Detalhe da pesquisa
1.
Challenges for gene editing in common variable immunodeficiency disorders: Current and future prospects.
Clin Immunol
; 258: 109854, 2024 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38013164
2.
Soluble wild-type ACE2 molecules inhibit newer SARS-CoV-2 variants and are a potential antiviral strategy to mitigate disease severity in COVID-19.
Clin Exp Immunol
; 214(3): 289-295, 2023 12 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-37565297
3.
First Identified Case of Fatal Fulminant Necrotizing Eosinophilic Myocarditis Following the Initial Dose of the Pfizer-BioNTech mRNA COVID-19 Vaccine (BNT162b2, Comirnaty): an Extremely Rare Idiosyncratic Hypersensitivity Reaction.
J Clin Immunol
; 42(3): 441-447, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-34978002
4.
New Therapies for Type 1 and Type 2 Hereditary Angioedema.
N Engl J Med
; 2024 May 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-38819650
5.
Droplet digital PCR for identifying copy number variations in patients with primary immunodeficiency disorders.
Clin Exp Immunol
; 207(3): 329-335, 2022 05 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-35553639
6.
Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations.
J Allergy Clin Immunol
; 146(4): 901-911, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32278790
7.
An Antisense Oligonucleotide for Hereditary Angioedema.
N Engl J Med
; 386(11): 1083-1085, 2022 03 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-35294818
8.
Haploinsufficiency of the NF-κB1 Subunit p50 in Common Variable Immunodeficiency.
Am J Hum Genet
; 97(3): 389-403, 2015 Sep 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-26279205
9.
Prospective Evaluation of the ESPGHAN Guidelines for Diagnosis of Celiac Disease in New Zealand Children.
J Pediatr Gastroenterol Nutr
; 67(6): 749-754, 2018 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-29916948
10.
Health Risks and Adverse Reactions to Functional Foods.
Crit Rev Food Sci Nutr
; 56(2): 318-25, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-25163007
11.
Profound Reversible Hypogammaglobulinemia Caused by Celiac Disease in the Absence of Protein Losing Enteropathy.
J Clin Immunol
; 35(6): 589-94, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-26318181
12.
Identification of germinal centres in the lymph node of a patient with hyperimmunoglobulin M syndrome associated with congenital rubella.
J Clin Immunol
; 34(7): 796-803, 2014 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-25113848
13.
Detection of interferon alpha and beta receptor subunit 1 (IFNAR1) loss-of-function Glu386∗ variant by tri-allelic genotyping.
Pathology
; 56(1): 92-97, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-37973454
14.
The autoimmune rheumatological presentation of Common Variable Immunodeficiency Disorders with an overview of genetic testing.
Semin Arthritis Rheum
; 65: 152387, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38330740
15.
Phenotypic spectrum in a family with a novel RAC2 p.I21S dominant-activating mutation.
Clin Transl Immunology
; 13(2): e1493, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38410820
16.
SARS-CoV-2 evolution has increased resistance to monoclonal antibodies and first-generation COVID-19 vaccines: Is there a future therapeutic role for soluble ACE2 receptors for COVID-19?
Antiviral Res
; 227: 105894, 2024 Apr 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-38677595
17.
Clinical variability of family members with the C104R mutation in transmembrane activator and calcium modulator and cyclophilin ligand interactor (TACI).
J Clin Immunol
; 33(1): 68-73, 2013 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-22983507
18.
Diagnostic utility of modified gliadin peptide antibody assays in New Zealand children.
J Pediatr Gastroenterol Nutr
; 57(1): 43-8, 2013 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-23403444
19.
Samter's triad in childhood: a warning for those prescribing NSAIDs.
Paediatr Anaesth
; 23(8): 757-9, 2013 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-23782034
20.
Selective IgA Deficiency May Be an Underrecognized Risk Factor for Severe COVID-19.
J Allergy Clin Immunol Pract
; 11(1): 181-186, 2023 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36241155