他的团队探讨骨髓增生异常综合征的患者血红蛋白合成异常的情况。
His team investigated the state of abnormal composition of hemoprotein in myelodysplastic syndrome.
骨髓增生异常综合征是一种造血干细胞克隆异常性疾病。
Myelodysplastic syndrome (MDS) is a clonal disorder of the hematopoietic stem cell.
目的探讨小儿骨髓增生异常综合征（MDS）的临床特点。
AbstractObjectiveTo study the clinical characteristics and prognosis factors of myelodysplastic syndrome (MDS) in children.
结论：骨髓活检是确诊低增生型骨髓增生异常综合征的必要手段。
Conclusion: the diagnose of hypoplastic MDS depends on the trephine biopsy.
目的探讨免疫细胞化学法在骨髓增生异常综合征（MDS）诊断价值。
Objective To explore the value of immunocytochemistry in diagnosis of myelodysplastic syndromes( MDS).
目的探讨骨髓增生异常综合征（MDS）合并自身免疫性疾病的特点。
Objective To explore the character of the myelodysplastic syndrome(MDS) with autoimmune disorders (AID).
抗利尿激素分泌异常综合征(SIADH)的诊断标准中那些是必须的？
What diagnostic criteria are necessary for the diagnosis of the syndrome of inappropriate antidiuretic hormone secretion (SIADH)?
我们研究了硼替佐米单药在骨髓增生异常综合征中应用的有效性和安全性。
We performed a study on efficacy and safety of bortezomib as a single agent in patients with myelodysplastic syndromes (MDS).
结果：20例符合抗利尿激素分泌异常综合征，其中治愈18例，死亡2例；
Results: Syndrome of inappropriate antidiuretic hormone was found in 20 cases, with which 18 patients were cured and 2 patients died.
多大剂量？多少频率？多长时间？骨髓增生异常综合征新疗法的临床应用指南。
How Much? How Frequent? How Long? A Clinical Guide to New Therapies in Myelodysplastic Syndromes.
目的：评估骨髓活检在骨髓增生异常综合征尤其是低增生型病例时的诊断价值。
Objective:To explore the value of bone marrow biopsy in diagnosing Myelodysplastic Syndrome(MDS) especially in the cases of MDS with hypoplasia.
方法10例19 ~58岁骨髓增生异常综合征的患者，选择部分脾动脉栓塞术治疗。
Methods 10 patients, ages: 19 ~ 58 years old, troubling with MDS, accepted splenic artery part embolization.
本研究探讨血小板糖蛋白特异性抗体在骨髓增生异常综合征（MDS）患者发病中的作用。
The aim of this study was to find platelet specific autoantibodies against glycoproteins in myelodysplastic syndrome(MDS)and to explore its role in pathogenesis of MDS.
氮杂胞苷（Azacitidine），用于治疗骨髓增生异常综合征（MDS）一种罕见的恶性血液肿瘤。
Azacitidine is used to treat patients with myelodysplastic syndromes (usually abbreviated, a bit oddly, to MDS), a group of rare and deadly blood malignancies.
骨髓增生异常综合征（MDS）患者的外周血白细胞减少、免疫功能低下和感染都是临床不可避免的问题。
The infection'manifestation with the decreased white blood cell and immune function is an unavoidable problem in the patients with myelodysplastic syndrome (MDS).
目的：调查白血病和骨髓增生异常综合征(MDS)患者红细胞酶和同工酶谱改变的患病率，并研究其临床意义。
Objective: To define the prevalence of acquired red cell enzymopathy in leukemia and MDS patients and explore its clinical significance.
结果联合治疗苯中毒中，再障2例均治愈，1例骨髓增生异常综合征(MDS)明显进步，1例急性造血停滞治愈。
Results 2 cases of aplastic anemia were cured and 1 case MDS was improved and 1 cured of stasis to produce blood.
目的：探讨糖基磷脂酰肌醇锚蛋白（GPIAP）在骨髓增生异常综合征（MDS）患者外周血细胞上的表达情况。
Objective:To investigate the expression of glycosylphosphatidylinositol anchored proteins(GPI AP:CD55, CD59) on peripheral erythrocytes and granulocytes in patients with myelodysplastic syndrome(MDS).
结论：骨髓活组织检查对于骨髓增生异常综合征（MDS）的阶段划分直观、明了，尤其在骨髓干抽病例更有其优越性；
Conclusion:It is simplicity and directly that to distinguished the stage of MDS with bone marrow biopsy; and for the cases of dry tap bone marrow aspiration was more useful.
Revlimid和类固醇地塞米松联合用药被批准用于多发性脊髓瘤和罕见病骨髓增生异常综合征的治疗。 其2009年的销售额为17亿美元。
Revlimid, which is approved for multiple myeloma patients in combination with the steroid dexamethasone, and for a rare condition called myelodysplastic syndromes, had revenue of $1.7 billion in 2009.
探讨儿童肾病综合征血脂代谢异常的特点及其与肾病临床状态和预后的关系。
Objective To investigate the abnormalities of lipid metabolism in children with nephrotic syndrome(NS), and relationship between the abnormalities and clinical state and prognosis of NS.
结论肾病综合征为一种自身免疫调节异常的疾病。
Conclusion Nephrotic syndrome is a kind of disease due to abnormal autoimmunity regulation.
结论过度通气综合征除呼吸困难外还常有其他众多症状，但查体都无异常，且常有明显的心因性诱因。
Conclusion Besides dyspnea, hyperventilation syndrome has many other symptoms as well as cardiac inducement, but it has no abnormal findings in physical and CT examination.
临床发现颈肋综合征的局部病理改变包括颈肋、斜角肌的异常和对臂丛神经的卡压。
The clinical local pathological findings of cervical rib syndrome were the cervical rib, abnormal scalenus and their compression on the brachial plexus.
结论原发性肾病综合征患儿血脂代谢发生明显异常，脂质三角出现明显变化。
Conclusion There were an obvious abnormal lipid metabolism and lipid trigone changes in children with primary nephrotic syndrome.
背景代谢综合征(MS)是多种代谢异常同时发生于同一个体的临床现象，可明显增加心血管疾病的危险性。
BackgroundMetabolic syndrome (MS) is the co-occurrence of multiple metabolic abnormalities in individuals and this clustering phenomenon drastically increase risk for cardiovascular disease.
尽管CAS是一种微创治疗方法，但仍然有许多潜在的并发症，如血流动力学异常、过度灌注综合征、脑梗死和再狭窄等。
Although CAS is a microinvasive technique, it has some potential complications, such as hemodynamic abnormalities, hyperperfusion syndrome, cerebral infarction, and restenosis.
尽管CAS是一种微创治疗方法，但仍然有许多潜在的并发症，如血流动力学异常、过度灌注综合征、脑梗死和再狭窄等。
Although CAS is a microinvasive technique, it has some potential complications, such as hemodynamic abnormalities, hyperperfusion syndrome, cerebral infarction, and restenosis.
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