Autori: Peterlin Borut
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 ![]() |
Info | WORLD JOURNAL OF MENS HEALTH, (2025), vol. br. , str. - |
Projekat | Slovenian Research and Inno-vation Agency [P3-0326] |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: |
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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] |
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 (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] |
Ispravka | Web of Science Elečas Rang časopisa |
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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 ![]() |
Info | MEDICINA-LITHUANIA, (2024), vol. 60 br. 12, str. - |
Projekat | University of Rijeka, Croatia; [uniri-iskusni-biomed-23-195] |
Ispravka | Web of Science Članak Elečas Rang časopisa |
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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 ![]() ![]() ![]() ![]() ![]() |
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] |
Ispravka | Web of Science Elečas Rang časopisa |
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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 ![]() ![]() ![]() ![]() ![]() ![]() |
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) |
Autori | Jovanovic Aleksa Lj ![]() ![]() ![]() ![]() ![]() ![]() |
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 ![]() |
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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