Detalhe da pesquisa
1.
Missing Heritability in Albinism: Deep Characterization of a Hungarian Albinism Cohort Raises the Possibility of the Digenic Genetic Background of the Disease.
Int J Mol Sci
; 25(2)2024 Jan 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-38279271
2.
Identification of two novel mutations in the SLC45A2 gene in a Hungarian pedigree affected by unusual OCA type 4.
BMC Med Genet
; 18(1): 27, 2017 03 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-28298193
3.
Methylchloroisothiazolinone/methylisothiazolinone and methylisothiazolinone hypersensitivity in 1122 patients: A national multicenter study organized by the Hungarian Contact Dermatitis Group.
Contact Dermatitis
; 81(6): 467-469, 2019 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-31373004
4.
International eDelphi Study to Reach Consensus on the Methotrexate Dosing Regimen in Patients With Psoriasis.
JAMA Dermatol
; 158(5): 561-572, 2022 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35353175
5.
Whole Exome Sequencing in a Series of Patients with a Clinical Diagnosis of Tuberous Sclerosis Not Confirmed by Targeted TSC1/TSC2 Sequencing.
Genes (Basel)
; 12(9)2021 09 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34573383
6.
Expansion of circulating follicular T helper cells associates with disease severity in childhood atopic dermatitis.
Immunol Lett
; 189: 101-108, 2017 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-28431963
7.
Delineating the genetic heterogeneity of OCA in Hungarian patients.
Eur J Med Res
; 22(1): 20, 2017 Jun 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-28629449
8.
From genomes to diaries: a 3-year prospective, real-life study of ragweed-specific sublingual immunotherapy.
Immunotherapy
; 9(15): 1279-1294, 2017 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-29130793
9.
CTSC and Papillon-Lefèvre syndrome: detection of recurrent mutations in Hungarian patients, a review of published variants and database update.
Mol Genet Genomic Med
; 2(3): 217-28, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24936511