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Index of Variant Human Fibrinogens
 
 
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Index of Variant Human Fibrinogens [Hardcover]

Ray F. Ebert (Author)

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Book Description

0849389984 978-0849389986 June 3, 1994
Whether you're a clinician concerned with patient management, a technician involved in diagnostic testing, or an investigator studying fibrinogen structure and function, you'll find that the 1994 Index of Variant Human Fibrinogens. is a valuable resource. It contains not only the most comprehensive compilation of the world literature and research on dyfibrinogenemia, but also includes a synopsis for health professionals and expert guidance for the diagnosis and treatment of dysfibrinogenemia, the study of genetically abnormal human fibrinogens. Furthermore, this book provides the latest DNA and protein sequences (including the AaE chain) and listings of available PCR primers and anti-fibrinogen antibodies. Add to this a set of 263 Dysfibrinogen Reports tracking more than 30 different characteristics for each variant, plus 9 summary tables and a comprehensive bibliography, and the result is an authoritative companion for the diagnosis and management of this multifaceted and complex disease.
Compare your patient's laboratory profile, clinical manifestations, or molecular defect with virtually all others in the literature. Consider all the options for treating bleeding or thrombotic complications. Determine if your data from a newly identified variant are unique. Spend an hour with this book and see if it doesn't save many hours of literature searching and summarizing!

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Inside This Book (learn more)
First Sentence:
At least 21 new variant fibrinogens have been identified and the literature on dysfibrinogenemia has increased by approximately 57 citations in the three years since the first edition of this book was published. Read the first page
Key Phrases - Statistically Improbable Phrases (SIPs): (learn more)
genetically abnormal fibrinogens, current characterisation strategies, recalcification time, vivo catabolism, euglobulin lysis time, congenital dysfibrinogenemia, fibrinopeptide analysis, abnormal fibrin monomer polymerization, congenital dysfibrinogenaemia, defective thrombin binding, haemostaseological aspects, defective fibrin monomer polymerization, defective stabilization, clinical laboratory results, strategies for structure elucidation, fibrinopeptide release, fibrinogen variant, abnormal fibrinopeptide, delayed polymerization, dysfibrinogenemia characterized, patient fibrinogen, excessive bleeding after dental extraction, thrombin time, abnormal fibrin polymerization, hereditary dysfibrinogenemia
Key Phrases - Capitalized Phrases (CAPs): (learn more)
Edition Remarks, Abnormal Normal, Dysfibrinogen Reports, Walter de Gruyter, Abnormal Abnormal, Monoclonal Mouse, Functional Aspects, Edition Last, Elsevier Science Publ, Remarks References, Blood Coag, Arg Cys, Polyclonal Rabbit, Biological Functions, Latin America, Excerpta Medica, Fibrinogen Bleeding, Fibrinogens London, Gene Sequence, Acta Haematol, Edition Clinical, Fibrinogen Structural Defect Mutation, Oligonucleotide Primers, Calcium Inhib, Chronometric Rate Independent Immunologic Hypodysfibrinogen
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