標(biāo)題: Titlebook: Aplastic Anemia and Other Bone Marrow Failure Syndromes; Nasrollah T. Shahidi Book 1990 Springer-Verlag Inc. 1990 Viruses.anemia.bone marr [打印本頁(yè)] 作者: JOLT 時(shí)間: 2025-3-21 19:01
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書目名稱Aplastic Anemia and Other Bone Marrow Failure Syndromes讀者反饋學(xué)科排名
作者: ANT 時(shí)間: 2025-3-21 21:58 作者: gangrene 時(shí)間: 2025-3-22 01:20 作者: Simulate 時(shí)間: 2025-3-22 08:26 作者: VEST 時(shí)間: 2025-3-22 11:11 作者: 關(guān)心 時(shí)間: 2025-3-22 16:54
Die Streumatrix und ihre Symmetrien,to failure of committed progenitor differentiation due perhaps to reduction of steroid-sensitive expression of a specific growth factor receptor gene. Finally, the response of aplastic anemia to antithymocyte globulin or cyclosporine or sometimes prednisone creates the impression that aplastic anemi作者: 確認(rèn) 時(shí)間: 2025-3-22 19:45 作者: Immunoglobulin 時(shí)間: 2025-3-22 23:37
Treatment of Severe Aplastic Anemia: A 12-Year Follow-Up of Patients after Bone Marrow Transplantat of the hip was seen in 4 patients and one developed breast cancer. The most serious late complication after BMT was chronic graft-versus-host disease (GvHD) in patients receiving methotrexate (MTX) for prophylaxis against GvHD.作者: daredevil 時(shí)間: 2025-3-23 03:50
Treatment of Severe Aplastic Anemia (SAA) with Bone Marrow Transplantation (BMT) or Immunosuppressits of ALG were superior to BMT for patients not infected (68 vs 60%) or with no hemorrhages at the time of treatment (77 vs 69%). A Cox regression analysis showed that the only significant pretreatment variables were a low neutrophil count (. = 0.001) and increasing age (. = 0.05).作者: 總 時(shí)間: 2025-3-23 06:08
Bone Marrow Transplantation for Fanconi Anemia,ase (GVHD).. This poor tolerance to alkylating agents has been related to a DNA defect with increased chromosomal instability. Recently, efforts have been made to modify the conditioning regimen according to the cell sensitivity to alkylating agents and to irradiation.作者: Vertical 時(shí)間: 2025-3-23 12:10
Treatment of Acquired Aplastic Anemia with Cyclosporine and Androgens, clinical grounds, it has been found that prior immunosuppressive conditioning is necessary for successful bone marrow transplantation in identical twins in approximately half of the cases.. In addition, some patients conditioned by immunosuppressive agents including antilymphocyte globulin (ALG) fo作者: Interlocking 時(shí)間: 2025-3-23 14:42 作者: 有特色 時(shí)間: 2025-3-23 18:48
Book 1990y alter normal cellular recog- nition sites by interacting with cellular components and result in loss of self tolerance. Immunologic mechanisms have long been advocated in many other organ failures, and the hemopoietic organ is no exception. It is of interest that parallel clinical and laboratory i作者: Excitotoxin 時(shí)間: 2025-3-24 01:50
agents may alter normal cellular recog- nition sites by interacting with cellular components and result in loss of self tolerance. Immunologic mechanisms have long been advocated in many other organ failures, and the hemopoietic organ is no exception. It is of interest that parallel clinical and laboratory i978-1-4612-7935-8978-1-4612-3254-4作者: 通情達(dá)理 時(shí)間: 2025-3-24 04:25
Aplastic Anemia and Other Bone Marrow Failure Syndromes作者: 動(dòng)脈 時(shí)間: 2025-3-24 09:07 作者: sebaceous-gland 時(shí)間: 2025-3-24 11:57
Rekonstruktive BildungsforschungThe diagnosis of aplastic anemia is based on the presence of pancytopenia combined with bone marrow hypocellularity. Aplastic anemia may be acquired or constitutional; in either case its occurrence may be indicative of a preleukemic condition.作者: 天空 時(shí)間: 2025-3-24 16:00
Cytogenetics in Constitutional Aplastic Anemia,The diagnosis of aplastic anemia is based on the presence of pancytopenia combined with bone marrow hypocellularity. Aplastic anemia may be acquired or constitutional; in either case its occurrence may be indicative of a preleukemic condition.作者: Entrancing 時(shí)間: 2025-3-24 21:42
https://doi.org/10.1007/978-1-4612-3254-4Viruses; anemia; bone marrow; cell; classification; cytogenetics; genetics; hematopoiesis; immunosuppression作者: SPER 時(shí)間: 2025-3-25 01:37 作者: 善變 時(shí)間: 2025-3-25 03:42
Prospects for the Treatment of Aplastic Anemia,n blood product support and in antibiotics. Many patients now are also cured by effective therapy of their underlying bone marrow failure. Despite improvements, many patients with severe disease will die of their disease due to inherent limitations of current therapy; some of these limits should be overcome in the next few years.作者: duplicate 時(shí)間: 2025-3-25 11:29 作者: eustachian-tube 時(shí)間: 2025-3-25 13:29 作者: Engaged 時(shí)間: 2025-3-25 17:46
https://doi.org/10.1007/978-3-322-83120-0tation and immunomodulatory therapies. Recently, cloned recombinant hematopoietic growth factors have been introduced into clinical trials with encouraging preliminary results. This review will summarize recent advances with each of these modalities and make recommendations regarding indications for each approach.作者: conscribe 時(shí)間: 2025-3-25 21:30
https://doi.org/10.1007/978-3-662-00246-9ation of the stem cell, the size of its bone marrow pool remains relatively fixed, while its differentiating progenies mature into various blood cells that are delivered into the circulation on demand. This entire process is known as hemopoiesis. Through this process, every day more than 200 billion作者: dragon 時(shí)間: 2025-3-26 02:10 作者: 壓艙物 時(shí)間: 2025-3-26 07:02
N. I. Koschkin,M. G. Schirkjewitsch this entire topic can be found in the recent textbook edited by Nathan and Oski.. The classification of the aplastic anemias is shown in Table 3.1. Although the majority of cases are acquired, this presentation will focus on the constitutional disorders, in an effort to increase awareness of these 作者: concubine 時(shí)間: 2025-3-26 10:22
https://doi.org/10.1007/978-3-658-04726-9nd cell-mediated events that normally function to maintain blood cell numbers within very narrow limits.. Significant changes in the rate of production of blood cells can occur when the rate of synthesis of the regulatory humoral factor(s) is altered. This is clearly demonstrated by the increased ci作者: 字謎游戲 時(shí)間: 2025-3-26 15:06
Rekonstruktive Bildungsforschunger to divide and produce blood elements. The microenvironment cells, or stromal cells, provide signals necessary for progenitor growth, maturation, and eventual release from the marrow. Stromal cells in turn are influenced by accessory cells consisting of lymphocytes and macrophages that are capable作者: 秘方藥 時(shí)間: 2025-3-26 18:40 作者: Substance 時(shí)間: 2025-3-26 20:59 作者: 客觀 時(shí)間: 2025-3-27 02:53
https://doi.org/10.1007/978-3-322-83120-0BMT) and the more recent results of “immunosuppressive therapy” (1ST), which usually includes antihuman thymocyte globulin (ATG) or antihuman lymphoblast globulin (ALG). Patient age and availability of a suitable marrow donor limit the number of patients who are potential candidates for marrow graft作者: 清澈 時(shí)間: 2025-3-27 06:00
Guy Coughlan,James Dodd,Hening Genzing donors and 291 patients with SAA treated with immunosuppressive therapy (IS) with antilymphocyte globulin (ALG). The overall actuarial survival was 63% after BMT and 61% after IS therapy at 6 years. Younger patients (under 20) had a significantly better survival with BMT (66%) compared to IS (56作者: Hormones 時(shí)間: 2025-3-27 11:55
https://doi.org/10.1007/978-3-322-83120-0tation and immunomodulatory therapies. Recently, cloned recombinant hematopoietic growth factors have been introduced into clinical trials with encouraging preliminary results. This review will summarize recent advances with each of these modalities and make recommendations regarding indications for作者: 密切關(guān)系 時(shí)間: 2025-3-27 17:33
Neutrale Kaonen und ,-Verletzungt common abnormalities are skin pigmentation, microcephaly, short stature, skeletal defects particularly of the lateral aspect of the forearms and hands, and kidney and cardiac malformations.. Multiple abnormalities of peripheral blood lymphocyte chromosomes are almost always present. In its natural作者: 躺下殘殺 時(shí)間: 2025-3-27 21:22 作者: Foolproof 時(shí)間: 2025-3-28 01:39 作者: exacerbate 時(shí)間: 2025-3-28 03:21 作者: 小口啜飲 時(shí)間: 2025-3-28 09:53
Hadronen in der Quantenchromodynamik,bsence of erythroblasts from an otherwise normal marrow.. In contrast to aplastic anemia in which there is a global marrow aplasia resulting in pancytopenia, in PRCA there is only a very selective aplasia of the erythroid cell line that results in anemia and reticulocytopenia but in the presence of 作者: myalgia 時(shí)間: 2025-3-28 12:31 作者: mitten 時(shí)間: 2025-3-28 18:21
Die Streumatrix und ihre Symmetrien,is heterogeneous and poorly understood. The field can be further confused by investigators who assign pathophysiologic mechanisms as a result of therapeutic experiences. For example, the response of aplastic anemia to androgen therapy implies to some that the disease might be due to a deficiency of 作者: Meager 時(shí)間: 2025-3-28 21:05
http://image.papertrans.cn/a/image/158973.jpg作者: Gorilla 時(shí)間: 2025-3-28 22:53 作者: inclusive 時(shí)間: 2025-3-29 06:50
Acquired Aplastic Anemia: Classification and Etiologic Considerations, associated with a normocellular bone marrow, in the vast majority of the cases, the bone marrow is hypoplastic and pancytopenia is pronounced. The aplastic anemia is referred to as severe when, in addition to a hypoplastic bone marrow (less than 25% cellularity), at least two of the following three作者: 新星 時(shí)間: 2025-3-29 08:57
Constitutional Aplastic Anemia, this entire topic can be found in the recent textbook edited by Nathan and Oski.. The classification of the aplastic anemias is shown in Table 3.1. Although the majority of cases are acquired, this presentation will focus on the constitutional disorders, in an effort to increase awareness of these 作者: 轉(zhuǎn)向 時(shí)間: 2025-3-29 11:24
Cellular Interactions in the Suppression of Hematopoiesis,nd cell-mediated events that normally function to maintain blood cell numbers within very narrow limits.. Significant changes in the rate of production of blood cells can occur when the rate of synthesis of the regulatory humoral factor(s) is altered. This is clearly demonstrated by the increased ci作者: CRAB 時(shí)間: 2025-3-29 16:34 作者: moribund 時(shí)間: 2025-3-29 22:48
Prospects for the Treatment of Aplastic Anemia,n blood product support and in antibiotics. Many patients now are also cured by effective therapy of their underlying bone marrow failure. Despite improvements, many patients with severe disease will die of their disease due to inherent limitations of current therapy; some of these limits should be 作者: EWE 時(shí)間: 2025-3-30 02:42
Treatment of Severe Aplastic Anemia: A 12-Year Follow-Up of Patients after Bone Marrow Transplantatts (BMT) and 111 were treated with antilymphocyte globulin (ALG). We have analyzed the incidence of late complications in both groups of patients. Thirty-two patients treated with ALG developed a hematological complication: 10 of them a myelodysplastic syndrome (MDS) and 18 paroxysmal nocturnal hemo作者: Provenance 時(shí)間: 2025-3-30 05:09
Long-Term Comparison of Immunosuppressive Therapy with Antithymocyte Globulin to Bone Marrow TranspBMT) and the more recent results of “immunosuppressive therapy” (1ST), which usually includes antihuman thymocyte globulin (ATG) or antihuman lymphoblast globulin (ALG). Patient age and availability of a suitable marrow donor limit the number of patients who are potential candidates for marrow graft作者: Arb853 時(shí)間: 2025-3-30 10:52
Treatment of Severe Aplastic Anemia (SAA) with Bone Marrow Transplantation (BMT) or Immunosuppressiing donors and 291 patients with SAA treated with immunosuppressive therapy (IS) with antilymphocyte globulin (ALG). The overall actuarial survival was 63% after BMT and 61% after IS therapy at 6 years. Younger patients (under 20) had a significantly better survival with BMT (66%) compared to IS (56作者: 知識(shí) 時(shí)間: 2025-3-30 14:41
Treatment of Aplastic Anemia: Bone Marrow Transplantation, Immunomodulatory Therapy, and Hematopoietation and immunomodulatory therapies. Recently, cloned recombinant hematopoietic growth factors have been introduced into clinical trials with encouraging preliminary results. This review will summarize recent advances with each of these modalities and make recommendations regarding indications for作者: BRIDE 時(shí)間: 2025-3-30 16:32 作者: 思考才皺眉 時(shí)間: 2025-3-30 23:43
The Use of Etiocholanolone and Antithymus Globulin to Treat Aplastic Anemia: An Uncontrolled Comparlete hematological recovery associated with bone marrow transplantation from sibling donors to patients less than 25 years of age.. In older patients the results with bone marrow transplantation have been less desirable because of the complications of graft-versus-host (GVH) disease and infection. I作者: Torrid 時(shí)間: 2025-3-31 03:11 作者: Inferior 時(shí)間: 2025-3-31 07:23 作者: 同來(lái)核對(duì) 時(shí)間: 2025-3-31 12:47
Pure Red Cell Aplasia,bsence of erythroblasts from an otherwise normal marrow.. In contrast to aplastic anemia in which there is a global marrow aplasia resulting in pancytopenia, in PRCA there is only a very selective aplasia of the erythroid cell line that results in anemia and reticulocytopenia but in the presence of 作者: CHART 時(shí)間: 2025-3-31 16:35 作者: hematuria 時(shí)間: 2025-3-31 19:11
Summary and Conclusions,is heterogeneous and poorly understood. The field can be further confused by investigators who assign pathophysiologic mechanisms as a result of therapeutic experiences. For example, the response of aplastic anemia to androgen therapy implies to some that the disease might be due to a deficiency of 作者: Expressly 時(shí)間: 2025-3-31 23:27
Constitutional Aplastic Anemia,conditions, and to emphasize that they are undoubtedly more common than is currently recognized. Among the genetic bone marrow failure syndromes, Fanconi’s anemia (FA) is the most common, and will be discussed in the most detail.作者: ALIEN 時(shí)間: 2025-4-1 05:27
Cellular Interactions in the Suppression of Hematopoiesis,rculating red cell mass in individuals producing elevated levels of erythropoietin (Ep) when subjected to hypoxia,. and by the anemia present in renoprival patients with decreased Ep production.. A direct association between altered cell-mediated events and hematopoiesis . has not been clearly established.
