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Autori: Milic-Rasic Vedrana M

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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 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  
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 ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Analysis of PMP22 duplication and deletion using a panel of six dinucleotide tandem repeats (Article)
Autori Gagic Milica  Keckarevic-Markovic Milica  Kecmanovic Miljana  Keckarevic Dusan P  Mladenovic Jelena M  Dackovic Jelena  Milic-Rasic Vedrana M  Romac Stanka P 
Info CLINICAL CHEMISTRY AND LABORATORY MEDICINE, (2016), vol. 54 br. 5, str. 773-780
Projekat Serbian Ministry of Education and Science [173016]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Joint effect of the SMN2 and SERF1A genes on childhood-onset types of spinal muscular atrophy in Serbian patients (Article)
Autori Brkusanin Milos  Kosac Ana P  Jovanovic Vladimir M  Pesovic Jovan  Brajuskovic Goran N  Dimitrijevic Nikola  Todorovic Slobodanka  Romac Stanka P  Milic-Rasic Vedrana M  Savic-Pavicevic Dusanka Lj 
Info JOURNAL OF HUMAN GENETICS, (2015), vol. 60 br. 11, str. 723-728
Projekat Ministry of Education, Science and Technological Development, Republic of Serbia [173016]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science  
Naslov The TREAT-NMD DMD Global Database: Analysis of More than 7,000 Duchenne Muscular Dystrophy Mutations (Article)
Autori Bladen Catherine L  ...  Monges Soledad  Milic-Rasic Vedrana M  Vojinovic Dina  ...  (broj koautora 61) 
Info HUMAN MUTATION, (2015), vol. 36 br. 4, str. 395-402
Projekat TREAT-NMD [FP6LSHM-CT-2006-036825, 20123307 UNEW_FY2013, AFM 16104]; European Union [305444, 305121]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Intellectual Ability in the Duchenne Muscular Dystrophy and Dystrophin Gene Mutation Location (Article)
Autori Milic-Rasic Vedrana M  Vojinovic Dina  Pesovic Jovan  Mijalkovic G  Lukic V  Mladenovic Jelena M  Kosac Ana P  Novakovic Ivana V  Maksimovic Nela S  Romac Stanka P  Todorovic Slobodanka  Pavicevic Savic D 
Info BALKAN JOURNAL OF MEDICAL GENETICS, (2014), vol. 17 br. 2, str. 25-35
Projekat Ministry of Education, Science and Technological Development, Republic of Serbia [173016, 17508]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Truncating and Missense Mutations in IGHMBP2 Cause Charcot-Marie Tooth Disease Type 2 (Article)
Autori Cottenie Ellen  ...  Milic-Rasic Vedrana M  ...  Nikolic Milos MI  ...  (broj koautora 40) 
Info AMERICAN JOURNAL OF HUMAN GENETICS, (2014), vol. 95 br. 5, str. 590-601
Projekat Medical Research Council (MRC UK); Wellcome Trust; Brain Research Trust (BRT); French Muscular Dystrophy Association (AFM); MRC Neuromuscular Diseases Centre grant [G0601943]; National Institutes of Neurological Diseases and Stroke and office of Rare Dise
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov ANO10 mutations cause ataxia and coenzyme Q(10) deficiency (Article)
Autori Balreira Andrea  ...  Milic-Rasic Vedrana M  ...  (broj koautora 17) 
Info JOURNAL OF NEUROLOGY, (2014), vol. 261 br. 11, str. 2192-2198
Projekat Medical Research Council (UK) [G1000848]; European Research Council [309548]; UK Parkinson's Disease Society; UK NIHR Biomedical Research Centre for Ageing and Age-related disease award; Wellcome Trust Centre for Mitochondrial Research [096919Z/11/Z]; UK
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Mapping the differences in care for 5,000 Spinal Muscular Atrophy patients, a survey of 24 national registries in North America, Australasia and Europe (Article)
Autori Bladen Catherine L  ...  Milic-Rasic Vedrana M  Kosac Ana P  ...  (broj koautora 62) 
Info JOURNAL OF NEUROLOGY, (2014), vol. 261 br. 1, str. 152-163
Projekat AFM [16104]; Jennifer Trust for Spinal Muscular Atrophy; EU [036825, VUL 317/2007]; German Ministry of Education and Research [01GM0302]; Italian Association of Patients with Neuromuscular Diseases (Italy); Neuromuscular Research Foundation Trust (New Zea
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
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