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Autori: Sarajlija Adrijan

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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 M  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  
Naslov Transatlantic combined and comparative data analysis of 1095 patients with urea cycle disordersA successful strategy for clinical research of rare diseases (Article)
Autori Posset Roland  ...  Sarajlija Adrijan  ...  (broj koautora 107) 
Info JOURNAL OF INHERITED METABOLIC DISEASE, (2019), vol. 42 br. 1, str. 93-106
Projekat University of Zurich; Kettering Foundation; Kettering Fund
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa  
Naslov Genetic characterization of GSD I in Serbian population revealed unexpectedly high incidence of GSD Ib and 3 novel SLC37A4 variants (Article)
Autori Skakic Anita  Djordjevic M  Sarajlija Adrijan  Klaassen Kristel M  Tosic Natasa M  Kecman Bozica  Ugrin Milena  Spasovski Vesna M  Pavlovic Sonja T  Stojiljkovic Maja M 
Info CLINICAL GENETICS, (2018), vol. 93 br. 2, str. 350-355
Projekat Ministry of Education, Science and Technological Development, Republic of Serbia [III41004]; European Commission [EU-FP7-REGPOT-316088]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa  
Naslov Appendiceal involvement in a patient with Gaucher disease (Article)
Autori Kocic Marija  Djuricic Slavisa M  Djordjevic Maja S  Savic Djordje  Kecman Bozica  Sarajlija Adrijan 
Info BLOOD CELLS MOLECULES AND DISEASES, (2018), vol. 68 br. , str. 109-111
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa  
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  
Naslov Postprandial hyperinsulinemic hypoglycemia in a child as a late complication of esophageal reconstruction (Article)
Autori Vukovic Rade M  Milenkovic Tatjana  Djordjevic Maja S  Mitrovic Katarina  Todorovic Sladjana  Sarajlija Adrijan  Hussain Khalid 
Info JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, (2017), vol. 30 br. 7, str. 791-795
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa  
Naslov Late-presenting congenital diaphragmatic hernia in a child with TMEM70 deficiency (Letter)
Autori Sarajlija Adrijan  Magner Martin  Djordjevic Maja  Kecman Bozica  Grujic Blagoje  Tesarova Marketa  Minic Predrag B 
Info CONGENITAL ANOMALIES, (2017), vol. 57 br. 2, str. 64-65
Projekat [RVO-VFN64165/2012]; [PRVOUK P24/LF1/3]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa  
Naslov Genotype-phenotype correlation in 44 Czech, Slovak, Croatian and Serbian patients with mucopolysaccharidosis type II (Article)
Autori Dvorakova L  ...  Sarajlija Adrijan  ...  Kecman Bozica  Djordjevic Maja S  ...  (broj koautora 19) 
Info CLINICAL GENETICS, (2017), vol. 91 br. 5, str. 787-796
Projekat Charles University [PRVOUK P24/LF1/3, UNCE 204011, GAUK 580716]; Ministry of Health, Czech Republic [64165/2012]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa  
Naslov Molecular and phenotypic characteristics of seven novel mutations causing branched-chain organic acidurias (Article)
Autori Stojiljkovic Maja M  Klaassen Kristel M  Djordjevic Maja S  Sarajlija Adrijan  Brasil S  Kecman Bozica  Grkovic Sanja  Kostic Jelena  Rodriguez-Pombo P  Desviat LR  Pavlovic Sonja T  Perez Belen 
Info CLINICAL GENETICS, (2016), vol. 90 br. 3, str. 252-257
Projekat Ministry of Education, Science and Technological Development, Serbia [III 41004]; European Commission [EU-FP7-REGPOT-316088]; Ministry of Economy and Competitiveness, Spain [PI13/01239]; Spanish-Serbian cooperation project - Ministry of Economy and Compet
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science  
Naslov Early Presentation of Hyperinsulinism/Hyperammonemia Syndrome in Three Serbian Patients (Article)
Autori Sarajlija Adrijan  Milenkovic Tatjana  Djordjevic Maja S  Mitrovic Katarina  Todorovic Sladjana  Kecman Bozica  Hussain Khalid 
Info JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY, (2016), vol. 8 br. 2, str. 228-231
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science  
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