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Autori: Milic-Rasic Vedrana M

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Vidi i: Rasic Vedrana M

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 Web of Science   Članak   Elečas   Rang časopisa  
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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 Web of Science   Članak   Elečas   Rang časopisa  
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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 Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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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 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 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 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 Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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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 Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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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 Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov Sphingosine 1-phosphate lyase deficiency causes Charcot-Marie-Tooth neuropathy (Article)
Autori Atkinson Derek Nikodinovic-Glumac Jelena Asselbergh Bob Ermanoska Biljana Blocquel David Steiner Regula Estrada-Cuzcano Alejandro Peeters Kristien Ooms Tinne De Vriendt Els Yang Xiang-Lei Hornemann Thorsten Milic-Rasic Vedrana M Jordanova Albena 
Info NEUROLOGY, (2017), vol. 88 br. 6, str. 533-542
Projekat University of Antwerp [TOP BOF 29069]; Fund for Scientific Research-Flanders (FWO) [G.0543.13, G0D7713N]; Belgian Association against Neuromuscular Disorders (ABMM); NIH [NS 085092]; Fund for Scientific Research-Flanders
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Vidi i: Rasic Vedrana M

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