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Autori: Radivojevic Danijela

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Naslov Townes-Brocks Syndrome With Consistent Renal Hypodysplasia and Variable Extrarenal Features Across Three Generations of Serbian Family (Article)
Autori Paripovic Aleksandra  Jankovic Aleksandar N  Ilic N  Ostojic Slavica B  Todorovic Sladjana  Radivojevic Danijela  Pejovic B  Naumovic Radomir T  Sarajlija Adrijan 
Info BALKAN JOURNAL OF MEDICAL GENETICS, (2025), vol. 28 br. 2, str. 93-100
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa  
Naslov Neuroblastoma Occurring in Nijmegen Breakage Syndrome (Article)
Autori Djurisic Marina  Sarajlija Adrijan  Radivojevic Danijela  Cirkovic Sanja  Djokic Dragoljub  Djuricic Slavisa M  Samardzija Gordana  Pasic Srdjan S 
Info JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, (2025), vol. 47 br. 1, str. e74-e76
Projekat Great Northern Children's Hospital, Newcastle upon Tyne
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa  
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 Genetic diagnosis of dup15q syndrome in a group of patients from Serbia (Meeting Abstract)
Autori Cupurdija Maja  Miskovic Marijana  Cirkovic Sanja S  Radivojevic Danijela  Ilic Nina  Lalic Tanja  Dobric Bojana  Djurisic Marina 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2024), vol. 32 br. , Suppl. 1, str. 231-232
Ispravka ISI/Web of Science   Elečas   Rang časopisa  
Naslov Prevalence of Variants in DFNB1 Locus in Serbian Patients with Autosomal Recessive Non-Syndromic Hearing Loss (Article)
Autori Dobric Bojana  Radivojevic Danijela  Jecmenica Jovana R  Fanis Pavlos  Neocleous Vassos  Phylactou Leonidas A  Djurisic Marina 
Info GENETIKA-BELGRADE, (2022), vol. 54 br. 1, str. 447-456
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
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 Audiological features in Serbian patients with hearing impairment identified with c.35delG in the GJB2 gene (Article)
Autori Dobric Bojana  Radivojevic Danijela  Jecmenica Jovana R  Neocleous Vassos  Fanis Pavlos  Phylactou Leonidas A  Djurisic Marina 
Info SRPSKI ARHIV ZA CELOKUPNO LEKARSTVO, (2021), vol. 149 br. 11-12, str. 685-690
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Incidence of Genetic Causes of Idiopathic Male Infertility in Serbia - Ten Years' Experience of Single Centre (Article)
Autori Dobric Bojana  Radivojevic Danijela  Lalic Tanja  Miskovic Marijana  Cirkovic Sanja S  Djordjevic Maja S  Djurisic Marina 
Info GENETIKA-BELGRADE, (2019), vol. 51 br. 3, str. 1009-1019
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov First results of genetic testing of non syndromic hearing impairment in patients from Serbia- case report of family with multiple affected members (Meeting Abstract)
Autori Dobric Bojana  Jecmenica Jovana R  Radivojevic Danijela  Djurisic Marina 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2018), vol. 26 br. , Suppl. S, str. 845-845
Ispravka ISI/Web of Science   Elečas   Rang časopisa   Citati: ISI/Web of Science  
Naslov Novel intragenic deletions within the UBE3A gene in two unrelated patients with Angelman syndrome: case report and review of the literature (Review)
Autori Aguilera Cinthia  Vinas-Jornet Marina  Baena Neus  Gabau Elisabeth  Fernandez Concepcion  Capdevila Nuria  Cirkovic Sanja S  Sarajlija Adrijan  Miskovic Marijana  Radivojevic Danijela  Ruiz Anna  Guitart Miriam 
Info BMC MEDICAL GENETICS, (2017), vol. 18 br. , str. -
Projekat Fundacio Parc Tauli- Institut d'Investigacio i Innovacio Parc Tauli I3PT [CIR2015/040]; Asociacion Espanola de Sindrome de Angelman; Instituto de Salud Carlos III [PI16/01411]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
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