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Naslov Characterization of 13 Novel Genetic Variants in Genes Associated with Epilepsy: Implications for Targeted Therapeutic Strategies (Article; Early Access)
Autori Andjelkovic Marina Z  Klaassen Kristel M  Skakic Anita G  Marjanovic Irena M  Kravljanac Ruzica M  Djordjevic Maja S  Vucetic-Tadic Biljana  Kecman Bozica  Pavlovic Sonja T  Stojiljkovic Maja M 
Info MOLECULAR DIAGNOSIS & THERAPY, (2024), vol. br. , str. -
Projekat Ministry of Science, Technological Development and Innovations Republic of Serbia [451-03-66/2024-03/200042]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati:
Naslov Reverse Phenotyping after Whole-Exome Sequencing in Children with Developmental Delay/Intellectual Disability-An Exception or a Necessity? (Article)
Autori Ilic Nikola A  Maric Nina  ...  Kravljanac Ruzica M  Cirkovic Jana  Krstic Jovana  Radivojevic Danijela  Cirkovic Sanja S  Ostojic Slavica B  Krasic Stasa D  Paripovic Aleksandra  Vukomanovic Vladislav A  ...  Maric Gorica D  Sarajlija Adrijan 
Info GENES, (2024), vol. 15 br. 6, str. -
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa  
Naslov Severe neurological complications in a child with multisystem inflammatory syndrome in children after asymptomatic COVID-19 (Article)
Autori Kravljanac Ruzica M  Stajic Natasa  Vukomanovic Vladislav A  Petrovic Gordana  Kuzmanovic Milos B 
Info SRPSKI ARHIV ZA CELOKUPNO LEKARSTVO, (2024), vol. 152 br. 3-4, str. 182-185
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa  
Naslov Main features and disease outcome of congenital myotonic dystrophy- experience from a single tertiary center (Article)
Autori Ostojic Slavica B  Kovacevic Gordana S  Meola Giovanni  Pesovic Jovan  Savic-Pavicevic Dusanka Lj  Brkusanin Milos  Kravljanac Ruzica M  Peric Marina  Martic Jelena M  Pejic Katarina  Ristic Snezana  Peric Stojan Z 
Info NEUROMUSCULAR DISORDERS, (2024), vol. 40 br. , str. 16-23
Projekat Ministry of Education, Science and Technological Development of the Republic of Serbia [175083]; Fondazione Malattie Miotoniche-FMM, Milan, Italy
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa  
Naslov "The Red Flags" in Clinical Approach to Acute Ataxia-the Experience in Cohort of 76 Children (Article; Early Access)
Autori Kravljanac Ruzica M  Golubovic Aleksa  Vucetic-Tadic Biljana  Ostojic Slavica B  Cerovic Ivana B  Savkic J 
Info CEREBELLUM, (2023), vol. br. , str. -
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati:
Naslov Acute disseminated encephalomyelitis in children and adolescents-20-year single-center experience in Serbia (Article)
Autori Ostojic Slavica B  Kravljanac Ruzica M  Kovacevic Gordana S  Vucetic-Tadic Biljana  Gazikalovic Slobodan  Sarajlija Adrijan 
Info SRPSKI ARHIV ZA CELOKUPNO LEKARSTVO, (2022), vol. 150 br. 9-10, str. 544-550
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa  
Naslov Acute disseminated encephalomyelitis in children and adolescents-20-year single-center experience in Serbia (Article)
Autori Ostojic Slavica B  Kravljanac Ruzica M  Kovacevic Gordana S  Vucetic-Tadic Biljana  Gazikalovic Slobodan  Sarajlija Adrijan 
Info SRPSKI ARHIV ZA CELOKUPNO LEKARSTVO, (2022), vol. 150 br. 9-10, str. 544-550
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 B  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 Provoked seizures at the onset of progressive disease contribute to diagnosis delay - A tertiary center experience in a cohort of 22 children with CLN2 (Article)
Autori Kravljanac Ruzica M  Vucetic-Tadic Biljana 
Info EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY, (2022), vol. 40 br. , str. 1-4
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Infantile hemiconvulsion-hemiplegia epilepsy syndrome associated with GRIN2A gene mutation (Article)
Autori Kravljanac Ruzica M  Gazikalovic Slobodan  Vucetic-Tadic Biljana 
Info SRPSKI ARHIV ZA CELOKUPNO LEKARSTVO, (2021), vol. 149 br. 7-8, str. 485-488
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
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