Autori: Sarajlija Adrijan
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 | WDR45 mutations may cause a MECP2 mutation-negative Rett syndrome phenotype (Editorial Material) |
Autori | Kulikovskaja Leonora Sarajlija Adrijan Savic-Pavicevic Dusanka Lj Dobricic Valerija S Klein Christine Westenberger Ana |
Info | NEUROLOGY-GENETICS, (2018), vol. 4 br. 2, str. - |
Projekat | Hermann and Lilly Schilling Foundation; Land Schleswig-Holstein within the funding programme Open Access Publikationsfonds |
Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
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 |
Naslov | Late-presenting congenital diaphragmatic hernia in a child with TMEM70 deficiency (Letter) |
Autori | Sarajlija Adrijan Magner Martin Djordjevic Maja S 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 Citati: ISI/Web of Science Scopus |
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 Citati: ISI/Web of Science Scopus |
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 Lourdes R 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 Scopus |
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 Scopus |