crescendo
发表于 2025-3-27 00:07:55
https://doi.org/10.1007/978-3-211-79892-8Myelodysplastic Syndroms; Myeloproliferative Disorders; Myeolid Disorders; Therapy; anemia; cell; epidemio
狂热文化
发表于 2025-3-27 03:26:04
978-3-7091-2003-3Springer-Verlag Vienna 2010
FOLLY
发表于 2025-3-27 05:57:47
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.
genesis
发表于 2025-3-27 09:51:40
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.
休战
发表于 2025-3-27 16:36:01
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 [.].
臭了生气
发表于 2025-3-27 21:49:51
http://reply.papertrans.cn/23/2264/226399/226399_36.png
伟大
发表于 2025-3-28 01:35:06
http://reply.papertrans.cn/23/2264/226399/226399_37.png
Assemble
发表于 2025-3-28 05:47:36
Essential Thrombocythemia (ET),n 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.
铁砧
发表于 2025-3-28 08:17:13
Rare Clonal Myeloid Diseases,yeloid 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.
artless
发表于 2025-3-28 13:13:04
,, “Classic” Paroxysmal Nocturnal Hemoglobinuria (PNH) (Marchiafava-Micheli Syndrome),t 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 [.].