Detalhe da pesquisa
1.
Protein Kinase C δ: a Gatekeeper of Immune Homeostasis.
J Clin Immunol
; 36(7): 631-40, 2016 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-27541826
2.
B-cell deficiency and severe autoimmunity caused by deficiency of protein kinase C δ.
Blood
; 121(16): 3112-6, 2013 Apr 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-23319571
3.
A novel immunodeficiency syndrome associated with partial trisomy 19p13.
J Med Genet
; 51(4): 254-63, 2014 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-24431329
4.
Early-onset inflammatory bowel disease and common variable immunodeficiency-like disease caused by IL-21 deficiency.
J Allergy Clin Immunol
; 133(6): 1651-9.e12, 2014 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-24746753
5.
Combined immunodeficiency evolving into predominant CD4+ lymphopenia caused by somatic chimerism in JAK3.
J Clin Immunol
; 34(8): 941-53, 2014 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-25205547
6.
Lymphocyte subsets in human immunodeficiency virus-unexposed Brazilian individuals from birth to adulthood.
Mem Inst Oswaldo Cruz
; 109(8): 989-98, 2014 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-25424448
7.
A novel mutation in the complement component 3 gene in a patient with selective IgA deficiency.
J Clin Immunol
; 33(1): 127-33, 2013 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-22996269
8.
Combined immunodeficiency with life-threatening EBV-associated lymphoproliferative disorder in patients lacking functional CD27.
Haematologica
; 98(3): 473-8, 2013 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-22801960
9.
Human ß-Defensin 2 Mutations Are Associated With Asthma and Atopy in Children and Its Application Prevents Atopic Asthma in a Mouse Model.
Front Immunol
; 12: 636061, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-33717182
10.
Symptoms, SARS-CoV-2 Antibodies, and Neutralization Capacity in a Cross Sectional-Population of German Children.
Front Pediatr
; 9: 678937, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34671582
11.
Biologicals in childhood severe asthma: the European PERMEABLE survey on the status quo.
ERJ Open Res
; 7(3)2021 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-34409097
12.
Publisher Correction: Human DEF6 deficiency underlies an immunodeficiency syndrome with systemic autoimmunity and aberrant CTLA-4 homeostasis.
Nat Commun
; 10(1): 4555, 2019 Oct 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31578334
13.
Human DEF6 deficiency underlies an immunodeficiency syndrome with systemic autoimmunity and aberrant CTLA-4 homeostasis.
Nat Commun
; 10(1): 3106, 2019 07 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-31308374
14.
Atypical manifestation of LRBA deficiency with predominant IBD-like phenotype.
Inflamm Bowel Dis
; 21(1): 40-7, 2015 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-25479458
15.
Biallelic loss-of-function mutation in NIK causes a primary immunodeficiency with multifaceted aberrant lymphoid immunity.
Nat Commun
; 5: 5360, 2014 Nov 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-25406581
16.
Lymphocyte subsets in human immunodeficiency virus-unexposed Brazilian individuals from birth to adulthood
Mem. Inst. Oswaldo Cruz
; 109(8): 989-998, 12/2014. tab, graf
Artigo
em Inglês
| LILACS | ID: lil-732605