Detalhe da pesquisa
1.
Wiskott-Aldrich Syndrome: A study on 577 patients defining the genotype as a predictive biomarker for disease severity.
Blood
; 2024 Apr 05.
Artigo
Inglês
| MEDLINE | ID: mdl-38579284
2.
Outcome of hematopoietic cell transplantation for DNA double-strand break repair disorders.
J Allergy Clin Immunol
; 141(1): 322-328.e10, 2018 01.
Artigo
Inglês
| MEDLINE | ID: mdl-28392333
3.
Long-term outcomes of 176 patients with X-linked hyper-IgM syndrome treated with or without hematopoietic cell transplantation.
J Allergy Clin Immunol
; 139(4): 1282-1292, 2017 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-27697500
4.
Nijmegen Breakage Syndrome: Clinical and Immunological Features, Long-Term Outcome and Treatment Options - a Retrospective Analysis.
J Clin Immunol
; 35(6): 538-49, 2015 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-26271390
5.
Severe combined immunodeficiency in Serbia and Montenegro between years 1986 and 2010: a single-center experience.
J Clin Immunol
; 34(3): 304-8, 2014 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-24481607
6.
The role of D-dimer in prediction of the course and outcome in pediatric acute pancreatitis.
Pancreatology
; 14(5): 330-4, 2014.
Artigo
Inglês
| MEDLINE | ID: mdl-25163808
7.
Atypical strain of Toxoplasma gondii causing fatal reactivation after hematopoietic stem cell transplantion in a patient with an underlying immunological deficiency.
J Clin Microbiol
; 51(8): 2686-90, 2013 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-23761151
8.
Therapeutic approaches for the treatment of renal disease in juvenile systemic lupus erythematosus: an international multicentre PRINTO study.
Ann Rheum Dis
; 72(9): 1503-9, 2013 Sep 01.
Artigo
Inglês
| MEDLINE | ID: mdl-23100607
9.
X-linked lymphoproliferative disease due to SAP/SH2D1A deficiency: a multicenter study on the manifestations, management and outcome of the disease.
Blood
; 117(1): 53-62, 2011 Jan 06.
Artigo
Inglês
| MEDLINE | ID: mdl-20926771
10.
Dominant-negative mutations in the DNA-binding domain of STAT3 cause hyper-IgE syndrome.
Nature
; 448(7157): 1058-62, 2007 Aug 30.
Artigo
Inglês
| MEDLINE | ID: mdl-17676033
11.
Association of Antiphospholipid Antibodies with Clinical Manifestations in Children with Systemic Lupus Erythematosus.
J Clin Med
; 12(4)2023 Feb 10.
Artigo
Inglês
| MEDLINE | ID: mdl-36835956
12.
Mechanisms of redox balance and inflammatory response after the use of methylprednisolone in children with multisystem inflammatory syndrome associated with COVID-19.
Front Immunol
; 14: 1249582, 2023.
Artigo
Inglês
| MEDLINE | ID: mdl-37646033
13.
Analysis of cardiac manifestation and treatment of multisystem inflammatory syndrome in children related to SARS-CoV-2.
Biomol Biomed
; 23(2): 335-343, 2023 Mar 16.
Artigo
Inglês
| MEDLINE | ID: mdl-36124439
14.
Performance of Birmingham Vasculitis Activity Score and disease extent index in childhood vasculitides.
Clin Exp Rheumatol
; 30(1 Suppl 70): S162-8, 2012.
Artigo
Inglês
| MEDLINE | ID: mdl-22640658
15.
Safety and efficacy of an oral histone deacetylase inhibitor in systemic-onset juvenile idiopathic arthritis.
Arthritis Rheum
; 63(5): 1452-8, 2011 May.
Artigo
Inglês
| MEDLINE | ID: mdl-21538322
16.
HHV-8-related hemophagocytic lymphohistiocytosis in a boy with XLP phenotype.
J Pediatr Hematol Oncol
; 34(6): 467-71, 2012 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-22258354
17.
Severe transient left ventricular pseudohypertrophy during treatment of hemophagocytic lymphohistiocytosis: a case report.
J Pediatr Hematol Oncol
; 34(6): 453-6, 2012 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-22735880
18.
Clinical heterogeneity and diagnostic delay of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome.
Clin Immunol
; 139(1): 6-11, 2011 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-21295522
19.
Case Report: Early Onset Systemic Lupus Erythematosus Due to Hereditary C1q Deficiency Treated With Fresh Frozen Plasma.
Front Pediatr
; 9: 756387, 2021.
Artigo
Inglês
| MEDLINE | ID: mdl-34993161
20.
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
Inglês
| MEDLINE | ID: mdl-31536830