Autori: Brankovic Vesna
| 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
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| Info | MOVEMENT DISORDERS, (2024), vol. br. , str. - |
| Projekat | International Parkinson and Movement Disorder Society; The Parkinson's Foundation; University of Luebeck; Projekt DEAL |
| Ispravka | Web of Science Članak Elečas Rang časopisa Citati: |
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| Naslov | Serum leptin levels in children and adolescents with spinal muscular atrophy types 2 and 3 (Article) |
| Autori | Djordjevic Stefan A Milic-Rasic Vedrana M Brankovic Vesna Kosac Ana P Dejanovic-Djordjevic Ivana Bijelic Maja Dimkic-Tomic Tijana J Markovic-Denic Ljiljana N Kovacevic Smiljka Petrovic Hristina Vitorovic S Dobric Z Zdravkovic Vera M
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| Info | ARCHIVES DE PEDIATRIE, (2022), vol. 29 br. 7, str. 480-483 |
| Ispravka | Web of Science Članak Elečas Rang časopisa |
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| Naslov | De Novo and Dominantly Inherited SPTAN1 Mutations Cause Spastic Paraplegia and Cerebellar Ataxia (Article) |
| Autori | Van de Vondel Liedewei ... Brankovic Vesna ... (broj koautora 38) |
| Info | MOVEMENT DISORDERS, (2022), vol. 37 br. 6, str. 1175-1186 |
| Projekat | European Reference Network for Rare Neuromuscular Diseases (ERN EURO-NMD) [870177]; EJPRD PREPARE Consortium; EJPRD PROSPAX consortium (EJP RD COFUND-EJP) [825575]; SPATAX network; TreatHSP network; European Reference Network for Rare Neurological Disease |
| Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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| Naslov | Refining the mutational spectrum and gene-phenotype correlates in pontocerebellar hypoplasia: results of a multicentric study (Article) |
| Autori | Nuovo Sara ... Brankovic Vesna ... (broj koautora 35) |
| Info | JOURNAL OF MEDICAL GENETICS, (2022), vol. 59 br. 4, str. 399-409 |
| Projekat | Ministry of Health [NET-2013-02356160, RC2018-2019-2020]; European Research Council (ERC Starting Grant)European Research Council (ERC) [260888]; Italian Ministry of University and Research (Progetto Dipartimenti di Eccellenza); Pierfranco and Luisa Maria |
| Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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| Naslov | A novel KCNA2 variant in a patient with cerebellar ataxia and epilepsy: functional characterization and sensitivity to 4-aminopyridine (Meeting Abstract) |
| Autori | Imbrici Paola Blunck Rikard Conte Elena Dinoi Giorgia Liantonio Antonella Brankovic Vesna Zanni Ginevra |
| Info | EPILEPSIA, (2021), vol. 62 br. , Suppl. 3, str. 109-109 |
| Ispravka | Web of Science Elečas Rang časopisa Citati: Web of Science Scopus |
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| Naslov | A Novel KCNA2 Variant in a Patient with Non-Progressive Congenital Ataxia and Epilepsy: Functional Characterization and Sensitivity to 4-Aminopyridine (Article) |
| Autori | Imbrici Paola Conte Elena Blunck Rikard Stregapede Fabrizia Liantonio Antonella Tosi Michele D'Adamo Maria Cristina De Luca Annamaria Brankovic Vesna Zanni Ginevra |
| Info | INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, (2021), vol. 22 br. 18, str. - |
| Projekat | Fondi Ateneo Universita degli Studi di Bari "Aldo Moro" |
| Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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| Naslov | Heterozygous KIF1A variants underlie a wide spectrum of neurodevelopmental and neurodegenerative disorders (Article) |
| Autori | Nicita Francesco ... Brankovic Vesna ... (broj koautora 25) |
| Info | JOURNAL OF MEDICAL GENETICS, (2021), vol. 58 br. 7, str. 475-483 |
| Projekat | Italian Ministry of HealthMinistry of Health, Italy [NET-2013-02356160]; European Research Council (ERC)European Research Council (ERC)European Commission [260888]; Italian Ministry of University and Research (Progetto Dipartimenti di Eccellenza to Dept. |
| Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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| Naslov | A novel de novo pathogenic variant in Kv1.2 potassium channel in a patient with cerebellar ataxia and epilepsy (Meeting Abstract) |
| Autori | Zanni Ginevra Blunck Rikard Conte Elena Brankovic Vesna Liantonio Antonella Imbrici Paola |
| Info | EUROPEAN JOURNAL OF CLINICAL INVESTIGATION, (2021), vol. 51 br. , Suppl. 1, str. 158-158 |
| Ispravka | Web of Science Elečas Rang časopisa Citati: Web of Science |
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| Naslov | Glucose and lipid metabolism disorders in children and adolescents with spinal muscular atrophy types 2 and 3 (Article) |
| Autori | Djordjevic Stefan A Milic-Rasic Vedrana M Brankovic Vesna Kosac Ana P Dejanovic-Djordjevic Ivana Markovic-Denic Ljiljana N Djuricic Goran J Milcanovic Natasa Kovacevic Smiljka Petrovic Hristina Djukic Milan M Zdravkovic Vera M
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| Info | NEUROMUSCULAR DISORDERS, (2021), vol. 31 br. 4, str. 291-299 |
| Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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| Naslov | Novel unconventional variants expand the allelic spectrum of OPHN1 gene (Article) |
| Autori | Nuovo Sara Brankovic Vesna Caputi Caterina Casella Antonella Nigro Vincenzo Leuzzi Vincenzo Valente Enza Maria |
| Info | AMERICAN JOURNAL OF MEDICAL GENETICS PART A, (2021), vol. 185 br. 5, str. 1575-1581 |
| Projekat | Fondazione Pierfranco e Luisa Mariani (PADAPORT project); Fondazione TelethonFondazione TelethonEuropean Commission [GP15001]; H2020 European Research Council (ERC)European Research Council (ERC) [260888]; Ministero della SaluteMinistry of Health, Italy; |
| Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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