Gal A - Search Results

1

Correlation of GAA Genotype and Acid-α-Glucosidase Enzyme Activity in Hungarian Patients with Pompe Disease.

Gal A, Grosz Z, Borsos B, Szatmari I, Sebők A, Jávor L, Harmath V, Szakszon K, Dezsi L, Balku E, Jobbagy Z, Herczegfalvi A, Almássy Z, Kerényi L, Molnar MJ. Gal A, et al. Life (Basel). 2021 May 31;11(6):507. doi: 10.3390/life11060507. Life (Basel). 2021. PMID: 34072668 Free PMC article.

2

Three novel mutations and genetic epidemiology analysis of the Gap Junction Beta 1 (GJB1) gene among Hungarian Charcot-Marie-Tooth disease patients.

Milley GM, Varga ET, Grosz Z, Bereznai B, Aranyi Z, Boczan J, Dioszeghy P, Kálmán B, Gal A, Molnar MJ. Milley GM, et al. Among authors: gal a. Neuromuscul Disord. 2016 Oct;26(10):706-711. doi: 10.1016/j.nmd.2016.07.012. Epub 2016 Jul 27. Neuromuscul Disord. 2016. PMID: 27544631

3

Genotypic and phenotypic spectrum of the most common causative genes of Charcot-Marie-Tooth disease in Hungarian patients.

Milley GM, Varga ET, Grosz Z, Nemes C, Arányi Z, Boczán J, Diószeghy P, Molnár MJ, Gál A. Milley GM, et al. Among authors: gal a. Neuromuscul Disord. 2018 Jan;28(1):38-43. doi: 10.1016/j.nmd.2017.08.007. Epub 2017 Sep 8. Neuromuscul Disord. 2018. PMID: 29174527

4

The Role of Genetic Testing in the Clinical Practice and Research of Early-Onset Parkinsonian Disorders in a Hungarian Cohort: Increasing Challenge in Genetic Counselling, Improving Chances in Stratification for Clinical Trials.

Illés A, Csabán D, Grosz Z, Balicza P, Gézsi A, Molnár V, Bencsik R, Gál A, Klivényi P, Molnar MJ. Illés A, et al. Among authors: gal a. Front Genet. 2019 Oct 31;10:1061. doi: 10.3389/fgene.2019.01061. eCollection 2019. Front Genet. 2019. PMID: 31737044 Free PMC article.

5

Implementation of personalized medicine in Central-Eastern Europe: pitfalls and potentials based on citizen's attitude.

Balicza P, Terebessy A, Grosz Z, Varga NA, Gal A, Fekete BA, Molnar MJ. Balicza P, et al. Among authors: gal a. EPMA J. 2018 Feb 9;9(1):103-112. doi: 10.1007/s13167-017-0125-3. eCollection 2018 Mar. EPMA J. 2018. PMID: 29515690 Free PMC article.

6

New Insights of Phospholipase A2 Associated Neurodegeneration Phenotype Based on the Long-Term Follow-Up of a Large Hungarian Family.

Toth-Bencsik R, Balicza P, Varga ET, Lengyel A, Rudas G, Gal A, Molnar MJ. Toth-Bencsik R, et al. Among authors: gal a. Front Genet. 2021 Jun 8;12:628904. doi: 10.3389/fgene.2021.628904. eCollection 2021. Front Genet. 2021. PMID: 34168672 Free PMC article.

7

Genetic landscape of early-onset dementia in Hungary.

Csaban D, Illes A, Renata TB, Balicza P, Pentelenyi K, Molnar V, Gezsi A, Grosz Z, Gal A, Kovacs T, Klivenyi P, Molnar MJ. Csaban D, et al. Among authors: gal a. Neurol Sci. 2022 Sep;43(9):5289-5300. doi: 10.1007/s10072-022-06168-8. Epub 2022 Jun 25. Neurol Sci. 2022. PMID: 35752680 Free PMC article.

8

The effect of the CYP 2C19*2 polymorphism on stroke care.

Nyírő G, Inczédy-Farkas G, Reményi V, Gál A, Pál Z, Molnár MJ. Nyírő G, et al. Among authors: gal a. Acta Physiol Hung. 2012 Mar;99(1):33-9. doi: 10.1556/APhysiol.99.2012.1.4. Acta Physiol Hung. 2012. PMID: 22425806

9

Asian-specific mitochondrial genome polymorphism (9-bp deletion) in Hungarian patients with mitochondrial disease.

Pentelenyi K, Remenyi V, Gal A, Milley GM, Csosz A, Mende BG, Molnar MJ. Pentelenyi K, et al. Among authors: gal a. Mitochondrial DNA A DNA Mapp Seq Anal. 2016 May;27(3):1697-700. doi: 10.3109/19401736.2014.961128. Epub 2014 Sep 22. Mitochondrial DNA A DNA Mapp Seq Anal. 2016. PMID: 25242187

10

Comprehensive Analysis of Rare Variants of 101 Autism-Linked Genes in a Hungarian Cohort of Autism Spectrum Disorder Patients.

Balicza P, Varga NÁ, Bolgár B, Pentelényi K, Bencsik R, Gál A, Gézsi A, Prekop C, Molnár V, Molnár MJ. Balicza P, et al. Among authors: gal a. Front Genet. 2019 May 8;10:434. doi: 10.3389/fgene.2019.00434. eCollection 2019. Front Genet. 2019. PMID: 31134136 Free PMC article.

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