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肺动脉高压自1973年第一次世界研讨会以来,一直是一种具有挑战性、慢性和复杂的疾病。且肺动脉高压人群基数较大,全球约有1%的人群受到影响[1]。欧洲心脏学会(ESC)与欧洲呼吸学会(ERS)以WHO分类为基础,将肺动脉高压(PH)分为:动脉性肺动脉高压、左心疾病所致肺动脉高压(PH-LHD)、肺部疾病和(或)低氧所致肺动脉高压、慢性血栓栓塞性肺动脉高压和其他肺动脉阻塞性疾病、未明和(或)多因素所致肺动脉高压[2]。
李依朔, 杨明, 刘佳辰, 王智慧
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[Clinical characteristics of DUX4-IGH fusion B-cell acute lymphoblastic leukemia in children]. [PDF]
Luo YX +4 more
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[Comprehensive considerations for the diagnosis, treatment, and management of osteogenesis imperfecta]. [PDF]
Lyu XH, Dong J.
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[Clinical and genetic characteristics of 14 children with sodium taurocholate co-transporting polypeptide deficiency]. [PDF]
Ma RX +7 more
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[A case of Harel-Yoon syndrome with seizures caused by an ATAD3A variant]. [PDF]
Yang Q, Pan Z, Chen C, Yin F, Peng J.
europepmc +1 more source
[Analysis of disease burden and changing trends of traumatic brain injury in China, 1990-2023]. [PDF]
Han Y, Sun K, Pan W, Luo X.
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[Primary familial and congenital polycythemia caused by EPOR gene mutation: two cases report and literature review]. [PDF]
Ning DH +10 more
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[Resistance to thyroid hormone syndrome with developmental disorders in two children]. [PDF]
Liao LY, Li XF, Zhang XX.
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