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Autori: Maver Ales

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Naslov Discovery of PHB1 as a Novel Candidate Gene in Dominant Optic Atrophy (Article; Early Access)
Autori Volk Marija  Maver Ales  Vidmar Martina Jarc  Trost Nusa  Visnjar Tanja  Fakin Ana  Kovac Lea  Habjan Maja Sustar  Malinar Lucija  Petrovic Pajic Sanja MI  Jerman Urska Dragin  Romih Rok  Hawlina Marko  Peterlin Borut 
Info CLINICAL GENETICS, (2026), vol. br. , str. -
Projekat Slovenian Research Agency [P3-0326, P3-0333]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati:
Naslov The role of DNA mismatch repair mutS/mutL homolog genes in spermatogenesis and male infertility: a systematic review and cohort study (Review)
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  Buretic-Tomljanovic Alena  Peterlin Borut 
Info REPRODUCTIVE BIOLOGY AND ENDOCRINOLOGY, (2025), vol. 23 br. 1, str. -
Projekat Slovenian Research and Innovation Agency [P3-0326]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa  
Naslov Genetic Testing for Monogenic Forms of Male Infertility Contributes to the Clinical Diagnosis of Men with Severe Idiopathic Male Infertility (Article)
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. 43 br. 4, str. 908-917
Projekat Slovenian Research and Innovation Agency [P3-0326]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science  
Naslov Increased burden of rare variants in GWAS associated genes in familial multiple sclerosis (Article)
Autori Turk Aleksander  Maver Ales  Juvan Peter  Drulovic Jelena S  Mesaros Sarlota T  Novakovic Ivana V  Starcevic-Cizmarevic Nada  Ristic Smiljana  Stankovic-Matic Ivana  Peterlin Borut 
Info SCIENTIFIC REPORTS, (2025), vol. 15 br. 1, str. -
Projekat Slovenian Research Agency [P3-0326, P4-0220]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa  
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 Noonan Syndrome: Relation of Genotype to Cardiovascular Phenotype-A Multi-Center Retrospective Study (Article)
Autori Ilic Nikola A  Krasic Stasa D  Maric Nina  Gasic Vladimir V  Krstic Jovana  Cvetkovic Dimitrije  Miljkovic Vesna  Zec Boris  Maver Ales  Vukomanovic Vladislav A  Sarajlija Adrijan 
Info GENES, (2024), vol. 15 br. 11, str. -
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa  
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 B  Alimpic Biljana  Ilic Nina  Sarajlija Adrijan 
Info BALKAN JOURNAL OF MEDICAL GENETICS, (2023), vol. 26 br. 2, str. 59-64
Ispravka ISI/Web of Science   Članak   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  
Naslov Sensorineural Hearing Loss in a Child with Succinic Semialdehyde Dehydrogenase Deficiency (Article)
Autori Parezanovic M  Ilic Nina  Ostojic Slavica B  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 ISI/Web of Science   Članak   Elečas   Rang časopisa  
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