Miljenko Kapovic
Miljenko Kapovic
Full professor, Department of Biology and Medical Genetics, School of Medicine, University of Rijeka
Potvrđena adresa e-pošte na
The role of iron and iron overload in chronic liver disease
S Milic, I Mikolasevic, L Orlic, E Devcic, N Starcevic-Cizmarevic, D Stimac, ...
Medical science monitor: international medical journal of experimental and …, 2016
Systematic review and meta-analysis of genetic association studies in idiopathic recurrent spontaneous abortion
N Pereza, S Ostojić, M Kapović, B Peterlin
Fertility and sterility 107 (1), 150-159. e2, 2017
Progesterone-dependent immunomodulation
J Szekeres-Bartho, B Polgar, N Kozma, E Miko, G Par, L Szereday, ...
Immunology of pregnancy 89, 118-125, 2005
Tolerance mechanisms in pregnancy: a reappraisal of the role of class I paternal MHC antigens
DA Clark, G Chaouat, K Wong, RM Gorczynski, R Kinsky
American Journal of Reproductive Immunology 63 (2), 93-103, 2010
Sex-specific differences of craniofacial traits in Croatia: the impact of environment in a small geographic area
A Buretić-Tomljanović, J Giacometti, S Ostojić, M Kapović
Annals of Human Biology 34 (3), 296-314, 2007
Secular change in body height and cephalic index of Croatian medical students (University of Rijeka)
A Buretić‐Tomljanović, S Ristić, B Brajenović‐Milić, S Ostojić, E Gombač, ...
American journal of physical anthropology 123 (1), 91-96, 2004
Matrix metalloproteinases 1, 2, 3 and 9 functional single-nucleotide polymorphisms in idiopathic recurrent spontaneous abortion
N Pereza, S Ostojić, M Volk, M Kapović, B Peterlin
Reproductive biomedicine online 24 (5), 567-575, 2012
Chromosomal anomalies in abnormal human pregnancies
B Brajenović-Milić, O Petrović, M Krašević, S Ristić, M Kapović
Fetal diagnosis and therapy 13 (3), 187-191, 1998
Identification of rare genetic variation of NLRP1 gene in familial multiple sclerosis
A Maver, P Lavtar, S Ristić, S Stopinšek, S Simčič, K Hočevar, J Sepčić, ...
Scientific reports 7 (1), 3715, 2017
Lipid classes and fatty acid composition of Diplodus vulgaris and Conger conger originating from the Adriatic Sea
J Varljen, S Šulić, J Brmalj, L Batičić, V Obersnel, M Kapović
Food Technology and Biotechnology 41 (2), 149-156, 2003
Secular change of craniofacial measures in Croatian younger adults
A Buretić‐Tomljanović, S Ostojić, M Kapović
American Journal of Human Biology: The Official Journal of the Human Biology …, 2006
Chromosome studies in patients with defective reproductive success
American Journal of Reproductive Immunology 44 (5), 279-283, 2000
Tumor necrosis factor-α-308 gene polymorphism in Croatian and Slovenian multiple sclerosis patients
S Ristić, L Lovrečić, N Starčević-Čizmarević, B Brajenović-Milić, ...
European neurology 57 (4), 203-207, 2007
Association of circadian rhythm genes ARNTL/BMAL1 and CLOCK with multiple sclerosis
P Lavtar, G Rudolf, A Maver, A Hodžić, N Starčević Čizmarević, M Živković, ...
PloS one 13 (1), e0190601, 2018
Genetic predisposition to idiopathic recurrent spontaneous abortion: contribution of genetic variations in IGF‐2 and H19 imprinted genes
S Ostojić, N Pereza, M Volk, M Kapović, B Peterlin
American Journal of Reproductive Immunology 60 (2), 111-117, 2008
Altered LINE-1 methylation in mothers of children with Down syndrome
I Babić Božović, A Stanković, M Živković, J Vraneković, M Kapović, ...
PLoS One 10 (5), e0127423, 2015
Polymorphisms in the interleukin‐12/18 genes and recurrent spontaneous abortion
S Ostojić, M Volk, I Medica, M Kapović, H Meden‐Vrtovec, B Peterlin
American journal of reproductive immunology 58 (5), 403-408, 2007
Region with persistent high frequency of multiple sclerosis in Croatia and Slovenia
KM Peterlin B, Ristić S, Sepčić J,Vracko BK, Rako A
Journal of the Neurological Sciences 247, 169-172, 2006
Angiotensin-converting enzyme insertion/deletion gene polymorphism in lung cancer patients
S Dević Pavlić, S Ristić, V Flego, M Kapović, A Radojčić Badovinac
Genetic testing and molecular biomarkers 16 (7), 722-725, 2012
Third case of 8q23.3‐q24.13 deletion in a patient with Langer–Giedion syndrome phenotype without TRPS1 gene deletion
N Pereza, S Severinski, S Ostojić, M Volk, A Maver, KB Dekanić, ...
American Journal of Medical Genetics Part A 158 (3), 659-663, 2012
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