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Acta Medico-Historica Adriatica : AMHA|October 29, 2025
Pharmacy on Cres: fragments of the history of the profession and cultureIgor Eterović, Toni Buterin, Juraj Sepčić, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|August 29, 2016
Angiotensin-converting enzyme insertion/deletion gene polymorphism in multiple sclerosis: a meta-analysisSmiljana Ristić, Nada Starčević Čizmarević, Juraj Sepčić, et al.Scientific Reports|June 26, 2019
Multiple Sclerosis patients carry an increased burden of exceedingly rare genetic variants in the inflammasome regulatory genesLovro Vidmar, Ales Maver, Jelena Drulović, et al.Pharmacogenetics and Genomics|April 22, 2017
Angiotensin-converting enzyme insertion/deletion gene polymorphism and interferon-β treatment response in multiple sclerosis patients: a preliminary reportSmiljana Ristić, Nada Starčević Čizmarević, Polona Lavtar, et al.Brain and Behavior|January 28, 2017
The lack of association between angiotensin-converting enzyme gene insertion/deletion polymorphism and nicotine dependence in multiple sclerosisSergej Nadalin, Alena Buretić-Tomljanović, Polona Lavtar, et al.Journal of Neuroimmunology|August 24, 2015
MMP-2 -1575G/A polymorphism modifies the onset of optic neuritis as a first presenting symptom in MS?Iva Gašparović, Nada Starčević Čizmarević, Luca Lovrečić, et al.Genetic Testing and Molecular Biomarkers|June 25, 2011
Angiotensin-converting enzyme gene polymorphism in patients with multiple sclerosis from Bosnia and HerzegovinaInge Klupka-Sarić, Borut Peterlin, Luca Lovrečić, et al.Plos One|January 12, 2018
Association of circadian rhythm genes ARNTL/BMAL1 and CLOCK with multiple sclerosisPolona Lavtar, Gorazd Rudolf, Aleš Maver, et al.Disease Markers|May 15, 2014
The role of TPA I/D and PAI-1 4G/5G polymorphisms in multiple sclerosisMaja Zivković, Nada Starčević Čizmarević, Luca Lovrečić, et al.Scientific Reports|June 18, 2017
Identification of rare genetic variation of NLRP1 gene in familial multiple sclerosisAles Maver, Polona Lavtar, Smiljana Ristić, et al.Pageof 1