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Autoimmune Thrombocytopenia [electronic resource] / edited by Yoji Ishida, Yoshiaki Tomiyama.

Medverkande: Materialtyp: TextUtgivningsuppgift: Singapore : Springer Singapore : Imprint: Springer, 2017Beskrivning: X, 229 p. 26 illus., 7 illus. in color. online resourceInnehållstyp:
  • text
Medietyp:
  • computer
Bärartyp:
  • online resource
ISBN:
  • 9789811041426
Ämnen: Fler format: Printed edition:: Ingen titelDDK-klassifikation:
  • 616.15 23
Library of Congress (LC) klassifikationskod:
  • RB45
Onlineresurser:
Innehåll:
Part 1 Introduction -- 1 Megakaryocytopoiesis and thrombocytopoisis -- Part 2 History -- 2 History -- Part 3 Epidemiology -- 3 Epidemiology -- Part 4 Pathophysiology -- 4 Platelet membrane glycoproteins -- 5 Autoantigens in ITP -- 6 T cell abnormalities -- Part 5 Clinical manifestation -- 7 ITP in adults -- 8 ITP in childhood -- Part 6 Diagnosis -- 9 Diagnosis in general -- 10 Differential Diagnosis: Secondary ITP -- 11 Differential Diagnosis: Hereditary thrombocytopenia -- 12 Differential Diagnosis: Aplastic thrombocytopenia -- Part 7 Treatment of Adults -- 13 Helicobacter pylori (H. pylori) eradication -- 14 Steroid -- 15 High dose Immunnoglobulin -- 16 Splenectomy -- 17 Rituximab -- 18 TPO-R agonist -- 19 Others (Syk inhibitor and Other medications) -- 20 Transfusion -- 21 Therapy in pregnancy -- Part 8 Treatment of Children -- 22 Treatment of Children.
I: Springer eBooksSammanfattning: This book provides a concise yet comprehensive summary of the current state of knowledge concerning the pathophysiology, differential diagnosis and treatment options that support day-to-day patient management. It reviews a variety of treatments including TOP-R antagonists, along with Syk inhibitor, which has recently proven to be effective, enabling readers to update and broaden their knowledge of the disease. Covering topics ranging from basic science to clinical practice, Autoimmune Thrombocytopenia will appeal to a wide readership, from medical interns and residents to clinicians and hematologists, offering them a thought-provoking, instructive and informative collection of cutting-edge works. Accordingly, readers will gain an overview of the autoimmune and other causes of the disease, and the book will serve as a foundation for new research directions that further our understanding of the pathophysiology and development of diagnosis and treatment options.
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Part 1 Introduction -- 1 Megakaryocytopoiesis and thrombocytopoisis -- Part 2 History -- 2 History -- Part 3 Epidemiology -- 3 Epidemiology -- Part 4 Pathophysiology -- 4 Platelet membrane glycoproteins -- 5 Autoantigens in ITP -- 6 T cell abnormalities -- Part 5 Clinical manifestation -- 7 ITP in adults -- 8 ITP in childhood -- Part 6 Diagnosis -- 9 Diagnosis in general -- 10 Differential Diagnosis: Secondary ITP -- 11 Differential Diagnosis: Hereditary thrombocytopenia -- 12 Differential Diagnosis: Aplastic thrombocytopenia -- Part 7 Treatment of Adults -- 13 Helicobacter pylori (H. pylori) eradication -- 14 Steroid -- 15 High dose Immunnoglobulin -- 16 Splenectomy -- 17 Rituximab -- 18 TPO-R agonist -- 19 Others (Syk inhibitor and Other medications) -- 20 Transfusion -- 21 Therapy in pregnancy -- Part 8 Treatment of Children -- 22 Treatment of Children.

This book provides a concise yet comprehensive summary of the current state of knowledge concerning the pathophysiology, differential diagnosis and treatment options that support day-to-day patient management. It reviews a variety of treatments including TOP-R antagonists, along with Syk inhibitor, which has recently proven to be effective, enabling readers to update and broaden their knowledge of the disease. Covering topics ranging from basic science to clinical practice, Autoimmune Thrombocytopenia will appeal to a wide readership, from medical interns and residents to clinicians and hematologists, offering them a thought-provoking, instructive and informative collection of cutting-edge works. Accordingly, readers will gain an overview of the autoimmune and other causes of the disease, and the book will serve as a foundation for new research directions that further our understanding of the pathophysiology and development of diagnosis and treatment options.

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