Detalhe da pesquisa
1.
Phenotypic and Genotypic Characterization of Hereditary Angioedema in Saudi Arabia.
J Clin Immunol
; 43(2): 479-484, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36348183
2.
The international WAO/EAACI guideline for the management of hereditary angioedema-The 2021 revision and update.
Allergy
; 77(7): 1961-1990, 2022 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-35006617
3.
Novel mutation in DOCK8-HIES with severe phenotype and successful transplantation.
Clin Immunol
; 178: 39-44, 2017 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-27890707
4.
Loss of NHEJ1 Protein Due to a Novel Splice Site Mutation in a Family Presenting with Combined Immunodeficiency, Microcephaly, and Growth Retardation and Literature Review.
J Clin Immunol
; 37(6): 575-581, 2017 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-28741180
5.
Evolving spectrum of LRBA deficiency-associated chronic arthritis: is there a causative role in juvenile idiopathic arthritis?
Clin Exp Rheumatol
; 35(2): 327-329, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28134088
6.
Unbiased targeted next-generation sequencing molecular approach for primary immunodeficiency diseases.
J Allergy Clin Immunol
; 137(6): 1780-1787, 2016 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-26915675
7.
Transmission of Middle East Respiratory Syndrome Coronavirus Infections in Healthcare Settings, Abu Dhabi.
Emerg Infect Dis
; 22(4): 647-56, 2016 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-26981708
8.
Detection of SARS-CoV-2 in COVID-19 Patient Nasal Swab Samples Using Signal Processing.
IEEE J Sel Top Signal Process
; 16(2): 164-174, 2022 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-35582704
9.
The international WAO/EAACI guideline for the management of hereditary angioedema - The 2021 revision and update.
World Allergy Organ J
; 15(3): 100627, 2022 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-35497649
10.
The Expanding Spectrum of Mutations in Hereditary Angioedema.
J Allergy Clin Immunol Pract
; 9(6): 2229-2234, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33746090
11.
Assessment of pain in patients with primary immune deficiency.
Saudi J Anaesth
; 15(4): 377-382, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34658722
12.
Admission levels of Soluble Urokinase Plasminogen Activator Receptor (suPAR) are Associated with the Development of Severe Complications in Hospitalised COVID-19 Patients: A Prospective Cohort Study.
Int J Infect Dis
; 107: 188-194, 2021 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-33862208
13.
Novel CARMIL2 Mutations in Patients with Variable Clinical Dermatitis, Infections, and Combined Immunodeficiency.
Front Immunol
; 9: 203, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29479355
14.
Familial Emberger Syndrome With Autoimmunity, Hyper-Immunoglobulin E and Lymphatic Impairment Caused by a Novel GATA2 Mutation.
Hematol Oncol Stem Cell Ther
; 15(2): 63-65, 2022 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32497548
15.
First study of pattern of anaphylaxis in a large tertiary care hospital in Saudi Arabia.
Asia Pac Allergy
; 5(4): 216-21, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-26539404
16.
Hereditary angioedema may be associated with the development of fatty liver.
J Allergy Clin Immunol Pract
; 7(6): 2082-2083, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-30825607
17.
Characteristics of epidemic and sporadic strains of Acinetobacter baumannii isolated in Abu Dhabi hospitals.
J Med Microbiol
; 62(Pt 4): 582-590, 2013 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-23264451