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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]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati:
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]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa  
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
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati:
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]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati:
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 ISI/Web of Science   Članak   Elečas   Rang časopisa  
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 ISI/Web of Science   Članak   Elečas   Rang časopisa  
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 
Info GENETIKA-BELGRADE, (2022), vol. 54 br. 3, str. 1351-1364
Projekat Serbian Ministry of education, science, and technological development [175090, 175091, 200]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa  
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 
Info BALKAN JOURNAL OF MEDICAL GENETICS, (2022), vol. 25 br. 1, str. 93-99
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa  
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 ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science  
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 ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
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