Detalhe da pesquisa
1.
Immunodeficiency associated with a novel functionally defective variant of SLC19A1 benefits from folinic acid treatment.
Genes Immun
; 24(1): 12-20, 2023 02.
Artigo
Inglês
| MEDLINE | ID: mdl-36517554
2.
Defective Treg generation and increased type 3 immune response in leukocyte adhesion deficiency 1.
Clin Immunol
; 253: 109691, 2023 08.
Artigo
Inglês
| MEDLINE | ID: mdl-37433423
3.
A Novel Biallelic LCK Variant Resulting in Profound T-Cell Immune Deficiency and Review of the Literature.
J Clin Immunol
; 44(1): 1, 2023 12 15.
Artigo
Inglês
| MEDLINE | ID: mdl-38100037
4.
Characterization of peripheral blood T follicular helper (TFH) cells in patients with type 1 Gaucher disease and carriers.
Blood Cells Mol Dis
; 100: 102728, 2023 05.
Artigo
Inglês
| MEDLINE | ID: mdl-36738539
5.
The Beneficial Clinical Effects of Teriflunomide in Experimental Autoimmune Myasthenia Gravis and the Investigation of the Possible Immunological Mechanisms.
Cell Mol Neurobiol
; 43(5): 2071-2087, 2023 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-36219379
6.
Synthesis and Comprehensive in Vivo Activity Profiling of Olean-12-en-28-ol, 3ß-Pentacosanoate in Experimental Autoimmune Encephalomyelitis: A Natural Remyelinating and Anti-Inflammatory Agent.
J Nat Prod
; 86(1): 103-118, 2023 01 27.
Artigo
Inglês
| MEDLINE | ID: mdl-36598820
7.
Evolution and long-term outcomes of combined immunodeficiency due to CARMIL2 deficiency.
Allergy
; 77(3): 1004-1019, 2022 03.
Artigo
Inglês
| MEDLINE | ID: mdl-34287962
8.
A Novel Intronic Mutation Reduces HAX1 Level and is Associated With Severe Congenital Neutropenia.
J Pediatr Hematol Oncol
; 44(1): e62-e67, 2022 01 01.
Artigo
Inglês
| MEDLINE | ID: mdl-33560082
9.
Circulating fibrocyte level in children with cystic fibrosis.
Pediatr Int
; 64(1): e15058, 2022 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-34779084
10.
Temporal overexpression of IL-22 and Reg3γ differentially impacts the severity of experimental autoimmune encephalomyelitis.
Immunology
; 164(1): 73-89, 2021 09.
Artigo
Inglês
| MEDLINE | ID: mdl-33876425
11.
Common Variable Immunodeficiency, Autoimmune Hemolytic Anemia, and Pancytopenia Associated With a Defect in IKAROS.
J Pediatr Hematol Oncol
; 43(3): e351-e357, 2021 04 01.
Artigo
Inglês
| MEDLINE | ID: mdl-33122583
12.
ILC3 deficiency and generalized ILC abnormalities in DOCK8-deficient patients.
Allergy
; 75(4): 921-932, 2020 04.
Artigo
Inglês
| MEDLINE | ID: mdl-31596517
13.
Genetic Deficiency and Biochemical Inhibition of ITK Affect Human Th17, Treg, and Innate Lymphoid Cells.
J Clin Immunol
; 39(4): 391-400, 2019 05.
Artigo
Inglês
| MEDLINE | ID: mdl-31025232
14.
Correction to: A Novel Biallelic LCK Variant Resulting in Profound T-Cell Immune Deficiency and Review of the Literature.
J Clin Immunol
; 44(1): 41, 2024 Jan 16.
Artigo
Inglês
| MEDLINE | ID: mdl-38225415
15.
A case of autoimmune lymphoproliferative syndrome with a novel de novo FAS variant.
Pediatr Hematol Oncol
; 41(4): 301-309, 2024 May.
Artigo
Inglês
| MEDLINE | ID: mdl-38047450
16.
A novel missense mutation outside the DNAJ domain of DNAJC21 is associated with Shwachman-Diamond syndrome.
Br J Haematol
; 197(6): e88-e93, 2022 06.
Artigo
Inglês
| MEDLINE | ID: mdl-35298850
17.
A novel gain-of-function mutation in STAT5B is associated with treatment-resistant severe atopic dermatitis.
Clin Exp Allergy
; 52(7): 907-910, 2022 07.
Artigo
Inglês
| MEDLINE | ID: mdl-35426955
18.
A rare cause of membranoproliferative patterns of injury in siblings with steroid-resistant nephrotic syndrome: Questions.
Pediatr Nephrol
; 36(12): 4027-4028, 2021 12.
Artigo
Inglês
| MEDLINE | ID: mdl-34185134
19.
A rare cause of membranoproliferative patterns of injury in siblings with steroid-resistant nephrotic syndrome: Answers.
Pediatr Nephrol
; 36(12): 4029-4032, 2021 12.
Artigo
Inglês
| MEDLINE | ID: mdl-34185135
20.
Alantolactone ameliorates graft versus host disease in mice.
Int Immunopharmacol
; 128: 111560, 2024 Feb 15.
Artigo
Inglês
| MEDLINE | ID: mdl-38246003