Detalhe da pesquisa
1.
Neuroimmune communication regulating pruritus in atopic dermatitis.
J Allergy Clin Immunol
; 149(6): 1875-1898, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35337846
2.
Epidemiology of Geriatric-Dermatology virtual clinic: Teledermatology-Based care for elderly patients with skin diseases in Qatar.
Qatar Med J
; 2023(2): 12, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-38025342
3.
Successful treatment of pachyonychia congenita with simvastatin.
J Eur Acad Dermatol Venereol
; 38(4): e356-e358, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-37994233
4.
Severe atopic dermatitis in an Asian-Arabic population treated with dupilumab: A retrospective observational study.
J Eur Acad Dermatol Venereol
; 2024 Apr 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-38651189
5.
Retrospective evaluation of a TEN/SJS series managed with a new treatment protocol.
J Eur Acad Dermatol Venereol
; 2024 May 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-38713099
6.
Itch in elderly patients: Origin, diagnostics, management.
J Allergy Clin Immunol
; 152(1): 42-49, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37220840
7.
Ion Transporters, Channelopathies, and Glucose Disorders.
Int J Mol Sci
; 20(10)2019 May 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-31137773
8.
Emerging Role of the IL-36/IL-36R Axis in Multiple Inflammatory Skin Diseases.
J Invest Dermatol
; 144(2): 206-224, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-38189700
9.
Homozygous Insulin Promotor Gene Mutation Causing Permanent Neonatal Diabetes Mellitus and Childhood Onset Autoantibody Negative Diabetes in the Same Family.
Int Med Case Rep J
; 15: 35-41, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35140529
10.
An induced pluripotent stem cell line derived from a patient with neonatal diabetes and Fanconi-Bickel syndrome caused by a homozygous mutation in the SLC2A2 gene.
Stem Cell Res
; 54: 102433, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-34171785
11.
Epidemiology, genetic landscape and classification of childhood diabetes mellitus in the State of Qatar.
J Diabetes Investig
; 12(12): 2141-2148, 2021 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-34101350
12.
Clinical features, epidemiology, autoantibody status, HLA haplotypes and genetic mechanisms of type 1 diabetes mellitus among children in Qatar.
Sci Rep
; 11(1): 18887, 2021 09 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-34556755
13.
Potential application of mesenchymal stem cells and their exosomes in lung injury: an emerging therapeutic option for COVID-19 patients.
Stem Cell Res Ther
; 11(1): 437, 2020 10 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-33059757
14.
Derivation of a human induced pluripotent stem cell line (QBRIi007-A) from a patient carrying a homozygous intronic mutation (c.613-7T>G) in the SLC2A2 gene.
Stem Cell Res
; 44: 101736, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-32146263
15.
Generation of two human iPSC lines from patients with maturity-onset diabetes of the young type 2 (MODY2) and permanent neonatal diabetes due to mutations in the GCK gene.
Stem Cell Res
; 48: 101991, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32971462
16.
Haploinsufficiency of the FOXA2 associated with a complex clinical phenotype.
Mol Genet Genomic Med
; 8(6): e1086, 2020 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32277595
17.
Generation of a human induced pluripotent stem cell line (QBRIi009-A) from a patient with a heterozygous deletion of FOXA2.
Stem Cell Res
; 42: 101705, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31991389
18.
Clinical Characteristics and Long-term Follow-up of Patients with Diabetes Due To PTF1A Enhancer Mutations.
J Clin Endocrinol Metab
; 105(12)2020 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32893856
19.
The Genetic and Molecular Mechanisms of Congenital Hyperinsulinism.
Front Endocrinol (Lausanne)
; 10: 111, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-30873120
20.
A Systematic Review of Childhood Diabetes Research in the Middle East Region.
Front Endocrinol (Lausanne)
; 10: 805, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31824422