Detalhe da pesquisa
1.
Phase 3 randomized trial of mavorixafor, CXCR4 antagonist, in WHIM syndrome.
Blood
; 2024 Apr 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-38643510
2.
Comprehensive phenotypic analysis of diverse FOXN1 variants.
J Allergy Clin Immunol
; 152(5): 1273-1291.e15, 2023 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-37419334
3.
CVID-Associated Intestinal Disorders in the USIDNET Registry: An Analysis of Disease Manifestations, Functional Status, Comorbidities, and Treatment.
J Clin Immunol
; 44(1): 32, 2023 12 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-38133694
4.
SARS-CoV-2 infection associated with hepatitis in an infant with X-linked severe combined immunodeficiency.
Clin Immunol
; 224: 108662, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33412294
5.
Connecting the Dots From Fever of Unknown Origin to Myelodysplastic Syndrome: GATA2 Haploinsufficiency.
J Pediatr Hematol Oncol
; 42(5): e365-e368, 2020 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-31033783
6.
Novel nonsense gain-of-function NFKB2 mutations associated with a combined immunodeficiency phenotype.
Blood
; 130(13): 1553-1564, 2017 09 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-28778864
7.
Macrophage Activation Syndrome Complicated by Toxic Epidermal Necrolysis Following SARS-CoV-2 mRNA Vaccination.
J Clin Immunol
; 43(3): 521-524, 2023 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-36441289
8.
What's in a name? The heterogeneous clinical spectrum and prognostic factors in a cohort of adults with hemophagocytic lymphohistiocytosis.
Transfus Apher Sci
; 57(6): 779-784, 2018 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-30327177
9.
Hypomorphic Janus kinase 3 mutations result in a spectrum of immune defects, including partial maternal T-cell engraftment.
J Allergy Clin Immunol
; 131(4): 1136-45, 2013 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-23384681
10.
CVID-associated intestinal disorders in the USIDNET registry: An analysis of disease manifestations, functional status, comorbidities, and treatment.
Res Sq
; 2023 May 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37214897
11.
Obstructive hydrocephalus and intracerebral mass secondary to Epicoccum nigrum.
Med Mycol Case Rep
; 35: 18-21, 2022 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-35036296
12.
Mesenchymal cell replacement corrects thymic hypoplasia in murine models of 22q11.2 deletion syndrome.
J Clin Invest
; 132(22)2022 11 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-36136514
13.
Cytoplasmic RNA quality control failure engages mTORC1-mediated autoinflammatory disease.
J Clin Invest
; 132(2)2022 01 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-35040435
14.
Lymphomatoid granulomatosis of the central nervous system (CNS-LYG) posing a management challenge.
Clin Case Rep
; 9(9): e04808, 2021 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-34512987
15.
Molecular Insights Into the Causes of Human Thymic Hypoplasia With Animal Models.
Front Immunol
; 11: 830, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32431714
16.
FOXN1 compound heterozygous mutations cause selective thymic hypoplasia in humans.
J Clin Invest
; 129(11): 4724-4738, 2019 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31566583
17.
Mesenchymal cell replacement corrects thymic hypoplasia in murine models of 22q11.2 deletion syndrome.
J Clin Invest
; 133(13)2023 07 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-37395280
18.
Comparing hemophagocytic lymphohistiocytosis in pediatric and adult patients.
Curr Opin Allergy Clin Immunol
; 17(6): 405-413, 2017 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-28957822
19.
Chronic Granulomatous Disease of the Upper Airway.
Ear Nose Throat J
; : 1455613211054635, 2021 Oct 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-34670444
20.
Autoimmune Disease in Primary Immunodeficiency: At the Crossroads of Anti-Infective Immunity and Self-Tolerance.
Immunol Allergy Clin North Am
; 35(4): 731-52, 2015 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-26454316