Works matching AU Dostálová, Gabriela


Results: 19
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    Nationwide screening of Fabry disease in patients with hypertrophic cardiomyopathy in Czech Republic.

    Published in:
    ESC Heart Failure, 2022, v. 9, n. 6, p. 4160, doi. 10.1002/ehf2.14135
    By:
    • Zemánek, David;
    • Januška, Jaroslav;
    • Honěk, Tomáš;
    • Čurila, Karol;
    • Kubánek, Miloš;
    • Šindelářová, Štěpánka;
    • Zahálková, Lucie;
    • Klofáč, Petr;
    • Laštůvková, Eliška;
    • Lichnerová, Eva;
    • Aiglová, Renata;
    • Lhotský, Jan;
    • Vondrák, Jiří;
    • Dostálová, Gabriela;
    • Táborský, Miloš;
    • Kasper, David;
    • Linhart, Aleš
    Publication type:
    Article
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    Pitfalls of X‐chromosome inactivation testing in females with Fabry disease.

    Published in:
    American Journal of Medical Genetics. Part A, 2022, v. 188, n. 7, p. 1979, doi. 10.1002/ajmg.a.62728
    By:
    • Řeboun, Martin;
    • Sikora, Jakub;
    • Magner, Martin;
    • Wiederlechnerová, Helena;
    • Černá, Alena;
    • Poupětová, Helena;
    • Štorkánova, Gabriela;
    • Mušálková, Dita;
    • Dostálová, Gabriela;
    • Goláň, Lubor;
    • Linhart, Aleš;
    • Dvořáková, Lenka
    Publication type:
    Article
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    Study of urinary proteomes in Anderson-Fabry disease.

    Published in:
    Renal Failure, 2010, v. 32, n. 10, p. 1202, doi. 10.3109/0886022X.2010.516859
    By:
    • Vojtová, Lucie;
    • Zima, Tomáš;
    • Tesař, Vladimír;
    • Michalová, Jana;
    • Přikryl, Petr;
    • Dostálová, Gabriela;
    • Linhart, Aleš
    Publication type:
    Article
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    Infekční aneurysma hrudní aorty.

    Published in:
    Intervencní a Akutní Kardiologie, 2023, v. 22, n. 2, p. 87, doi. 10.36290/kar.2023.017
    By:
    • Veselá, Michaela;
    • Procházka, Pavel;
    • Klika, Tomáš;
    • Ambrož, David;
    • Dostálová, Gabriela;
    • Chocholová, Barbora;
    • Karetová, Debora;
    • Linhart, Aleš
    Publication type:
    Article
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    Detailed Phenotype of GLA Variants Identified by the Nationwide Neurological Screening of Stroke Patients in the Czech Republic.

    Published in:
    Journal of Clinical Medicine, 2021, v. 10, n. 16, p. 3543, doi. 10.3390/jcm10163543
    By:
    • Reková, Petra;
    • Dostálová, Gabriela;
    • Kemlink, David;
    • Paulasová Schwabová, Jaroslava;
    • Dubská, Zora;
    • Vaneckova, Manuela;
    • Mašek, Martin;
    • Kodet, Ondřej;
    • Poupětová, Helena;
    • Mazurová, Stella;
    • Rajdova, Aneta;
    • Vlckova, Eva;
    • Táboříková, Alena;
    • Fafejtová, Štěpánka;
    • Nevsimalova, Miroslava;
    • Linhart, Aleš;
    • Tomek, Aleš
    Publication type:
    Article
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    Safety and efficacy of pegunigalsidase alfa in patients with Fabry disease who were previously treated with agalsidase alfa: results from BRIDGE, a phase 3 open-label study.

    Published in:
    Orphanet Journal of Rare Diseases, 2023, v. 18, n. 1, p. 1, doi. 10.1186/s13023-023-02937-6
    By:
    • Linhart, Aleš;
    • Dostálová, Gabriela;
    • Nicholls, Kathy;
    • West, Michael L.;
    • Tøndel, Camilla;
    • Jovanovic, Ana;
    • Giraldo, Pilar;
    • Vujkovac, Bojan;
    • Geberhiwot, Tarekegn;
    • Brill-Almon, Einat;
    • Alon, Sari;
    • Chertkoff, Raul;
    • Rocco, Rossana;
    • Hughes, Derralynn
    Publication type:
    Article
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