Zobrazeno 1 - 10
of 345
pro vyhledávání: '"P. Domsik"'
Autor:
Attila Nemes, Árpád Kormányos, Péter Domsik, Anita Kalapos, Nándor Gyenes, Lajos Kemény, Győző Szolnoky
Publikováno v:
Advances in Dermatology and Allergology, Vol 39, Iss 3, Pp 580-586 (2022)
Externí odkaz:
https://doaj.org/article/8778e40ffd4f4fc38bf900fe66fca0d2
Autor:
Attila Nemes, Árpád Kormányos, Péter Domsik, Anita Kalapos, Csaba Lengyel, Nóra Ambrus, Zsuzsanna Valkusz
Publikováno v:
Revista Portuguesa de Cardiologia, Vol 40, Iss 4, Pp 253-258 (2021)
Introduction and Objective: Acromegaly is a rare, chronic and slowly developing endocrine disorder caused by hypersecretion of human growth hormone and consequently of insulin-like growth factor-1 during adulthood. The present study was conducted to
Externí odkaz:
https://doaj.org/article/0436e03cb75145c0a08f3c09f725318d
Autor:
Árpád Kormányos, Péter Domsik, Anita Kalapos, Nándor Gyenes, Zsuzsanna Valkusz, Csaba Lengyel, Tamás Forster, Attila Nemes
Publikováno v:
Revista Portuguesa de Cardiologia, Vol 39, Iss 4, Pp 189-196 (2020)
Introduction: Acromegaly is a relatively rare chronic hormonal disease resulting in disfigurement. In 90% of cases, acromegaly is caused by a benign pituitary monoclonal human growth hormone-secreting tumor. The aim of the present study was to determ
Externí odkaz:
https://doaj.org/article/a27488e52332419a8dc904f3869ae08c
Autor:
Attila Nemes, Árpád Kormányos, Péter Domsik, Isabel Forner-Cordero, Lajos Kemény, Győző Szolnoky
Publikováno v:
Revista Colombiana de Cardiología, Vol 26, Iss 4, Pp 218-221 (2019)
Resumen: El lipedema es un trastorno crónico que se caracteriza por una hiperplasia del tejido adiposo subcutáneo simétrico, deformante, asociado a hematomas y dolor, que afecta fundamentalmente a mujeres tras la pubertad, que suele ser familiar y
Externí odkaz:
https://doaj.org/article/cb011ca78b8e4d4ba8d8592dc65dc7de
Autor:
Dóra Földeák, Árpád Kormányos, Péter Domsik, Anita Kalapos, Györgyike Á. Piros, Nóra Ambrus, Zénó Ajtay, Róbert Sepp, Zita Borbényi, Tamás Forster, Attila Nemes
Publikováno v:
Revista Portuguesa de Cardiologia, Vol 36, Iss 12, Pp 905-913 (2017)
Introduction: While cardiac amyloidosis (CA) is a rare systemic disease characterized by extracellular deposition of protein-derived fibrils, hypertrophic cardiomyopathy (HCM) is histopathologically characterized by myocyte hypertrophy and disarray,
Externí odkaz:
https://doaj.org/article/4ade6f260fd54e0eb8b9dbe37ec9aa61
Autor:
Attila Nemes, Péter Domsik, Anita Kalapos, Henriette Gavallér, Mónika Oszlánczi, Tamás Forster
Publikováno v:
Revista Portuguesa de Cardiologia, Vol 35, Iss 10, Pp 515-521 (2016)
Objective: Isolated left ventricular noncompaction (ILVNC) is a rare cardiomyopathy characterized by a prominent trabecular meshwork and deep intertrabecular recesses. The present study aimed to examine right atrial (RA) volumes, volume-based functio
Externí odkaz:
https://doaj.org/article/818af533ec33440fa3611ff33cd900fb
Autor:
Attila Nemes, Imelda Marton, Péter Domsik, Anita Kalapos, Éva Pósfai, Szabolcs Modok, Zita Borbényi, Tamás Forster
Publikováno v:
Revista Portuguesa de Cardiologia, Vol 35, Iss 5, Pp 277-283 (2016)
Introduction: The present study was designed to compare three-dimensional speckle tracking echocardiography (3DSTE)-derived left atrial (LA) volumetric, volume-based functional and strain parameters between patients with hypereosinophilic syndrome (H
Externí odkaz:
https://doaj.org/article/2203bbc2ff574bcd8861424e492ffdd7
Autor:
Györgyike Ágnes Piros, Péter Domsik, Anita Kalapos, Csaba Lengyel, Andrea Orosz, Tamás Forster, Attila Nemes
Publikováno v:
Revista Portuguesa de Cardiologia, Vol 35, Iss 2, Pp 83-91 (2016)
Introduction and Objective: Three-dimensional (3D) speckle tracking echocardiography (3DSTE) is a novel method for assessment of left atrial (LA) volumes and function without geometrical assumptions. 3DSTE allows detailed assessment of LA features in
Externí odkaz:
https://doaj.org/article/6907d50aacb3425ba3fed7b8232add59
Publikováno v:
Hellenic Journal of Cardiology, Vol 57, Iss 1, Pp 23-29 (2016)
Noncompaction cardiomyopathy (NCCM) is a rare congenital cardiomyopathy characterised by a distinctive 2-layered appearance of the myocardium due to hypertrabecularisation and deep intertrabecular recesses. The present study was designed to assess le
Externí odkaz:
https://doaj.org/article/529ba7fbd69441359cce6cdf50d91f61
Publikováno v:
Türk Kardiyoloji Derneği Arşivi, Vol 43, Iss 7, Pp 655-658 (2015)
Three-dimensional speckle-tracking echocardiography (3DSTE) is accepted as a reliable and feasible method in the quantification of left ventricular (LV) volumes, strains and rotational characteristics. This case aimed to demonstrate the diagnostic im
Externí odkaz:
https://doaj.org/article/04aa8cbc34ca47139ca5d2b77af7933f