Artykuły udostępnione publicznie: - Seza OzenWięcej informacji
Niedostępne w żadnym miejscu: 11
Sprawdź
A monogenic disease with a variety of phenotypes: deficiency of adenosine deaminase 2
S Özen, ED Batu, EZ Taşkıran, HA Özkara, Ş Ünal, N Güleray, A Erden, ...
The Journal of rheumatology 47 (1), 117-125, 2020
Upoważnienia: Scientific and Technological Research Council of Turkey
Sprawdź
Expression of ASC in renal tissues of familial mediterranean fever patients with amyloidosis: postulating a role for ASC in AA type amyloid deposition
B Balci-Peynircioglu, AL Waite, P Schaner, ZE Taskiran, N Richards, ...
Experimental biology and medicine 233 (11), 1324-1333, 2008
Upoważnienia: US National Institutes of Health
Sprawdź
Autoinflammation in addition to combined immunodeficiency: SLC29A3 gene defect
D Çağdaş, N Sürücü, Ç Tan, B Kayaoğlu, RK Özgül, YZ Akkaya-Ulum, ...
Molecular Immunology 121, 28-37, 2020
Upoważnienia: Scientific and Technological Research Council of Turkey
Sprawdź
A retrospective study comparing the phenotype and outcomes of patients with polyarteritis nodosa between UK and Turkish cohorts
O Karadag, A Erden, Y Bilginer, S Gopaluni, A Sari, B Armagan, I Ertenli, ...
Rheumatology International 38 (10), 1833-1840, 2018
Upoważnienia: National Institute for Health Research, UK
Sprawdź
Whole exome sequencing in unclassified autoinflammatory diseases: more monogenic diseases in the pipeline?
C Kosukcu, EZ Taskiran, ED Batu, E Sag, Y Bilginer, M Alikasifoglu, ...
Rheumatology 60 (2), 607-616, 2021
Upoważnienia: Scientific and Technological Research Council of Turkey
Sprawdź
Clinical characteristics and outcomes of polyarteritis nodosa: an international study
O Karadag, EC Bolek, G Ayan, AJ Mohammad, PC Grayson, C Pagnoux, ...
Arthritis & Rheumatology 76 (7), 1120-1129, 2024
Upoważnienia: National Institute for Health Research, UK
Sprawdź
Epigenetics for clinicians from the perspective of pediatric rheumatic diseases
TH Akbaba, E Sag, B Balci-Peynircioglu, S Ozen
Current rheumatology reports 22, 1-14, 2020
Upoważnienia: Scientific and Technological Research Council of Turkey
Sprawdź
Juvenile idiopathic arthritis: lymphocyte activation gene-3 is a central immune receptor in children with oligoarticular subtypes
E Sag, S Demir, M Aspari, MA Nielsen, C Skejø, M Hvid, E Turhan, ...
Pediatric Research 90 (4), 744-751, 2021
Upoważnienia: Scientific and Technological Research Council of Turkey
Sprawdź
Structural, electronic and vibrational properties of ultra-thin octahedrally coordinated structure of EuO2
M Ozcan, S Ozen, M Yagmurcukardes, H Sahin
Journal of Magnetism and Magnetic Materials 493, 165668, 2020
Upoważnienia: Research Foundation (Flanders), Scientific and Technological Research …
Sprawdź
Drug metabolism and inflammation related distinct miRNA signature of colchicine resistant familial Mediterranean fever patients
BŞ Tümerdem, TH Akbaba, ED Batu, YZ Akkaya-Ulum, P Mutlu, S Ozen, ...
International Immunopharmacology 124, 111011, 2023
Upoważnienia: Scientific and Technological Research Council of Turkey
Sprawdź
Editorial Board, Chinese Edition
GBJ Andersson, X Baraliakos, R Ruhrgebiet, F Berenbaum, ...
RHEUMATOLOGY 5 (2), 2019
Upoważnienia: US National Institutes of Health
Dostępne w jakimś miejscu: 81
Sprawdź
Genetic diagnosis by whole exome capture and massively parallel DNA sequencing
M Choi, UI Scholl, W Ji, T Liu, IR Tikhonova, P Zumbo, A Nayir, ...
Proceedings of the National Academy of Sciences 106 (45), 19096-19101, 2009
Upoważnienia: US National Institutes of Health, Howard Hughes Medical Institute
Sprawdź
Early-onset stroke and vasculopathy associated with mutations in ADA2
Q Zhou, D Yang, AK Ombrello, AV Zavialov, C Toro, AV Zavialov, ...
New England Journal of Medicine 370 (10), 911-920, 2014
Upoważnienia: US National Institutes of Health
Sprawdź
Two randomized trials of canakinumab in systemic juvenile idiopathic arthritis
N Ruperto, HI Brunner, P Quartier, T Constantin, N Wulffraat, G Horneff, ...
New England Journal of Medicine 367 (25), 2396-2406, 2012
Upoważnienia: Versus Arthritis, UK
Sprawdź
Loss-of-function mutations in TNFAIP3 leading to A20 haploinsufficiency cause an early-onset autoinflammatory disease
Q Zhou, H Wang, DM Schwartz, M Stoffels, YH Park, Y Zhang, D Yang, ...
Nature genetics 48 (1), 67-73, 2016
Upoważnienia: US National Institutes of Health
Sprawdź
JAK1/2 inhibition with baricitinib in the treatment of autoinflammatory interferonopathies
GAM Sanchez, A Reinhardt, S Ramsey, H Wittkowski, PJ Hashkes, ...
The Journal of clinical investigation 128 (7), 3041-3052, 2018
Upoważnienia: US Department of Defense, US National Institutes of Health
Sprawdź
Consensus-based recommendations for the management of juvenile dermatomyositis
FB Enders, B Bader-Meunier, E Baildam, T Constantin, P Dolezalova, ...
Annals of the rheumatic diseases 76 (2), 329-340, 2017
Upoważnienia: UK Medical Research Council, National Institute for Health Research, UK
Sprawdź
Management and treatment of glomerular diseases (part 1): conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference
J Floege, SJ Barbour, DC Cattran, JJ Hogan, PH Nachman, SCW Tang, ...
Kidney international 95 (2), 268-280, 2019
Upoważnienia: US National Institutes of Health, Wellcome Trust
Sprawdź
Diagnostic criteria for cryopyrin-associated periodic syndrome (CAPS)
JB Kuemmerle-Deschner, S Ozen, PN Tyrrell, I Kone-Paut, ...
Annals of the rheumatic diseases 76 (6), 942-947, 2017
Upoważnienia: US National Institutes of Health
Sprawdź
Biallelic hypomorphic mutations in a linear deubiquitinase define otulipenia, an early-onset autoinflammatory disease
Q Zhou, X Yu, E Demirkaya, N Deuitch, D Stone, WL Tsai, HS Kuehn, ...
Proceedings of the National Academy of Sciences 113 (36), 10127-10132, 2016
Upoważnienia: US National Institutes of Health
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