Diagnostic outcomes of exome sequencing in patients with syndromic or non-syndromic hearing loss
Likar, Tina, Hasanhodžić, Mensuda, Teran, Nataša, Maver, Aleš, Peterlin, Borut, Writzl, Karin
Published in PloS one (02.01.2018)
Published in PloS one (02.01.2018)
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A novel splice-site FHOD3 founder variant is a common cause of hypertrophic cardiomyopathy in the population of the Balkans-A cohort study
Vodnjov, Nina, Toplišek, Janez, Maver, Aleš, Čuturilo, Goran, Jaklič, Helena, Teran, Nataša, Višnjar, Tanja, Škrjanec Pušenjak, Maruša, Hodžić, Alenka, Miljanović, Olivera, Peterlin, Borut, Writzl, Karin
Published in PloS one (05.12.2023)
Published in PloS one (05.12.2023)
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Clinical and Histopathological Features of Gelsolin Amyloidosis Associated with a Novel GSN Variant p.Glu580Lys
Potrč, Maja, Volk, Marija, de Rosa, Matteo, Pižem, Jože, Teran, Nataša, Jaklič, Helena, Maver, Aleš, Drnovšek-Olup, Brigita, Bollati, Michela, Vogelnik, Katarina, Hočevar, Alojzija, Gornik, Ana, Pfeifer, Vladimir, Peterlin, Borut, Hawlina, Marko, Fakin, Ana
Published in International journal of molecular sciences (22.01.2021)
Published in International journal of molecular sciences (22.01.2021)
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Journal Article
A multicenter study of genetic testing for Parkinson’s disease in the clinical setting
Kovanda, Anja, Rački, Valentino, Bergant, Gaber, Georgiev, Dejan, Flisar, Dušan, Papić, Eliša, Brankovic, Marija, Jankovic, Milena, Svetel, Marina, Teran, Nataša, Maver, Aleš, Kostic, Vladimir S, Novakovic, Ivana, Pirtošek, Zvezdan, Rakuša, Martin, Vuletić, Vladimira, Peterlin, Borut
Published in NPJ Parkinson's Disease (04.11.2022)
Published in NPJ Parkinson's Disease (04.11.2022)
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Journal Article
A case of avoidable heterotopic pregnancy after single embryo transfer
Gergolet, Marco, Klanjšček, Jure, Steblovnik, Lili, Teran, Nataša, Bizjak, Neda, Di Bon, Nika, Budihna, Teja, Zavrtanik-Čelan, Alenka, Tul Mandić, Nataša, Vrtačnik-Bokal, Eda
Published in Reproductive biomedicine online (01.06.2015)
Published in Reproductive biomedicine online (01.06.2015)
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Clinical Outcome of Hypertrophic Cardiomyopathy in Probands with the Founder Variant c.913_914del in MYBPC3: A Slovenian Cohort Study
Vodnjov, Nina, Maver, Aleš, Teran, Nataša, Peterlin, Borut, Toplišek, Janez, Writzl, Karin
Published in Journal of cardiovascular translational research (19.08.2024)
Published in Journal of cardiovascular translational research (19.08.2024)
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CTG amplification in the DM1PK gene is not associated with idiopathic male subfertility
Kunej, Tanja, Teran, Nataša, Zorn, Branko, Peterlin, Borut
Published in Human reproduction (Oxford) (01.09.2004)
Published in Human reproduction (Oxford) (01.09.2004)
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Journal Article
The -429 T/C and -374 T/A gene polymorphisms of the receptor of advanced glycation end products gene (RAGE) are not risk factors for coronary artery disease in Slovene population with type 2 diabetes
Kirbis, Janez, Milutinović, Aleksandra, Steblovnik, Klemen, Teran, Natasa, Terzić, Rifet, Zorc, Marjeta
Published in Collegium antropologicum (01.12.2004)
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Published in Collegium antropologicum (01.12.2004)
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Frequency of HFE gene mutations C282Y and H63D in Bosnia and Herzegovina
Terzić, Rifet, Sehić, Amela, Teran, Natasa, Terzić, Ibrahim, Peterlin, Borut
Published in Collegium antropologicum (01.09.2006)
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Published in Collegium antropologicum (01.09.2006)
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P182: Arteries in Patients with Huntington’s Disease
Melik, Ziva, Kobal, Jan, Cankar, Ksenija, Pretnar, Janja, Zaletel, Marjan, Kobal, Lucijan, Teran, Natasa
Published in Artery research (01.12.2017)
Published in Artery research (01.12.2017)
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Journal Article
Insertion/deletion polymorphism of angiotensin-converting enzyme gene--risk factor for coronary artery disease in the Tuzla region population (Bosnia and Herzegovina)
Terzić, Rifet, Letonja, Mitja, Terzić, Ibrahim, Sehić, Amela, Merić, Muharem, Teran, Natasa
Published in Collegium antropologicum (01.12.2003)
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Published in Collegium antropologicum (01.12.2003)
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Multisite Verification of a Targeted CFTR Polymerase Chain Reaction/Capillary Electrophoresis Assay That Evaluates Pathogenic Variants Across Diverse Ethnic and Ancestral Groups
Hall, Bradley, Milligan, John N, Kelnar, Kevin, Hallmark, Elliot, Ashton, Jacob D, Parker, Connor A, Filipovic-Sadic, Stela, Sharp, Abigail, Eagle, Samantha, Rodgers, Nissa, Leung, Marco, Mathew, Mariam T, Grissom, Luke, Post, Rebecca, Teran, Nataša, Latham, Gary J
Published in Archives of pathology & laboratory medicine (1976) (08.01.2024)
Published in Archives of pathology & laboratory medicine (1976) (08.01.2024)
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The ScaI gene polymorphism of the atrial natriuretic factor and essential arterial hypertension in childhood
Zorc-Plesković, Ruda, Bidovec, Matjaz, Bregar, Dejan, Milutinović, Aleksandra, Terzić, Rifet, Teran, Natasa
Published in Collegium antropologicum (01.12.2004)
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Published in Collegium antropologicum (01.12.2004)
Journal Article
A novel splice-site FHOD3 founder variant is a common cause of hypertrophic cardiomyopathy in the population of the Balkans–A cohort study
Nina Vodnjov, Janez Toplišek, Aleš Maver, Goran Čuturilo, Helena Jaklič, Nataša Teran, Tanja Višnjar, Maruša Škrjanec Pušenjak, Alenka Hodžić, Olivera Miljanović, Borut Peterlin, Karin Writzl
Published in PloS one (01.01.2023)
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Published in PloS one (01.01.2023)
Journal Article
Patients with primary cataract as a genetic pool of DMPK protomutation
Medica, Igor, Teran, Natasa, Volk, Marija, Pfeifer, Vladimir, Ladavac, Edi, Peterlin, Borut
Published in Journal of human genetics (01.02.2007)
Published in Journal of human genetics (01.02.2007)
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Journal Article
Deletion/Deletion genotype of angiotensin-I converting enzyme gene is not associated with coronary artery disease in caucasians with type 2 diabetes
Zorc-Pleskovic, Ruda, Teran, Natasa, Plesković, Ales, Terzić, Rifet, Milutinović, Aleksandra
Published in Collegium antropologicum (01.06.2005)
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Published in Collegium antropologicum (01.06.2005)
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