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Showing results (171-180 of 200) with videos related to

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Transplantation Proceedings|February 12, 2008
Outcome of primary glomerular disease in pediatric renal transplantation: a single-center experienceY Bilginer, R Topaloglu, F T Aki, et al.
Clinical and Experimental Rheumatology|October 28, 2006
Are carriers for MEFV mutations "healthy"?M Kalyoncu, B C Acar, N Cakar, et al.
Arthritis and Rheumatism|October 23, 2001
Higher frequency of allele 2 of the interleukin-1 receptor antagonist gene in patients with juvenile idiopathic arthritisJ Vencovský, K Jarosová, S Růzicková, et al.
Transplantation Proceedings|April 14, 2011
Follow-up of patients with juvenile nephronophthisis after renal transplantation: a single center experienceA C Tayfur, N Besbas, Y Bilginer, et al.
Rheumatology (Oxford, England)|June 17, 1999
Evaluation of tumour necrosis factor alpha, interferon gamma and granulocyte-macrophage colony stimulating factor levels in juvenile chronic arthritisS Yetgin, S Ozen, U Saatci, et al.
Scandinavian Journal of Rheumatology|July 19, 2022
A novel variant in severe disease of DADA2: involving vasculitic and haematologic featuresG Ayan, B Yagiz, O E Cinar, et al.
European Journal of Human Genetics : EJHG|June 15, 2000
Familial Mediterranean fever in the 'Chuetas' of Mallorca: a question of Jewish origin or genetic heterogeneityC Domingo, I Touitou, A Bayou, et al.
Transplantation Proceedings|February 12, 2008
Renal transplantation in children with lower urinary tract dysfunction of different origin: a single-center experienceY Bilginer, F T Aki, R Topaloglu, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|February 24, 2001
Association of nitric oxide production and apoptosis in a model of experimental nephropathyS Ozen, Y Usta, I Sahin-Erdemli, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|January 13, 2016
Familial partial lipodystrophy linked to a novel peroxisome proliferator activator receptor -γ (PPARG) mutation, H449L: a comparison of people with this mutation and those with classic codon 482 Lamin A/C (LMNA) mutationsT Demir, H Onay, D B Savage, et al.
Pageof 20

Showing results (171-180 of 200) with videos related to

Sort By:
Pageof 20
Transplantation Proceedings|February 12, 2008
Outcome of primary glomerular disease in pediatric renal transplantation: a single-center experienceY Bilginer, R Topaloglu, F T Aki, et al.
Clinical and Experimental Rheumatology|October 28, 2006
Are carriers for MEFV mutations "healthy"?M Kalyoncu, B C Acar, N Cakar, et al.
Arthritis and Rheumatism|October 23, 2001
Higher frequency of allele 2 of the interleukin-1 receptor antagonist gene in patients with juvenile idiopathic arthritisJ Vencovský, K Jarosová, S Růzicková, et al.
Transplantation Proceedings|April 14, 2011
Follow-up of patients with juvenile nephronophthisis after renal transplantation: a single center experienceA C Tayfur, N Besbas, Y Bilginer, et al.
Rheumatology (Oxford, England)|June 17, 1999
Evaluation of tumour necrosis factor alpha, interferon gamma and granulocyte-macrophage colony stimulating factor levels in juvenile chronic arthritisS Yetgin, S Ozen, U Saatci, et al.
Scandinavian Journal of Rheumatology|July 19, 2022
A novel variant in severe disease of DADA2: involving vasculitic and haematologic featuresG Ayan, B Yagiz, O E Cinar, et al.
European Journal of Human Genetics : EJHG|June 15, 2000
Familial Mediterranean fever in the 'Chuetas' of Mallorca: a question of Jewish origin or genetic heterogeneityC Domingo, I Touitou, A Bayou, et al.
Transplantation Proceedings|February 12, 2008
Renal transplantation in children with lower urinary tract dysfunction of different origin: a single-center experienceY Bilginer, F T Aki, R Topaloglu, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|February 24, 2001
Association of nitric oxide production and apoptosis in a model of experimental nephropathyS Ozen, Y Usta, I Sahin-Erdemli, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|January 13, 2016
Familial partial lipodystrophy linked to a novel peroxisome proliferator activator receptor -γ (PPARG) mutation, H449L: a comparison of people with this mutation and those with classic codon 482 Lamin A/C (LMNA) mutationsT Demir, H Onay, D B Savage, et al.
Pageof 20