Autori: Brankovic Vesna
Naslov | ANO10-Related Spinocerebellar Ataxia: MDSGene Systematic Literature Review and a Romani Case Series (Article) |
Autori | Milovanovic Andona ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
Info | MOVEMENT DISORDERS, (2024), vol. 39 br. 5, str. 887-892 |
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 ![]() ![]() ![]() ![]() |
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 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 | Glucose and lipid metabolism disorders in children and adolescents with spinal muscular atrophy types 2 and 3 (Article) |
Autori | Djordjevic Stefan A ![]() ![]() ![]() ![]() ![]() ![]() |
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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Naslov | Cardiac findings in pediatric patients with spinal muscular atrophy types 2 and 3 (Article) |
Autori | Djordjevic Stefan A ![]() ![]() ![]() ![]() ![]() |
Info | MUSCLE & NERVE, (2021), vol. 63 br. 1, str. 75-83 |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science |
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Naslov | Cardiac phenotype in ATP1A3-related syndromes A multicenter cohort study (Article) |
Autori | Balestrini Simona ... Brankovic Vesna ... Potic Ana D ... (broj koautora 54) |
Info | NEUROLOGY, (2020), vol. 95 br. 21, str. E2866-E2879 |
Projekat | Epilepsy Society, UK; National Institute for Health Research Biomedical Research Centres funding scheme; Muir Maxwell Trust; National Institute of Neurological Disorders and Stroke [R01NS058949]; National Institute for Health Research Biomedical Centre at Great Ormond Street Hospital for Children NHS Foundation Trust; University College London; DFG-Grant [TR-128]; Duke Institute of Brain Sciences, Duke Research and discretionary funds; National Health and Medical Research Council of Australia; National Heart, Lung, and Blood Institute grant [F30 HL131217]; British Heart Foundation [RG/15/15/31742]; AHC UK; Max's Foundation (via the Great Ormond Street Hospital Children's Charity); MRC [MR/T024062/1] Funding Source: UKRI |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science |
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