@article{MTMT:34815635,
	title = {Exhaled and Systemic Biomarkers to Aid the Diagnosis of Bronchial Asthma in Elite Water Sports Athletes},
	url = {https://m2.mtmt.hu/api/publication/34815635},
	author = {Csoma, Balázs and Sydó, Nóra and Szűcs, Gergő and Seres, Éva and Erdélyi, Tamás and Horváth, Gábor and Csulak, Emese and Merkely, Béla Péter and Müller, Veronika},
	doi = {10.1249/MSS.0000000000003419},
	journal-iso = {MED SCI SPORT EXER},
	journal = {MEDICINE AND SCIENCE IN SPORTS AND EXERCISE},
	volume = {56},
	unique-id = {34815635},
	issn = {0195-9131},
	year = {2024},
	eissn = {1530-0315},
	pages = {1256-1264},
	orcid-numbers = {Csoma, Balázs/0000-0002-9425-1219; Szűcs, Gergő/0000-0002-3446-0406; Seres, Éva/0000-0001-8518-6729; Erdélyi, Tamás/0000-0002-5025-8769; Horváth, Gábor/0000-0003-4079-1698; Csulak, Emese/0000-0001-7683-8000; Merkely, Béla Péter/0000-0001-6514-0723; Müller, Veronika/0000-0002-1398-3187}
}

@article{MTMT:34441434,
	title = {Pneumocystis diagnosztizálása nem ismert HIV fertőzött betegnél - Esetismertetés},
	url = {https://m2.mtmt.hu/api/publication/34441434},
	author = {Szűcs, Gergő and Komáromi, Tamás and Matics, Zsombor Zoltán and Erdélyi, Tamás and Pápay, Judit and Kristóf, Katalin and Bohács, Anikó and Müller, Veronika},
	journal-iso = {MED THORAC (BP)},
	journal = {MEDICINA THORACALIS (BUDAPEST)},
	volume = {76},
	unique-id = {34441434},
	issn = {0238-2571},
	year = {2023},
	pages = {323-326},
	orcid-numbers = {Szűcs, Gergő/0000-0002-3446-0406; Komáromi, Tamás/0000-0002-8083-7243; Erdélyi, Tamás/0000-0002-5025-8769; Pápay, Judit/0000-0003-2642-2060; Kristóf, Katalin/0000-0002-5189-4636; Bohács, Anikó/0000-0002-8229-4254; Müller, Veronika/0000-0002-1398-3187}
}

@article{MTMT:34441154,
	title = {Circulating apelin, IL22RA2 and VEGF in pre-capillary pulmonary hypertension},
	url = {https://m2.mtmt.hu/api/publication/34441154},
	author = {Csósza, Györgyi and Szűcs, Gergő and Rozgonyi, Zsolt Dezső and Csoma, Balázs and Losonczy, György and Müller, Veronika and Karlócai, Kristóf and Lázár, Zsófia},
	doi = {10.1556/2060.2023.00264},
	journal-iso = {PHYSIOL INT},
	journal = {PHYSIOLOGY INTERNATIONAL},
	volume = {110},
	unique-id = {34441154},
	issn = {2498-602X},
	year = {2023},
	eissn = {2677-0164},
	pages = {356-370},
	orcid-numbers = {Csósza, Györgyi/0000-0002-5510-5868; Szűcs, Gergő/0000-0002-3446-0406; Rozgonyi, Zsolt Dezső/0000-0002-6395-7139; Csoma, Balázs/0000-0002-9425-1219; Losonczy, György/0000-0002-5340-360X; Müller, Veronika/0000-0002-1398-3187; Karlócai, Kristóf/0000-0003-2162-2039; Lázár, Zsófia/0000-0003-2444-9040}
}

@misc{MTMT:33925821,
	title = {Kétoldali, infiltratív tüdőbetegség esete COVID-19 infekció után},
	url = {https://m2.mtmt.hu/api/publication/33925821},
	author = {Horváth, Péter and Kiss, Judit and Jenei, Alex and Szűcs, Gergő and Lakatos, Gergely},
	unique-id = {33925821},
	year = {2023},
	orcid-numbers = {Szűcs, Gergő/0000-0002-3446-0406}
}

@misc{MTMT:33925652,
	title = {A BMI és a túlélési idő közötti összefüggés korai stádiumú NSCLC-ben},
	url = {https://m2.mtmt.hu/api/publication/33925652},
	author = {Szűcs, Gergő and Szentkereszty, Márton and Tóvári, István and Ladányi, Andrea and Gálffy, Gabriella and Losonczy, György},
	unique-id = {33925652},
	year = {2023},
	orcid-numbers = {Szűcs, Gergő/0000-0002-3446-0406; Szentkereszty, Márton/0000-0001-8891-8657; Ladányi, Andrea/0000-0001-9304-8473; Losonczy, György/0000-0002-5340-360X}
}

@{MTMT:33620477,
	title = {Mikrobiológiai, laboratóriumi citológiai és szövettani vizsgálatok},
	url = {https://m2.mtmt.hu/api/publication/33620477},
	author = {Tóth, Nóra Melinda and Szűcs, Gergő},
	booktitle = {Tüdőgyógyászat},
	unique-id = {33620477},
	year = {2022},
	pages = {89-96},
	orcid-numbers = {Tóth, Nóra Melinda/0000-0002-5665-4631; Szűcs, Gergő/0000-0002-3446-0406}
}

@article{MTMT:33168673,
	title = {Helminthiasis diagnosztizálása tüdőrákos beteg esetén},
	url = {https://m2.mtmt.hu/api/publication/33168673},
	author = {Szűcs, Gergő and Bohács, Anikó and Varga, János Tamás and Bogyó, Levente Zoltán and Müller, Veronika and Vincze, Krisztina},
	journal-iso = {MED THORAC (BP)},
	journal = {MEDICINA THORACALIS (BUDAPEST)},
	volume = {75},
	unique-id = {33168673},
	issn = {0238-2571},
	year = {2022},
	pages = {312-315},
	orcid-numbers = {Szűcs, Gergő/0000-0002-3446-0406; Bohács, Anikó/0000-0002-8229-4254; Varga, János Tamás/0000-0002-8552-1336; Bogyó, Levente Zoltán/0000-0003-1207-2258; Müller, Veronika/0000-0002-1398-3187; Vincze, Krisztina/0000-0002-3667-5371}
}

@article{MTMT:33032862,
	title = {Peripheral blood and bronchoalveolar leukocyte profile in lung transplant recipients and their changes according to immunosuppressive regimen: A single-center experience},
	url = {https://m2.mtmt.hu/api/publication/33032862},
	author = {Jáky-Kováts, Zsuzsanna Ágnes and Vámos, Melinda and Komlósi, Zsolt and Bikov, András and Madurka, Ildikó Eszter and Szűcs, Gergő and Müller, Veronika and Bohács, Anikó},
	doi = {10.1002/iid3.673},
	journal-iso = {IMMUN INFLAM DIS},
	journal = {IMMUNITY INFLAMMATION AND DISEASE},
	volume = {10},
	unique-id = {33032862},
	abstract = {Background: After lung transplantation (LuTX), lower respiratory tract infections (LRTI) and acute cellular rejection (ACR) are associated with changes in peripheral blood and bronchoalveolar lavage fluid mononuclear cell profile (PBMC and BALIC). PBMC is also influenced by immunosuppressive regimen and its changes with postoperative time. First-year PBMC and BALIC changes were evaluated in this study with rabbit anti-thymocyte globulin (ATG) and alemtuzumab (AL) induction therapy. Methods: In total, 64 LuTX recipients were included, 53 of them received AL and 11 ATG as induction therapy. PBMC and BALIC were examined routinely and in cases suspicious of infection and/or rejection. A PBMC- and BALIC-based algorithm for infection and rejection prediction was also tested. Results: In the AL group, peripheral blood lymphocyte and basophil cell numbers were significantly reduced, while the neutrophil cell number elevation during LRTI was significantly higher compared to the control. Early postoperative measurements showed a lower BALIC lymphocyte count. The algorithm had 17% sensitivity and 94% specificity for ACR in all patients and 33% sensitivity and 95% specificity for ACR with coexisting LRTI. Conclusion: BALIC is not significantly influenced by the immunosuppressive regimen. PBMC- and BALIC-based algorithm may improve the differential diagnosis of ACR.},
	keywords = {INDUCTION; Differential diagnosis; alemtuzumab; REJECTION; Bronchoalveolar lavage; Lung transplant; acute cellular rejection; WORKING FORMULATION},
	year = {2022},
	eissn = {2050-4527},
	orcid-numbers = {Jáky-Kováts, Zsuzsanna Ágnes/0000-0001-6145-6595; Vámos, Melinda/0000-0001-8653-7500; Komlósi, Zsolt/0000-0002-4149-1497; Bikov, András/0000-0002-8983-740X; Madurka, Ildikó Eszter/0000-0002-7083-0638; Szűcs, Gergő/0000-0002-3446-0406; Müller, Veronika/0000-0002-1398-3187; Bohács, Anikó/0000-0002-8229-4254}
}

@article{MTMT:32151365,
	title = {Cellular and molecular mechanisms of allergic asthma},
	url = {https://m2.mtmt.hu/api/publication/32151365},
	author = {Komlósi, Zsolt and van, de Veen W. and Kovács, N. and Szűcs, Gergő and Sokolowska, M. and O'Mahony, L. and Akdis, M. and Akdis, C.A.},
	doi = {10.1016/j.mam.2021.100995},
	journal-iso = {MOL ASPECTS MED},
	journal = {MOLECULAR ASPECTS OF MEDICINE},
	volume = {85},
	unique-id = {32151365},
	issn = {0098-2997},
	abstract = {Asthma is a chronic disease of the airways, which affects more than 350 million people worldwide. It is the most common chronic disease in children, affecting at least 30 million children and young adults in Europe. Asthma is a complex, partially heritable disease with a marked heterogeneity. Its development is influenced both by genetic and environmental factors. The most common, as well as the most well characterized subtype of asthma is allergic eosinophilic asthma, which is characterized by a type 2 airway inflammation. The prevalence of asthma has substantially increased in industrialized countries during the last 60 years. The mechanisms underpinning this phenomenon are incompletely understood, however increased exposure to various environmental pollutants probably plays a role. Disease inception is thought to be enabled by a disadvantageous shift in the balance between protective and harmful lifestyle and environmental factors, including exposure to protective commensal microbes versus infection with pathogens, collectively leading to airway epithelial cell damage and disrupted barrier integrity. Epithelial cell-derived cytokines are one of the main drivers of the type 2 immune response against innocuous allergens, ultimately leading to infiltration of lung tissue with type 2 T helper (TH2) cells, type 2 innate lymphoid cells (ILC2s), M2 macrophages and eosinophils. This review outlines the mechanisms responsible for the orchestration of type 2 inflammation and summarizes the novel findings, including but not limited to dysregulated epithelial barrier integrity, alarmin release and innate lymphoid cell stimulation. © 2021 The Authors},
	year = {2022},
	eissn = {1872-9452},
	orcid-numbers = {Komlósi, Zsolt/0000-0002-4149-1497; Szűcs, Gergő/0000-0002-3446-0406}
}

@article{MTMT:32245954,
	title = {Measurements of upper and lower airway nitric oxide in healthy adults},
	url = {https://m2.mtmt.hu/api/publication/32245954},
	author = {Csoma, Balázs and Beringer, Filippa and Szűcs, Gergő and Bikov, András and Müller, Veronika and Lázár, Zsófia},
	doi = {10.1088/1752-7163/ac2567},
	journal-iso = {J BREATH RES},
	journal = {JOURNAL OF BREATH RESEARCH},
	volume = {15},
	unique-id = {32245954},
	issn = {1752-7155},
	abstract = {Introduction. Nasal nitric oxide (NO) measurement can be a useful tool for monitoring upper airway diseases. However, there is a considerable lack of validation data. Aims. To evaluate the repeatability and intra-subject variations of nasal NO output (nV (NO)) in healthy adults and to study its correlation with lower airway NO parameters. Methods. nV (NO) was measured in healthy non-smokers at baseline (N = 31, age: 28 +/- 6 years), after 1 h (N = 15), 1 d (N = 15), 1 week (N = 17), and compared using the Bland-Altman method. At baseline, lower airway NO parameters (F (ENO), flux of NO in the conducting airways and alveolar NO concentration) were also measured and correlated to nV (NO) (Spearman correlation). Multivariate regression analysis was used to assess the factors influencing nV (NO). Results. Baseline median nV (NO) was 465 (interquartile range (IQR) = 404-536) nL min(-1). The mean differences between the baseline and repeated measurements were not significant (p > 0.05). The coefficient of repeatability (mean: 118, IQR = 88-181 nL min(-1)) and coefficient of variation (mean: 9.1%) were low. We found no correlation between nV (NO) and lower airway NO parameters (p > 0.05). Sex (beta = -0.52, p = 0.02) and body weight (beta = -0.65, p = 0.03) influenced nV (NO) (model: p = 0.04, R (2) = 0.31). Conclusion. nasal NO output has good repeatability in healthy adults. The NO productions of lower and upper airways are not related in health, but nasal NO output seems to be affected by sex and body weight.},
	keywords = {Adult; Biomarkers; nitric oxide; nasal mucosa; PRIMARY CILIARY DYSKINESIA; Chronic rhinosinusitis; Biochemical Research Methods; individual biological variation},
	year = {2021},
	eissn = {1752-7163},
	orcid-numbers = {Csoma, Balázs/0000-0002-9425-1219; Beringer, Filippa/0000-0003-4693-4012; Szűcs, Gergő/0000-0002-3446-0406; Bikov, András/0000-0002-8983-740X; Müller, Veronika/0000-0002-1398-3187; Lázár, Zsófia/0000-0003-2444-9040}
}