Remenyi V - Search Results

1

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. Among authors: remenyi v. 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

2

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: remenyi v. Acta Physiol Hung. 2012 Mar;99(1):33-9. doi: 10.1556/APhysiol.99.2012.1.4. Acta Physiol Hung. 2012. PMID: 22425806

3

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: remenyi v. Ideggyogy Sz. 2011 Nov 30;64(11-12):399-403. Ideggyogy Sz. 2011. PMID: 22611618

4

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. Mitochondrial DNA. 2015 Aug;26(4):572-8. doi: 10.3109/19401736.2013.878901. Epub 2014 Jan 17. Mitochondrial DNA. 2015. PMID: 24438288

5

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: remenyi v. 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

6

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: remenyi v. 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

7

Interleukin-4 receptor alpha polymorphisms in autoimmune myasthenia gravis in a Caucasian population.

Pál Z, Varga Z, Semsei Á, Reményi V, Rózsa C, Falus A, Illes Z, Buzás EI, Molnar MJ. Pál Z, et al. Among authors: remenyi v. Hum Immunol. 2012 Feb;73(2):193-5. doi: 10.1016/j.humimm.2011.11.001. Epub 2011 Nov 12. Hum Immunol. 2012. PMID: 22119518

8

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: remenyi v. Behav Brain Funct. 2012 Feb 13;8:9. doi: 10.1186/1744-9081-8-9. Behav Brain Funct. 2012. PMID: 22329956 Free PMC article.

9

Mitochondrial dysfunction and autism: comprehensive genetic analyses of children with autism and mtDNA deletion.

Varga NÁ, Pentelényi K, Balicza P, Gézsi A, Reményi V, Hársfalvi V, Bencsik R, Illés A, Prekop C, Molnár MJ. Varga NÁ, et al. Among authors: remenyi v. Behav Brain Funct. 2018 Feb 20;14(1):4. doi: 10.1186/s12993-018-0135-x. Behav Brain Funct. 2018. PMID: 29458409 Free PMC article.

10

Bcl-2 or bcl-XL gene therapy increases neural plasticity proteins nestin and c-fos expression in PC12 cells.

Gal A, Pentelenyi K, Remenyi V, Wappler EA, Safrany G, Skopal J, Nagy Z. Gal A, et al. Among authors: remenyi v. Neurochem Int. 2009 Sep;55(5):349-53. doi: 10.1016/j.neuint.2009.04.003. Epub 2009 Apr 16. Neurochem Int. 2009. PMID: 19375463

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