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Autori: Sarajlija Adrijan

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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  
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   Citati: ISI/Web of Science  
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 G  Djordjevic Maja S  Sarajlija Adrijan  Klaassen Kristel M  Tosic Natasa M  Kecman Bozica  Ugrin Milena M  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   Citati: ISI/Web of Science   Scopus  
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   Citati: ISI/Web of Science   Scopus  
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  
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   Citati: ISI/Web of Science   Scopus  
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