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Cells|January 8, 2023
Expression of Markers of Endometrial Receptivity in Obese Infertile PCOS Women before and after the Weight Loss Program-A Preliminary StudyGaber Bergant, Dzhamilyat Abdulkhalikova, Ana Šuštaršič, et al.
Current Issues in Molecular Biology|August 27, 2021
Disease Progression in <i>CNGA3</i> and <i>CNGB3</i> Retinopathy; Characteristics of Slovenian Cohort and Proposed OCT Staging Based on Pooled Data from 126 Patients from 7 StudiesManca Tekavčič Pompe, Nika Vrabič, Marija Volk, et al.
Journal of Applied Genetics|March 23, 2018
Diagnostic efficacy and new variants in isolated and complex autism spectrum disorder using molecular karyotypingLuca Lovrečić, Polona Rajar, Marija Volk, et al.
Neurobiology of Aging|July 29, 2011
Histamine N-methyltransferase Thr105Ile polymorphism is associated with Parkinson's diseaseVinko Palada, Janoš Terzić, Joseph Mazzulli, et al.
Neuroscience Letters|June 16, 2005
Mutations in the hemochromatosis gene (HFE) and multiple sclerosisSmiljana Ristić, Luca Lovrecić, Bojana Brajenović-Milić, et al.
Journal of Child Neurology|October 19, 2019
Diagnostic and Clinical Utility of Clinical Exome Sequencing in Children With Moderate and Severe Global Developmental Delay / Intellectual DisabilityJelena Ruml Stojanovic, Aleksandra Miletic, Borut Peterlin, et al.
European Neurology|February 3, 2007
Tumor necrosis factor-alpha-308 gene polymorphism in Croatian and Slovenian multiple sclerosis patientsSmiljana Ristić, Luca Lovrecić, Nada Starcević-Cizmarević, et al.
Collegium Antropologicum|November 29, 2007
HLA class II polymorphism in autochthonous population of Gorski kotar, CroatiaMarija Crnić-Martinović, Blazenka Grahovac, Blanka Vidan Jeras, et al.
Andrology|August 30, 2020
De novo mutations in idiopathic male infertility-A pilot studyAlenka Hodžić, Aleš Maver, Dijana Plaseska-Karanfilska, et al.
Medical Science Monitor : International Medical Journal of Experimental and Clinical Research|October 1, 2011
Low frequency of HFE gene mutations in Croatian patients suspected of having hereditary hemochromatosisSandra Milić, Smiljana Ristić, Nada Starčević-Čizmarević, et al.
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