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Autori: Maver Ales

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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]
Ispravka Web of Science   Elečas   Rang časopisa  
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Naslov Expanding the Phenotypic Spectrum: Chronic Kidney Disease in a Patient with Combined Oxidative Phosphorylation Defect 21 (Article)
Autori Paripovic Aleksandra Maver Ales Stajic Natasa Putnik Jovana  Ostojic Slavica  Alimpic Biljana Ilic Nina Sarajlija Adrijan  
Info BALKAN JOURNAL OF MEDICAL GENETICS, (2023), vol. 26 br. 2, str. 59-64
Ispravka Web of Science   Članak   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 Sensorineural Hearing Loss in a Child with Succinic Semialdehyde Dehydrogenase Deficiency (Article)
Autori Parezanovic M Ilic Nina Ostojic Slavica  Stevanovic Galina B Jecmenica Jovana R Maver Ales Sarajlija Adrijan  
Info BALKAN JOURNAL OF MEDICAL GENETICS, (2023), vol. 26 br. 1, str. 63-67
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 
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 
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 
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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