Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Meral, Kayikcioglu"'
Autor:
Meral Kayikcioglu, Hasan Selcuk Ozkan, Burcu Yagmur, Selen Bayraktaroglu, Asli Tetik Vardarli
Publikováno v:
Frontiers in Genetics, Vol 13 (2023)
Background: Homozygous familial hypercholesterolemia (HoFH) is a rare and devastating genetic condition characterized by extremely elevated levels of low-density lipoprotein cholesterol (LDL-C) leading to an increased risk of premature atherosclerosi
Externí odkaz:
https://doaj.org/article/ac9efca3cd094e67a3ac09feae2ca231
Publikováno v:
Balkan Medical Journal, Vol 39, Iss 2, Pp 83-95 (2022)
Myocardial infarction mostly presents with atypical signs and symptoms and has different risk factors in young individuals compared to older individuals. These risk factors are often preventable, therefore recognizing them and taking precautions can
Externí odkaz:
https://doaj.org/article/8adff7251db046779a21380c6d1725c7
Autor:
Laura D’Erasmo, Antonina Giammanco, Patrizia Suppressa, Chiara Pavanello, Gabriella Iannuzzo, Alessia Di Costanzo, Daniele Tramontano, Ilenia Minicocci, Simone Bini, Anja Vogt, Kim Stewards, Jeanine Roeters Van Lennep, Stefano Bertolini, Marcello Arca, the Italian and European Working Group on Lomitapide in HoFH, Maurizio Averna, Eric Boersma, Katia Bonomo, Marco Bucci, Laura Calabresi, Paolo Calabrò, Angelo Baldassare Cefalù, Jaimini Cegla, Arturo Cesaro, Sergio D’Addato, Eugene Daphnis, Maria Donata Di Taranto, Avishay Ellis, Fabio Fimiani, Giuliana Fortunato, Marco Gentile, Meral Kayikcioglu, Genovefa Kolovou, Evangelos Liberopoulos, Karin Littmann, Sergio Martínez-Hervás, Tiziana Montalcini, Fabio Nota, Livia Pisciotta, Arturo Puja, Giovanni José Real, Jeanine Roeters van Lennep, Joost Rutten, Carlo Sabbà, Tiziana Sampietro, Francesco Sbrana, Kim Steward, Fulvio Ventura, Battista Vigna, Shahenaz Walji
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Backgroundand aim: Autosomal recessive hypercholesterolemia (ARH) is a rare autosomal recessive disorder of low-density lipoprotein (LDL) metabolism caused by pathogenic variants in the LDLRAP1 gene. Like homozygous familial hypercholesterolemia, ARH
Externí odkaz:
https://doaj.org/article/c310a706a0ae42eda26ba363b9582898
Autor:
Meral Kayikcioglu, Lale Tokgozoglu
Publikováno v:
Pharmaceuticals, Vol 16, Iss 1, p 64 (2022)
Homozygous familial hypercholesterolemia (HoFH) is the rare form of familial hypercholesterolemia causing extremely high low-density lipoprotein cholesterol (LDL-C) levels, leading to atherosclerotic cardiovascular disease (ASCVD) in the first decade
Externí odkaz:
https://doaj.org/article/97690322e7614b4b9409090f368cbcad
Publikováno v:
Journal of Clinical Sleep Medicine. 19:889-898
Publikováno v:
American Journal of Preventive Cardiology, Vol 6, Iss , Pp 100184- (2021)
Turkey, like many countries, is facing a growing burden of non-communicable disease (NCD)s and is among the countries with high cardiovascular mortality in Europe. Moreover, Turkey currently has the highest rate of premature cardiovascular disease (C
Externí odkaz:
https://doaj.org/article/548e84ba612d4e61a3b8fd58b48b0108
Publikováno v:
American Journal of Preventive Cardiology, Vol 4, Iss , Pp 100128- (2020)
Objectives: The coronavirus-disease-2019 (COVID-19) pandemic has led to the restructuring of health-services to prioritize the treatment of COVID-19. The severe restrictions on daily life affected the management of chronic diseases. Patients with a p
Externí odkaz:
https://doaj.org/article/fd673d4d1bbc46c4a88edeacdfbf7dcf
Autor:
Alper Sonmez, Ibrahim Demirci, Cem Haymana, Ilker Tasci, Mustafa Okan Ayvalı, Naim Ata, Fatih Suheyl Ezgu, Fahri Bayram, Cem Barcin, Murat Caglayan, Mustafa Mahir Ülgü, Suayip Birinci, Lale Tokgozoglu, Ilhan Satman, Meral Kayikcioglu
Background and aims: Familial hypercholesterolemia (FH) is the most common cause of premature atherosclerotic cardiovascular disease (ASCVD). Türkiye is among the countries with the highest rate of ASCVD. However, no population-based study has been
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f90dd87ac9dbdf65ad18cd6cff1368a
https://avesis.erciyes.edu.tr/publication/details/3599a56c-e9fb-4c8b-97d1-34d9bae49c64/oai
https://avesis.erciyes.edu.tr/publication/details/3599a56c-e9fb-4c8b-97d1-34d9bae49c64/oai
Autor:
Marina Cuchel, Frederick J Raal, Robert A Hegele, Khalid Al-Rasadi, Marcello Arca, Maurizio Averna, Eric Bruckert, Tomas Freiberger, Daniel Gaudet, Mariko Harada-Shiba, Lisa C Hudgins, Meral Kayikcioglu, Luis Masana, Klaus G Parhofer, Jeanine E Roeters van Lennep, Raul D Santos, Erik S G Stroes, Gerald F Watts, Albert Wiegman, Jane K Stock, Lale S Tokgözoğlu, Alberico L Catapano, Kausik K Ray
Publikováno v:
European Heart Journal.
This 2023 statement updates clinical guidance for homozygous familial hypercholesterolaemia (HoFH), explains the genetic complexity, and provides pragmatic recommendations to address inequities in HoFH care worldwide. Key strengths include updated cr
Publikováno v:
European Atherosclerosis Journal. 1
Lipoprotein (a) (Lp(a)) attests to be of interest as a new lipoprotein target. However, Lp(a) was discovered in 1963 and since then was recognized as a low-density lipoprotein (LDL)-like lipoprotein with a structurally similar domain to plasminogen.