Zobrazeno 1 - 10
of 144
pro vyhledávání: '"Anita Kalapos"'
Publikováno v:
ESC Heart Failure, Vol 8, Iss 5, Pp 4328-4333 (2021)
Abstract Aims Lower body half compression of bilateral secondary leg lymphoedema (LE) without relevant cardiac insufficiency gives rise to whether external leg compression may influence left ventricular (LV) function. Patients with LE were subjected
Externí odkaz:
https://doaj.org/article/48bba35aabd644a5a7ddfeb0455b975d
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:
Gloria Kafui Esi Zodanu, Mónika Oszlánczi, Kálmán Havasi, Anita Kalapos, Gergely Rácz, Márta Katona, Anikó Ujfalusi, Orsolya Nagy, Márta Széll, Dóra Nagy
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
Congenital heart defects (CHD) are the most common developmental abnormalities, affecting approximately 0.9% of livebirths. Genetic factors, including copy number variations (CNVs), play an important role in their development. The most common CNVs ar
Externí odkaz:
https://doaj.org/article/4f1e7a1d50c74cb0a782585c82c728d2
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
Autor:
Attila Nemes, Dóra Földeák, Péter Domsik, Anita Kalapos, Árpád Kormányos, Zita Borbényi, Tamás Forster
Publikováno v:
Arquivos Brasileiros de Cardiologia, Iss 0 (2018)
Abstract Background: Light-chain (AL) cardiac amyloidosis (CA) is characterized by fibril deposits, which are composed of monoclonal immunoglobulin light chains. The right ventricle is mostly involved in AL-CA and impairment of its function is a pred
Externí odkaz:
https://doaj.org/article/1dd245d510d0482fb604be404a889e42