Detalhe da pesquisa
1.
A Novel Homozygous Germline Mutation in Transferrin Receptor 1 (TfR1) Leads to Combined Immunodeficiency and Provides New Insights into Iron-Immunity Axis.
J Clin Immunol
; 44(2): 55, 2024 Jan 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-38270687
2.
Heterogeneity in RAG1 and RAG2 deficiency: 35 cases from a single-centre.
Clin Exp Immunol
; 215(2): 160-176, 2024 02 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37724703
3.
Expanding the clinical and immunological phenotypes of PAX1-deficient SCID and CID patients.
Clin Immunol
; 255: 109757, 2023 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-37689091
4.
Expanding the Clinical and Immunological Phenotypes and Natural History of MALT1 Deficiency.
J Clin Immunol
; 42(3): 634-652, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35079916
5.
Extended clinical and immunological phenotype and transplant outcome in CD27 and CD70 deficiency.
Blood
; 136(23): 2638-2655, 2020 12 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-32603431
6.
Invasive Saprochaete capitata Infection in a Patient with Autosomal Recessive CARD9 Deficiency and a Review of the Literature.
J Clin Immunol
; 40(3): 466-474, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-32020378
7.
IgE and IgG4 binding to lentil epitopes in children with red and green lentil allergy.
Pediatr Allergy Immunol
; 31(2): 158-166, 2020 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31598994
8.
A Novel Homozygous Six Base Pair Deletion Found in the NFATC2 Gene in a Patient with EBV-Associated Lymphoproliferation.
J Clin Immunol
; 44(3): 74, 2024 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38427060
9.
Two siblings with PRKDC defect who presented with cutaneous granulomas and review of the literature.
Clin Immunol
; 197: 1-5, 2018 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-30121298
10.
Corrigendum to "Expanding the clinical and immunological phenotypes of PAX1-deficient SCID and CID patients" [Clinical Immunology 255 (2023) 109757].
Clin Immunol
; 256: 109799, 2023 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-37845128
11.
COVID-19 Induced Hemophagocytic Lymphohistiocytosis in a Patient with Novel Homozygous UNC13D Gene Variant.
Klin Padiatr
; 235(4): 258-260, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37493977
12.
Diagnosis of Interstitial Lung Disease Caused by Possible Hypersensitivity Pneumonitis in a Child: Think CGD.
J Clin Immunol
; 37(3): 269-272, 2017 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-28224353
13.
STK4 (MST1) deficiency in two siblings with autoimmune cytopenias: A novel mutation.
Clin Immunol
; 161(2): 316-23, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26117625
14.
Biallelic Form of a Known CD3E Mutation in a Patient with Severe Combined Immunodeficiency.
J Clin Immunol
; 40(3): 539-542, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-32016651
15.
Experimental Investigation of Microfluidic Device for Platelet Activation.
IEEE Trans Biomed Eng
; 70(3): 954-961, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36103447
16.
Combined immunodeficiency with CD4 lymphopenia and sclerosing cholangitis caused by a novel loss-of-function mutation affecting IL21R.
Haematologica
; 100(6): e216-9, 2015 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-25769540
17.
Genetic Screening of the Patients with Primary Immunodeficiency by Whole-Exome Sequencing.
Pediatr Allergy Immunol Pulmonol
; 33(1): 19-24, 2020 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33406023
18.
Role of natural killer cells in lung cancer.
J Cancer Res Clin Oncol
; 144(6): 997-1003, 2018 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-29616326
19.
Defective pneumococcal antibody response in patients with recurrent respiratory tract infections.
Turk J Pediatr
; 59(5): 555-560, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-29745117
20.
Statins and IL-1ß, IL-10, and MPO Levels in Gingival Crevicular Fluid: Preliminary Results.
Inflammation
; 39(4): 1547-57, 2016 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-27290718