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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  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
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Naslov Whole exome sequencing in Serbian patients with hereditary spastic paraplegia (Article; Early Access)
Autori Brankovic Marija  Ivanovic Vukan Basta Ivana Z ... Stevic Zorica D Ralic Branislav M Tubic Radoje M ... Markovic Vladana V  Bozovic Ivo Svetel Marina V  Marjanovic Ana  Veselinovic Nikola D Mesaros Sarlota T Jankovic Milena Z  Savic-Pavicevic Dusanka Lj  Jovin Zita B Novakovic Ivana V  ... Peric Stojan Z  
Info NEUROGENETICS, (2024), vol. br. , str. -
Projekat Yonsei University
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Naslov ANO10-Related Spinocerebellar Ataxia: MDSGene Systematic Literature Review and a Romani Case Series (Article; Early Access)
Autori Milovanovic Andona  ...  Stankovic Iva D  Tamas Olivera S Brankovic Marija  Marjanovic Ana  ... Brankovic Vesna Novakovic Ivana V  Petrovic Igor N Svetel Marina V  ... Kostic Vladimir S Dragasevic-Miskovic Natasa T 
Info MOVEMENT DISORDERS, (2024), vol. br. , str. -
Projekat International Parkinson and Movement Disorder Society; The Parkinson's Foundation; University of Luebeck; Projekt DEAL
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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; 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 MULTIPLE SCLEROSIS AND RELATED DISORDERS, (2024), vol. 82 br. , str. -
Projekat Ministry of Science, Technological Development and Innovations of the Republic of Serbia [200110]
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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]
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Naslov Yield of GATOR1 gene sequencing in a Serbian focal epilepsy cohort (Meeting Abstract)
Autori Kovacevic Masa  Jankovic M Brankovic Marija  Milicevic Ognjen S Novakovic Ivana V  Sokic Dragoslav V Ristic Aleksandar J  Berisavac I Vojvodic Nikola M 
Info EPILEPSIA, (2023), vol. 64 br. , Suppl. 2, str. 386-386
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Naslov Clinical and Genetic Features of Huntington's Disease Patients From Republic of Serbia: A Single-Center Experience (Letter)
Autori Kresojevic Nikola D  Perovic Ivana Stankovic Iva D  Tomic Aleksandra D Jecmenica-Lukic Milica V  Markovic Vladana V  Stojkovic Tanja  Mandic Gorana B Jankovic Milena Z  Marjanovic Ana  Brankovic Marija  Novakovic Ivana V  Petrovic Igor N Dragasevic Natasa T Stefanova Elka D  Svetel Marina V  Kostic Vladimir K 
Info JOURNAL OF MOVEMENT DISORDERS, (2023), vol. 16 br. 3, str. 333-335
Projekat Ministry of Education and Science of the Republic of Serbia [175090]
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Naslov Whole exome sequencing in Serbian patients with hereditary spastic paraplegia (Meeting Abstract)
Autori Ivanovic Vukan Brankovic Marija  Bozovic Ivo Stevic Zorica D Basta Ivana Z Markovic Vladana V  Svetel Marina V  Tubic Radoje M Marjanovic Ana  Veselinovic Nikola D Mesaros Sarlota T Jankovic Milena Z  Rakocevic-Stojanovic Vidosava M Savic-Pavicevic Dusanka Lj  Novakovic Ivana V  Peric Stojan Z  
Info EUROPEAN JOURNAL OF NEUROLOGY, (2023), vol. 30 br. , Suppl. 1, str. 260-260
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Naslov Motor neuron involvement in facial muscles as characteristic of ANO10 mutation (Meeting Abstract)
Autori Dragasevic-Miskovic Natasa T Milovanovic Andona  Stankovic I Marjanovic Ana  Brankovic Marija  Dobricic Valerija S Petrovic Igor N Svetel Marina V  Novakovic Ivana V  Kostic V 
Info EUROPEAN JOURNAL OF NEUROLOGY, (2023), vol. 30 br. , Suppl. 1, str. 234-234
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Naslov The importance of direct genetic testing for determining female carriers of the mutation in dystrophinopathies (Article)
Autori Maksic Jasmina  Maksimovic Nela S  Rasulic Lukas G  Milankov Olgica Marjanovic Ana  Cvetkovic Dragana D Rakocevic-Stojanovic Vidosava M Novakovic Ivana V  
Info VOJNOSANITETSKI PREGLED, (2023), vol. 80 br. 3, str. 201-207
Projekat Serbian Ministry of Education, Science, and Technological Development [ON175091]; [ON175083]
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