Browsing by Author Duma, Filip


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PreviewTitleAuthor(s)Issue DateType
Autistic spectrum disorder-neuropediatric approach and treatmentAngelkova N; Zorcec, T ; Dukovska V; Duma, F ; Sabolic V2017Proceeding article
CASE REPORT OF DOUBLE HETEROZYGOUS PATIENTC WITH SPINAL MUSCULAR ATROPHYNonkulovski, Danilo ; Duma, Filip ; Muaremoska-Kanzoska, Lejla; Kirovski, Ilija ; Sofijanova, Aspazija ; Zhivkovska, Liljana; Dukovska, Valentina2023Article
Children with special needs review of public information at www as a parental guidance in choosing learning resourcesDuma, Filip ; Zorcec, Tatjana ; Angelkova, Natalija; Bojadzeva, Sonja2018Proceeding article
COMPOUND HETEROZYGOTE REASON FOR JUVENILE FORM OF TAY-SACHIS DISEASE -CASE REPORTNonkulovski, Danilo ; Duma, Filip ; Dicoska, Mateja; Kirovski, Ilija ; Maneva Kuzeska, Konstandina; Muaremoska-Kanzoska, Lejla2022Article
Early onset of complex seizures as a first sign of 16p11.2 deletion syndromeShukarova Angelovska, Elena ; Anastasovska, Violeta ; Duma, Filip ; Muaremovska, Ljelja; Nestoroska, Dragica; Ilieva, Gordana; Pesevska, Milica; Velkov, Milan6-Jun-2020Proceeding article
EPILEPSY WITH HETEROZYGOUS ALDH7A1 AND SLC6A1 MUTATIONSAlili Ademi, Learta; Duma, Filip ; Ademi, Blerim; Muaremoska Kanzoska, Lejla; Nonkulovski, Danilo 2020Article
GANGLIOMA ASSOCIATED WITH FOCAL EPILEPSYDanilo Nonkulovski ; Filip Duma ; Lejla Muaremoska Kanzoska; Learta Adili Ademi; Matilda Stojanovska; Maja Tankoska; Julijana Georgievska; Ivona Petkovska Ivanovska; Boro Ilievski 2020Article
GENETIC TESTING ESSENTIAL IN EARLY DIAGNOSIS AND TREATMENT IN TUBEROUS SCLEROSIS COMPLEXNonkulovski Danilo ; Duma Filip ; Muaremoska Kanzoska Lejla; Alili Ademi Learta; Cilevska Mladenovska Sanja; Cilevska Sandra; Serafimova Emilija; Kirovski Ilija ; Pandovska Bisera2021Article
Identification, characteristics and early treatment of autism spectrum disorder in pediatric populationZorcec, T ; Sofijanova, A ; Duma, F ; Angelkova, N2014Proceeding article
Importance of 6 minute walk test in diagnostics of rare metabolic myophaty a case reportNatalija Angelkova; Elena Shukarova Angelkova; Mirjana Kocova; Filip Duma ; Vesna Sabolic; Hristina Mandzukovska Dec-2017Article
IMPORTANCE OF 6-MINUTE WALK TEST IN DIAGNOSTICS OF RARE METABOLIC MYOPATHY - A CASE REPORT OF CARNITINE PALMITOYLTRANSFERASE II DEFICIENCYAngelkova Natalija; Shukarova Angelovska, Elena ; Kocova Mirjana ; Duma, Filip ; Sabolich Vesna; Mandjukovska HristinaDec-2017Article
Late diagnosis of phenylketonuria-time for changesNatalija Angelkova; Vesna Sabolic; Elena Sukarova Angelkovska ; Tatjana Zorchec ; Elena Kochova; Filip Duma 2015Proceeding article
Myopathic form of carnitine palmitoyltransferase II deficiency – Case reportAngelkova, N.; Sukarova-Angelovska, E.; Kocova, M. ; Duma, F. ; Sabolic, V.Jun-2017Proceeding article
POST COVID-19 NEUROLOGICAL SYNDROME (PCNS) IN AN 11 YEARS OLD BOY,A CASE REPORTLearta Alili Ademi; Filip Duma ; Aspazija Sofijanova ; Sonja Bojadjieva ; Blerim Ademi; Lejla Muaremoska Kanzoska; Danilo Nonkulovski ; Katerina Abrasheva; Vesna Jovicic Fidanovska2021Article
Psychological characteristics and treatment of children with tension type headacheZorcec, T ; Duma, F ; Angelkova, N2012Proceeding article
Special needs children: from exclusion to inclusionZorcec, Tatjana ; Duma, Filip 2018Proceeding article
Tic disorder in the pediatric populationZorcec, T ; Duma, F ; Angelkova N2017Article
West Nile EncephalitisDuma, F ; Sofijanova, A ; Bojnovska, T; Grozdanovski, K ; Zorcec, Tatjana ; Saboliц V; Lekovska, O; Angelkovska, N; Dimovska, K; Andonovski, A; Spirkoska, M2012Article
ВИСОКОРИЗИЧНИ НОВОРОДЕНИ И ПЕРВАЗИВНИ РАЗВОЈНИ НАРУШУВАЊАDukovska Valentina; Duma, Filip ; Angelkova Natalija; Avramovska Vesna; Zorcec, Tatjana ; Sofijanova, Aspazija ; Bojadzieva, Sonja ; Popovska, Ana ; Spasovska Anastazija2017Article
Превенција, рана детекција, и лекување на развојни проблеми во детската возраст во склоп на перинаталниот проект-основни препоставкиDuma, F ; Kuturec M; Sabolic-Avramovska V; Lekovska O; Pop-Jordanova N; Zorcec, Tatjana 2001Article