fred F. Ferri, MD, FACP, and featuring high-quality images from Drs. Studdiford and Tully - faculty members at Jefferson Medical College, Ferri's Fast Facts in Dermatology presents "need-to-know" information on nearly 200 dermatologic disorders. Each topic includes color images displaying the disease, and the accompanying bulleted text provides an at-a-glance view. This useful, clinical resource helps you hone your developing diagnostic skills and sharpen your clinical acumen. Its concise, user-friendly format lets you get to the information you need fast, and its convenient size makes reference a snap. Covers nearly 200 disorders that help you better diagnose and recognize the most common dermatologic diseases. Includes high-quality full-color images that provide optimal visual guidance for diagnoses. Presents a consistent organization for each disorder that includes Definitions, Etiology, Clinical Manifestations, Physical Examination, Diagnostic Tests, Differential Diagnosis, Treatment, and Clinical Pearls. Uses bulleted text that makes reference easy. Comes in a convenient 4" x 6" format for on-the-go reference. Makes the perfect study or review tool for exams for students or a focused point-of-care reference for residents and practitioners of all levels.
Author: B. Glader Publisher: Karger Medical and Scientific Publishers ISBN: 1912776839 Category : Medical Languages : en Pages : 66
Book Description
Vielleicht ist Ihnen das Krankheitsbild des Pyruvatkinase-Mangels noch unbekannt. Es handelt sich um einen seltenen erblichen Enzymdefekt, der die Energiegewinnung in den Erythrozyten über die Glykolyse betrifft und zu einer hämolytischen Anämie führt. Die Symptome sind von Patient zu Patient sehr unterschiedlich, was die Diagnosestellung erschwert, und die Behandlung besteht im Wesentlichen in supportiven Massnahmen. 'Fast Facts: Pyruvatkinase-Mangel' wurde von Experten verfasst und liefert eine umfassende Einführung in das Krankheitsbild. Behandelte Themen umfassen: • den zugrunde liegenden Enzymdefekt • den Vererbungsweg und die Beziehung zwischen Genotyp und Phänotyp • die Manifestationen der Erkrankung • die Grundlagen der Diagnosestellung und die Differentialdiagnose innerhalb einer heterogenen Gruppe von hämolytischen Erkrankungen • Monitoring und Behandlung möglicher Komplikationen. 'Fast Facts: Pyruvatkinase-Mangel' wurde für Allgemeinmediziner, Hämatologen, Onkologen, Kinderärzte, Internisten, Hämatologie-Fachpflegepersonal und Medizinstudenten geschrieben: kurzum für alle, die mehr über diese seltene genetische Blutkrankheit erfahren möchten.
Author: National Organization for Rare Disorders Publisher: Lippincott Williams & Wilkins ISBN: 9780781730631 Category : Medical Languages : en Pages : 982
Book Description
NORD Guide to Rare Disorders is a comprehensive, practical, authoritative guide to the diagnosis and management of more than 800 rare diseases. The diseases are discussed in a uniform, easy-to-follow format--a brief description, signs and symptoms, etiology, related disorders, epidemiology, standard treatment, investigational treatment, resources, and references.The book includes a complete directory of orphan drugs, a full-color atlas of visual diagnostic signs, and a Master Resource List of support groups and helpful organizations. An index of symptoms and key words offers physicians valuable assistance in finding the information they need quickly.
Author: Lippincott Williams & Wilkins Publisher: Lippincott Williams & Wilkins ISBN: 9781582556857 Category : Medical Languages : en Pages : 260
Book Description
Diagnostic Test Facts Made Incredibly Quick! provides instant access to essential information on more than 400 diagnostic tests. The book fits comfortably into a pocket, and the wipeable page surface allows nurses to write notes and remove them easily. Distinctively colored tabs identify the major sections: Basics, Blood, Urine, Cultures, Imaging, and Other including ECG and EEG. Tests are listed alphabetically within each section. Each listing includes the purpose of the test; normal reference values for men, women, and children, including SI values; critical values; and nursing considerations. Scores of quick-reference charts and illustrations are included.
Author: Kathryn Foucar Publisher: Elsevier Health Sciences ISBN: 0323879071 Category : Medical Languages : en Pages : 1005
Book Description
This expert volume in the Diagnostic Pathology series is an excellent point-of-care resource for practitioners at all levels of experience and training. Covering the full range of nonneoplastic and neoplastic conditions of blood and bone marrow, it incorporates the most recent scientific and technical knowledge in the field to provide a comprehensive overview of all key issues relevant to today’s practice. Richly illustrated and easy to use, the third edition of Diagnostic Pathology: Blood and Bone Marrow is a visually stunning, one-stop resource for every practicing pathologist, hematopathologist, oncologist, hematologist, resident, student, or fellow as an ideal day-to-day reference or as a reliable training resource. Provides practicing pathologists with key details about new entities, newly recognized causes of morphologic change in blood and bone marrow abnormalities, and new strategies for appropriate workup of neoplastic processes—all with a focus on key tests and key differential diagnostic considerations Helps pathologists recognize unique blood and bone marrow findings that can be an indicator for specific exposures, such as new medications, new targeted therapies, or toxins Integrates updated technologies, newly recognized disorders, complications/features in blood and bone marrow, new targeted therapies, and the increased use of homeopathic remedies Contains new chapters covering SARS-CoV-2 infection features in blood and bone marrow, myelodysplastic syndrome (MDS) mimics, blood and bone marrow findings linked to targeted therapies, blood and bone marrow findings linked to other medications, and more Updates all existing chapters and contains expanded information on T-cell neoplasms in blood and bone marrow and intravascular large B-cell lymphoma in blood and bone marrow Includes details from the World Health Organization (WHO) fifth edition Classification of Haematolymphoid Tumours and the very latest 2023 International Consensus Classification (ICC) publications, reflecting new and renamed diagnostic entities, tumor classification changes and updates, and terminology changes and updates Discusses molecular testing strategies based on specific neoplasms and specific differential diagnostic consideration Clearly delineates numerous genetic disorders often found in blood and bone marrow Features more than 2,500 superb images, including histology and gross pathology photographs, full-color illustrations and graphics, clinical photographs and radiologic images, and many new tables and charts/algorithms Employs consistently templated chapters, bulleted content, key facts, a variety of tables, annotated images, pertinent references, and an extensive index for quick, expert reference at the point of care Includes the enhanced eBook version, which allows you to search all text, figures, and references on a variety of devices
Author: Wilma Barcellini
Author: Wilma Barcellini
Author: C. Buske
Author: Bertil Glader
Author: Shirley D'Sa
Author: Fred F. Ferri
Author: Fred F. Ferri
Author: B. Glader
Author: National Organization for Rare Disorders
Author: Lippincott Williams & Wilkins
Author: Kathryn Foucar