Výpis publikací

AYGOEREN-PUERSUEN, Emel, Andrea ZANICHELLI, Danny M COHN, Mauro CANCIAN, Roman HAKL, Tamar KINACIYAN, Markus MAGERL, Inmaculada MARTINEZ-SAGUER, Marcin STOBIECKI, Henriette FARKAS, Sorena KIANI-ALIKHAN, Vesna GRIVCHEVA-PANOVSKA, Jonathan A BERNSTEIN, H Henry LI, Hilary J LONGHURST, Paul K AUDHYA, Michael SMITH, Christopher M YEA, Andreas MAETZEL, Daniel K LEE, Edward P FEENER, Richard GOWER, William R LUMRY, Aleena BANERJI, Marc A RIEDL a Marcus MAURER. An investigational oral plasma kallikrein inhibitor for on-demand treatment of hereditary angioedema: atwo-part, randomised, double-blind, placebo-controlled, crossover phase 2 trial. Lancet. New York: Elsevier Science Inc., 2023, roč. 401, č. 10375, s. 458-469. ISSN 0140-6736. Dostupné z: https://dx.doi.org/10.1016/S0140-6736(22)02406-0.

BALLONOVÁ, Lucie, Přemysl SOUČEK, Peter SLANINA, Kamila RÉBLOVÁ, Ondřej ZAPLETAL, Marcela VLKOVÁ, Roman HAKL, Viktor BÍLY, Hana GROMBIŘÍKOVÁ, Eliška SVOBODOVÁ, Petra KULÍŠKOVÁ, Julie ŠTÍCHOVÁ, Marta SOBOTKOVÁ, Zachová RADANA, Jana HANZLÍKOVÁ, Martina VACHOVÁ, Pavlína KRÁLÍČKOVÁ, Irena KRČMOVÁ, Miloš JESEŇÁK a Tomáš FREIBERGER. Myeloid lineage cells evince distinct steady-state level of certain gene groups in dependence on hereditary angioedema severity. FRONTIERS IN GENETICS. LAUSANNE: FRONTIERS MEDIA SA, 2023, roč. 14, July 2023, s. 1-15. ISSN 1664-8021. Dostupné z: https://dx.doi.org/10.3389/fgene.2023.1123914.

BALLONOVÁ, Lucie, Petra KULÍŠKOVÁ, Peter SLANINA, Julie ŠTÍCHOVÁ, Marcela VLKOVÁ, Roman HAKL, Jiří LITZMAN, Přemysl SOUČEK a Tomáš FREIBERGER. PLAUR splicing pattern in hereditary angioedema patients' monocytes and macrophages. Molecular Biology Reports. DORDRECHT: Springer, 2023, roč. 50, č. 6, s. 4975-4982. ISSN 0301-4851. Dostupné z: https://dx.doi.org/10.1007/s11033-023-08391-8.

SLANINA, Peter, Julie ŠTÍCHOVÁ, Petra KULÍŠKOVÁ, Lucie BALLONOVÁ, Jan BAROŠ, Jiří LITZMAN, Marcela VLKOVÁ, Přemysl SOUČEK, Tomáš FREIBERGER a Roman HAKL. Porovnanie diferenciácie a aktivácie monocytov a sledovanie funkčných zmien mitochondrií monocytov prietokovou cytometriou pred analýzou expresie génu PLAUR. In 40. sjezd ČSAKI. 2023.

GROMBIŘÍKOVÁ, Hana, Viktor BÍLY, Přemysl SOUČEK, Michal KRAMÁREK, Roman HAKL, Lucie BALLONOVÁ, Barbora RAVCUKOVA, Dita RICNA, Karolína KOŽENÁ, Lucie KRATOCHVÍLOVÁ, Marta SOBOTKOVA, Radana ZACHOVA, Pavel KUKLÍNEK, Pavlina KRALICKOVA, Irena KRCMOVA, Jana HANZLIKOVA, Martina VACHOVA, Olga KRYSTUFKOVA, Eva DANKOVA, Milos JESENAK, Martina NOVACKOVA, Michal SVOBODA, Jiří LITZMAN a Tomáš FREIBERGER. Systematic Approach Revealed SERPING1 Splicing-Affecting Variants to be Highly Represented in the Czech National HAE Cohort. Journal of Clinical Immunology. NEW YORK: SPRINGER, 2023, roč. 43, č. 8, s. 1974-1991. ISSN 0271-9142. Dostupné z: https://dx.doi.org/10.1007/s10875-023-01565-w.

BALLONOVÁ, Lucie, Přemysl SOUČEK, Roman HAKL, Peter SLANINA, Marcela VLKOVÁ, Marta SOBOTKOVÁ, Pavlína KRÁLÍČKOVÁ, I. KRČMOVÁ, Jana HANZLÍKOVÁ, M. VACHOVÁ, Miloš JESENÁK, Hana GROMBIŘÍKOVÁ, Kamila RÉBLOVÁ, Viktor BÍLY, Ondřej ZAPLETAL a Tomáš FREIBERGER. Different patterns of immune system activation in hereditary angioedema based on disease severity. In 20th Biennial Meeting of the European Society for Immunodeficiencies. 2022.

SLANINA, Peter, Julie ŠTÍCHOVÁ, Petra KULÍŠKOVÁ, Lucie BALLONOVÁ, Jan BAROŠ, Jiří LITZMAN, Marcela VLKOVÁ, Přemysl SOUČEK, Tomáš FREIBERGER a Roman HAKL. OPTIMALIZÁCIA IN VITRO DIFERENCIÁCIE A AKTIVÁCIE MONOCYTOV PRED ANALÝZOU EXPRESIE GÉNU PLAUR. In XXXIX sjezd českých a slovenských alergologů a klinických imunologů. 2022.

SLANINA, Peter, Julie ŠTÍCHOVÁ, Petra KULÍŠKOVÁ, Lucie BALLONOVÁ, Jan BAROŠ, Jiří LITZMAN, Marcela VLKOVÁ, Přemysl SOUČEK, Tomáš FREIBERGER a Roman HAKL. OPTIMIZATION OF IN-VITRO DIFFERENTIATION AND ACTIVATION OF MONOCYTES BEFORE THE ANALYSIS OF PLAUR GENE EXPRESSION. In MESIA PRAGUE 2022. 2022.

HAKL, Roman, Pavel KUKLÍNEK, Marta SOBOTKOVA, Irena KRCMOVA, Pavlina KRALICKOVA, Martina VACHOVA, Jana HANZLIKOVA, Martina NOVACKOVA, Michal SVOBODA, Ingrid KOVÁČOVÁ a Jiří LITZMAN. Registry-based analysis of Icatibant and C1-inhibitor use in treatment of laryngeal attacks of hereditary angioedema. CLINICAL AND EXPERIMENTAL ALLERGY. HOBOKEN: WILEY, 2022, roč. 52, č. 8, s. 994-997. ISSN 0954-7894. Dostupné z: https://dx.doi.org/10.1111/cea.14182.

MILOTA, Tomas, Marta SOBOTKOVA, Jitka SMETANOVA, Marketa BLOOMFIELD, Jana VYDLAKOVA, Zita CHOVANCOVÁ, Jiří LITZMAN, Roman HAKL, Jiri NOVAK, Ivana MALKUSOVA, Jana HANZLIKOVA, Dalibor JILEK, Beata HUTYROVA, Vitezslav NOVAK, Irena KRCMOVA, Anna SEDIVA a Pavlina KRALICKOVA. Risk Factors for Severe COVID-19 and Hospital Admission in Patients With Inborn Errors of Immunity-Results From a Multicenter Nationwide Study. Frontiers in Immunology. Laussane: Frontiers, 2022, roč. 13, February 2022, s. 1-8. ISSN 1664-3224. Dostupné z: https://dx.doi.org/10.3389/fimmu.2022.835770.

GROMBIŘÍKOVÁ, Hana, Barbora RAVČUKOVÁ, Lucie GRODECKÁ, Pavla HUJOVÁ, Roman HAKL, Pavel KUKLÍNEK, Radana ZACHOVÁ, M. SOBOTKOVÁ, Pavlína KRÁLÍČKOVÁ, Olga KRYŠTŮVKOVÁ, Anna ŠEDIVÁ, Jiří LITZMAN a Tomáš FREIBERGER. A spectrum of SERPING1 mutations and clinical characterisation of Czech Hereditary Angioedema patients. In 12th C1-inhibitor deficiency and angioedema workshop 2021. 2021.

SOBOTKOVA, Marta, Radana ZACHOVA, Roman HAKL, Pavel KUKLÍNEK, Pavlina KRALICKOVA, Irena KRCMOVA, Jana HANZLIKOVA, Martina VACHOVA a Jirina BARTUNKOVA. Acquired Angioedema with C1 Inhibitor Deficiency: Occurrence, Clinical Features, and Management: A Nationwide Retrospective Study in the Czech Republic Patients. International archives of allergy and immunology. Basel: Karger, 2021, roč. 182, č. 7, s. 642-649. ISSN 1018-2438. Dostupné z: https://dx.doi.org/10.1159/000512933.

BALLONOVÁ, Lucie, Přemysl SOUČEK, Peter SLANINA, Roman HAKL, Marcela VLKOVÁ a Tomáš FREIBERGER. Alternative splicing of PLAUR gene in macrophage differentiation stages of hereditary angioedema patients. In 4th International Caparica Conference in Splicing. 2021.

ZURAW, B., W. R. LUMRY, D. T. JOHNSTON, E. AYGOREN-PURSUN, A. BANERJI, J. A. BERNSTEIN, S. C. CHRISTIANSEN, J. S. JACOBS, K. V. SITZ, R. G. GOWER, R. GAGNON, H. J. WEDNER, T. KINACIYAN, Roman HAKL, Jana HANZLIKOVA, J. T. ANDERSON, D. L. MCNEIL, S. B. FRITZ, W. H. YANG, R. TACHDJIAN, P. J. BUSSE, T. J. CRAIG, H. H. LI, H. FARKAS, J. M. BEST, D. CLEMONS, M. CORNPROPST, S. M. DOBO, H. A. IOCCA, D. KARGL, E. NAGY, S. C. MURRAY, P. COLLIS, W. P. SHERIDAN, M. MAURER a M. A. RIEDL. Oral once-daily berotralstat for the prevention of hereditary angioedema attacks: A randomized, double-blind, placebo-controlled phase 3 trial. Journal of allergy and clinical immunology. New York: Mosby-Elsevier, 2021, roč. 148, č. 1, s. "164"-"172.e9", 18 s. ISSN 0091-6749. Dostupné z: https://dx.doi.org/10.1016/j.jaci.2020.10.015.

VALERIEVA, A., M. T. STAEVSKA, V. GRIVCHEVA-PANOVSKA, M. JESENAK, K. V. KOHALMI, K. HRUBISKOVA, A. ZANICHELLI, L. BELLIZZI, A. RELAN, Roman HAKL a H. FARKAS. Recombinant human C1 esterase inhibitor for hereditary angioedema attacks: A European registry. WORLD ALLERGY ORGANIZATION JOURNAL. AMSTERDAM: ELSEVIER, 2021, roč. 14, č. 4, s. 1-8. ISSN 1939-4551. Dostupné z: https://dx.doi.org/10.1016/j.waojou.2021.100535.

HUJOVÁ, Pavla, Přemysl SOUČEK, Lucie GRODECKÁ, Hana GROMBIŘÍKOVÁ, Barbora RAVČUKOVÁ, Pavel KUKLÍNEK, Roman HAKL, Jiří LITZMAN a Tomáš FREIBERGER. Deep Intronic Mutation in SERPING1 Caused Hereditary Angioedema Through Pseudoexon Activation. Journal of Clinical Immunology. New York: Springer, 2020, roč. 40, č. 3, s. 435-446. ISSN 0271-9142. Dostupné z: https://dx.doi.org/10.1007/s10875-020-00753-2.

VALERIEVA, Anna, Maria STAEVSKA, Milos JESENAK, Katarina HRUBISKOVA, Marta SOBOTKOVA, Radana ZACHOVA, Roman HAKL, Sladjana ANDREJEVIC, Tobias SUITER, Vesna GRIVCHEVA-PANOVSKA, Ljerka KARADZA-LAPIC, Daniel SOTERES, Ralph SHAPIRO, Jeffrey RUMBYRT, Raffi TACHDJIAN, Vinay MEHTA, F. Ida HSU a Andrea ZANICHELLI. Recombinant human C1 esterase inhibitor as short-term prophylaxis in patients with hereditary angioedema. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY-IN PRACTICE. AMSTERDAM: ELSEVIER, 2020, roč. 8, č. 2, s. 799-802. ISSN 2213-2198. Dostupné z: https://dx.doi.org/10.1016/j.jaip.2019.08.011.

BALLONOVÁ, Lucie, Přemysl SOUČEK, Peter SLANINA, Roman HAKL, Marcela VLKOVÁ a Tomáš FREIBERGER. The splicing pattern of PLAUR gene changes during monocyte differentiation in patients with hereditary angioedema. In EMBO | EMBL Symposium: The Complex Life of RNA. 2020.

GRYMOVÁ, Tereza, Marcela VLKOVÁ, Přemysl SOUČEK, Roman HAKL, Jana NECHVÁTALOVÁ, Peter SLANINA, Julie ŠTÍCHOVÁ, Jiří LITZMAN a Tomáš FREIBERGER. Neutrophils Are Dysregulated in Patients with Hereditary Angioedema Types I and II in a Symptom-Free Period. Mediators of Inflammation. New York: Hindawi Publishing Corporation, 2019, roč. 2019, č. 9515628, s. 1-12. ISSN 0962-9351. Dostupné z: https://dx.doi.org/10.1155/2019/9515628.

MOLDOVAN, Dumitru, Jonathan A. BERNSTEIN, Roman HAKL, Grzegorz POREBSKI, Kimberly POARCH, William R. LUMRY a Anurag RELAN. Safety of recombinant human C1 esterase inhibitor for hereditary angioedema attacks during pregnancy. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY-IN PRACTICE. AMSTERDAM: ELSEVIER, 2019, roč. 7, č. 8, s. 2938-2940. ISSN 2213-2198. Dostupné z: https://dx.doi.org/10.1016/j.jaip.2019.05.042.

HUJOVÁ, Pavla, Lucie GRODECKÁ, Přemysl SOUČEK, Hana GROMBIŘÍKOVÁ, Barbora RAVČUKOVÁ, Pavel KUKLÍNEK, Roman HAKL a Tomáš FREIBERGER. A new deep intronic mutation caused aberrant splicing in a family diagnosed with hereditary angioedema. In RNA and Diseases conference, Uppsala, Švédsko. 2018.

HAKL, Roman, Pavel KUKLÍNEK a Jiří LITZMAN. Hereditární angioedém laryngealní ataky: data z Národního registru primárních imunodeficiencí. In ČSAKI. 2018.

HAKL, Roman. Perioperative management of Hereditary Angioedema. In CEE HAE Expert meeting. 2018.

HAKL, Roman, Pavel KUKLÍNEK, Irena KRČMOVÁ, Pavlína KRÁLÍČKOVÁ, Tomáš FREIBERGER, Petr JANKŮ, Marcela VLKOVÁ a Jiří LITZMAN. Treatment of Hereditary Angioedema Attacks with Icatibant and Recombinant C1 Inhibitor During Pregnancy. Journal of Clinical Immunology. New York: Springer, 2018, roč. 38, č. 7, s. 810-815. ISSN 0271-9142. Dostupné z: https://dx.doi.org/10.1007/s10875-018-0553-4.

FREIBERGER, Tomáš, Barbora RAVČUKOVÁ, Hana GROMBIŘÍKOVÁ, Lucie GRODECKÁ, Pavla HUJOVÁ, Roman HAKL, Pavel KUKLÍNEK, R ZACHOVA, M SOBOTKOVA, P KRALICKOVA, O KRYSTUFKOVA, A SEDIVA a Jiří LITZMAN. Clinical and molecular characterisation of czech hereditary angioedema patients. In Meeting of the European Society for Immunodeficiencies, Edinburgh. 2017.

HUJOVÁ, Pavla, Hana GROMBIŘÍKOVÁ, Přemysl SOUČEK, Lucie GRODECKÁ, Barbora RAVČUKOVÁ, Pavel KUKLÍNEK, Roman HAKL a Tomáš FREIBERGER. New deep intronic mutation c.1029+384 A>G in SERPING1 gene creates de novo donor splice site and causes aberrant splicing. In ESHG, Dánsko. 2017.

HAKL, Roman, P. KUKLÍNEK, P. KADLECOVÁ a Jiří LITZMAN. Hereditary angio-oedema with C1 inhibitor deficiency: Characteristics and diagnostic delay of Czech patients from one centre. Allergologia et immunopathologia. Barcelona: Elsevier Doyma SL, 2016, roč. 44, č. 3, s. 241-245. ISSN 0301-0546. Dostupné z: https://dx.doi.org/10.1016/j.aller.2015.09.003.

HAKL, Roman. Současné možnosti léčby hereditárního angioedému. Vnitřní lékařství. Praha: Česká lékařská společnost J. E. Purkyně, 2016, roč. 62, č. 9, s. 736-739. ISSN 0042-773X.

BŘEZINOVÁ, Eva, Miroslav NEČAS, Roman HAKL, Vojtěch THON, Tomáš FREIBERGER, Barbora RAVČUKOVÁ a Vladimír VAŠKŮ. A novel STAT3 gene mutation revealed in a patient with hyper IgE syndrome and severe eczema. In 24th EADV Congress, 7.-11.10.2015, Copenhagen, Denmark. 2015.

HLAVÁČKOVÁ, Eva, Olga TICHÁ, Roman HAKL a Jiří LITZMAN. Activation of granulocytes in common variable immunodeficiency and hereditary angioedema. In Allergy. 2015. ISSN 0105-4538.