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Screening for Fabry disease using genetic testing

机译：使用基因测试筛查法布里病

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《European Journal of Heart Failure》 |2010年第6期|p.530-531|共2页
作者
Markus Niemann;
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University of Wuerzburg, @%@Corresponding author. Tel: @%@, Fax: @%@, Email:;

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1. Screening for Fabry disease using genetic testing. [J] . Weidemann F, Niemann M European journal of heart failure: journal of the Working Group on Heart Failure of the European Society of Cardiology . 2010,第6期

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2. Screening for Fabry Disease in Patients with Chronic Kidney Disease: Limitations of Plasma ?±-Galactosidase Assay as a Screening Test [J] . Adeera Levin, Bee-Chin Toh, Hilary D. Vallance, Clinical journal of the American Society of Nephrology: CJASN . 2008,第1期

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3. The benefits, challenges and regional differences of family screening in rare genetic diseases: Lessons from Fabry disease [J] . Molecular genetics and metabolism . 2020,第2期

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5. Newborn Screening for Fabry Disease in the United States: Evaluation of the Psychosocial Impacts on Family Members [D] . Momohara, Christie-Brianna K. 2015

机译：美国法布里病的新生儿筛查：对家庭成员的社会心理影响的评估
6. Prevalence of Fabry disease in dialysis patients: Western Australia Fabry disease screening study - the FoRWARD study [O] . Sadia Jahan, Subashini Sarathchandran, Shamina Akhter, 2020

机译：透析患者中法布里病的流行：西澳大利亚州法布里病筛查研究-FoRWARD研究
7. Screening for Fabry Disease in Patients with Chronic Kidney Disease: Limitations of Plasma α-Galactosidase Assay as a Screening Test [O] . Andrade, Jason, Waters, Paula J., Singh, R. Suneet, 2008

机译：慢性肾脏病患者的法布里病筛查：血浆α-半乳糖苷酶测定的局限性

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