標(biāo)題: Titlebook: Concise Guide to Hematology; Hillard M. Lazarus,Alvin H. Schmaier Book 2019Latest edition Springer Nature Switzerland AG 2019 hematopoiesi [打印本頁] 作者: DEIFY 時(shí)間: 2025-3-21 17:19
書目名稱Concise Guide to Hematology影響因子(影響力)
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書目名稱Concise Guide to Hematology網(wǎng)絡(luò)公開度學(xué)科排名
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書目名稱Concise Guide to Hematology讀者反饋
書目名稱Concise Guide to Hematology讀者反饋學(xué)科排名
作者: 供過于求 時(shí)間: 2025-3-21 20:27
,Sickle Cell Disease and the?Hemoglobinopathies,ical complications and therapies for sickle cell disease and the thalassemias. Outcomes for patients affected by hemoglobinopathies are improving as our ability to treat and cure these disorders becomes more sophisticated.作者: GLIB 時(shí)間: 2025-3-22 03:10 作者: 追逐 時(shí)間: 2025-3-22 07:17 作者: 高興一回 時(shí)間: 2025-3-22 10:28
Lene Auestad,Amal Treacher Kabesholysis-augmenting event and ranges from asymptomatic to life-threatening anemia. Even fully compensated non-anemic congenital hemolytic conditions increase the risk of gallstones and erythroferrone/hepcidin-mediated iron overload and its associated complications.作者: enumaerate 時(shí)間: 2025-3-22 13:55
https://doi.org/10.1007/978-3-662-42322-6 major roles in hemostasis. This chapter focuses on platelet structure and function and on inherited disorders of platelet number and function, which are generally associated with an increased bleeding risk with hemostatic challenges.作者: enumaerate 時(shí)間: 2025-3-22 18:56
Hematopoiesis,tic ontogeny and mechanisms responsible for hematopoietic homeostasis have important implications for day-to-day clinical practice. This chapter reviews the biology of normal hematopoiesis and how they contribute to pathological findings in disease states.作者: 確定 時(shí)間: 2025-3-22 21:17 作者: Expostulate 時(shí)間: 2025-3-23 05:21
Platelet Function in Hemostasis and Inherited Disorders of Platelet Number and Function, major roles in hemostasis. This chapter focuses on platelet structure and function and on inherited disorders of platelet number and function, which are generally associated with an increased bleeding risk with hemostatic challenges.作者: 混雜人 時(shí)間: 2025-3-23 06:32
https://doi.org/10.1007/978-981-13-6864-6cyte count provide particularly useful information when considered together and sometimes point toward the specific cause of anemia present. This knowledge minimizes the amount of additional laboratory investigation required. Accurate and timely diagnosis facilitates appropriate therapeutic intervention.作者: atrophy 時(shí)間: 2025-3-23 09:45 作者: 意外的成功 時(shí)間: 2025-3-23 16:04
https://doi.org/10.1007/978-3-642-71665-2and consumption coagulopathies. Antithrombotic treatment may be another frequent cause of an acquired bleeding disorder, and in case of severe or even life-threatening bleeding, immediate reversal may be required.作者: embolus 時(shí)間: 2025-3-23 21:44 作者: prolate 時(shí)間: 2025-3-24 01:16 作者: CRANK 時(shí)間: 2025-3-24 03:42
Iron Deficiency,tory tests to diagnose the condition. The importance of determining the cause of the patient’s iron deficiency and the approach to treatment is summarized. The final section focused on the anemia of inflammation and its differentiation from iron deficiency.作者: hieroglyphic 時(shí)間: 2025-3-24 07:28
Acquired Bleeding Disorders,and consumption coagulopathies. Antithrombotic treatment may be another frequent cause of an acquired bleeding disorder, and in case of severe or even life-threatening bleeding, immediate reversal may be required.作者: 簡(jiǎn)略 時(shí)間: 2025-3-24 11:49 作者: 外來 時(shí)間: 2025-3-24 14:54
.Written by a diverse range of experts in the field, .Concise Guide to Hematology, Second Edition. is a valuable resource for clinicians, residents, trainees, and entry-level fellows who work in or are just entering the field of hematology..978-3-319-97873-4作者: 踉蹌 時(shí)間: 2025-3-24 21:05 作者: 首創(chuàng)精神 時(shí)間: 2025-3-25 00:13 作者: Ingest 時(shí)間: 2025-3-25 06:12
The Influence of Glacial Meltwater,acteristics and laboratory tests to reach diagnosis, determine the underlying causes, and proceed to treatments to avoid the often significant mortality and morbidity risks of acquired hemolytic anemias.作者: 全等 時(shí)間: 2025-3-25 11:12
The Next Cold Period Is Coming,logic states, vessel occlusion or thrombosis arises from both expression of tissue factor and factor VIIa or activation of factor XII upon contact with various physiologic or pathophysiologic anionic biologic surfaces. The goal of hemostasis is to generate thrombin in a kinetically fast manner to st作者: 重疊 時(shí)間: 2025-3-25 14:22 作者: FECT 時(shí)間: 2025-3-25 17:57
https://doi.org/10.1007/978-3-319-67867-2coagulability, and a prothrombotic state. When faced with a thrombocytopenic patient, the clinician must ask: what is the probable cause of the patient’s thrombocytopenia? The answer to that question indicates whether the patient’s major risk is bleeding, thrombosis, or increased mortality (due to m作者: ABASH 時(shí)間: 2025-3-25 22:17
Giovannina Botez,Jürgen Wincklerhe bulk of venous thrombosis..In 1856, Virchow described the three causes of thrombosis: blood hypercoagulability, stasis, and vessel wall abnormalities (Virchow’s triad). Blood components (including blood cells and plasma proteins) are the best studied of this triad, and the importance of alteratio作者: AWE 時(shí)間: 2025-3-26 03:03 作者: Opponent 時(shí)間: 2025-3-26 04:52
Odjan Assadian,Matthias Leonhard clinical trials that have established the efficacy and safety profile of these treatments. This chapter will review the role of platelets in cardiovascular disease, the pharmacology of antiplatelet drugs, and the clinical evidence that guides their use.作者: dilute 時(shí)間: 2025-3-26 08:47
Introduction to Hematology,ecific organ for hematologic disorders, and its diseases arise within the bone marrow, the lymph nodes, or the intravascular compartment. The latter includes the endothelial cells lining blood vessels and the proteins in the blood plasma. The circulating cell-endothelial cell interface and the rheol作者: Debrief 時(shí)間: 2025-3-26 15:05 作者: Tincture 時(shí)間: 2025-3-26 16:59 作者: garrulous 時(shí)間: 2025-3-27 00:09
Physiology of Hemostasis,logic states, vessel occlusion or thrombosis arises from both expression of tissue factor and factor VIIa or activation of factor XII upon contact with various physiologic or pathophysiologic anionic biologic surfaces. The goal of hemostasis is to generate thrombin in a kinetically fast manner to st作者: 注射器 時(shí)間: 2025-3-27 02:00
Congenital Bleeding Disorders,d quality of life. Modifications to the recombinant factor proteins have prolonged the half-life of these factors, hence reducing the number of doses and increasing the residual trough levels in patients on prophylaxis. Newer therapies for patients with hemophilia A and B include alternative substit作者: probate 時(shí)間: 2025-3-27 08:35 作者: flutter 時(shí)間: 2025-3-27 11:41 作者: 背景 時(shí)間: 2025-3-27 17:05 作者: notice 時(shí)間: 2025-3-27 20:42
Antiplatelet Therapy in Cardiovascular Disease, clinical trials that have established the efficacy and safety profile of these treatments. This chapter will review the role of platelets in cardiovascular disease, the pharmacology of antiplatelet drugs, and the clinical evidence that guides their use.作者: obeisance 時(shí)間: 2025-3-28 00:33
The topological residue homomorphism,nts as well as a liquid portion consisting of proteins, amino acids, carbohydrates, lipids, and other macromolecules and low-molecular-weight precursors. The hematopoietic system is characterized by high cell turnover and replenishment throughout one’s life. The pluripotent hematopoietic stem cell (作者: Exposure 時(shí)間: 2025-3-28 02:46 作者: Accord 時(shí)間: 2025-3-28 07:04 作者: 空洞 時(shí)間: 2025-3-28 10:29 作者: Missile 時(shí)間: 2025-3-28 17:20
https://doi.org/10.1007/978-981-13-6864-6 an explanation of the pathophysiology of iron depletion. The phases of the development of iron-deficiency anemia and its prevalence in different populations at risk are outlined. The clinical manifestations of iron deficiency and the resulting anemia are reviewed, along with a description of labora作者: 監(jiān)禁 時(shí)間: 2025-3-28 22:37 作者: 濃縮 時(shí)間: 2025-3-28 23:12
Traces of Violence and Freedom of Thoughtia are the most common inherited hemoglobinopathies. The clinical phenotype of these hemolytic disorders are contingent on the number and type of mutations or deletions inherited. Both qualitative and quantitative disorders occur. Understanding the genetic basis for these disorders facilitates repro作者: Disk199 時(shí)間: 2025-3-29 04:09 作者: GOAT 時(shí)間: 2025-3-29 07:53
The Influence of Glacial Meltwater,ally by increased reticulocytosis. In contrast to hereditary hemolytic anemias, the decreased erythrocyte survival due to increased red blood cell destruction is caused typically by extrinsic factors including immune-mediated mechanisms (autoimmune or alloimmune causes), mechanical injury to erythro作者: 小卷發(fā) 時(shí)間: 2025-3-29 11:26 作者: ironic 時(shí)間: 2025-3-29 18:51
K. Gdanietz,K. Vorpahl,G. Piehl,A. H?ckof fibrinogen; prothrombin; factors V, VII, X, XI, and XIII; and PAI-1 constitute rare bleeding disorders (RBDs). Inherited deficiencies of inhibitors of fibrinolysis are extremely rare bleeding disorders and are included under the “miscellaneous” category. The clinical spectrum of bleeding symptoms作者: 英寸 時(shí)間: 2025-3-29 21:27
https://doi.org/10.1007/978-3-642-71665-2e coagulation tests, such as the platelet count, prothrombin time, or activated partial thromboplastin time. Acquired bleeding disorders can be categorized in quantitative or qualitative platelet defects, impaired clotting factor synthesis or low coagulation factors caused by inhibiting antibodies, 作者: GREG 時(shí)間: 2025-3-30 03:24
https://doi.org/10.1007/978-3-662-42322-6ng events involving the blood vessel, platelets, and plasma coagulation system. Platelets are anucleate fragments derived from megakaryocytes and have major roles in hemostasis. This chapter focuses on platelet structure and function and on inherited disorders of platelet number and function, which 作者: foreign 時(shí)間: 2025-3-30 05:01
https://doi.org/10.1007/978-3-319-67867-2ative), sequestration (hypersplenism), increased platelet consumption, and increased platelet destruction. Consumptive thrombocytopenic disorders include thrombin-mediated (disseminated intravascular coagulation), septicemia, and thrombotic microangiopathy (thrombotic thrombocytopenic purpura, hemol作者: pester 時(shí)間: 2025-3-30 08:22
Giovannina Botez,Jürgen Wincklerd pulmonary embolism) is worse than the expected survival in age- and sex-matched controls [1, 2]. Moreover, the risk of death after a pulmonary embolism (PE) is 18-fold higher than after a deep vein thrombosis (DVT) [3]. VTE also poses a significant burden globally in terms of disability-adjusted l作者: induct 時(shí)間: 2025-3-30 13:04 作者: pus840 時(shí)間: 2025-3-30 16:41
Odjan Assadian,Matthias Leonhard and peripheral vascular disease. Cardiovascular disease is the leading cause of death in most regions of the world, and antiplatelet therapy is an essential part of the treatment of acute coronary syndromes and stable coronary artery disease. Drugs that inhibit platelet function block key receptors作者: 鬼魂 時(shí)間: 2025-3-30 20:59 作者: Anthem 時(shí)間: 2025-3-31 02:37 作者: 膽汁 時(shí)間: 2025-3-31 08:26
Physiological Roles of Leukocytes and Disorders, their basic physiology and important disease states associated with defects of each of these entities. Each of these cells arises from a common bone marrow myeloid or lymphoid progenitor to differentiate into their unique types.作者: Rustproof 時(shí)間: 2025-3-31 11:32
Social Media and Ambient Social Distanceocess of hematopoiesis and the structure of hemoglobin. It also characterizes the structure and function of the red cell membrane and the various intracellular metabolic pathways. Both are of critical importance for red blood cell function and survival.作者: 金盤是高原 時(shí)間: 2025-3-31 16:56 作者: Canvas 時(shí)間: 2025-3-31 20:00
Treatment of Congenital Cricoid Stenosis,This chapter aims to provide a simple diagnostic framework in which the physician can approach most patients with abnormal bleeding in a logical fashion to recognize the underlying cause. The diagnostic approach to bleeding disorders is based upon a full understanding of what the current screening assays for bleeding states measure.作者: 抵押貸款 時(shí)間: 2025-3-31 23:16
,Approach to the?Bleeding Patient,This chapter aims to provide a simple diagnostic framework in which the physician can approach most patients with abnormal bleeding in a logical fashion to recognize the underlying cause. The diagnostic approach to bleeding disorders is based upon a full understanding of what the current screening assays for bleeding states measure.作者: 放縱 時(shí)間: 2025-4-1 05:51 作者: 小卷發(fā) 時(shí)間: 2025-4-1 06:11
Springer Nature Switzerland AG 2019作者: circumvent 時(shí)間: 2025-4-1 10:21 作者: Badger 時(shí)間: 2025-4-1 15:56
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