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LIBRERIA STUDIUM
Libreria medica internazionale
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LIBRERIA STUDIUM
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Nonmalignant Hematology
Expert Clinical Review: Questions and Answers
Abutalib, Connors, Ragni
Editore
Springer
Anno
2016
Pagine
718
ISBN
9783319303505
170,00 €
I prezzi indicati possono subire variazioni poiché soggetti all'oscillazione dei cambi delle valute e/o agli aggiornamenti effettuati dagli Editori.

This book, in Q&A format, addresses a wide range of clinically relevant topics and issues in Nonmalignant Hematology, or “Benign Hematology,” with a view to offering a robust, engaging tool that will assist every hematologist and oncologist (pediatric and adult equally) in making decisions during day-to-day practice. The entire spectrum of the specialty is covered in more than 60 exceptional chapters written by acknowledged authorities in the field. The content is organized into well-designed broad sections on red cell disorders, platelet and coagulation disorders, coagulopathy in systemic diseases, thromboembolic disease and its management (including surgical), immune system and related disorders, hemostasis and thrombosis during pregnancy and in the newborn and elderly, and Transfusion Medicine. A key aspect of the book is the opportunity it affords expert physicians to express well-reasoned opinions regarding complex issues in Nonmalignant Hematology. Readers will find that it provides a practical and immediately applicable compendium of answers to often complex and vexing questions. It will appeal to residents, fellows, house officers and more experienced practitioners around the globe.

  • Evaluation of Anemia in Children and Adults

    Marks, Peter W.

    Pages 3-12

     
  • Iron Homeostasis and the Pathophysiology and Management of Iron Deficiency

    McLaren, Gordon D. (et al.)

    Pages 13-22

  • Porphyrias: Diagnosis and Management

    Tishler, Peter V.

    Pages 23-28

  • Disorders of Hemoglobin Synthesis: Pathophysiology and Diagnostic Evaluation

    Cassinerio, Elena (et al.)

    Pages 29-37

  • Management of Thalassemias

    Badawy, Sherif M. (et al.)

    Pages 39-51

  • Allogeneic Hematopoietic Cell Transplant in β-Thalassemia Major

    Abutalib, Syed A.

    Pages 53-61

  • Sickle Cell Disease: Prevention of Complications

    Novelli, Enrico Maria

    Pages 63-73

  • Sickle Cell Disease: Management of Complications

    Winstead, Michael (et al.)

    Pages 75-87

  • Allogeneic Hematopoietic Cell Transplant in Sickle Cell Disease

    Saraf, Santosh L.

    Pages 89-96

  • Anemia of Inflammation

    Means, Robert T.

    Pages 97-102

  • Iron Overload: Diagnosis, Complications, and Management

    Brissot, Pierre

    Pages 103-112

  • Megaloblastic and Nutritional Anemias

    Stabler, Sally P.

    Pages 113-123

  • Sideroblastic Anemias: Diagnosis and Management

    Werner, Eric J. (et al.)

    Pages 125-135

  • Primary Autoimmune Warm Antibody Hemolytic Anemias

    Krauth, Maria Theresa (et al.)

    Pages 137-152

  • Intrinsic Hemolytic Anemias: Pathophysiology, Diagnosis, and Management

    Quinn, Charles T.

    Pages 153-167

  • Platelet Disorders: Diagnostic Tests and Their Interpretations

    Huntington, Scott F. (et al.)

    Pages 171-183

  • Inherited Platelet Disorders: Diagnosis and Management

    Songdej, Natthapol (et al.)

    Pages 185-197

  • Acquired Platelet Disorders: Diagnosis and Management

    Neunert, Cindy

    Pages 199-207

  • Immune-Mediated Thrombocytopenia

    Papadantonakis, Nikolaos (et al.)

    Pages 209-220

  • Coagulation Cascade and Fibrinolysis Pathway: Assessment in the Laboratory

    George, Lindsey A. (et al.)

    Pages 221-233

  • Abnormalities in the Fibrinolysis Pathway and Clinical Implications

    Kwaan, Hau C. (et al.)

    Pages 235-242

  • Congenital Disorders of Fibrinogen: Clinical Presentations, Diagnosis and Management

    Casini, Alessandro (et al.)

    Pages 243-254

  • Hemophilia A and B: Diagnosis and Management

    Brown, Deborah

    Pages 255-262

  • Coagulation Factor Inhibitors: Diagnosis and Management

    Reipert, Birgit M. (et al.)

    Pages 263-272

  • Rare Coagulation Factor Deficiencies: Diagnosis and Management

    Green, David (et al.)

    Pages 273-283

  • von Willebrand Disease: Differential Diagnosis and Diagnostic Approach to Specific Subtypes

    Ragni, Margaret V.

    Pages 285-293

  • von Willebrand Disease: Prevention of Complications and Management of the Disease

    Kouides, Peter A.

    Pages 295-311

  • Antifibrinolytics: Indications and Precautions

    Harthy, Munjid (et al.)

    Pages 313-319

  • Gene Therapy for Bleeding Disorders

    Monahan, Paul E. (et al.)

    Pages 321-336

  • Disseminated Intravascular Coagulation

    Mandernach, Molly W. (et al.)

    Pages 339-347

  • Coagulopathy in Critically Ill Subjects

    Levi, Marcel

    Pages 349-359

  • Trauma-Associated Coagulopathy

    Hess, John R.

    Pages 361-367

  • Coagulation-Related Issues in Malignant Hematology: Diagnosis and Management

    Barreto, Jason N. (et al.)

    Pages 369-378

  • Unmet Clinical Needs of Antithrombotic Treatment in BCR/ABL-Negative Myeloproliferative Neoplasms

    Rocca, Bianca (et al.)

    Pages 379-393

  • Bleeding and Thrombosis in a Cancer Patient

    Fogerty, Annemarie E. (et al.)

    Pages 395-402

  • Management of the Surgical Patient with Thrombotic and Bleeding Diathesis

    Pruthi, Rajiv K.

    Pages 403-413

  • Prevention and Treatment of Arterial Thromboembolism

    Weinreich, Michael (et al.)

    Pages 417-428

  • Prevention of Venous Thromboembolism

    Dittus, Christopher (et al.)

    Pages 429-443

  • Diagnostic, Prognostic, and Therapeutic Challenges in Venous Thromboembolism

    Kopolovic, Ilana (et al.)

    Pages 445-461

  • Complications of Venous Thromboembolic Disease

    Connolly, Gregory C. (et al.)

    Pages 463-474

  • Hereditary Thrombophilias: Pathophysiology, Timing of Testing and Familial Testing

    Curnow, Jennifer (et al.)

    Pages 475-484

  • Antiphospholipid Antibodies and Syndrome: Complexities in Diagnosis and Management

    Schreiber, Karen (et al.)

    Pages 485-494

  • Unidentifiable Thrombophilia

    Mantha, Simon (et al.)

    Pages 495-502

  • Anticoagulation Drugs: Indications, Therapeutic Monitoring, and Antidotes

    Sharda, Anish V. (et al.)

    Pages 503-517

  • Heparin-Induced Thrombocytopenia: Diagnosis and Management

    Sun, Lova (et al.)

    Pages 519-529

  • Thrombotic Thrombocytopenic Purpura and Hemolytic Uremic Syndrome

    Tsai, Han-Mou

    Pages 531-547

  • Surgical Treatment of Thromboembolic Disease

    Karimi, Kamran M. (et al.)

    Pages 549-560

  • Nonmalignant Leukocyte Disorders

    Rice, Lawrence (et al.)

    Pages 563-573

  • Primary Immunodeficiency Disorders: Diagnosis and Management

    Maggina, Paraskevi (et al.)

    Pages 575-584

  • Disorders of Phagocytic Function: Diagnosis and Treatment

    Gansner, John M. (et al.)

    Pages 585-594

  • Inherited Bone Marrow Failure Syndromes

    Olson, Timothy S. (et al.)

    Pages 595-609

  • Hemophagocytic Lymphohistiocytosis: Diagnosis and Management Challenges

    Henry, Michael M. (et al.)

    Pages 611-617

  • Lysosomal Storage Disorders: Haematology Perspective

    Beaton, Brendan (et al.)

    Pages 619-631

  • Cryoglobulins and Cryoglobulinemia

    Gonsalves, Wilson I. (et al.)

    Pages 633-645

  • Reproductive Issues in Women with Bleeding and Thrombotic Disorders

    Williams, Stella G. (et al.)

    Pages 649-659

  • Pregnancy in Subjects with Hemoglobinopathies: Precautions and Management

    Naik, Rakhi P. (et al.)

    Pages 661-668

  • Neonatal Thrombosis and Coagulopathies

    Zaidi, Ahmar U. (et al.)

    Pages 669-676

  • Bleeding and Thrombosis in the Elderly

    Gaddh, Manila

    Pages 677-684

  • Transfusion Support: Indications, Efficacy, and Complications

    West, Kamille A. (et al.)

    Pages 687-696

  • Human Blood Antigens and Antibodies: Diagnostic and Therapeutic Implications

    Sheppard, Chelsea A. (et al.)

    Pages 697-705

  • Therapeutic Apheresis in Hematologic Disorders: When and Why?

    West, Kamille A. (et al.)

    Pages 707-718

 

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