Detalhe da pesquisa
1.
DNA polymerase-α regulates the activation of type I interferons through cytosolic RNA:DNA synthesis.
Nat Immunol
; 17(5): 495-504, 2016 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-27019227
2.
Clinical and genetic characteristics of patients with congenital hyperinsulinism in 21 non-consanguineous families from Serbia.
Eur J Pediatr
; 180(9): 2815-2821, 2021 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-33770274
3.
Appendiceal involvement in a patient with Gaucher disease.
Blood Cells Mol Dis
; 68: 109-111, 2018 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-27717752
4.
Novel intragenic deletions within the UBE3A gene in two unrelated patients with Angelman syndrome: case report and review of the literature.
BMC Med Genet
; 18(1): 137, 2017 11 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-29162042
5.
Epidemiology of Rett syndrome in Serbia: prevalence, incidence and survival.
Neuroepidemiology
; 44(1): 1-5, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-25571926
6.
Age-specific causes of upper gastrointestinal bleeding in children.
World J Gastroenterol
; 29(47): 6095-6110, 2023 Dec 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-38186684
7.
Impact of genotype on neutropenia in a large cohort of Serbian patients with glycogen storage disease type Ib.
Eur J Med Genet
; 63(3): 103767, 2020 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-31536830
8.
Postprandial hyperinsulinemic hypoglycemia in a child as a late complication of esophageal reconstruction.
J Pediatr Endocrinol Metab
; 30(7): 791-795, 2017 Jul 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-28672750
9.
Early Presentation of Hyperinsulinism/Hyperammonemia Syndrome in Three Serbian Patients.
J Clin Res Pediatr Endocrinol
; 8(2): 228-31, 2016 Jun 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-26759084
10.
Tetrahydrobiopterin deficiency among Serbian patients presenting with hyperphenylalaninemia.
J Pediatr Endocrinol Metab
; 28(3-4): 477-80, 2015 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-25418970
11.
Assessment of health status and quality of life of homeless persons in Belgrade, Serbia.
Vojnosanit Pregl
; 71(2): 167-74, 2014 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-24665575
12.
Health-related quality of life and depression in Rett syndrome caregivers.
Vojnosanit Pregl
; 70(9): 842-7, 2013 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-24266312
13.
Vitamin D deficiency in Serbian patients with Rett syndrome.
J Clin Endocrinol Metab
; 98(12): E1972-8, 2013 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-24106287
14.
WDR45 mutations may cause a MECP2 mutation-negative Rett syndrome phenotype.
Neurol Genet
; 4(2): e227, 2018 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-29600274
15.
Molecular Genetics and Genotype-Based Estimation of BH4-Responsiveness in Serbian PKU Patients: Spotlight on Phenotypic Implications of p.L48S.
JIMD Rep
; 9: 49-58, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23430547
16.
Late-presenting congenital diaphragmatic hernia in a child with TMEM70 deficiency.
Congenit Anom (Kyoto)
; 57(2): 64-65, 2017 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-27649480
17.
Pulmonary involvement in siblings with Gaucher disease type III.
Vojnosanit Pregl
; 68(12): 1071-4, 2011 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-22352271
18.
Clinical characteristics of respiratory syncytial virus infection in neonates and young infants.
Vojnosanit Pregl
; 68(3): 220-4, 2011 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-21524004
19.
[Use of mechanical ventilation in pediatric patients].
Vojnosanit Pregl
; 65(12): 876-81, 2008 Dec.
Artigo
em Sr
| MEDLINE | ID: mdl-19160980