Researchers
Sarajlija, Adrijan
Results 21-40 of 62
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2023 | Three case reports of patients with rare copy number variations in the recurrent 2q11.1-q11.2 region | Perović, Dijana   ; Maksimović, Nela ; Damnjanović, Tatjana ; Đuranović, Ana ; Sarajlija, Adrijan ; Mijović, Marija | Conference Paper | Mp. category will be shown later |
| 2023 | Age-specific causes of upper gastrointestinal bleeding in children | Kocić, Marija; Rašić, Petar; Marušić, Vuk P. ; Prokić, Dragan; Savić, Đorđe ; Miličković, Maja ; Kitić, Ivana; Mijović, Tanja; Sarajlija, Adrijan | Article | 21M21 |
| 2022 | Acute disseminated encephalomyelitis in children and adolescents – 20-year single-center experience in Serbia | Ostojić, Slavica; Kravljanac, Ružica ; Kovačević, Gordana ; Vučetić-Tadić, Biljana ; Gazikalović, Slobodan; Sarajlija, Adrijan | Article | 23M23 |
| 2022 | A Novel Variant in the LIPA Gene Associated with Distinct Phenotype | Sarajlija, Adrijan ; Armengol, L.; Maver, Ales; Kitić, Ivana; Prokić, Dragan; Cehić, Maja; Đuričić, MS; Peterlin, Borut | Article | 23M23 |
| 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 |
| 2021 | Ambiguous Genitalia and Lissencephaly in a 46,xy Neonate with a Novel Variant of Aristaless Gene | Basa, Mihail; Vuković, Rade; Sarajlija, Adrijan ; Milenković, Tatjana; Đorđević, Maja ; Vučetić, Biljana ; Martić, Jelena | Article | 23M23 |
| 2020 | Manufaktura G | Sarajlija, Adrijan | Other | Mp. category will be shown later |
| 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 |
| 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 |
| 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 | 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 |
| 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 | 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 | 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 | 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 | 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 | 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 |
| 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 |
| 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+ |
| 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 |