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Autori: Sarajlija Adrijan

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Naslov Noonan Syndrome: Relation of Genotype to Cardiovascular Phenotype-A Multi-Center Retrospective Study (Article)
Autori Ilic Nikola A  Krasic Stasa D  Maric Nina  Gasic Vladimir V  Krstic Jovana  Cvetkovic Dimitrije  Miljkovic Vesna  Zec Boris  Maver Ales  Vukomanovic Vladislav A  Sarajlija Adrijan 
Info GENES, (2024), vol. 15 br. 11, str. -
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Naslov Treatment of RAF1-Related Biventricular Hypertrophy and Double Chamber Right Ventricle by MEK Inhibition Using Trametinib (Letter; Early Access)
Autori Krasic Stasa D  Djuric Ivana  Ilic Nikola A  Sarajlija Adrijan  Nesic Dejan M  Vukomanovic Vladislav A 
Info INDIAN JOURNAL OF PEDIATRICS, (2024), vol. br. , str. -
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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. -
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Naslov Expanding the Phenotypic Spectrum: Chronic Kidney Disease in a Patient with Combined Oxidative Phosphorylation Defect 21 (Article)
Autori Paripovic Aleksandra  Maver Ales  Stajic Natasa  Putnik Jovana  Ostojic Slavica B  Alimpic Biljana  Ilic Nina  Sarajlija Adrijan 
Info BALKAN JOURNAL OF MEDICAL GENETICS, (2023), vol. 26 br. 2, str. 59-64
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Naslov Age-specific causes of upper gastrointestinal bleeding in children (Review)
Autori Kocic Marija  Rasic Petar  Marusic Vuk P  Prokic Dragan  Savic Djordje  Milickovic Maja  Kitic Ivana  Mijovic Tanja  Sarajlija Adrijan 
Info WORLD JOURNAL OF GASTROENTEROLOGY, (2023), vol. 29 br. 47, str. -
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Naslov Three case reports of patients with rare copy number variations in the recurrent 2q11.1-q11.2 region (Meeting Abstract)
Autori Perovic Dijana  Maksimovic Nela S  Damnjanovic Tatjana M  Djuranovic Ana S  Sarajlija Adrijan  Mijovic Marija 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2023), vol. 31 br. , Suppl. 1, str. 267-268
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Naslov Sensorineural Hearing Loss in a Child with Succinic Semialdehyde Dehydrogenase Deficiency (Article)
Autori Parezanovic M  Ilic Nina  Ostojic Slavica B  Stevanovic Galina B  Jecmenica Jovana R  Maver Ales  Sarajlija Adrijan 
Info BALKAN JOURNAL OF MEDICAL GENETICS, (2023), vol. 26 br. 1, str. 63-67
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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
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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
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Naslov A Novel Variant in the LIPA Gene Associated with Distinct Phenotype (Article)
Autori Sarajlija Adrijan  Armengol L  Maver Ales  Kitic Ivana  Prokic Dragan  Cehic Maja  Djuricic MS  Peterlin Borut 
Info BALKAN JOURNAL OF MEDICAL GENETICS, (2022), vol. 25 br. 1, str. 93-99
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