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Autori: Savic-Pavicevic Dusanka Lj

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Naslov WDR45 mutations may cause a MECP2 mutation-negative Rett syndrome phenotype (Editorial Material)
Autori Kulikovskaja Leonora Sarajlija Adrijan  Savic-Pavicevic Dusanka Lj  Dobricic Valerija S Klein Christine Westenberger Ana 
Info NEUROLOGY-GENETICS, (2018), vol. 4 br. 2, str. -
Projekat Hermann and Lilly Schilling Foundation; Land Schleswig-Holstein within the funding programme Open Access Publikationsfonds
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov NOS3 gene variants and male infertility: Association of 4a/4b with oligoasthenozoospermia (Article)
Autori Vucic Nemanja L Nikolic Zorana Z Vukotic Vinka D Tomovic Sasa M Vukovic Ivan I Kanazir Selma D  Savic-Pavicevic Dusanka Lj  Brajuskovic Goran N  
Info ANDROLOGIA, (2018), vol. 50 br. 1, str. -
Projekat Ministry of Education, Science and Technological Development of the Republic of Serbia [173016]
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov Metabolic syndrome in myotonic dystrophy type 2 (Meeting Abstract)
Autori Vujnic Milorad Calic Z Bucma Tatjana Peric Stojan Z  Pesovic Jovan Basta Ivana Z Nikolic Aleksandra L  Kacar Aleksandra S Savic-Pavicevic Dusanka Lj  Rakocevic-Stojanovic Vidosava M 
Info JOURNAL OF THE NEUROLOGICAL SCIENCES, (2017), vol. 381 br. , Suppl. S, str. 828-828
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science  
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Naslov Molecular genetic and clinical characterization of myotonic dystrophy type 1 patients carrying variant repeats within DMPK expansions (Article)
Autori Pesovic Jovan Peric Stojan Z  Brkusanin Milos Brajuskovic Goran N  Rakocevic-Stojanovic Vidosava M Savic-Pavicevic Dusanka Lj  
Info NEUROGENETICS, (2017), vol. 18 br. 4, str. 207-218
Projekat Ministry of Education, Science and Technological Development, Republic of Serbia [173016, 175083]
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov Genetic testing of individuals with pre-senile cataract identifies patients with myotonic dystrophy type 2 (Letter)
Autori Rakocevic-Stojanovic Vidosava M Peric Stojan Z  Pesovic Jovan Sencanic Ivan Bozic Marija M  Svikovic Sasa Brkusanin Milos Savic-Pavicevic Dusanka Lj  
Info EUROPEAN JOURNAL OF NEUROLOGY, (2017), vol. 24 br. 11, str. E79-E80
Projekat Ministry of Education, Science and Technological Development, Republic of Serbia [175083, 173016]
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov Magnetic resonance imaging of leg muscles in patients with myotonic dystrophies (Article)
Autori Peric Stojan Z  Maksimovic Ruzica M Banko Bojan Djurdjic Milica Bjelica Bogdan Bozovic Ivo Balcik Yunus Pesovic Jovan Savic-Pavicevic Dusanka Lj  Rakocevic-Stojanovic Vidosava M 
Info JOURNAL OF NEUROLOGY, (2017), vol. 264 br. 9, str. 1899-1908
Projekat Ministry of Education, Science and Technological Development of Serbia [175083]
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov Myotonic dystrophy type 2-data from the Serbian Registry (Meeting Abstract)
Autori Peric Stojan Z  Pesovic Jovan Basta Ivana Z Kacar Aleksandra S Nikolic Aleksandra L  Peric Marina Marjanovic Ivan V Stevic Zorica D Lavrnic Dragana V Savic-Pavicevic Dusanka Lj  Rakocevic-Stojanovic Vidosava M 
Info EUROPEAN JOURNAL OF NEUROLOGY, (2017), vol. 24 br. , Suppl. 1, str. 582-582
Ispravka Web of Science   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov Novel GNB1 mutations disrupt assembly and function of G protein heterotrimers and cause global developmental delay in humans (Article)
Autori Lohmann Katja ... Dobricic Valerija S ... Savic-Pavicevic Dusanka Lj  ... (broj koautora 18) 
Info HUMAN MOLECULAR GENETICS, (2017), vol. 26 br. 6, str. 1078-1086
Projekat NIH [NS081282, HL105550]; German Ministry of Education and Research (BMBF, DYSTRACT consortium) [01GM1514B]; Ministry of Education, Science and Technological Development, Republic of Serbia [173016, 175090]; Hermann and Lilly Schilling Foundation
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov Effect of childhood general traumas on suicide attempt depends on TPH2 and ADARB1 variants in psychiatric patients (Article)
Autori Karanovic Jelena  Ivkovic Maja Jovanovic Vladimir M  Svikovic Sasa Pantovic-Stefanovic Maja M  Brkusanin Milos Damjanovic Aleksandar G Brajuskovic Goran N  Savic-Pavicevic Dusanka Lj  
Info JOURNAL OF NEURAL TRANSMISSION, (2017), vol. 124 br. 5, str. 621-629
Projekat Ministry of Education, Science and Technological Development, Republic of Serbia [173016]
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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Vidi i: Savic Dusanka Lj

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