Publications by authors named "Beata Fabos"

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Real-World Study of Ragweed Sublingual Immunotherapy in Hungary.
Adrienne Nagy, Katalin Balogh, Csilla Csáki, Beáta Fábos, Edit Mohácsi

Allergol Immunopathol (Madr)· September 2024

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Missing Heritability in Albinism: Deep Characterization of a Hungarian Albinism Cohort Raises the Possibility of the Digenic Genetic Background of the Disease.
Nikoletta Nagy, Margit Pal, Jozsef Kun, Bence Galik, Peter Urban, Beata Fabos

Int J Mol Sci· January 2024

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International eDelphi Study to Reach Consensus on the Methotrexate Dosing Regimen in Patients With Psoriasis.
Astrid M van Huizen, Stef P Menting, Rolland Gyulai, Lars Iversen, Gayle E van der Kraaij

JAMA Dermatol· May 2022

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Whole Exome Sequencing in a Series of Patients with a Clinical Diagnosis of Tuberous Sclerosis Not Confirmed by Targeted Sequencing.
Erzsebet Kovesdi, Reka Ripszam, Etelka Postyeni, Emese Beatrix Horvath, Anna Kelemen, Beata Fabos

Genes (Basel)· September 2021

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Methylchloroisothiazolinone/methylisothiazolinone and methylisothiazolinone hypersensitivity in 1122 patients: A national multicenter study organized by the Hungarian Contact Dermatitis Group.
Györgyi Pónyai, Ilona Németh, Gabriella Nagy, Beáta Fábos, Beatrix Irinyi

Contact Dermatitis· December 2019

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From genomes to diaries: a 3-year prospective, real-life study of ragweed-specific sublingual immunotherapy.
Viktor Molnár, Adrienne Nagy, Lilla Tamási, Gabriella Gálffy, Renáta Böcskei

Immunotherapy· November 2017

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Expansion of circulating follicular T helper cells associates with disease severity in childhood atopic dermatitis.
Krisztina Szabó, Krisztián Gáspár, Zsolt Dajnoki, Gábor Papp, Beáta Fábos

Immunol Lett· September 2017

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Delineating the genetic heterogeneity of OCA in Hungarian patients.
Beáta Fábos, Katalin Farkas, Lola Tóth, Adrienn Sulák, Kornélia Tripolszki

Eur J Med Res· June 2017

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Identification of two novel mutations in the SLC45A2 gene in a Hungarian pedigree affected by unusual OCA type 4.
Lola Tóth, Beáta Fábos, Katalin Farkas, Adrienn Sulák, Kornélia Tripolszki

BMC Med Genet· March 2017

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CTSC and Papillon-Lefèvre syndrome: detection of recurrent mutations in Hungarian patients, a review of published variants and database update.
Nikoletta Nagy, Péter Vályi, Zsanett Csoma, Adrienn Sulák, Kornélia Tripolszki

Mol Genet Genomic Med· May 2014

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