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Autori: Sarajlija Adrijan

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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
Ispravka ISI/Web of Science   Elečas   Rang časopisa  
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
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 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 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
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa  
Naslov Ambiguous Genitalia and Lissencephaly in a 46,xy Neonate with a Novel Variant of Aristaless Gene (Article)
Autori Basa Mihail I  Vukovic Rade M  Sarajlija Adrijan  Milenkovic Tatjana  Djordjevic M  Vucetic Biljana  Martic Jelena M 
Info ACTA ENDOCRINOLOGICA-BUCHAREST, (2021), vol. 17 br. 3, str. -
Ispravka ISI/Web of Science   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Clinical and genetic characteristics of patients with congenital hyperinsulinism in 21 non-consanguineous families from Serbia (Article)
Autori Raicevic Maja  Milenkovic Tatjana  Hussain Khalid  Djordjevic Maja S  Martic Jelena M  Todorovic Sladjana  Mitrovic Katarina  Sarajlija Adrijan  Vukovic Rade M 
Info EUROPEAN JOURNAL OF PEDIATRICS, (2021), vol. 180 br. 9, str. 2815-2821
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Impact of genotype on neutropenia in a large cohort of Serbian patients with glycogen storage disease type Ib (Article)
Autori Sarajlija Adrijan  Djordjevic Maja S  Kecman Bozica  Skakic Anita G  Pavlovic Sonja T  Pasic Srdjan S  Stojiljkovic Maja M 
Info EUROPEAN JOURNAL OF MEDICAL GENETICS, (2020), vol. 63 br. 3, str. -
Projekat Ministry of Education, Science and Technological Development, Republic of Serbia [III41004]; European Commission Joint Research Centre [EU-FP7-REGPOT-316088]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Evaluation of dietary treatment and amino acid supplementation in organic acidurias and urea-cycle disorders: On the basis of information from a European multicenter registry (Article; Proceedings Paper)
Autori Molema Femke  ...  Djordjevic Maja S  Sarajlija Adrijan  ...  (broj koautora 68) 
Info JOURNAL OF INHERITED METABOLIC DISEASE, (2019), vol. 42 br. 6, str. 1162-1175
Projekat Metakids; Erasmus University Medical Center; European Union (EU) [2010 12 01]; Kindness-for-Kids Foundation (Munich, Germany); Dietmar Hopp Foundation (St. Leon-Rot, Germany)
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Decreased plasma L-arginine levels in organic acidurias (MMA and PA) and decreased plasma branched-chain amino acid levels in urea cycle disorders as a potential cause of growth retardation: Options for treatment (Article)
Autori Molema Femke  ...  Djordjevic Maja S  Sarajlija Adrijan  ...  (broj koautora 67) 
Info MOLECULAR GENETICS AND METABOLISM, (2019), vol. 126 br. 4, str. 397-405
Projekat Metakids and Erasmus University Medical Center; European Union within the framework of the Health Programme [2010 12 01]; Kindness-for-Kids Foundation (Munich, Germany); Dietmar Hopp Foundation (St. Leon-Rot, Germany); EU
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
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