Detalhe da pesquisa
1.
T-follicular helper cell expansion and chronic T-cell activation are characteristic immune anomalies in Evans syndrome.
Blood
; 139(3): 369-383, 2022 01 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-34424963
2.
Infections in Infants with SCID: Isolation, Infection Screening, and Prophylaxis in PIDTC Centers.
J Clin Immunol
; 41(1): 38-50, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33006109
3.
Diagnostic interpretation of genetic studies in patients with primary immunodeficiency diseases: A working group report of the Primary Immunodeficiency Diseases Committee of the American Academy of Allergy, Asthma & Immunology.
J Allergy Clin Immunol
; 145(1): 46-69, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31568798
4.
NAPDH Oxidase-Specific Flow Cytometry Allows for Rapid Genetic Triage and Classification of Novel Variants in Chronic Granulomatous Disease.
J Clin Immunol
; 40(1): 191-202, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31813112
5.
Noninfectious complications of common variable immune deficiency.
Allergy Asthma Proc
; 40(2): 129-132, 2019 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30819283
6.
Hypogammaglobulinemia with decreased class-switched B-cells and dysregulated T-follicular-helper cells in IPEX syndrome.
Clin Immunol
; 197: 219-223, 2018 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-30368009
7.
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
8.
Use of Genetic Testing for Primary Immunodeficiency Patients.
J Clin Immunol
; 38(3): 320-329, 2018 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-29675737
9.
Long-term outcomes of 176 patients with X-linked hyper-IgM syndrome treated with or without hematopoietic cell transplantation.
J Allergy Clin Immunol
; 139(4): 1282-1292, 2017 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-27697500
10.
Long-Term Tolerability, Safety, and Efficacy of Recombinant Human Hyaluronidase-Facilitated Subcutaneous Infusion of Human Immunoglobulin for Primary Immunodeficiency.
J Clin Immunol
; 36(6): 571-82, 2016 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-27220317
11.
Correction to: Infections in Infants with SCID: Isolation, Infection Screening and Prophylaxis in PIDTC Centers.
J Clin Immunol
; 41(2): 498-500, 2021 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-33274413
12.
MALDI-TOF-MS Assay to Detect the Hemizygous 22q11.2 Deletion in DNA from Dried Blood Spots.
Clin Chem
; 62(1): 287-92, 2016 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-26585925
13.
Cost-Effectiveness/Cost-Benefit Analysis of Newborn Screening for Severe Combined Immune Deficiency in Washington State.
J Pediatr
; 172: 127-35, 2016 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-26876279
14.
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
15.
Subcutaneous Immunoglobulin Replacement Therapy with Hizentra® is Safe and Effective in Children Less Than 5 Years of Age.
J Clin Immunol
; 35(6): 558-65, 2015 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-26336818
16.
The effect of hypocalcemia in early childhood on autism-related social and communication skills in patients with 22q11 deletion syndrome.
Eur Arch Psychiatry Clin Neurosci
; 265(6): 519-24, 2015 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-25267002
17.
Management of ADA-Deficient SCID Patient on Adagen During Pregnancy.
J Clin Immunol
; 39(8): 846-848, 2019 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-31620946
18.
Prevalence and morbidity of primary immunodeficiency diseases, United States 2001-2007.
J Clin Immunol
; 34(8): 954-61, 2014 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-25257253
19.
ICON: the early diagnosis of congenital immunodeficiencies.
J Clin Immunol
; 34(4): 398-424, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24619621
20.
Malakoplakia and primary immunodeficiency.
J Pediatr
; 165(5): 1053-6, 2014 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-25155967