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Autori: Peterlin Borut

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Naslov Genetic Testing for Monogenic Forms of Male Infertility Contributes to the Clinical Diagnosis of Men with Severe Idiopathic Male Infertility (Article; Early Access)
Autori Podgrajsek Rebeka Hodzic Alenka Maver Ales Stimpfel Martin Andjelic Aleksander Miljanovic Olivera Ristanovic Momcilo Novakovic Ivana V  Plaseska-Karanfilska Dijana Noveski Predrag Ostojic Sasa Grskovic Antun Buretic-Tomljanovic Alena Peterlin Borut 
Info WORLD JOURNAL OF MENS HEALTH, (2025), vol. br. , str. -
Projekat Slovenian Research and Inno-vation Agency [P3-0326]
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Naslov A novel splice-site FHOD3 founder variant is a common cause of hypertrophic cardiomyopathy in the population of the Balkans - a cohort study (Meeting Abstract)
Autori Vodnjov Nina Toplisek Janez Maver Ales Cuturilo Goran Jaklic Helena Teran Natasa Visnjar Tanja Skrjanec-Pusenjak Marusa Hodzic Alenka Miljanovic Olivera Peterlin Borut Writzl Karin 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2024), vol. 32 br. , Suppl. 2, str. 1390-1390
Projekat [P3-0326]
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Naslov A novel splice-site FHOD3 founder variant is a common cause of hypertrophic cardiomyopathy in the population of the Balkans - a cohort study (Meeting Abstract)
Autori Vodnjov Nina Toplisek Janez Maver Ales Cuturilo Goran Jaklic Helena Teran Natasa Visnjar Tanja Pusenjak Marusa Skrjanec Hodzic Alenka Miljanovic Olivera Peterlin Borut Writzl Karin 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2024), vol. 32 br. , Suppl. 2, str. 1390-1390
Projekat [P3-0326]
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Naslov MTHFR Gene Polymorphisms and DNA Methylation in Idiopathic Spontaneous Preterm Birth (Article)
Autori Devic-Pavlic Sanja Sverko Roberta Barisic Anita Mladenic Tea Vranekovic Jadranka Stankovic Aleksandra D  Peterlin Ana Peterlin Borut Ostojic Sasa Pereza Nina 
Info MEDICINA-LITHUANIA, (2024), vol. 60 br. 12, str. -
Projekat University of Rijeka, Croatia; [uniri-iskusni-biomed-23-195]
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Naslov Rare and Uncommon Gene Variants Associated with Familial Multiple Sclerosis: A Case-Control Study (Meeting Abstract)
Autori Jovanovic Aleksa Lj  Turk Aleksander Novakovic Ivana V  Mesaros Sarlota T Veselinovic Nikola D Tamas Olivera S Maric Gorica D  Andabaka Marko M Momcilovic Nikola Pekmezovic Tatjana D  Peterlin Borut Drulovic Jelena S  
Info MULTIPLE SCLEROSIS JOURNAL, (2024), vol. 30 br. 3, Suppl. S, str. 866-867
Projekat Ministry of Science, Technological development and Innovation of the Republic of Serbia [200110]
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Naslov Earlier age of symptom onset in younger generation of familial cases of multiple sclerosis (Article; Early Access)
Autori Jovanovic Aleksa Lj  Pekmezovic Tatjana D  Mesaros Sarlota T Novakovic Ivana V  Peterlin Borut Veselinovic Nikola D Tamas Olivera S Ivanovic Jovana B  Maric Gorica D  Andabaka Marko M Momcilovic Nikola Drulovic Jelena S  
Info NEUROLOGICAL SCIENCES, (2024), vol. br. , str. -
Projekat Ministarstvo Prosvete, Nauke i Tehnoloscaron;kog Razvoja
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Naslov Exclusive breastfeeding may be a protective factor in individuals with familial multiple sclerosis. A population registry-based case-control study (Article)
Autori Jovanovic Aleksa Lj  Pekmezovic Tatjana D  Mesaros Sarlota T Novakovic Ivana V  Peterlin Borut Veselinovic Nikola D Tamas Olivera S Ivanovic Jovana B  Maric Gorica D  Andabaka Marko M Momcilovic Nikola Drulovic Jelena S  
Info MULTIPLE SCLEROSIS AND RELATED DISORDERS, (2024), vol. 82 br. , str. -
Projekat Ministry of Science, Technological Development and Innovations of the Republic of Serbia [200110]
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Naslov Genetic testing for monogenic forms of male infertility contributes to the clinical diagnosis of men with idiopathic severe male infertility (Meeting Abstract)
Autori Podgrajsek Rebeka Hodzic Alenka Maver Ales Stimpfel Martin Andjelic Aleksander Miljanovic Olivera Ristanovic Momcilo Novakovic Ivana V  Plaseska-Karanfilska Dijana Noveski Predrag Ostojic Sasa Grskovic Antun Buretic-Tomljanovic Alena Peterlin Borut 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2024), vol. 32 br. , Suppl. 1, str. 356-357
Projekat Slovenian Research Agency [P3-0326]
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Naslov A novel splice-site FHOD3 founder variant is a common cause of hypertrophic cardiomyopathy in the population of the Balkans-A cohort study (Article)
Autori Vodnjov Nina Toplisek Janez Maver Ales Cuturilo Goran Jaklic Helena Teran Natasa Visnjar Tanja Skrjanec Pusenjak Marusa Hodzic Alenka Miljanovic Olivera Peterlin Borut Writzl Karin Mahdieh Nejat 
Info PLOS ONE, (2023), vol. 18 br. 12, str. -
Projekat Slovenian Research and Innovation Agency [P3-0326]
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Naslov Leber Hereditary Optic Neuropathy in a Family of Carriers of MT-ND5 m.13042G>T (A236S) Novel Variant (Article)
Autori Petrovic Pajic Sanja MI Habjan Maja Sustar Brecelj Jelka Fakin Ana Volk Marija Maver Ales Jezernik Gregor Peterlin Borut Glavac Damjan Hawlina Marko Jarc-Vidmar Martina 
Info JOURNAL OF NEURO-OPHTHALMOLOGY, (2023), vol. 43 br. 3, str. 341-347
Projekat Slovenian Research Agency (ARRS Program) [P3-0333, P3-0427]
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