Autori: Peterlin Borut
| 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
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| Info | NEUROLOGICAL SCIENCES, (2024), vol. br. , str. - |
| Projekat | Ministarstvo Prosvete, Nauke i Tehnoloscaron;kog Razvoja |
| Ispravka | Web of Science Članak Elečas Rang časopisa Citati: |
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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; 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
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| 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] |
| Ispravka | Web of Science Članak Elečas Rang časopisa Citati: |
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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
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| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2024), vol. 32 br. , Suppl. 1, str. 356-357 |
| Projekat | Slovenian Research Agency [P3-0326] |
| Ispravka | Web of Science Elečas Rang časopisa |
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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] |
| Ispravka | Web of Science Članak Elečas Rang časopisa |
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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] |
| Ispravka | Web of Science Članak Elečas Rang časopisa |
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| Naslov | Analysis of "Clinical Exome" Panel in Serbian Patients with Cognitive Disorders (Article) |
| Autori | Brankovic Marija Stefanova Elka D Mandic Gorana B Marjanovic Ana Dobricic Valerija S Maver Ales Bergant Gaber Stevic Zorica D Jankovic Milena Z Novakovic Ivana V Peterlin Borut Kostic Vladimir K
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| Info | GENETIKA-BELGRADE, (2022), vol. 54 br. 3, str. 1351-1364 |
| Projekat | Serbian Ministry of education, science, and technological development [175090, 175091, 200] |
| Ispravka | Web of Science Članak Elečas Rang časopisa |
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| Naslov | A Novel Variant in the LIPA Gene Associated with Distinct Phenotype (Article) |
| Autori | Sarajlija Adrijan Armengol L Maver Ales Kitic Ivana Prokic Dragan Cehic Maja Djuricic MS Peterlin Borut
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| Info | BALKAN JOURNAL OF MEDICAL GENETICS, (2022), vol. 25 br. 1, str. 93-99 |
| Ispravka | Web of Science Članak Elečas Rang časopisa |
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| Naslov | Case report: Long-term follow-up of two patients with LHON caused by DNAJC30:c.152G > A pathogenic variant-case series (Article) |
| Autori | Petrovic Pajic Sanja MI Jarc-Vidmar Martina Fakin Ana Sustar-Habjan Maja Brecelj Jelka Volk Marija Maver Ales Peterlin Borut Hawlina Marko |
| Info | FRONTIERS IN NEUROLOGY, (2022), vol. 13 br. , str. - |
| Projekat | Slovenian Research Agency; [P3-0333] |
| Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science |
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| Naslov | The Relative Preservation of the Central Retinal Layers in Leber Hereditary Optic Neuropathy (Article) |
| Autori | Petrovic Pajic Sanja MI Lapajne Luka Vratanar Bor Fakin Ana Jarc-Vidmar Martina Sustar-Habjan Maja Volk Marija Maver Ales Peterlin Borut Hawlina Marko |
| Info | JOURNAL OF CLINICAL MEDICINE, (2022), vol. 11 br. 20, str. - |
| Projekat | Slovenian Research Agency [P3-0333] |
| Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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| Naslov | Clinical Exome Sequencing in Serbian Patients with Movement Disorders - Single Centre Experience (Article) |
| Autori | Brankovic Marija Dragasevic Natasa T Dobricic Valerija S Maver Ales Bergant Gaber Petrovic Igor N Peric Stojan Z Marjanovic Ana Jankovic Milena Z Jancic Jasna B Novakovic Ivana V Peterlin Borut Svetel Marina V Kostic Vladimir K
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| Info | GENETIKA-BELGRADE, (2022), vol. 54 br. 1, str. 395-409 |
| Projekat | Serbian Ministry of education, science, and technological development [175090, 175091] |
| Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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