Ataxia Telangiectasia: A Rare Neurodegenerative Disease with Variable Immunodeficiency and Recurrent Infections

Cataletto Mary

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Ataxia Telangiectasia: A Rare Neurodegenerative Disease with Variable Immunodeficiency and Recurrent Infections

机译：Ataxia Telanciectasia：一种罕见的神经变性疾病，具有可变免疫缺陷和反复感染

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"Ataxia Telangiectasia: A Rare Neurodegenerative Disease with Variable Immunodeficiency and Recurrent Infections." Pediatric Allergy, Immunology, and Pulmonology , 31(1), p. 1

机译：“共济失调毛细血管扩张症：一种罕见的神经退行性疾病，伴有可变免疫缺陷和反复感染。”儿科过敏、免疫学和肺脏学，31（1），第1页

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《Pediatric allergy, immunology, and pulmonology》 |2018年第1期|共1页
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Cataletto Mary;
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正文语种 eng
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1. Molecular basis of ataxia telangiectasia and related diseases [J] . Lindsay G BALL, Wei XIAO 中国药理学报：英文版 . 2005,第008期
2. Ataxia Telangiectasia: A Rare Neurodegenerative Disease with Variable Immunodeficiency and Recurrent Infections [J] . Cataletto Mary Pediatric allergy, immunology, and pulmonology . 2018,第1期

机译：Ataxia Telanciectasia：一种罕见的神经变性疾病，具有可变免疫缺陷和反复感染
3. A master protocol to investigate a novel therapy acetyl-l-leucine for three ultra-rare neurodegenerative diseases: Niemann-Pick type C, the GM2 gangliosidoses, and ataxia telangiectasia [J] . T. Fields, M. Patterson, T. Bremova-Ertl, Trials . 2021,第1期

机译：用于研究三种超罕见神经变性疾病的新疗法乙酰-L亮氨酸的母料方案：Niemann-Pick型C，GM2神经节性和Ataxia Telangiectasia
4. A CASE OF ATAXIA TELANGIECTASIA WITH IMMUNODEFICIENCY DUE TO A RARE VRIANT [J] . Rampur Lahari, Shliozberg Jenny Journal of Clinical Immunology . 2016,第3期

机译：一例因稀有变异导致免疫缺陷的阿塔克氏囊病
5. A Patient with Paroxysmal Nocturnal Hemoglobinuria in whom G-CSF Administration was Remarkably Effective against Recurrent Gastrointestinal Infections and Hemolytic Episodes Caused by Cellular Immunodeficiency [C] . T. Matsunaga, A. Fujimi, N. Takemoto, International Symposium on PNH and Related Disorders . 2003

机译：患有阵发性夜间血红蛋白尿的患者，G-CSF给药对由细胞免疫缺陷引起的复发性胃肠道感染和溶血发作显着有效
6. The ataxia-telangiectasia gene product: Expression, purification, and characterization of recombinant ATM and a diagnostic discussion of the ATM ELISA and disease pathogenesis. [D] . Chun, Helen Hyun Kyung. 2002

机译：共济失调-毛细血管扩张基因产品：重组ATM的表达，纯化和表征，以及ATM ELISA和疾病发病机理的诊断性讨论。
7. Brain hypometabolism in rare genetic neurodegenerative disease: Niemann-Pick disease type C spinocerebellar ataxia and Huntington disease assessed by FDG PET [O] . Yung Hsiang Kao, Melissa Cheng, Dennis Velakoulis, 2021

机译：稀有遗传神经变性疾病中的脑抑郁症状：Niemann-pick型C型CSpinocerebellar Ataxia和FDG PET评估的亨廷顿病
8. A master protocol to investigate a novel therapy acetyl-l-leucine for three ultra-rare neurodegenerative diseases: Niemann-Pick type C, the GM2 gangliosidoses, and ataxia telangiectasia [O] . T. Fields, M. Patterson, T. Bremova-Ertl, 2021

机译：探讨乙酰-L-L-亮氨酸三种超罕见神经变性疾病的母料方案：Niemann-Pick型C，GM2神经节性和Ataxia Telangiectasia
9. (Molecular approaches to the study of the radiation-sensitive disease ataxia-telangiectasia (AT)). Final technical report. [R] . 1991

机译：（分子方法研究辐射敏感性疾病共济失调 - 毛细血管扩张症（aT））。最终技术报告。

Ataxia Telangiectasia: A Rare Neurodegenerative Disease with Variable Immunodeficiency and Recurrent Infections

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