Researchers
Sarajlija, Adrijan
Results 21-40 of 57
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2021 | Clinical and genetic characteristics of patients with congenital hyperinsulinism in 21 non-consanguineous families from Serbia | Raičević, Maja; Milenković, Tatjana; Hussain, Khalid; Đorđević, Maja   ; Martić, Jelena ; Todorović, Slađana; Mitrović, Katarina; Sarajlija, Adrijan ; Vuković, Rade | Article | 21aM21a |
| 2020 | Impact of genotype on neutropenia in a large cohort of Serbian patients with glycogen storage disease type Ib | Sarajlija, Adrijan ; Đorđević, Maja ; Kecman, Božica; Skakić, Anita ; Pavlović, Sonja ; Pašić, Srđan ; Stojiljković, Maja | Article | 22M22 |
| 2020 | Manufaktura G | Sarajlija, Adrijan | Other | Mp. category will be shown later |
| 2019 | 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 | Molema, Femke; ...; Đorđević, Maja S. ; Sarajlija, Adrijan ; ...; (broj koautora 67) | Article | 21M21 |
| 2019 | Transatlantic combined and comparative data analysis of 1095 patients with urea cycle disordersA successful strategy for clinical research of rare diseases | Posset, Roland; ...; Sarajlija, Adrijan ; ...; (broj koautora 70) | Article | 21M21 |
| 2019 | 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 | Molema, Femke; ...; Đorđević, Maja S. ; Sarajlija, Adrijan ; ...; (broj koautora 68) | Article | 21M21 |
| 2018 | Genetic characterization of GSD I in Serbian population revealed unexpectedly high incidence of GSD Ib and 3 novel SLC37A4 variants | Skakić, Anita ; Đorđević, M.; Sarajlija, A. ; Klaassen, Kristel ; Tošić, Nataša ; Kecman, B.; Ugrin, Milena ; Spasovski, Vesna ; Pavlović, Sonja ; Stojiljković, Maja | Article | 21M21 |
| 2018 | Appendiceal involvement in a patient with Gaucher disease | Kocić, Marija; Đuričić, Slaviša M.; Đorđević, Maja ; Savić, Đorđe ; Kecman, Božica; Sarajlija, Adrijan | Article | 22M22 |
| 2018 | WDR45 mutations may cause a MECP2 mutation-negative Rett syndrome phenotype | Kulikovskaja, Leonora; Sarajlija, Adrijan ; Savić Pavićević, Dušanka ; Dobričić, Valerija ; Klein, Christine; Westenberger, Ana | Article | Mp. category will be shown later |
| 2017 | Postprandial hyperinsulinemic hypoglycemia in a child as a late complication of esophageal reconstruction | Vuković, Rade M.; Milenković, Tatjana; Đorđević, Maja S. ; Mitrović, Katarina; Todorović, Slađana; Sarajlija, Adrijan ; Hussain, Khalid | Article | 22M22 |
| 2017 | Genotype-phenotype correlation in 44 Czech, Slovak, Croatian and Serbian patients with mucopolysaccharidosis type II | Dvorakova, L.; Vlaskova, H.; Sarajlija, Adrijan ; Ramadza, D. P.; Poupetova, H.; Hruba, E.; Hlavata, A.; Bzduch, V.; Peskova, K.; Storkanova, G.;
Kecman, Božica; Đorđević, Maja
; Baric, I.; Fumic, K.; Barisic, I.; Reboun, M.; Kulhanek, J.; Zeman, J.; Magner, M.; | Article | 21M21 |
| 2017 | Late-presenting congenital diaphragmatic hernia in a child with TMEM70 deficiency | Sarajlija, Adrijan ; Magner, Martin; Đorđević, Maja ; Kecman, Božica; Grujić, Blagoje ; Tesarova, Marketa; Minić, Predrag | Contribution to periodical | 22M22 |
| 2017 | Novel intragenic deletions within the UBE3A gene in two unrelated patients with Angelman syndrome: case report and review of the literature | Aguilera, Cinthia; Vinas-Jornet, Marina; Baena, Neus; Gabau, Elisabeth; Fernandez, Concepcion; Capdevila, Nuria; Ćirković, Sanja S.; Sarajlija, Adrijan ; Mišković, Marijana; Radivojević, Danijela ;
Ruiz, Anna; Guitart, Miriam;
| Article | 22M22 |
| 2016 | Molecular and phenotypic characteristics of seven novel mutations causing branched-chain organic acidurias | Stojiljković, Maja ; Klaassen, Kristel ; Đorđević, Maja ; Sarajlija, Adrijan ; Brasil, S.; Kecman, Božica; Grković, Sanja; Perić, Jelena ; Rodriguez-Pombo, P.; Desviat, L.R.;
Pavlović, Sonja
; Perez, B.; | Article | 21M21 |
| 2016 | Early Presentation of Hyperinsulinism/Hyperammonemia Syndrome in Three Serbian Patients | Sarajlija, Adrijan ; Milenković, Tatjana; Đorđević, Maja ; Mitrović, Katarina; Todorović, Slađana; Kecman, Božica; Hussain, Khalid | Article | 22M22 |
| 2016 | DNA polymerase-alpha regulates the activation of type I interferons through cytosolic RNA:DNA synthesis | Starokadomskyy, Petro; ...; Sarajlija, Adrijan ; ...; (broj koautora 31) | Article | 21a+M21a+ |
| 2015 | Epidemiology of Rett Syndrome in Serbia: Prevalence, Incidence and Survival | Sarajlija, Adrijan ; Kisić Tepavčević, Darija ; Nikolic, Zorana ; Savic, Pavicevic Dusanka ; Obradovic, Slobodan; Djuric, Milena; Pekmezović, Tatjana | Article | 21M21 |
| 2015 | Non-renal indications for the continuous renal replacement therapy in the intensive care unit of terciary care center: eleven years of experience | Stajić, Nataša; Putnik, Jovana; Paripović, Aleksandra; Đorđević, Maja ; Martić, Jelena ; Kecman, Božica; Sarajlija, Adrijan ; Pejić, Katarina; Prokić, Dragan; Višekruna, Jelena;
Bogdanović, Radovan;
| Conference Paper | Mp. category will be shown later |
| 2015 | Addictions among homeless in Belgrade | Sarajlija, Marija; Jugović, Aleksandar ; Živaljević, Dragan; Merdović, Boro ; Sarajlija, Adrijan | Conference Paper | Mp. category will be shown later |
| 2015 | Tetrahydrobiopterin deficiency among Serbian patients presenting with hyperphenylalaninemia | Stojiljković, Maja ; Klaassen, Kristel ; Đorđević, Maja; Sarajlija, Adrijan ; Kecman, Bozica; Ugrin, Milena ; Zukić, Branka ; Desviat, Lourdes R.; Pavlović, Sonja ; Perez, Belen | Article | 23M23 |