bifurcate
发表于 2025-3-25 04:24:42
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喊叫
发表于 2025-3-25 07:40:47
Thomas Kron,Christian W. G. Lasarczykn platelets in the peripheral blood, with ensuing thrombohemorrhagic symptoms. Furthermore, mild leukocytosis, lack of hepatosplenomegaly and excellent prognosis with only rare transformation to acute leukemia are typical characteristics of this disease.
Nutrient
发表于 2025-3-25 14:13:13
Thomas Kron,Christian W. G. LasarczykPV in the state of Connecticut is 22 per 100,000 [.]. Only ∼5% of the patients are <40 years at diagnosis. Several studies report a higher incidence in males. The prevalence is ∼30/100,000. The incidence of thrombosis is ∼18 per 1,000 person-years [.]. If left untreated, the survival time of patient
Phenothiazines
发表于 2025-3-25 16:58:09
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工作
发表于 2025-3-25 22:30:46
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谈判
发表于 2025-3-26 02:07:41
Diktumscharakterisierung als Sprechakt?,s. MDS is characterized by an increased but ineffective and dysplastic hematopoiesis as well as peripheral cytopenias. The abnormal hematopoietic clone partly gives rise to mature, but functionally and morphologically abnormal blood cells, and, at least in some cases, is capable of both myeloid and
fastness
发表于 2025-3-26 04:23:45
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赞成你
发表于 2025-3-26 08:44:25
https://doi.org/10.1057/978-1-137-54642-5yeloid leukemia (CML) are relatively rare disorders. Due to the long life span of most patients with these diseases however, the prevalence is quite high, so that patients with these diseases are commonly seen in hematological outpatient departments.
驾驶
发表于 2025-3-26 14:31:20
https://doi.org/10.1057/978-1-137-54642-5t can be present in adolescence or childhood on rare occasions [.]. Overall both genders are affected in approximately equivalent numbers. However, some Asian studies report a strong male preponderance [.]. The median age at diagnosis is 30 years in Caucasians and 45 years in Asian patients [.].
配偶
发表于 2025-3-26 17:18:41
https://doi.org/10.1057/978-1-137-54642-5hemoglobinuria (PNH) and T-cell large granular lymphocytic leukemia (T-LGL) (see .). All these entities are bone marrow failure disorders1 in which oligoclonal T-cell-mediated immune responses are without doubt pathophysiologically relevant. These overlap syndromes seem to form some kind of disease-