Nagy D - Search Results

1

Cerebrovascular Pathology in Hypertriglyceridemic APOB-100 Transgenic Mice.

Hoyk Z, Tóth ME, Lénárt N, Nagy D, Dukay B, Csefová A, Zvara Á, Seprényi G, Kincses A, Walter FR, Veszelka S, Vígh J, Barabási B, Harazin A, Kittel Á, Puskás LG, Penke B, Vígh L, Deli MA, Sántha M. Hoyk Z, et al. Among authors: nagy d. Front Cell Neurosci. 2018 Oct 25;12:380. doi: 10.3389/fncel.2018.00380. eCollection 2018. Front Cell Neurosci. 2018. PMID: 30410436 Free PMC article.

2

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.

Zodanu GKE, Oszlánczi M, Havasi K, Kalapos A, Rácz G, Katona M, Ujfalusi A, Nagy O, Széll M, Nagy D. Zodanu GKE, et al. Among authors: nagy d, nagy o. Front Genet. 2021 Apr 29;12:635480. doi: 10.3389/fgene.2021.635480. eCollection 2021. Front Genet. 2021. PMID: 33995479 Free PMC article.

3

Comprehensive Genetic Analysis of a Hungarian Amyotrophic Lateral Sclerosis Cohort.

Tripolszki K, Gampawar P, Schmidt H, Nagy ZF, Nagy D, Klivényi P, Engelhardt JI, Széll M. Tripolszki K, et al. Among authors: nagy zf, nagy d. Front Genet. 2019 Aug 16;10:732. doi: 10.3389/fgene.2019.00732. eCollection 2019. Front Genet. 2019. PMID: 31475037 Free PMC article.

4

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

Nagy O, Szakszon K, Biró BO, Mogyorósy G, Nagy D, Nagy B, Balogh I, Ujfalusi A. Nagy O, et al. Among authors: nagy d, nagy b. J Biotechnol. 2019 Jun 20;299:86-95. doi: 10.1016/j.jbiotec.2019.04.025. Epub 2019 May 1. J Biotechnol. 2019. PMID: 31054299

5

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

Tripolszki K, Danis J, Padhi AK, Gomes J, Bozó R, Nagy ZF, Nagy D, Klivényi P, Engelhardt JI, Széll M. Tripolszki K, et al. Among authors: nagy zf, nagy d. Brain Behav. 2019 Jun;9(6):e01293. doi: 10.1002/brb3.1293. Epub 2019 Apr 25. Brain Behav. 2019. PMID: 31025543 Free PMC article.

6

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

Tripolszki K, Csányi B, Nagy D, Ratti A, Tiloca C, Silani V, Kereszty É, Török N, Vécsei L, Engelhardt JI, Klivényi P, Nagy N, Széll M. Tripolszki K, et al. Among authors: nagy d, nagy n. Neurobiol Aging. 2017 May;53:195.e1-195.e5. doi: 10.1016/j.neurobiolaging.2017.01.016. Epub 2017 Jan 29. Neurobiol Aging. 2017. PMID: 28222900 Free article.

7

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

Büki G, Zsigmond A, Czakó M, Szalai R, Antal G, Farkas V, Fekete G, Nagy D, Széll M, Tihanyi M, Melegh B, Hadzsiev K, Bene J. Büki G, et al. Among authors: nagy d. Front Genet. 2021 Jun 8;12:673025. doi: 10.3389/fgene.2021.673025. eCollection 2021. Front Genet. 2021. PMID: 34168676 Free PMC article.

8

[Genetic heterogeneity and complexity of congenital heart defects].

Nagy D, Széll M. Nagy D, et al. Orv Hetil. 2018 Apr;159(17):661-670. doi: 10.1556/650.2018.31054. Orv Hetil. 2018. PMID: 29681176 Review. Hungarian.

9

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

Nagy D, Farkas K, Armengol L, Segura M, Esi Zodanu GK, Csányi B, Zimmermann A, Vámos B, Széll M. Nagy D, et al. Eur J Med Genet. 2020 Apr;63(4):103800. doi: 10.1016/j.ejmg.2019.103800. Epub 2019 Oct 31. Eur J Med Genet. 2020. PMID: 31678216 Review. No abstract available.

10

[Genetic aspects of Gorlin‒Goltz syndrome].

Vetró É, Oláh J, Nagy D, Széll M, Piffkó J, Seres L. Vetró É, et al. Among authors: nagy d. Orv Hetil. 2020 Dec 6;161(49):2072-2077. doi: 10.1556/650.2020.31933. Print 2020 Dec 6. Orv Hetil. 2020. PMID: 33279882 Review. Hungarian.

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