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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]
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 (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 ISI/Web of Science   Elečas   Rang časopisa  
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 ISI/Web of Science   Elečas   Rang časopisa  
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 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]
Ispravka ISI/Web of Science   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 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]
Ispravka ISI/Web of Science   Elečas   Rang časopisa  
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  
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