Detalhe da pesquisa
1.
Inborn Errors of RNA Lariat Metabolism in Humans with Brainstem Viral Infection.
Cell
; 172(5): 952-965.e18, 2018 02 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-29474921
2.
Transendothelial migration of lymphocytes mediated by intraendothelial vesicle stores rather than by extracellular chemokine depots.
Nat Immunol
; 13(1): 67-76, 2011 Dec 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-22138716
3.
Adherence to Immunization: Rebuttal of Vaccine Hesitancy.
Acta Haematol
; 144(4): 413-417, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-33202404
4.
Correction to: Human Inborn Errors of Immunity: 2019 Update on the Classification from the International Union of Immunological Societies Expert Committee.
J Clin Immunol
; 40(1): 65, 2020 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-32086639
5.
Human Inborn Errors of Immunity: 2019 Update of the IUIS Phenotypical Classification.
J Clin Immunol
; 40(1): 66-81, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32048120
6.
Human Inborn Errors of Immunity: 2019 Update on the Classification from the International Union of Immunological Societies Expert Committee.
J Clin Immunol
; 40(1): 24-64, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31953710
7.
Leucocyte adhesion deficiency-A multicentre national experience.
Eur J Clin Invest
; 49(2): e13047, 2019 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-30412664
8.
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
9.
The 2017 IUIS Phenotypic Classification for Primary Immunodeficiencies.
J Clin Immunol
; 38(1): 129-143, 2018 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29226301
10.
International Union of Immunological Societies: 2017 Primary Immunodeficiency Diseases Committee Report on Inborn Errors of Immunity.
J Clin Immunol
; 38(1): 96-128, 2018 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29226302
11.
Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotype.
Blood
; 127(25): 3154-64, 2016 06 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-27114460
12.
Immune defects caused by mutations in the ubiquitin system.
J Allergy Clin Immunol
; 139(3): 743-753, 2017 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-28270366
13.
Ataxia-telangiectasia: Immunodeficiency and survival.
Clin Immunol
; 178: 45-55, 2017 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-28126470
14.
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
15.
The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency.
J Allergy Clin Immunol
; 136(2): 402-12, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-25724123
16.
Deleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunity.
Am J Hum Genet
; 90(6): 986-1001, 2012 Jun 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-22608502
17.
Lazy Leukocyte Syndrome-an Enigma Finally Solved?
J Clin Immunol
; 40(1): 9-12, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31768891
18.
Primary Immunodeficiency Diseases: an Update on the Classification from the International Union of Immunological Societies Expert Committee for Primary Immunodeficiency 2015.
J Clin Immunol
; 35(8): 696-726, 2015 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-26482257
19.
The 2015 IUIS Phenotypic Classification for Primary Immunodeficiencies.
J Clin Immunol
; 35(8): 727-38, 2015 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-26445875
20.
Leukocyte adhesion deficiency type III: clinical features and treatment with stem cell transplantation.
J Pediatr Hematol Oncol
; 37(4): 264-8, 2015 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-25072369