Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Ferhat Guzel"'
Autor:
Ferhat Guzel, Micol Romano, Erdi Keles, David Piskin, Seza Ozen, Hakan Poyrazoglu, Ozgur Kasapcopur, Erkan Demirkaya
Publikováno v:
Frontiers in Immunology, Vol 12 (2021)
BackgroundDuring the last decade, remarkable progress with massive sequencing has been made in the identification of disease-associated genes for AIDs using next-generation sequencing technologies (NGS). An international group of experts described th
Externí odkaz:
https://doaj.org/article/87b3f73b55c34c45ab5858bc36ffd5c7
Autor:
Sezgin Sahin, Micol Romano, Ferhat Guzel, David Piskin, Dimitri Poddighe, Siren Sezer, Ozgur Kasapcopur, C. Thomas Appleton, Ilker Yilmaz, Erkan Demirkaya
Publikováno v:
Life, Vol 12, Iss 5, p 631 (2022)
Cardiovascular disease (CVD) remains underestimated in familial Mediterranean fever-associated AA amyloidosis (FMF-AA). We aimed to compare early markers of endothelial dysfunction and atherosclerosis in FMF-AA with a homozygous M694V mutation (Group
Externí odkaz:
https://doaj.org/article/09a68ce2277c4bab97129db2a5920061
Publikováno v:
Paediatrics Publications
Behçet’s disease (BD) is a polygenic condition with a complex immunopathogenetic background and challenging diagnostic and therapeutic concepts. Advances in genomic medicine have provided intriguing insights into disease pathogenesis over the last
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76a1f3f5e44efbf867d3f675485c6641
https://ir.lib.uwo.ca/paedpub/1106
https://ir.lib.uwo.ca/paedpub/1106
Autor:
Ferhat Guzel, Roberta A. Berard, Micol Romano, Sezgin Sahin, Erkan Demirkaya, Mahmut Ilker Yilmaz, Zehra Serap Arici, David Piskin
Publikováno v:
Paediatrics Publications
Journal of Clinical Medicine, Vol 10, Iss 3511, p 3511 (2021)
Journal of Clinical Medicine
Volume 10
Issue 16
Journal of Clinical Medicine, Vol 10, Iss 3511, p 3511 (2021)
Journal of Clinical Medicine
Volume 10
Issue 16
The aim of the study was to compare the clinical phenotype of patients with familial Mediterranean fever (FMF)-related AA amyloidosis, according to the age of FMF diagnosis and E148Q genotype. Patients with biopsy-confirmed FMF-related AA amyloidosis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a895de9b30d9142c4b2ebc2fab418803
https://ir.lib.uwo.ca/paedpub/790
https://ir.lib.uwo.ca/paedpub/790
Autor:
Sezgin Sahin, David Piskin, Ferhat Guzel, Ozgur Kasapcopur, I. Yilmaz, Micol Romano, Erkan Demirkaya
Publikováno v:
Annals of the Rheumatic Diseases. 80:969.2-970
Background:There are limited data in FMF associated AA amyloidosis patients regarding the vascular abnormalities including atherosclerosis and endothelial dysfunction, all of which are contributors of cardiovascular disease (CVD) risk. And, this risk
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::702a35abb6201f69c0f418b3b89e1447
https://doi.org/10.1136/annrheumdis-2021-eular.3582
https://doi.org/10.1136/annrheumdis-2021-eular.3582
Autor:
Dan Yang, Qing Zhou, Mario Abinun, Xiaomin Yu, Ferhat Guzel, Manfred Boehm, Mary Blake, Steven B. Welch, Hye Sun Kuehn, Daniel L. Kastner, Jae Jin Chae, Natalie Deuitch, Elaine F. Remmers, Seza Ozen, Hongying Wang, Wanxia Li Tsai, Rezan Topaloglu, Joshua D. Milner, Massimo Gadina, Amanda K. Ombrello, Ivona Aksentijevich, Yong Hwan Park, Erkan Demirkaya, Tina Romeo, James C. Mullikin, Sergio D. Rosenzweig, Deborah L. Stone
Publikováno v:
Paediatrics Publications
Systemic autoinflammatory diseases are caused by mutations in genes that function in innate immunity. Here, we report an autoinflammatory disease caused by loss-of-function mutations in OTULIN (FAM105B), encoding a deubiquitinase with linear linkage
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::807a95d0c05a6c6fce481b6580dbeddd
https://ir.lib.uwo.ca/context/paedpub/article/2121/viewcontent/pnas.1612594113.pdf
https://ir.lib.uwo.ca/context/paedpub/article/2121/viewcontent/pnas.1612594113.pdf