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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: linhart a. 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
Right ventricular involvement in Fabry disease.
Palecek T, Dostalova G, Kuchynka P, Karetova D, Bultas J, Elleder M, Linhart A. Palecek T, et al. Among authors: linhart a. J Am Soc Echocardiogr. 2008 Nov;21(11):1265-8. doi: 10.1016/j.echo.2008.09.002. Epub 2008 Oct 4. J Am Soc Echocardiogr. 2008. PMID: 18835697
Study of urinary proteomes in Anderson-Fabry disease.
Vojtová L, Zima T, Tesař V, Michalová J, Přikryl P, Dostálová G, Linhart A. Vojtová L, et al. Among authors: linhart a. Ren Fail. 2010;32(10):1202-9. doi: 10.3109/0886022X.2010.516859. Ren Fail. 2010. PMID: 20954982
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. Among authors: linhart a. 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.
A high frequency of viral agents yet absence of Borrelia burgdorferi is seen within the myocardium of subjects with normal left ventricular systolic function: an electron microscopy study.
Kuchynka P, Palecek T, Grus T, Schramlova J, Krsek D, Vitkova I, Rohn V, Lindner J, Wicks E, Nemecek E, Dostalova G, Podzimkova J, Linhart A. Kuchynka P, et al. Among authors: linhart a. Folia Microbiol (Praha). 2016 Mar;61(2):129-35. doi: 10.1007/s12223-015-0417-8. Epub 2015 Jul 24. Folia Microbiol (Praha). 2016. PMID: 26205424
Time to treatment benefit for adult patients with Fabry disease receiving agalsidase β: data from the Fabry Registry.
Ortiz A, Abiose A, Bichet DG, Cabrera G, Charrow J, Germain DP, Hopkin RJ, Jovanovic A, Linhart A, Maruti SS, Mauer M, Oliveira JP, Patel MR, Politei J, Waldek S, Wanner C, Yoo HW, Warnock DG. Ortiz A, et al. Among authors: linhart a. J Med Genet. 2016 Jul;53(7):495-502. doi: 10.1136/jmedgenet-2015-103486. Epub 2016 Mar 18. J Med Genet. 2016. PMID: 26993266 Free PMC article. Clinical Trial.
412 results