The influence of a polymorphism in the gene encoding angiotensin converting enzyme (ACE) on treatment outcomes in late-onset Pompe patients receiving alglucosidase alfa
Author:
Publisher
Elsevier BV
Subject
Endocrinology,Genetics,Molecular Biology
Reference17 articles.
1. Pompe's disease;van der Ploeg;Lancet,2008
2. Glycogen storage disease type II: acid α-glucosidase (acid maltase deficiency);Hirschhorn,2001
3. Consensus treatment recommendations for late-onset Pompe disease;Cupler;Muscle Nerve,2012
4. Enzyme replacement therapy in late-onset Pompe disease: a systematic literature review;Toscano;J. Neurol.,2013
5. A randomized study of alglucosidase alfa in late-onset Pompe's disease;van der Ploeg;New. Engl. J. Med.,2010
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1. Polymorphism in exercise genes and respiratory function in late-onset Pompe disease;Journal of Applied Physiology;2021-12-01
2. Gene therapy with secreted acid alpha-glucosidase rescues Pompe disease in a novel mouse model with early-onset spinal cord and respiratory defects;EBioMedicine;2020-11
3. Molecular genetics of Pompe disease: a comprehensive overview;Annals of Translational Medicine;2019-07
4. A genetic modifier of symptom onset in Pompe disease;EBioMedicine;2019-05
5. Assessing the Role of Anti rh-GAA in Modulating Response to ERT in a Late-Onset Pompe Disease Cohort from the Italian GSDII Study Group;Advances in Therapy;2019-03-16
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