@article{MTMT:34725548,
	title = {A perindopril alapú kettős és hármas fix kombinációk napi többszöri alkalmazása},
	url = {https://m2.mtmt.hu/api/publication/34725548},
	author = {Légrády, Péter},
	journal-iso = {METABOLIZMUS},
	journal = {METABOLIZMUS},
	volume = {21},
	unique-id = {34725548},
	issn = {1589-7311},
	year = {2023},
	pages = {138-140}
}

@article{MTMT:34725540,
	title = {A perindropil alapú kettős és hármas fix kombinációk napi többszöri alkalmazása},
	url = {https://m2.mtmt.hu/api/publication/34725540},
	author = {Légrády, Péter},
	journal-iso = {HÁZIORVOS TOVÁBBKÉPZŐ SZEMLE},
	journal = {HÁZIORVOS TOVÁBBKÉPZŐ SZEMLE},
	volume = {28},
	unique-id = {34725540},
	issn = {1219-8641},
	year = {2023},
	pages = {254-257}
}

@article{MTMT:34560639,
	title = {SGLT2-GÁTLÓ DAPAGLIFLOZIN EREDMÉNYES ALKALMAZÁSA NEPHROSIS SZINDRÓMÁVAL JÁRÓ, SZÖVETTANILAG IGAZOLT DIABETESES VESEBETEGSÉGBEN},
	url = {https://m2.mtmt.hu/api/publication/34560639},
	author = {Fejes, Imola and Bajcsi, Dóra and Czakó, László and Turkevi-Nagy, Sándor and Iványi, Béla and Ábrahám, György and Várkonyi, Tamás and Lengyel, Csaba Attila and Légrády, Péter},
	journal-iso = {MBA},
	journal = {MAGYAR BELORVOSI ARCHIVUM},
	volume = {76},
	unique-id = {34560639},
	issn = {0133-5464},
	year = {2023},
	pages = {306-306},
	orcid-numbers = {Czakó, László/0000-0002-6331-0802; Ábrahám, György/0000-0002-2272-2317; Várkonyi, Tamás/0000-0001-6833-3563; Lengyel, Csaba Attila/0000-0002-0434-0067}
}

@article{MTMT:34476417,
	title = {Komplex terápiás védelem SGLT-2-gátlókkal -- fókuszban a vese},
	url = {https://m2.mtmt.hu/api/publication/34476417},
	author = {Légrády, Péter},
	doi = {10.33668/hn.27.033},
	journal-iso = {HYPERTONIA NEPHROLOGIA},
	journal = {HYPERTONIA ÉS NEPHROLOGIA},
	volume = {27},
	unique-id = {34476417},
	issn = {1418-477X},
	year = {2023},
	eissn = {2498-6259},
	pages = {282-287}
}

@article{MTMT:34441379,
	title = {Phenotype–Genotype Correlations in Three Different Cases of Adult-Onset Genetic Focal Segmental Glomerulosclerosis},
	url = {https://m2.mtmt.hu/api/publication/34441379},
	author = {Kalmár, Tibor and Turkevi-Nagy, Sándor and Bitó, László and Kaizer, László and Maróti, Zoltán and Jakab, Dániel and Letoha, Annamária and Légrády, Péter and Iványi, Béla},
	doi = {10.3390/ijms242417489},
	journal-iso = {INT J MOL SCI},
	journal = {INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES},
	volume = {24},
	unique-id = {34441379},
	issn = {1661-6596},
	abstract = {This study highlights the importance of a combined diagnostic approach in the diagnosis of rare diseases, such as adult-onset genetic FSGS. We present three adult patient cases evaluated with kidney biopsy for proteinuria, chronic kidney disease, and hypertension, which were suggestive of adult-onset genetic FSGS. Renal biopsy samples and formalin-fixed, paraffin-embedded fetal kidneys were evaluated using standard light microscopical stainings, direct immunofluorescence on cryostat sections, and electron microscopy. Clinical exome sequencing was performed for each case, and 45 FSGS-related genes were analyzed. Identifying mutations in the PAX2, ACTN4, and COL4A5 genes have prompted a re-evaluation of the previous histopathological examinations. The PAX2 mutation led to a thinner nephrogenic zone and decreased number of glomeruli, resulting in oligohydramnios during fetal development and oligomeganephronia and adaptive focal-segmental glomerulosclerosis in adulthood. The ACTN4 mutation caused distinct electron-dense aggregates in podocyte cell bodies, while the COL4A5 mutation led to segmental sclerosis of glomeruli with marked interstitial fibrosis and tubular atrophy. The identification of specific mutations and their histopathological consequences can lead to a better understanding of the disease and its progression, as well as potential treatment options.},
	year = {2023},
	eissn = {1422-0067},
	orcid-numbers = {Kalmár, Tibor/0000-0002-0419-2009; Maróti, Zoltán/0000-0002-0515-117X}
}

@article{MTMT:34435133,
	title = {COMPARISON OF FIRST RESULTS OF RADIOFREQUENCY RENAL DENERVATIONS WITH FIRST AND SECOND GENERATION TECHNIQUES},
	url = {https://m2.mtmt.hu/api/publication/34435133},
	author = {Légrády, Péter and Fejes, Imola and Schulcz, Domonkos and Nagy, Ferenc Tamás and Ungi, Imre and Ruzsa, Zoltán and Ábrahám, György},
	journal-iso = {J HYPERTENSION},
	journal = {JOURNAL OF HYPERTENSION},
	volume = {41},
	unique-id = {34435133},
	issn = {0263-6352},
	year = {2023},
	eissn = {1473-5598},
	pages = {E255},
	orcid-numbers = {Ungi, Imre/0000-0002-2011-0069; Ruzsa, Zoltán/0000-0002-2474-5723; Ábrahám, György/0000-0002-2272-2317}
}

@article{MTMT:34224666,
	title = {Clinical and pathological characteristics of primary focal segmental glomerulosclerosis in adults: A single-center retrospective study},
	url = {https://m2.mtmt.hu/api/publication/34224666},
	author = {Manafzadeh, Amir Reza and Fejes, Imola and Bitó, László and Bajcsi, Dóra and Letoha, Annamária and Turkevi-Nagy, Sándor and Kemény, Éva and Ábrahám, György and Iványi, béla and Légrády, Péter},
	journal-iso = {HYPERTONIA NEPHROLOGIA},
	journal = {HYPERTONIA ÉS NEPHROLOGIA},
	volume = {27},
	unique-id = {34224666},
	issn = {1418-477X},
	year = {2023},
	eissn = {2498-6259},
	pages = {33-33},
	orcid-numbers = {Ábrahám, György/0000-0002-2272-2317}
}

@article{MTMT:34224661,
	title = {Minimális elváltozású nefropátia felnőttkorban},
	url = {https://m2.mtmt.hu/api/publication/34224661},
	author = {Légrády, Péter and Vantara, Henrietta and Fejes, Imola and Bajcsi, Dóra and Bitó, László and Letoha, Annamária and Kemény, Éva and Turkevi-Nagy, Sándor and Iványi, Béla and Ábrahám, György},
	journal-iso = {HYPERTONIA NEPHROLOGIA},
	journal = {HYPERTONIA ÉS NEPHROLOGIA},
	volume = {27},
	unique-id = {34224661},
	issn = {1418-477X},
	year = {2023},
	eissn = {2498-6259},
	pages = {33-33},
	orcid-numbers = {Ábrahám, György/0000-0002-2272-2317}
}

@article{MTMT:34224658,
	title = {SGLT2-gátló dapagliflozin eredményes alkalmazása nefrózis szindrómával járó, szövettanilag igazolt diabéteszes vesebetegségben},
	url = {https://m2.mtmt.hu/api/publication/34224658},
	author = {Fejes, Imola and Bajcsi, Dóra and Czakó, László and Turkevi-Nagy, Sándor and Iványi, Béla and Várkonyi, Tamás and Lengyel, Csaba Attila and Ábrahám, György and Légrády, Péter},
	journal-iso = {HYPERTONIA NEPHROLOGIA},
	journal = {HYPERTONIA ÉS NEPHROLOGIA},
	volume = {27},
	unique-id = {34224658},
	issn = {1418-477X},
	year = {2023},
	eissn = {2498-6259},
	pages = {27-28},
	orcid-numbers = {Czakó, László/0000-0002-6331-0802; Várkonyi, Tamás/0000-0001-6833-3563; Lengyel, Csaba Attila/0000-0002-0434-0067; Ábrahám, György/0000-0002-2272-2317}
}

@misc{MTMT:34118786,
	title = {Diagnostic approach to genetic diseases of the nephron},
	url = {https://m2.mtmt.hu/api/publication/34118786},
	author = {Turkevi-Nagy, Sándor and Kalmár, Tibor and Jakab, Dániel and Bitó, László and Légrády, Péter and Bereczki, Csaba and Iványi, Béla},
	unique-id = {34118786},
	year = {2023},
	orcid-numbers = {Kalmár, Tibor/0000-0002-0419-2009; Bereczki, Csaba/0000-0003-0091-3558}
}