Lavoisier S.A.S.
14 rue de Provigny
94236 Cachan cedex
FRANCE

Heures d'ouverture 08h30-12h30/13h30-17h30
Tél.: +33 (0)1 47 40 67 00
Fax: +33 (0)1 47 40 67 02


Url canonique : www.lavoisier.fr/livre/medecine/congenital-bleeding-disorders/descriptif_3833517
Url courte ou permalien : www.lavoisier.fr/livre/notice.asp?ouvrage=3833517

0 article 

 Frais de port 0,01€*

Exclusivité web : à partir de 35 euros d’achat, frais de port à 1 centime pour les expéditions vers la France métropolitaine, la Suisse et l’UE avec Colissimo ou GLS

Congenital Bleeding Disorders, Softcover reprint of the original 1st ed. 2018 Diagnosis and Management

Langue : Anglais

Coordonnateur : Dorgalaleh Akbar

Couverture de l’ouvrage Congenital Bleeding Disorders
This book describes in detail the clinical presentation, diagnosis, and management of a wide range of congenital bleeding disorders. It will assist readers in overcoming the significant challenges involved in clinical and laboratory diagnosis and in providing effective clinical care that makes optimal use of new products, including recombinant factorconcentrate. The coverage ranges from hemophilia A and B and von Willebrand disease to rare bleeding disorders such as congenital factor V, factor X, factor XI, and factor XIII deficiency and inherited platelet function disorders. The exceptional attention to rarer conditions is of particular importance given the considerable risk of overlooking them during diagnosis, with potential consequences for disease-related morbidity and mortality. The authors are acknowledged specialists in the field from across the world who have particular expertise in the disorder that they discuss. The book will be of value to hematologists, oncologists, pediatricians, laboratory specialists and technicians, general physicians, and trainees. 

Part I: Common bleeding disorders.- 1. Von Willebrand disease.- 2. Hemophilia A (congenital factor VIII deficiency).- 3. Hemophilia B (congenital factor IX deficiency) Part II: Rare bleeding disorders.- 4. Congenital factor I (fibrinogen) disorders.- 5. Congenital factor II deficiency.- 6. Congenital factor V deficiency.- 7. Combined coagulation factor deficiencies.- 8.  Congenital factor VII deficiency.- 9. Congenital factor X deficiency.- 10.   Congenital factor XI deficiency.- 11. Congenital factor XIII deficiency Part III: Inherited platelet function disorders .- 12. Glanzmann thrombasthenia .- 13. Bernard–Soulier syndrome.- 14. Gray platelet syndrome.- 15. Quebec platelet disorder.

 

 

Akbar Dorgalaleh, hematologist and scientific researcher in the field of congenital bleeding disorders in the Department of Hematology and Blood Transfusion, Iran University of Medical Sciences (IUMS). Dr. Dorgalaleh’s primary interest is the diagnosis and management of congenital bleeding disorders, and he has a special interest in congenital factor XIII deficiency. He acts as a reviewer for several international journals in the field of Hematology and to date has authored about 100 papers that cover all the congenital bleeding disorders, including hemophilia, rare bleeding disorders, and inherited platelet function disorders. He has reported the clinical, laboratory, and molecular characteristics of a very large number of patients with congenital bleeding disorders.  

Offers detailed assistance in the diagnosis and management of bleeding disorders Includes extensive coverage of rare disorders and the challenges that they pose Provides up-to-date guidance on use of the latest treatment options and new products