國立虎尾科技大學 |

Congenital Bleeding Disorders = Diagnosis and Management /

Record Type:	Language materials, printed : Monograph/item
Title/Author:	Congenital Bleeding Disorders / edited by Akbar Dorgalaleh.
Reminder of title:	Diagnosis and Management /
other author:	Dorgalaleh, Akbar.
Description:	XIV, 396 p. 93 illus., 85 illus. in color.online resource. :
Contained By:	Springer Nature eBook
Subject:	Hematology. -
Online resource:	https://doi.org/10.1007/978-3-319-76723-9
ISBN:	9783319767239

Congenital Bleeding Disorders = Diagnosis and Management /
Congenital Bleeding Disorders Diagnosis and Management /[electronic resource] :edited by Akbar Dorgalaleh. - 1st ed. 2018. - XIV, 396 p. 93 illus., 85 illus. in color.online resource.

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. .

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 factor concentrate. 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. .

ISBN: 9783319767239

Standard No.: 10.1007/978-3-319-76723-9doiSubjects--Topical Terms:

645254
Hematology.

LC Class. No.: RB45

Dewey Class. No.: 616.15

Congenital Bleeding Disorders = Diagnosis and Management /
LDR:03130nam a22003975i 4500 001 987603
003 DE-He213
005 20200706063228.0
007 cr nn 008mamaa
008 201225s2018 gw | s |||| 0|eng d
020 $a 9783319767239 $9 978-3-319-76723-9
024 7 $a 10.1007/978-3-319-76723-9 $2 doi
035 $a 978-3-319-76723-9
050 4 $a RB45
072 7 $a MJF $2 bicssc
072 7 $a MED038000 $2 bisacsh
072 7 $a MJF $2 thema
082 0 4 $a 616.15 $2 23
245 1 0 $a Congenital Bleeding Disorders $h [electronic resource] : $b Diagnosis and Management / $c edited by Akbar Dorgalaleh.
250 $a 1st ed. 2018.
264 1 $a Cham : $b Springer International Publishing : $b Imprint: Springer, $c 2018.
300 $a XIV, 396 p. 93 illus., 85 illus. in color. $b online resource.
336 $a text $b txt $2 rdacontent
337 $a computer $b c $2 rdamedia
338 $a online resource $b cr $2 rdacarrier
347 $a text file $b PDF $2 rda
505 0 $a 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. .
520 $a 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 factor concentrate. 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. .
650 0 $a Hematology. $3 645254
650 0 $a Pediatrics. $3 644839
700 1 $a Dorgalaleh, Akbar. $4 edt $4 http://id.loc.gov/vocabulary/relators/edt $3 1207725
710 2 $a SpringerLink (Online service) $3 593884
773 0 $t Springer Nature eBook
776 0 8 $i Printed edition: $z 9783319767222
776 0 8 $i Printed edition: $z 9783319767246
776 0 8 $i Printed edition: $z 9783030095659
856 4 0 $u https://doi.org/10.1007/978-3-319-76723-9
912 $a ZDB-2-SME
912 $a ZDB-2-SXM
950 $a Medicine (SpringerNature-11650)
950 $a Medicine (R0) (SpringerNature-43714)