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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.
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.
Journal of Molecular and Cellular Cardiology|December 13, 2000
SSeCKS gene expression in vascular smooth muscle cells: regulation by angiotensin II and a potential role in the regulation of PAI-1 gene expressionS R Coats, J W Covington, M Su, et al.
International Angiology : a Journal of the International Union of Angiology|December 11, 2012
Femoral pseudoaneurysm in patients undergoing primary percutaneous coronary intervention for ST-elevation myocardial infarction: incidence, clinical course and risk factorsE Ayhan, T Isik, H Uyarel, et al.
Human Psychopharmacology|December 6, 2005
Nitric oxide, adenosine deaminase, xanthine oxidase and superoxide dismutase in patients with panic disorder: alterations by antidepressant treatmentHasan Herken, Omer Akyol, H Ramazan Yilmaz, et al.
Biochemistry|February 11, 1997
Control of oxidation-reduction potentials in flavodoxin from Clostridium beijerinckii: the role of conformation changesM L Ludwig, K A Pattridge, A L Metzger, 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.
International Journal of Immunopathology and Pharmacology|January 10, 2013
Pharmacokinetics of colchicine in pediatric and adult patients with familial Mediterranean feverY Berkun, S Wason, R Brik, et al.
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