Detalhe da pesquisa
1.
Conversion of monoclonal IgG to dimeric and secretory IgA restores neutralizing ability and prevents infection of Omicron lineages.
Proc Natl Acad Sci U S A
; 121(3): e2315354120, 2024 Jan 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-38194459
2.
Prospective Newborn Screening for SCID in Germany: A First Analysis by the Pediatric Immunology Working Group (API).
J Clin Immunol
; 43(5): 965-978, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-36843153
3.
Long-Term Follow-Up of Newborns with 22q11 Deletion Syndrome and Low TRECs.
J Clin Immunol
; 42(3): 618-633, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35080750
4.
Gut Microbiota Perturbation in IgA Deficiency Is Influenced by IgA-Autoantibody Status.
Gastroenterology
; 160(7): 2423-2434.e5, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33662387
5.
Sensitive and specific serological ELISA for the detection of SARS-CoV-2 infections.
Virol J
; 19(1): 50, 2022 03 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-35305688
6.
Impaired polysaccharide responsiveness without agammaglobulinaemia in three patients with hypomorphic mutations in Bruton Tyrosine Kinase-No detection by newborn screening for primary immunodeficiencies.
Scand J Immunol
; 91(1): e12811, 2020 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-31378960
7.
Study of an extended family with CTLA-4 deficiency suggests a CD28/CTLA-4 independent mechanism responsible for differences in disease manifestations and severity.
Clin Immunol
; 188: 94-102, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29305966
8.
Newborn screening using TREC/KREC assay for severe T and B cell lymphopenia in Iran.
Scand J Immunol
; : e12699, 2018 Jun 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-29943473
9.
Newborn Screening for Severe Primary Immunodeficiency Diseases in Sweden-a 2-Year Pilot TREC and KREC Screening Study.
J Clin Immunol
; 37(1): 51-60, 2017 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27873105
10.
The Extended Clinical Phenotype of 26 Patients with Chronic Mucocutaneous Candidiasis due to Gain-of-Function Mutations in STAT1.
J Clin Immunol
; 36(1): 73-84, 2016 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-26604104
11.
Deficiency of innate and acquired immunity caused by an IKBKB mutation.
N Engl J Med
; 369(26): 2504-14, 2013 Dec 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-24369075
12.
Prospective neonatal screening for severe T- and B-lymphocyte deficiencies in Seville.
Pediatr Allergy Immunol
; 27(1): 70-7, 2016 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-26498110
13.
Novel mutations in TNFRSF7/CD27: Clinical, immunologic, and genetic characterization of human CD27 deficiency.
J Allergy Clin Immunol
; 136(3): 703-712.e10, 2015 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-25843314
14.
SYK expression endows human ZAP70-deficient CD8 T cells with residual TCR signaling.
Clin Immunol
; 161(2): 103-9, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26187144
15.
Diagnosis of immunodeficiency caused by a purine nucleoside phosphorylase defect by using tandem mass spectrometry on dried blood spots.
J Allergy Clin Immunol
; 134(1): 155-9, 2014 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-24767876
16.
Clinical picture and treatment of 2212 patients with common variable immunodeficiency.
J Allergy Clin Immunol
; 134(1): 116-26, 2014 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-24582312
17.
Newborn screening for severe T and B cell lymphopenia identifies a fraction of patients with Wiskott-Aldrich syndrome.
Clin Immunol
; 155(1): 74-78, 2014 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-25217881
18.
Novel NLRP12 mutations associated with intestinal amyloidosis in a patient diagnosed with common variable immunodeficiency.
Clin Immunol
; 154(2): 105-11, 2014 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-25064839
19.
Retrospective analysis of TREC based newborn screening results and clinical phenotypes in infants with the 22q11 deletion syndrome.
J Clin Immunol
; 34(4): 514-9, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24610337
20.
Neonatal screening for severe primary immunodeficiency diseases using high-throughput triplex real-time PCR.
Blood
; 119(11): 2552-5, 2012 Mar 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-22130802