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1 improved therapies for benign and malignant hematologic disease.
2 in patients with malignant and non-malignant hematologic disease.
3 -4.3) for trauma to 8.7 (95% CI, 6.8-11) for hematologic disease.
4 provide insights into inherited and acquired hematologic disease.
5 l transplantation, in patients with advanced hematologic disease.
6 te hematopoiesis but may also be relevant to hematologic disease.
7 geted therapy as a new treatment modality in hematologic disease.
8 en given to its effect on the development of hematologic disease.
9 d diagnosis and treatment for this important hematologic disease.
10 f choice for treatment of intractable benign hematologic disease.
11 ne of the affected patients had a history of hematologic disease.
12 n the microbiota's role in hematopoiesis and hematologic diseases.
13 antation, a potentially curative therapy for hematologic diseases.
14 berrant PKA signaling in the pathogenesis of hematologic diseases.
15 ved as a curative modality for patients with hematologic diseases.
16 thought to contribute to the development of hematologic diseases.
17 at promise for cell-based therapies to treat hematologic diseases.
18 investigation and for clinical diagnosis of hematologic diseases.
19 is a curative procedure for life-threatening hematologic diseases.
20 cyte (MN) recruitment in immune-mediated and hematologic diseases.
21 s too low for effective gene therapy of most hematologic diseases.
22 deal treatment strategy for many genetic and hematologic diseases.
23 he treatment of a large number of congenital hematologic diseases.
24 th laparoscopic splenectomy in patients with hematologic diseases.
25 ng nonmalignant non-primary immunodeficiency hematologic disease (15.4%; p = 0.020), metabolic disord
26 rge and were alive and in remission of their hematologic disease after a follow-up of 18 (range, 5-30
27 of patients with several types of malignant hematologic disease and hematologic disorders; however,
28 und in PB lymphocytes of patients with other hematologic diseases and heavy transfusion burdens or in
31 ans for studying the role of phytosterols in hematologic diseases and testing therapeutic interventio
32 mal HSC biology, featuring aspects of aging, hematologic disease, and how this circuitry may be explo
34 comparable to those of open splenectomy for hematologic diseases, and it appears to retain other pat
35 e a treatment for patients with nonmalignant hematologic diseases, and may tolerize patients to organ
36 type I, which is seen exclusively in clonal hematologic diseases, and type II/III, which is called m
38 nd, but diagnostic criteria for MDS or other hematologic diseases are not fulfilled, a condition term
39 the prophylactic transfusion of platelets in hematologic diseases are well described, relatively litt
40 ia is a critical problem that occurs in many hematologic diseases, as well as after cancer therapy an
41 uired severe aplastic anemia (SAA) is a rare hematologic disease associated with significant morbidit
46 juvenile myelomonocytic leukemia, are clonal hematologic diseases characterized by myeloid dysplasia,
47 omes (MDSs) are collections of heterogeneous hematologic diseases characterized by refractory cytopen
48 estigation of how biophysical alterations in hematologic disease collectively lead to microvascular o
51 lobinuria (PNH), a rare but life-threatening hematologic disease, has fundamentally improved with the
56 alized patient dying with advanced cancer or hematologic disease in which the limitation of life-sust
59 entiation, and iron overload in a variety of hematologic diseases is associated with excessive bone r
61 inactive granulomata, or even the underlying hematologic disease itself (especially in patients with
62 native for patients with high-risk malignant hematologic diseases, lacking an HLA identical sibling a
63 take-associated alterations in patients with hematologic disease on triazol antifungal medication.
64 eukemia (AML) varies as a result of previous hematologic disease or can be explained by differences i
65 have been implicated in the pathogenesis of hematologic diseases other than chronic myelogenous leuk
66 ause of the association of mastocytosis with hematologic disease, plasma levels were measured for sol
68 CMV reactivation had no preventive effect on hematologic disease relapse irrespective of diagnosis.
72 astic anemia (AA) is its evolution to clonal hematologic diseases such as myelodysplasia (MDS) and le
73 bers has been associated with multiple human hematologic diseases such as neutrophil dysfunction, leu
76 ute promyelocytic leukemia is one of the few hematologic diseases that must be recognized under the m
77 n factors V and VIII (F5F8D) are the 2 known hematologic diseases that result from defects in the end
78 antation mortality is greater than for other hematologic diseases, treatment leads to durable hematol
81 topoietic stem cell source for patients with hematologic diseases who can be cured by allogeneic hema
82 e only curative treatment for many malignant hematologic diseases, with an often critical graft-versu
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