Detalhe da pesquisa
1.
Impaired Response to Polysaccharide Vaccine in Selective IgE Deficiency.
J Clin Immunol
; 43(6): 1448-1454, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37169968
2.
Dysregulated Lymphocyte Antigen Receptor Signaling in Common Variable Immunodeficiency with Granulomatous Lymphocytic Interstitial Lung Disease.
J Clin Immunol
; 43(6): 1311-1325, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37093407
3.
Germline IKAROS dimerization haploinsufficiency causes hematologic cytopenias and malignancies.
Blood
; 137(3): 349-363, 2021 01 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-32845957
4.
Role of GATA2 in Human NK Cell Development.
Crit Rev Immunol
; 41(2): 21-33, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34348000
5.
Rituximab and antimetabolite treatment of granulomatous and lymphocytic interstitial lung disease in common variable immunodeficiency.
J Allergy Clin Immunol
; 147(2): 704-712.e17, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-32745555
6.
Novel Hemizygous IL2RG p.(Pro58Ser) Mutation Impairs IL-2 Receptor Complex Expression on Lymphocytes Causing X-Linked Combined Immunodeficiency.
J Clin Immunol
; 40(3): 503-514, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-32072341
7.
Clinical and histologic presentation of pediatric reactive granulomatous dermatitis.
Pediatr Dermatol
; 37(3): 498-503, 2020 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-32115758
8.
Identification of molecular signatures of cystic fibrosis disease status with plasma-based functional genomics.
Physiol Genomics
; 51(1): 27-41, 2019 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30540547
9.
Correction to: Use of Genetic Testing for Primary Immunodeficiency Patients.
J Clin Immunol
; 38(4): 540-541, 2018 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-29781065
10.
Use of Genetic Testing for Primary Immunodeficiency Patients.
J Clin Immunol
; 38(3): 320-329, 2018 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-29675737
11.
Low Serum IgE Is a Sensitive and Specific Marker for Common Variable Immunodeficiency (CVID).
J Clin Immunol
; 38(3): 225-233, 2018 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-29453744
12.
Newborn Screening for Severe Combined Immunodeficiency.
Curr Allergy Asthma Rep
; 18(6): 34, 2018 05 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-29749587
13.
Internuclear Ophthalmoplegia in a Child With Deficiency of Adenosine Deaminase 2.
J Neuroophthalmol
; 43(1): e12-e13, 2023 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34629408
14.
The Use of Salmonella Typhim Vaccine to Diagnose Antibody Deficiency.
J Clin Immunol
; 37(5): 427-433, 2017 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-28589420
15.
Early-onset stroke and vasculopathy associated with mutations in ADA2.
N Engl J Med
; 370(10): 911-20, 2014 Mar 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-24552284
16.
Early-onset lymphoproliferation and autoimmunity caused by germline STAT3 gain-of-function mutations.
Blood
; 125(4): 591-9, 2015 Jan 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-25359994
17.
X-linked Hyper IgM Syndrome Presenting as Pulmonary Alveolar Proteinosis.
J Clin Immunol
; 36(6): 564-70, 2016 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-27324886
18.
Intact Regulatory T-Cell Function but Defective Generation of IL-17A-Producing CD4+ T Cells in XIAP Deficiency.
J Pediatr Gastroenterol Nutr
; 63(2): 218-25, 2016 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-26825770
19.
Practice parameter for the diagnosis and management of primary immunodeficiency.
J Allergy Clin Immunol
; 136(5): 1186-205.e1-78, 2015 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-26371839
20.
Gain of Function Mutations of PIK3CD as a Cause of Primary Sclerosing Cholangitis.
J Clin Immunol
; 35(1): 11-4, 2015 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-25352054