Overview

Von Willebrand Disease: Basic and Clinical Aspects provides an insight into all aspects of the condition. Since its discovery, von Willebrand disease has been extensively studied and the causative factor deficiency, the understanding of the condition and its treatment has greatly improved. This book summarizes recent research and will help to optimize the management of patients with von Willebrand disease.

This valuable book describes the important and complex role of von ...

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Von Willebrand Disease: Basic and Clinical Aspects

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Overview

Von Willebrand Disease: Basic and Clinical Aspects provides an insight into all aspects of the condition. Since its discovery, von Willebrand disease has been extensively studied and the causative factor deficiency, the understanding of the condition and its treatment has greatly improved. This book summarizes recent research and will help to optimize the management of patients with von Willebrand disease.

This valuable book describes the important and complex role of von Willebrand factor in hemostasis and thrombosis. In addition to the current understanding of its molecular biology, this book gives particular focus to the association between genetic variants of von Willebrand factor and different von Willebrand disease phenotypes. It also reviews the important area of the obstetric and gynecological manifestations of von Willebrand disease, as well as the treatment of acute bleeding.

Written by an international team of contributors it describes the progress in, and difficulties of diagnosing phenotypes and genotypes. Molecular diagnosis of type 1, type 2 and its subgroups, and type 3 von Willebrand disease are presented as well as discussion of the potential future role of gene therapy.

Von Willebrand Disease: Basic and Clinical Aspects is a valuable resource for hematologists in practice and in training, and specialists in thrombosis and hemostasis.

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Editorial Reviews

From the Publisher
"This book certainly helped to enhance my knowledge about von Willebrand disease and even prompted me to present a review of the disease to my colleagues. It is excellently written, appeals to a broad category of readers, and exceeds its stated objectives. I would definitely recommend the book to colleagues." (Doody's, 23 September 2011)
From The Critics
Reviewer: Oluwatoyosi Fatunase, MD(Northwestern University Feinberg School of Medicine)
Description: This book presents a broad, but detailed, overview of the history, pathophysiology, clinical aspects, advances, and future directions in von Willebrand disease.
Purpose: The purpose is to provide hematologists who care for patients with von Willebrand disease a useful clinical tool that is evidence-based, up-to-date, and comprehensive. This is a much-needed resource, not only for hematologists, but also for an increasing number of generalists and primary care providers who care for patients with von Willebrand disease in the face of a growing shortage of classically-trained benign hematologists.
Audience: According to the editors, this book is written for hematologists, but it is accessible to a broader audience including students, residents, and general internal medicine physicians.
Features: The book starts off with a history of the discovery of von Willebrand disease. Then it goes into detail about the pathophysiology of von Willebrand factor and other mediators involved in the pathogenesis of the disease. A few chapters are devoted to the classification and diagnosis of the disease, followed by a discussion of various treatment options. Space is devoted to special populations and considerations in management of disease. I was especially pleased with the inclusion of a chapter dedicated to acquired von Willebrand disease, and I enjoyed the chapter on the history of the disease because it helps puts the rest of the information in the book into perspective. However, there is quite a bit of repetition as several of the contributors chose to begin their chapters with a brief history of the disease. The figures and tables are very reader-friendly and help to augment the text.
Assessment: This book certainly helped to enhance my knowledge about von Willebrand disease and even prompted me to present a review of the disease to my colleagues. It is excellently written, appeals to a broad category of readers, and exceeds its stated objectives. I would definitely recommend the book to colleagues.
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Product Details

  • ISBN-13: 9781444329940
  • Publisher: Wiley, John & Sons, Incorporated
  • Publication date: 1/31/2011
  • Sold by: Barnes & Noble
  • Format: eBook
  • Edition number: 1
  • Pages: 268
  • Product dimensions: 5.91 (w) x 9.84 (h) x 0.59 (d)
  • File size: 6 MB

Meet the Author

Augusto B. Federici, MD, Associate Professor of Hematology, Angelo Bianchi Bonomi Hemophilia Thrombosis Center, Department of Internal Medicine, University of Milan, Milan, Italy.

Christine A. Lee, Emeritus Professor of Haemophilia, University of London, Honorary Consultant Haematologist, Oxford Haemophilia Centre

Erik Berntorp, Department of Coagulation Disorders, Malmö University Hospital, Malmö, Sweden.

David Lillicrap, Department of Pathology and Molecular Medicine, Queen's University, Kingston, Ontarion, Canada.

Bob Montgomery, Professor, Pediatrics (Hematology) and Vice Chair, Blood Research Institute, Medical College of Wisconsin, Milwaukee, USA

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Table of Contents

List of Contributors.

Foreword.

Preface.

1 Historical perspective on von Willebrand disease (Erik Berntorp and Margareta Blombäck).

2 Biosynthesis and organization of von Willebrand factor (Sandra L. Haberichter).

3 von Willebrand factor Structure and Function (Robert R. Montgomery and Sandra L. Haberichter).

4 Modulation of von Willebrand factor by ADAMTS13 (Jennifer Barr and David Motto).

5 Animal models in von Willebrand disease (Cécile V. Denis, Olivier D. Christophe and Peter J Lenting).

6 Classification of von Willebrand Disease (Javier Batlle, Almudena Pérez-Rodríguez and María Fernanda López-Fernández).

7 The epidemiology of von Willebrand disease (Giancarlo Castaman and Francesco Rodeghiero).

8 Clinical Aspects of von Willebrand Disease: Bleeding History (Paula D. James and Alberto Tosetto).

9 Laboratory diagnosis of von Willebrand Disease: the phenotype (Ulrich Budde and Emmanuel J Favaloro).

10 Molecular Diagnosis of von Willebrand Disease: the Genotype (Anne C Goodeve and Reinhard Schneppenheim).

11 Clinical, Laboratory and Molecular Markers of Type 1 von Willebrand disease (David Lillicrap, Francesco Rodeghiero and Ian Peake).

12 Clinical, laboratory and molecular markers of von Willebrand disease type 2 (Dominique Meyer, Edith Fressinaud and Claudine Mazurier).

13 Clinical, laboratory and molecular markers of von Willebrand disease type 3 (Luciano Baronciani, Augusto B. Federici and Jeroen C.J. Eikenboom).

14 Pediatric Aspects of von Willebrand Disease (Jorge Di Paola and Thomas Abshire).

15 Women with von Willebrand Disease (Christine A. Lee, Rezan A. Kadir and Peter A. Kouides).

16 The use of desmopressin in von Willebrand disease (Stefan Lethagen, Augusto B. Federici and Giancarlo Castaman).

17 The use of plasma-derived concentrates (Pier Mannuccio Mannucci, Massimo Franchini).

18 Prophylaxis in von Willebrand disease (Erik Berntorp).

19 Pathophysiology, Epidemiology, Diagnosis and Treatment of the Acquired von Willebrand Syndrome (Ulrich Budde, Augusto B. Federici and Jacob H. Rand).

20 Gene therapy for von Willebrand disease (Marinee K.L. Chuah, Inge Petrus and Thierry VandenDriessche).

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