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Multiple Sclerosis (Houndmills, Basingstoke, England)|November 8, 2007
PAI and TPA gene polymorphisms in multiple sclerosisLuca Lovrecic, Smiljana Ristić, Nada Starcević-Cizmarević, et al.
Genes|April 3, 2021
Cone Dystrophy Associated with a Novel Variant in the Terminal Codon of the <i>RPGR</i>-<i>ORF15</i>Vlasta Hadalin, Maja Šuštar, Marija Volk, 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.
Radiology and Oncology|September 25, 2015
The influence of cytokine gene polymorphisms on the risk of developing gastric cancer in patients with Helicobacter pylori infectionDavid Stubljar, Samo Jeverica, Tomislav Jukic, 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.
Frontiers in Aging Neuroscience|December 26, 2022
The effects of microbiota abundance on symptom severity in Parkinson's disease: A systematic reviewEliša Papić, Valentino Rački, Mario Hero, et al.
Plos One|September 18, 2020
Genetic testing offer for inherited neuromuscular diseases within the EURO-NMD reference network: A European survey studyBorut Peterlin, Francesca Gualandi, Ales Maver, et al.
Neurology. Genetics|May 6, 2022
Biallelic <i>ATOH1</i> Gene Variant in Siblings With Pontocerebellar Hypoplasia, Developmental Delay, and Hearing LossTanja Višnjar, Aleš Maver, Karin Writzl, et al.
Frontiers in Neurology|November 17, 2022
Case report: Long-term follow-up of two patients with LHON caused by DNAJC30:c.152G>A pathogenic variant-case seriesSanja Petrovic Pajic, Martina Jarc-Vidmar, Ana Fakin, et al.
Cells|June 25, 2025
Exome Study of Single Nucleotide Variations in Patients with Syndromic and Non-Syndromic Autism Reveals Potential Candidate Genes for Diagnostics and Novel Single Nucleotide VariantsLyudmila Belenska-Todorova, Milen Zamfirov, Tihomir Todorov, et al.
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