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Fabry disease - Vascular manifestations.
Karetova D, Bultas J, Dostalova G, Palecek T, Kovarnik T, Golan L, Linhart A. Karetova D, et al. Among authors: golan l. Vasa. 2010 May;39(2):123-31. doi: 10.1024/0301-1526/a000017. Vasa. 2010. PMID: 20464667 Review.
Pitfalls of X-chromosome inactivation testing in females with Fabry disease.
Řeboun M, Sikora J, Magner M, Wiederlechnerová H, Černá A, Poupětová H, Štorkánova G, Mušálková D, Dostálová G, Goláň L, Linhart A, Dvořáková L. Řeboun M, et al. Among authors: golan l. Am J Med Genet A. 2022 Jul;188(7):1979-1989. doi: 10.1002/ajmg.a.62728. Epub 2022 Mar 26. Am J Med Genet A. 2022. PMID: 35338595
Uric Acid as a Marker of Mortality and Morbidity in Fabry Disease.
Rob D, Marek J, Dostálová G, Goláň L, Linhart A. Rob D, et al. Among authors: golan l. PLoS One. 2016 Nov 11;11(11):e0166290. doi: 10.1371/journal.pone.0166290. eCollection 2016. PLoS One. 2016. PMID: 27835692 Free PMC article.
Evaluation of the efficacy and safety of three dosing regimens of agalsidase alfa enzyme replacement therapy in adults with Fabry disease.
Goláň L, Goker-Alpan O, Holida M, Kantola I, Klopotowski M, Kuusisto J, Linhart A, Musial J, Nicholls K, Gonzalez-Rodriguez D, Sharma R, Vujkovac B, Chang P, Wijatyk A. Goláň L, et al. Drug Des Devel Ther. 2015 Jul 8;9:3435-44. doi: 10.2147/DDDT.S80928. eCollection 2015. Drug Des Devel Ther. 2015. PMID: 26185417 Free PMC article. Clinical Trial.
56 results