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Naslov ANO10-Related Spinocerebellar Ataxia: MDSGene Systematic Literature Review and a Romani Case Series (Article)
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. 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  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  
Info ARCHIVES DE PEDIATRIE, (2022), vol. 29 br. 7, str. 480-483
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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  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  
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  Milic-Rasic Vedrana M Brankovic Vesna Kosac Ana P  Vukomanovic Goran V Topalovic Mirko Marinkovic Dejan Mladenovic Jelena M Pavlovic Andrija S  Bijelic Maja Djukic Milan M  Markovic-Denic Ljiljana N  
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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