Gal A - Search Results

1

Oestrogen receptor alpha gene intronic polymorphisms and autoimmune myasthenia gravis in Caucasian women.

Pal Z, Gal A, Remenyi V, Tordai A, Molnar MJ. Pal Z, et al. Among authors: gal a. Neuromuscul Disord. 2009 Dec;19(12):822-4. doi: 10.1016/j.nmd.2009.09.002. Epub 2009 Sep 29. Neuromuscul Disord. 2009. PMID: 19793653

2

Psychiatric symptoms of patients with primary mitochondrial DNA disorders.

Inczedy-Farkas G, Remenyi V, Gal A, Varga Z, Balla P, Udvardy-Meszaros A, Bereznai B, Molnar MJ. Inczedy-Farkas G, et al. Among authors: gal a. Behav Brain Funct. 2012 Feb 13;8:9. doi: 10.1186/1744-9081-8-9. Behav Brain Funct. 2012. PMID: 22329956 Free PMC article.

3

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

4

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

5

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

6

Novel heteroplasmic mutation in the anticodon stem of mitochondrial tRNA(Lys) associated with dystonia and stroke-like episodes.

Gal A, Pentelenyi K, Remenyi V, Pal Z, Csanyi B, Tomory G, Rasko I, Molnar MJ. Gal A, et al. Acta Neurol Scand. 2010 Oct;122(4):252-6. doi: 10.1111/j.1600-0404.2009.01297.x. Epub 2009 Nov 20. Acta Neurol Scand. 2010. PMID: 19930207

7

Genetically determined neuropathy (CMT 1A) accompanied by immune dysfunction: a case report.

Pál Z, Kiss E, Gál A, Csépány T, Lengyel A, Molnar MJ. Pál Z, et al. Among authors: gal a. Inflamm Res. 2009 Jul;58(7):359-61. doi: 10.1007/s00011-009-0025-7. Epub 2009 Mar 10. Inflamm Res. 2009. PMID: 19274435

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

A8344G mutation of the mitochondrial DNA with typical mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes syndrome.

Vastagh I, Gál A, Reményi V, Semjén J, Lukács T, Valikovics A, Molnár MJ. Vastagh I, et al. Among authors: gal a. Ideggyogy Sz. 2011 Nov 30;64(11-12):399-403. Ideggyogy Sz. 2011. PMID: 22611618

10

Retrospective assessment of the most common mitochondrial DNA mutations in a large Hungarian cohort of suspect mitochondrial cases.

Remenyi V, Inczedy-Farkas G, Komlosi K, Horvath R, Maasz A, Janicsek I, Pentelenyi K, Gal A, Karcagi V, Melegh B, Molnar MJ. Remenyi V, et al. Among authors: gal a. Mitochondrial DNA. 2015 Aug;26(4):572-8. doi: 10.3109/19401736.2013.878901. Epub 2014 Jan 17. Mitochondrial DNA. 2015. PMID: 24438288

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