Results 1-20 of 86
Issue DateTitleAuthor(s)TypeМp-cat.
2024Characterization of 13 Novel Genetic Variants in Genes Associated with Epilepsy: Implications for Targeted Therapeutic StrategiesAnđelković, Marina  ; Klaassen, Kristel  ; Skakić, Anita  ; Marjanović, Irena  ; Kravljanac, Ružica  ; Đorđević, Maja  ; Vučetić-Tadić, Biljana  ; Kecman, Božica; Pavlović, Sonja  ; Stojiljković, Maja  Article
21M21
2024Characterization of 16 novel genetic variants in genes associated with paediatric epilepsy: implications for targeted therapeutic strategiesAnđelković, Marina  ; Klaassen, Kristel  ; Skakić, Anita  ; Marjanović, Irena  ; Kravljanac, Ružica  ; Đorđević, Maja  ; Vučetić Tadić, Biljana  ; Kecman, Božica; Pavlović, Sonja  ; Stojiljković, Maja  Conference Paper
Mp. category will be shown later
2024Schinzel-Giedion syndrome: a rare cause of psychomotor delay and refractory seizuresKovačević, Gordana; Kravljanac, Ružica  ; Vučetić-Tadić, Biljana  ; Ostojić, Slavica; Ryu, Seung WooArticle
Mp. category will be shown later
2024“The Red Flags” in Clinical Approach to Acute Ataxia—the Experience in Cohort of 76 ChildrenKravljanac, Ružica  ; Golubović, Aleksa; Vučetić-Tadić, Biljana  ; Ostojić, Slavica; Cerović, Ivana; Savkić, Jana Article
22M22
2024Reverse Phenotyping after Whole-Exome Sequencing in Children with Developmental Delay/Intellectual Disability-An Exception or a Necessity?Ilić, Nikola A.; Marić, Nina; Maver, Aleš; Armengol, Lluis; Kravljanac, Ružica M.  ; Ćirković, Jana; Krstić, Jovana; Radivojević, Danijela ; Ćirković, Sanja S.; Ostojić, Slavica B.;
Krasić, Staša D.; Paripović, Aleksandra; Vukomanović, Vladislav A.  ; Peterlin, Borut; Marić, Gorica D.  ; Sarajlija, Adrijan  ;
Article
22M22
2024Complications of pneumococcal meningitis in a child with proteus syndrome: A case report and literature reviewOstojić, Slavica; Kravljanac, Ružica  ; Kovačević, Gordana; Vučetić-Tadić, Biljana  ; Kuzmanović, Miloš  ; Prijić, Sergej  ; Gazikalović, Slobodan; Paripović, Aleksandra; Sarajlija, Adrijan  Article
53M53
2024Main features and disease outcome of congenital myotonic dystrophy- experience from a single tertiary centerOstojić, Slavica B.; Kovačević, Gordana S.  ; Meola, Giovanni; Pešović, Jovan  ; Savić-Pavicević, Dušanka Lj.  ; Brkušanin, Miloš  ; Kravljanac, Ružica M.  ; Perić, Marina; Martić, Jelena M.  ; Pejić, Katarina;
Ristić, Snežana; Perić, Stojan Z.  ;
Article
22M22
2024Severe neurological complications in a child with multisystem inflammatory syndrome in children after asymptomatic COVID-19Kravljanac, Ružica  ; Stajić, Nataša; Vukomanović, Vladislav  ; Petrović, Gordana S.; Kuzmanović, Miloš  Article
23M23
2023Subacute sclerosing panencephalitis: Changes in phenotype during the last decadeKravljanac, Ružica  ; Palić, Ilija; Vučetić-Tadić, Biljana  Article
53M53
2022Acute disseminated encephalomyelitis in children and adolescents – 20-year single-center experience in SerbiaOstojić, Slavica; Kravljanac, Ružica  ; Kovačević, Gordana  ; Vučetić-Tadić, Biljana  ; Gazikalović, Slobodan; Sarajlija, Adrijan  Article
23M23
2022 LTBP4, SPP1, and CD40 Variants: Genetic Modifiers of Duchenne Muscular Dystrophy Analyzed in Serbian PatientsKosac, Ana ; Pešović, Jovan  ; Radenković, Lana  ; Brkušanin, Miloš  ; Radovanović, Nemanja  ; Đurišić, Marina; Radivojević, Danijela; Mladenović, Jelena; Ostojić, Slavica; Kovačević, Gordana;
Kravljanac, Ružica  ; Savić-Pavićević, Dušanka  ; Milić-Rašić, Vedrana ;
Article
22M22
2022Very early and atypical presentation of Triple A (Allgrove) syndromeCehić, Maja; Kovačević, Gordana  ; Milenković, Tatjana; Kravljanac, Ružica  ; Todorović, Slađana; Vuković, Rade; Panić-Zarić, Sanja; Mitrović, KatarinaConference Paper
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2022Epilepsy in children with neurocutaneous disorders – a tertiary center experienceKravljanac, Ružica  ; Vučetić-Tadić, Biljana  ; Bedjik, J; Cerović, Ivana; Ostojić, Slavica; Kovačević, Gordana  ; Kravljanac, ĐorđeConference Paper
Mp. category will be shown later
2022Provoked seizures at the onset of progressive disease contribute to diagnosis delay - A tertiary center experience in a cohort of 22 children with CLN2Kravljanac, Ružica  ; Vučetić-Tadić, Biljana  Article
21M21
2022Intracardiac Thrombosis in the Three-Year-Old Boy with Normal Left Ventricle Systolic Function in MIS-C Associated with COVID-19Krasić, Staša; Popović, Saša; Kravljanac, Ružica  ; Prijić, Sergej  ; Vukomanović, Vladislav  Other
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2021The features of initial seizures and a further epilepsy course in a cohort of 22 children with CLN2-A single center experienceKravljanac, Ružica  ; Sims, Katherine; Vucetić-Tadić, Biljana  Conference Paper
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2021Infantile hemiconvulsion-hemiplegia epilepsy syndrome associated with GRIN2A gene mutationKravljanac, Ružica  ; Gazikalović, Slobodan; Vučetić-Tadić, Biljana  Article
23M23
2021Problemi u pedijatriji 2020Kravljanac, Ružica  ; Kuzmanović, Miloš  Monograph
Mp. category will be shown later
2021Super-refractory status epilepticus and pharmacoresistant epilepsy in an infant with hemorrhagic shock and encephalopathy syndromeKravljanac, Ružica  ; Đaković, Marija; Vučetić-Tadić, Biljana  ; Kravljanac, ĐorđeArticle
23M23
2021A case of juvenile CLN1-challenge in diagnosis and epilepsy treatmentKravljanac, Ružica  ; Sims, KatherineArticle
23M23