Detalhe da pesquisa
1.
Loss of function of ENT3 drives histiocytosis and inflammation through TLR-MAPK signaling.
Blood
; 142(20): 1740-1751, 2023 11 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-37738562
2.
Hypoparathyroidism-Retardation-Dysmorphism Syndrome due to a Variant in the Tubulin-Specific Chaperone E Gene as a Cause of Combined Immune Deficiency.
J Clin Immunol
; 43(2): 350-357, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36258138
3.
SLP76 Mutation Associated with Combined Immunodeficiency and EBV-Related Lymphoma.
J Clin Immunol
; 43(3): 625-635, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36474126
4.
Unusual phenotype in patients with a hypomorphic mutation in the DCLRE1C gene: IgG hypergammaglobulinemia with IgA and IgE deficiency.
Clin Immunol
; 213: 108366, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-32092471
5.
Efficacy of omalizumab treatment for pediatric chronic spontaneous urticaria: A multi-center retrospective case series.
Pediatr Dermatol
; 37(6): 1051-1054, 2020 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-32951239
6.
Gastric Drainage in the Treatment of Near-Fatal Food-Induced Anaphylaxis.
Pediatr Emerg Care
; 36(3): e166-e167, 2020 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-29016518
7.
Neutrophil Functions in Immunodeficiency Due to DOCK8 Deficiency.
Immunol Invest
; 48(4): 431-439, 2019 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-30689480
8.
Risk factors for congenital heart defects in two populations residing in the same geographic area: a long-term population-based study, Southern Israel.
Cardiol Young
; 29(8): 1040-1044, 2019 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-31287039
9.
Analysis of Chronic Granulomatous Disease in the Kavkazi Population in Israel Reveals Phenotypic Heterogeneity in Patients with the Same NCF1 mutation (c.579G>A).
J Clin Immunol
; 38(2): 193-203, 2018 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-29411231
10.
Incidence of typically Severe Primary Immunodeficiency Diseases in Consanguineous and Non-consanguineous Populations.
J Clin Immunol
; 37(3): 295-300, 2017 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-28299599
11.
Chronic granulomatous disease: Clinical, functional, molecular, and genetic studies. The Israeli experience with 84 patients.
Am J Hematol
; 92(1): 28-36, 2017 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-27701760
12.
Anomalous Left Coronary Artery From the Pulmonary Artery in Infants and Toddlers Misdiagnosed as Myocarditis.
Pediatr Emerg Care
; 32(4): 232-4, 2016 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-26414630
13.
Defining the biological responses of IL-6 by the study of a novel IL-6 receptor chain immunodeficiency.
J Allergy Clin Immunol
; 145(3): 1011-1015.e6, 2020 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-31778705
14.
Anaphylactic reactions in adult patients in Southern Israel.
Asian Pac J Allergy Immunol
; 34(1): 44-50, 2016 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-26994625
15.
Clinical features of Candidiasis in patients with inherited interleukin 12 receptor ß1 deficiency.
Clin Infect Dis
; 58(2): 204-13, 2014 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-24186907
16.
The effects of Bruton tyrosine kinase inhibition on chemotaxis and superoxide generation in human neutrophils.
J Clin Immunol
; 34(5): 555-60, 2014 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-24771458
17.
Thymic function in MHC class II-deficient patients.
J Allergy Clin Immunol
; 131(3): 831-9, 2013 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-23228244
18.
[Allergy to non-steroidal antiinflammatory drugs: recommendations of the Israeli allergy and clinical immunology association].
Harefuah
; 153(10): 605-9, 623, 2014 Oct.
Artigo
em Hebraico
| MEDLINE | ID: mdl-25518080
19.
IL-12Rß1 deficiency: mutation update and description of the IL12RB1 variation database.
Hum Mutat
; 34(10): 1329-39, 2013 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-23864330
20.
A novel epsilon gamma delta beta thalassemia presenting with pregnancy complications and severe neonatal anemia.
Eur J Haematol
; 90(2): 127-33, 2013 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-23206178