Pronađeno: 21-30 / 99 radova

Autori: Dobricic Valerija S

>> Filter: Samo Article i Review

Naslov Use of clinical exome analysis in rare neurodegenerative disorders in Serbian population: Firs experience (Meeting Abstract)
Autori Brankovic M  Dobricic Valerija S  Svetel Marina V  Peric Stojan Z  Stefanova Elka D  Marjanovic Ana  Petrovic Igor N  Novakovic Ivana V  Kostic Vladimir S 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2019), vol. 27 br. , Suppl. 1, str. 292-292
Ispravka ISI/Web of Science   Elečas   Rang časopisa   Citati: ISI/Web of Science  
Naslov Genomic variants in the FTO gene are associated with sporadic amyotrophic lateral sclerosis in Greek patients (Meeting Abstract)
Autori Mitropoulos Konstantinos  ...  Dobricic Valerija S  Novakovic Ivana V  Kostic Vladimir S  ...  (broj koautora 33) 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2019), vol. 27 br. , Suppl. 1, str. 252-253
Ispravka ISI/Web of Science   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov The pattern of inheritance and genetic status in early onset Alzheimer's disease and frontotemporal dementia (Meeting Abstract)
Autori Mandic-Stojmenovic Gorana B  Stefanova Elka D  Novakovic Ivana V  Dobricic Valerija S  Stojkovic Tanja  Kostic Vladimir K 
Info EUROPEAN JOURNAL OF NEUROLOGY, (2019), vol. 26 br. , Suppl. 1, str. 120-120
Ispravka ISI/Web of Science   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Identification of mutations in PARK2 gene in Serbian patients with Parkinson's disease (Meeting Abstract)
Autori Jankovic Milena Z  Dobricic Valerija S  Kresojevic Nikola D  Markovic Vladana V  Petrovic Igor N  Svetel Marina V  Pekmezovic Tatjana D  Novakovic Ivana V  Kostic Vladimir K 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2018), vol. 26 br. , Suppl. S, str. 410-411
Ispravka ISI/Web of Science   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov C9ORF72 genetic screening in Serbian patients with neurodegenerative disorders (Meeting Abstract)
Autori Marjanovic Ana  Dobricic Valerija S  Marjanovic Ivan V  Brankovic Marija  Jankovic Milena Z  Mandic Gorana B  Stevic Zorica D  Novakovic Ivana V  Stefanova Elka D  Kostic Vladimir K 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2018), vol. 26 br. , Suppl. S, str. 376-376
Ispravka ISI/Web of Science   Elečas   Rang časopisa   Citati: ISI/Web of Science  
Naslov Contribution to the knowledge on the distribution of freshwater sponges - the Danube and Sava rivers case study (Article)
Autori Andjus Stefan P  Nikolic Nadja S  Dobricic Valerija S  Marjanovic Ana  Gacic Zoran M  Brankovic Goran O  Akovic Maja R  Paunovic Momir M 
Info JOURNAL OF LIMNOLOGY, (2018), vol. 77 br. 2, str. 199-208
Projekat Ministry of Education, Science and Technological Development of the Republic of Serbia [176018]; European Union [603629-ENV-2013-6.2.1-GLOBAQUA]; European Commission
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Identification of mutations in the PARK2 gene in Serbian patients with Parkinson's disease (Article)
Autori Jankovic Milena Z  Dobricic Valerija S  Kresojevic Nikola D  Markovic Vladana V  Petrovic Igor N  Svetel Marina V  Pekmezovic Tatjana D  Novakovic Ivana V  Kostic Vladimir K 
Info JOURNAL OF THE NEUROLOGICAL SCIENCES, (2018), vol. 393 br. , str. 27-30
Projekat Serbian Ministry of Science and Technological Development [ON175090, ON175091]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Genomic Variants in the FTO Gene are Associated with Sporadic Amyotrophic Lateral Sclerosis in Greek Patients (Meeting Abstract)
Autori Mitropoulos Konstantinos  ...  Dobricic Valerija S  Novakovic Ivana V  Kostic Vladimir S  ...  (broj koautora 30) 
Info PUBLIC HEALTH GENOMICS, (2018), vol. 21 br. , Suppl. 1, str. 17-17
Ispravka ISI/Web of Science   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
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 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  
Ispis zapisa u formatu:TXT | BibTeX