D. Nagy

发表

Toxocariasis associated with chronic cough in childhood: a longitudinal study in Hungary

K. Gyurkovits, O. Bede, J. Danka, 2008, Journal of Helminthology.

Analysis of serum cytokine levels in children with chronic cough associated with Toxocara canis infection

S. Sipka, O. Bede, J. Danka, 2012, Parasite immunology.

Effects of magnesium supplementation on the glutathione redox system in atopic asthmatic children

K. Gyurkovits, O. Bede, A. Surányi, 2008, Inflammation Research.

Genotype-Phenotype Associations in Patients With Type-1, Type-2, and Atypical NF1 Microdeletions

A. Zsigmond, J. Bene, B. Melegh, 2021, Frontiers in Genetics.

Human Epididymis Protein 4: A Novel Serum Inflammatory Biomarker in Cystic Fibrosis.

L. Clarke, M. Macek, M. Amaral, 2016, Chest.

Further delineation of the phenotype of PAK3-associated x-linked intellectual disability: Identification of a novel missense mutation and review of literature.

L. Armengol, M. Széll, Alíz Zimmermann, 2020, European journal of medical genetics.

Copy number variants detection by microarray and multiplex ligation-dependent probe amplification in congenital heart diseases.

B. Nagy, I. Balogh, G. Mogyorósy, 2019, Journal of biotechnology.

Retinal and optic nerve functions in incontinentia pigmenti: long-term elctrophysiological follow-up

G. Benedek, Á. Jánossy, D. Török, 2020 .

SJOVS, December 2020, Vol. 13, No. 2

G. Benedek, A. Kovács, Á. Jánossy, 2020 .

Comparison of lactase persistence polymorphism in ancient and present-day Hungarian populations.

C. Downes, I. Rasko, L. Bartosiewicz, 2011, American journal of physical anthropology.

Prevalence of adult-type hypolactasia as diagnosed with genetic and lactose hydrogen breath tests in Hungarians

I. Rasko, O. Bede, Á. Czibula, 2009, European Journal of Clinical Nutrition.

Skin wipe test: A simple, inexpensive, and fast approach in the diagnosis of cystic fibrosis

P. Dřevínek, M. Dastych, F. Foret, 2020, Pediatric pulmonology.

Comprehensive Genetic Analysis of a Hungarian Amyotrophic Lateral Sclerosis Cohort

H. Schmidt, P. Klivényi, M. Széll, 2019, Front. Genet..

Genotype-Phenotype Comparison in POGZ-Related Neurodevelopmental Disorders by Using Clinical Scoring

W. Chung, Kristen Wigby, C. Fagerberg, 2022, Genes.

Membranous NECTIN-4 Expression Frequently Decreases during Metastatic Spread of Urothelial Carcinoma and Is Associated with Enfortumab Vedotin Resistance

G. Kristiansen, P. Adam, W. Weichert, 2022, Clinical cancer research : an official journal of the American Association for Cancer Research.

Genetic Etiology of Nonsyndromic Hearing Loss in Hungarian Patients

A. Németh, N. Nagy, M. Széll, 2023, International journal of molecular sciences.

Angiogenin mutations in Hungarian patients with amyotrophic lateral sclerosis: Clinical, genetic, computational, and functional analyses

P. Klivényi, J. Gomes, M. Széll, 2019, Brain and behavior.

Genetic analysis of the SOD1 and C9ORF72 genes in Hungarian patients with amyotrophic lateral sclerosis

P. Klivényi, L. Vécsei, C. Tiloca, 2017, Neurobiology of Aging.

Genetic analysis of the SOD 1 and C 9 ORF 72 genes in Hungarian patients with amyotrophic lateral sclerosis

P. Klivényi, L. Vécsei, C. Tiloca, 2017 .

Whole-Exome Sequencing Identified Two Novel Pathogenic Mutations in the PTCH1 Gene in BCNS

J. Piffkó, N. Nagy, M. Széll, 2023, Current issues in molecular biology.

Systemic Screening for 22q11.2 Copy Number Variations in Hungarian Pediatric and Adult Patients With Congenital Heart Diseases Identified Rare Pathogenic Patterns in the Region

M. Széll, G. Racz, A. Kalapos, 2021, Frontiers in Genetics.

Inflammatory fibroid polyp of the renal pelvis: first report at an extra-gastrointestinal site with molecular confirmation

G. Kristiansen, M. Ritter, D. Nagy, 2023, Virchows Archiv.