Canlyniadau Chwilio - Markéta Pavlı́ková

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  1. 1
    Metabolic Syndrome, Alcohol Consumption and Genetic Factors Are Associated with Serum Uric Acid Concentration

    Metabolic Syndrome, Alcohol Consumption and Genetic Factors Are Associated with Serum Uric Acid Concentration gan Blanka Stibůrková, Markéta Pavlı́ková, Jitka Sokolová, Viktor Kožich

    Cyhoeddwyd 2014
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    Artigo
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  2. 2
    Circulating microRNA alternations in primary hyperuricemia and gout

    Circulating microRNA alternations in primary hyperuricemia and gout gan Jana Bohatá, Veronika Horváthová, Markéta Pavlı́ková, Blanka Stibůrková

    Cyhoeddwyd 2021
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    Artigo
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  3. 3
    The impact of dysfunctional variants of ABCG2 on hyperuricemia and gout in pediatric-onset patients

    The impact of dysfunctional variants of ABCG2 on hyperuricemia and gout in pediatric-onset patients gan Blanka Stibůrková, Kateřina Pavelcová, Markéta Pavlı́ková, Pavel Ješina, Karel Pavelká

    Cyhoeddwyd 2019
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    Artigo
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  4. 4
    Evaluation of the Influence of Genetic Variants of SLC2A9 (GLUT9) and SLC22A12 (URAT1) on the Development of Hyperuricemia and Gout

    Evaluation of the Influence of Genetic Variants of SLC2A9 (GLUT9) and SLC22A12 (URAT1) on the Development of Hyperuricemia and Gout gan Kateřina Pavelcová, Jana Bohatá, Markéta Pavlı́ková, Eliška Bubeníková, Karel Pavelká, Blanka Stibůrková

    Cyhoeddwyd 2020
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    Artigo
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  5. 5
    A comprehensive validation study of the latest version of BoneXpert on a large cohort of Caucasian children and adolescents

    A comprehensive validation study of the latest version of BoneXpert on a large cohort of Caucasian children and adolescents gan Klára Maratová, D Zemková, Petr Sedlák, Markéta Pavlı́ková, Shenali Anne Amaratunga, H Krásnicanová, Ondřej Souček, Zdenĕk Šumnı́k

    Cyhoeddwyd 2023
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    Artigo
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  6. 6
    Functional non-synonymous variants of ABCG2 and gout risk

    Functional non-synonymous variants of ABCG2 and gout risk gan Blanka Stibůrková, Kateřina Pavelcová, Jakub Závada, Lenka Petrů, Pavel Šimek, Pavel Čepek, Markéta Pavlı́ková, Hirotaka Matsuo, Tony R. Merriman, Karel Pavelká

    Cyhoeddwyd 2017
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    Artigo
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  7. 7
    Alterations in lipidome profiles distinguish early-onset hyperuricemia, gout, and the effect of urate-lowering treatment

    Alterations in lipidome profiles distinguish early-onset hyperuricemia, gout, and the effect of urate-lowering treatment gan Aleš Kvasnička, David Friedecký, Radana Brumarová, Markéta Pavlı́ková, Kateřina Pavelcová, Jana Mašínová, Lenka Hasíková, Jakub Závada, Karel Pavelká, Pavel Ješina, Blanka Stibůrková

    Cyhoeddwyd 2023
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    Artigo
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  8. 8
    Functional Characterization of Clinically-Relevant Rare Variants in ABCG2 Identified in a Gout and Hyperuricemia Cohort

    Functional Characterization of Clinically-Relevant Rare Variants in ABCG2 Identified in a Gout and Hyperuricemia Cohort gan Yu Toyoda, Andrea Mančíková, Vladimír Krylov, Keito Morimoto, Kateřina Pavelcová, Jana Bohatá, Karel Pavelká, Markéta Pavlı́ková, Hiroshi Suzuki, Hirotaka Matsuo, Tappei Takada, Blanka Stibůrková

    Cyhoeddwyd 2019
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    Artigo
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  9. 9
    Cystathionine β‐Synthase Deficiency in the E‐<scp>HOD</scp> Registry—Part <scp>II</scp>: Dietary and Pharmacological Treatment

    Cystathionine β‐Synthase Deficiency in the E‐<scp>HOD</scp> Registry—Part <scp>II</scp>: Dietary and Pharmacological Treatment gan Andrew A. M. Morris, Jitka Sokolová, Markéta Pavlı́ková, Florian Gleich, Stefan Kölker, Carlo Dionisi‐Vici, Matthias R. Baumgartner, Luciana Hannibal, Henk J. Blom, Martina Huemer, Viktor Kožich

    Cyhoeddwyd 2025
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    Artigo
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  10. 10
    Are all HCL systems the same? long term outcomes of three HCL systems in children with type 1 diabetes: real-life registry-based study

    Are all HCL systems the same? long term outcomes of three HCL systems in children with type 1 diabetes: real-life registry-based study gan Alzbeta Šantová, Lukáš Plachý, Vít Neuman, Markéta Pavlı́ková, Lenka Petruželková, Petra Konečná, Petra Venháčová, Jaroslav Škvor, Renata Pomahačová, David L. Neumann, Jan Vosáhlo, Jiří Strnadel, Kamila Kocourková, Barbora Obermannová, Štěpánka Průhová, Ondřej Cinek, Zdenĕk Šumnı́k

    Cyhoeddwyd 2023
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    Artigo
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  11. 11
    Guidelines for the diagnosis and management of cystathionine beta‐synthase deficiency

    Guidelines for the diagnosis and management of cystathionine beta‐synthase deficiency gan Andrew A. M. Morris, Viktor Kožich, Saikat Santra, Generoso Andria, Tawfeg Ben‐Omran, Anupam Chakrapani, Ellen Crushell, Mick Henderson, Michel Hochuli, Martina Huemer, Miriam C Janssen, F. Maillot, Philip Mayne, Jenny McNulty, Tara M. Morrison, Hélène Ogier, Siobhán O’Sullivan, Markéta Pavlı́ková, Isabel Tavares de Almeida, Allyson Terry, Sufin Yap, Henk J. Blom, Kimberly A. Chapman

    Cyhoeddwyd 2016
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    Revisão
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  12. 12
    Newborn screening for homocystinurias: Recent recommendations versus current practice

    Newborn screening for homocystinurias: Recent recommendations versus current practice gan Rebecca Keller, Petr Chrastina, Markéta Pavlı́ková, Sofía Gouveia, Antònia Ribes, Stefan Kölker, Henk J. Blom, Matthias R. Baumgartner, Josef Bártl, Carlo Dionisi‐Vici, Florian Gleich, Andrew A. M. Morris, Viktor Kožich, Martina Huemer, Ivo Barić, Tawfeq Ben‐Omran, Javier Blasco‐Alonso, María Andrea Delgado, Claudia Carducci, Michela Cassanello, R. Cerone, María L. Couce, Ellen Crushell, Carmen Delgado Pecellín, Elena Dulín, Mercedes Espada, Giulio Ferino, Ralph Fingerhut, I. García Jiménez, Immaculada Gonzalez Gallego, Yolanda González, Gwendolyn Gramer, María Jesús Juan Fita, Eszter Karg, Jeanette Klein, Vassiliki Konstantopoulou, Giancarlo la Marca, Elisa Leão Teles, Vincenzo Leuzzi, Franco Lilliu, Rosa María López, Allan M. Lund, Philip Mayne, Silvia Meavilla, Stuart J. Moat, Jürgen G. Okun, Elisabeta Pasquini, Consuelo Pedrón‐Giner, Gábor Rácz, María Ángeles Ruiz Gómez, Laura Vilarinho, Raquel Yahyaoui, Moja Zerjav Tansek, Rolf Zetterström, Maximilian Zeyda

    Cyhoeddwyd 2019
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    Artigo
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