Detalhe da pesquisa
1.
Sensory neurons promote immune homeostasis in the lung.
Cell;
187(1): 44-61.e17, 2024 01 04.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38134932
2.
Dominant negative variants in IKZF2 cause ICHAD syndrome, a new disorder characterised by immunodysregulation, craniofacial anomalies, hearing impairment, athelia and developmental delay.
J Med Genet;
60(11): 1092-1104, 2023 Nov.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37316189
3.
Inborn errors of immunity manifesting as atopic disorders.
J Allergy Clin Immunol;
148(5): 1130-1139, 2021 11.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34428518
4.
All hands on deck: A multidisciplinary approach to SARS-CoV-2-associated MIS-C.
Paediatr Child Health;
27(Suppl 1): S53-S58, 2022 Jun.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35620558
5.
Ruxolitinib as adjunctive therapy for secondary hemophagocytic lymphohistiocytosis: A case series.
Eur J Haematol;
106(5): 654-661, 2021 May.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33523540
6.
Diverse clinical features and diagnostic delay in monogenic inborn errors of immunity: A call for access to genetic testing.
Pediatr Allergy Immunol;
32(8): 1796-1803, 2021 11.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34097760
7.
Idiopathic splenomegaly in childhood and the spectrum of RAS-associated lymphoproliferative disease: a case report.
BMC Pediatr;
21(1): 45, 2021 01 21.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33472608
8.
Recurrent sterile abscesses in a case of X-linked neutropenia.
Pediatr Dermatol;
37(4): 742-744, 2020 Jul.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32202653
9.
Should 'primary immune disorder' replace 'inborn error of immunity'? Names matter but there's room for both.
J Allergy Clin Immunol;
2024 Apr 20.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38649118
10.
Germline CBM-opathies: From immunodeficiency to atopy.
J Allergy Clin Immunol;
143(5): 1661-1673, 2019 05.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31060714
11.
Expanding the molecular and phenotypic spectrum of CTLA-4 insufficiency.
Pediatr Allergy Immunol;
35(2): e14077, 2024 Feb.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38351878
12.
Homozygous RMRP Promoter Duplications Cause Severely Reduced Transcript Abundance and SCID Associated with Cartilage Hair Hypoplasia.
J Clin Immunol;
43(6): 1139-1142, 2023 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37115363
13.
DOCK8 deficiency: Insights into pathophysiology, clinical features and management.
Clin Immunol;
181: 75-82, 2017 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28625885
14.
Targeted treatment of immune thrombocytopenia in CTLA-4 insufficiency: a case report.
Br J Haematol;
196(3): e42-e45, 2022 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34628649
15.
Hematopoietic stem cell transplantation outcomes for 11 patients with dedicator of cytokinesis 8 deficiency.
J Allergy Clin Immunol;
138(3): 852-859.e3, 2016 09.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27130861
16.
Tout le monde sur le pont : une approche multidisciplinaire du SRAS-CoV-2 associé au SIME.
Paediatr Child Health;
27(Suppl 2): S136-S142, 2022 Sep.
Artigo
em Francês
| MEDLINE
| ID: mdl-36092300
17.
Amelioration of COVID-19-related cytokine storm syndrome: parallels to chimeric antigen receptor-T cell cytokine release syndrome.
Br J Haematol;
190(3): e150-e154, 2020 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32584416
18.
Innate immune control of EBV-infected B cells by invariant natural killer T cells.
Blood;
122(15): 2600-8, 2013 Oct 10.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23974196
19.
Inborn errors of immunity in adulthood.
Allergy Asthma Clin Immunol;
20(1): 6, 2024 Jan 17.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38233962
20.
Gain-of-function MARK4 variant associates with pediatric neurodevelopmental disorder and dysmorphism.
HGG Adv;
5(1): 100259, 2024 Jan 11.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38041405