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Naslov Phosphorylated neurofilament heavy chain in cerebrospinal fluid and plasma as a Nusinersen treatment response marker in childhood-onset SMA individuals from Serbia (Article)
Autori Brkusanin Milos  Kosac Ana P  Brankovic-Sreckovic Vesna  Jovanovic Kristina  Peric Stojan Z  Karanovic Jelena  Matijasevic-Jokovic Suzana  Garai Nemanja  Pesovic Jovan  Nikolic Dimitrije M  Stevic Zorica D  Brajuskovic Goran N  Milic-Rasic Vedrana M  Savic-Pavicevic Dusanka Lj 
Info FRONTIERS IN NEUROLOGY, (2024), vol. 15 br. , str. -
Projekat Ministry of Science, Technological Development and Innovation of the Republic of Serbia [451-03-66/2024-03/ 200178]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa  
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
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa  
Naslov LTBP4, SPP1, and CD40 Variants: Genetic Modifiers of Duchenne Muscular Dystrophy Analyzed in Serbian Patients (Article)
Autori Kosac Ana P  Pesovic Jovan  Radenkovic Lana  Brkusanin Milos  Radovanovic Nemanja  Djurisic Marina  Radivojevic Danijela  Mladenovic Jelena M  Ostojic Slavica  Kovacevic Gordana S  Kravljanac Ruzica M  Savic-Pavicevic Dusanka Lj  Milic-Rasic Vedrana M 
Info GENES, (2022), vol. 13 br. 8, str. -
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa  
Naslov Frameshift Mutation in Polar Rich Domain (PRD) of PQBP1 Gene Associated with Asymmetric Cerebellar Hemispheres: A Case Report of Renpenning Syndrome (Article)
Autori Aleksic Dejan Z  Borkovic Milan P  Krivacic Jelena  Petrusic Igor P  Milic-Rasic Vedrana M 
Info IRANIAN JOURNAL OF PEDIATRICS, (2021), vol. 31 br. 4, str. -
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Biallelic ADPRHL2 mutations in complex neuropathy affect ADP ribosylation and DNA damage response (Article)
Autori Beijer Danique  Agnew Thomas  Rack Johannes Gregor Matthias  Prokhorova Evgeniia  Deconinck Tine  Ceulemans Berten  Peric Stojan Z  Milic-Rasic Vedrana M  De Jonghe Peter  Ahel Ivan  Baets Jonathan 
Info LIFE SCIENCE ALLIANCE, (2021), vol. 4 br. 11, str. -
Projekat Association Belge contre les Maladies Neuromusculaire (ABMM) -Aide a la Recherche ASBL [2017-2018/05]; EU FP7/2007-2013 [2012-305121]; EU Horizon 2020 program [779257]; Wellcome TrustEuropean Commission [101794, 210634]; Biotechnology and Bi
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
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 ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
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 ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science  
Naslov Analysis of duplications versus deletions in the dystrophin gene in Serbian cohort with dystrophinopathies (Article)
Autori Maksic Jasmina  Dobricic Valerija S  Rasulic Lukas G  Maksimovic Nela S  Brankovic Marija  Milic-Rasic Vedrana M  Rakocevic-Stojanovic Vidosava M  Novakovic Ivana V 
Info VOJNOSANITETSKI PREGLED, (2020), vol. 77 br. 4, str. 387-394
Projekat Serbian Ministry of Education, Science and Technological Development [175083, 175091]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov GCH1 mutations are common in Serbian patients with dystonia-parkinsonism: Challenging previously reported prevalence rates of DOPA-responsive dystonia (Article)
Autori Dobricic Valerija S  Tomic Aleksandra D  Brankovic Vesna  Kresojevic Nikola D  Jankovic Milena Z  Westenberger Ana  Milic-Rasic Vedrana M  Klein Christine  Novakovic Ivana V  Svetel Marina V  Kostic Vladimir S 
Info PARKINSONISM & RELATED DISORDERS, (2017), vol. 45 br. , str. 81-84
Projekat Ministry of Education and Science, Republic of Serbia [ON175090, ON175091]; Hermann and Lilly Schilling Foundation; German Research Foundation (DFG) Research Unit [FOR2488]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov A novel recessive TTN founder variant is a common cause of distal myopathy in the Serbian population (Article)
Autori Peric Stojan Z  Nikodinovic-Glumac Jelena  ...  Savic-Pavicevic Dusanka Lj  ...  Brkusanin Milos  Milenkovic Sanja M  Milic-Rasic Vedrana M  Banko Bojan  Maksimovic Ruzica M  ...  Rakocevic-Stojanovic Vidosava M  (broj koautora 19) 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2017), vol. 25 br. 5, str. 572-581
Projekat Sanofi Genzyme; Ultragenyx Pharmaceutical; LGMD2I Research Fund; Kurt+Peter Foundation; LGMD2D Foundation; Samantha J Brazzo Foundation; Medical Research Council UK [G1002274, 98482]; European Union [305444, 305121]; Ministry of Education, Science and Tec
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
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