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The International Journal of Biological Markers|March 9, 2016
Polymorphisms in cancer susceptibility genes XRCC1, RAD51 and TP53 and the risk of breast cancer in Serbian womenAna M Krivokuca, Milena R Cavic, Emina J Malisic, et al.
European Journal of Vascular and Endovascular Surgery : the Official Journal of the European Society for Vascular Surgery|February 11, 2016
Morphological Differences in the Aorto-iliac Segment in AAA Patients of Caucasian and Asian OriginI Banzic, Q Lu, L Zhang, et al.
Journal of B.U.ON. : Official Journal of the Balkan Union of Oncology|April 3, 2017
Nitric oxide synthesis modulation - a possible diagnostic and therapeutic target in colorectal cancerBranko Brankovic, Goran Stanojevic, Ivana Stojanovic, et al.
Scientific Reports|February 3, 2023
The effects of being told you are in the intervention group on training results: a pilot studyKolbjørn Lindberg, Thomas Bjørnsen, Fredrik T Vårvik, et al.
BMC Cancer|October 13, 2010
Screening of the DNA mismatch repair genes MLH1, MSH2 and MSH6 in a Greek cohort of Lynch syndrome suspected familiesGeorgia Thodi, Florentia Fostira, Raphael Sandaltzopoulos, et al.
Life Science Alliance|March 10, 2021
Arterial stiffness and cardiac dysfunction in Hutchinson-Gilford Progeria Syndrome corrected by inhibition of lysyl oxidaseRyan von Kleeck, Emilia Roberts, Paola Castagnino, et al.
Clinical Genetics|April 11, 2016
Mutations in the IRBIT domain of ITPR1 are a frequent cause of autosomal dominant nonprogressive congenital ataxiaS Barresi, M Niceta, P Alfieri, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 16, 2019
Neuropathic pain in patients with Charcot-Marie-Tooth type 1ABogdan Bjelica, Stojan Peric, Ivana Basta, et al.
Scientific Reports|March 8, 2024
Clinical electromagnetic brain scannerAmin Abbosh, Konstanty Bialkowski, Lei Guo, et al.
Revista Espanola De Cardiologia (English Ed.)|November 13, 2025
Impact of SGLT2 inhibitors on long-term outcomes in TAVI patients with heart failure: a propensity-matched analysisOmar Obeidat, Ahmad Alayyat, Abdallah Naser, et al.
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