The establishment of facial telangiectasia animal modle by ultraviolet irradition

紫外线诱导的面部 毛细血管 扩张动物模型的建立

Ultra-high field 3.0T MR susceptibility weighted imaging in diagnosis of intracerebral capillary telangiectasia

超高场3.0T磁共振磁敏感加权成像诊断颅内 毛细血管 扩张 症

PVA microspheres embolization : a case of hepatic involvement in hereditary hemorrhagic telangiectasia

PVA微球栓塞肝脏遗传性出血性 毛细血管 扩张 症1例

It has now been confirmed that Ataxia Telangiectasia mutated ( ATM ) protein plays a crucial role in the regulation of cell cycle which is regulated by corresponding cyclin .

细胞周期由相应的周期蛋白进行调控，现已证实共济失调 毛细血管 扩张突变蛋白（ Ataxia Telangiectasia mutated protein，ATMprotein）在这一过程中发挥着关键的调控作用。

Conclusion Endoscopic heat probe is an effective method in colon telangiectasia .

结论内镜下热极治疗结肠 毛细血管 扩张 症是一种 微创有效 安全的方法。

Symptomatic children with hereditary hemorrhagic telangiectasia : A pediatric center experience

有症状的遗传性出血性 毛细血管 扩张 症患儿的临床和 遗传学 特征： 来自儿科中心的经验

ATM gene mutations in Chinese patients with ataxia - telangiectasia

中国人共济失调 毛细血管 扩张 症ATM基因突变研究

Objective To investigate the value of different MR sequences in diagnosing intracerebral capillary telangiectasia ( ICT ) .

目的探讨磁共振成像不同序列对颅内 毛细血管 扩张 症 的 影像诊断价值。

By electron microscope different degree of glial cell swelling and telangiectasia on the experimental side was seen . But on the control side no obvious glial cell swelling or telangiectasia was seen .

在电镜下，实验侧脑组织见不同程度的胶质细胞肿胀及 毛细血管 扩张，而对照侧未见明显的胶质细胞肿胀或毛细血管扩张。

Ataxia Telangiectasia ( AT ) as a genetic disorder results from single gene mutation characterized by radiosensitivity progressive nerve degeneration immunodeficiency premature aging and cancer predisposition .

共济失调性 毛细血管 扩张 综合症（ AT）是一种单基因突变引起的遗传性疾病，表现为高辐射敏感性、进行性神经退变、免疫缺陷、早衰及易患癌症等。

Metasilicate acid can improve telangiectasia decrease incidence of cardiovascular and avoid skin diseases gynecopathy & diabetes .

偏硅酸：能改善 血管 扩张，降低心血管发病率，可防治皮肤病、妇科病、糖尿病。

Treatment of facial telangiectasia by using XL-radiofrequency skin ablation apparatus

XL-射频皮肤治疗仪消融在 毛细血管 扩张治疗中的应用

Objective To study the radiosensitivity of fibroblast cells ( AT cells ) from the skin of the patients with ataxia telangiectasia ( AT ) .

目的研究 源于 毛细血管 扩张性共济失调症（ ataxia telangiectasia，AT）患者皮肤的成纤维细胞 系AT5BIVA（AT细胞）的辐射敏感性。

Objective : To study the treatment of nosebleed caused by hereditary hemorrhagic telangiectasia ( HHT ) .

目的：探讨遗传性出血性 毛细血管 扩张 症所引起鼻出血的治疗方法。

Analysis of angiogenesis related proteins and its implication in type-2 hereditary hemorrhagic telangiectasia

Ⅱ型遗传性出血性 毛细血管 扩张 症血管生长 发育相关蛋白质分析及意义

Objective To localize the pathogenic gene of hereditary hemorrhagic telangiectasia ( HHT ) in a Chinese family of Han Nationality .

目的定位一个中国汉族遗传性出血性 毛细血管 扩张 症家系的致病基因。

Because people sleep after muscle relaxation telangiectasia porokeratosis large central temperature regulation function easy to catch a cold or other diseases ;

因为人睡后肌肉松弛、 毛细血管 扩张、汗孔张大，体温调节中枢功能减退、易患感冒或其他疾病；

Caspase 3 mediated Cleavage of Ataxia Telangiectasia Mutated Protein in Induction of Apoptosis

毛细血管 扩张性共济失调突变蛋白在细胞凋亡过程中被Caspase┐3降解

RCM indicated that a week after treatment telangiectasia and edema were observed . After the inflammation has subsided collagens were mesh-shape aligned .

RCM检测示治疗后在1周可见 毛细血管 扩张、水肿等炎性反应，1个月后可见到胶原纤维呈网状排列。

Hereditary hemorrhagic telangiectasia resulted from a nonsense mutation Arg 479 Stop in the ALK-1 gene

ALK-1基因无义突变Arg479Stop导致的遗传性出血性 毛细血管 扩张症

The genetic disorder ataxia telangiectasia ( AT ) is characterized by immunodeficiency progressive cerebellar ataxia gonadal abnormalities radiosensitivity and cancer predisposition .

基因缺陷所致共济失调- 毛细血管 扩张 症（ AT）表现为免疫缺陷、进行性共济失调、性腺发育异常、辐射敏感和易患癌症等。

Tumor were 6 cases ( leiomyoma or leiomyosarcoma 5 adenoma 1 ) . Vascular lesion were 11 cases ( AVM 6 small intestinal telangiectasia 4 gastric varices 1 ) .

其中肿瘤6例（胃肠平滑肌瘤或肉瘤5例，腺瘤1例），血管病变11例（AVM6例，小肠 毛细血管 扩张 症4 症，胃底静脉曲张1例）；

Ultrasonographic Application in Diagnosing Hereditary Hemorrhagic Telangiectasia Involving Liver

超声在遗传性出血性 毛细血管 扩张 症肝受累中的应用价值

The Treatment of Nosebleed Caused by Hereditary Hemorrhagic Telangiectasia

中西 医 结合治疗遗传性出血性 毛细血管 扩张 症致鼻出血 疗效 观察

Objective To investigate the characteristics of the cytogenetic anomalies of ataxia telangiectasia .

目的探讨共济失调 毛细血管 扩张 症的细胞遗传学异常特点。

Mutation analysis of the ATM gene in two Chinese patients with ataxia telangiectasia

2例华裔共济失调 毛细血管 扩张 症患者的ATM基因突变分析

Color Doppler ultrasound in diagnosis of hereditary hemorrhagic telangiectasia with hepatic involvement

彩超诊断累及肝脏的遗传性出血性 毛细血管 扩张 症