Pentelenyi K - Search Results

1

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: pentelenyi k. 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

2

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: pentelenyi k. 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

3

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

4

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. 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

5

[Maternally inherited diabetes mellitus, deafness, chronic progressive external ophthalmoplegia and myopathy as the result of A3243G mutation of mtDNA].

Gál A, Szabó A, Pentelényi K, Pál Z. Gál A, et al. Among authors: pentelenyi k. Orv Hetil. 2008 Aug 24;149(34):1593-8. doi: 10.1556/OH.2008.28398. Orv Hetil. 2008. PMID: 18708313 Review. Hungarian.

6

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: pentelenyi k. 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.

7

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: pentelenyi k. Front Genet. 2019 May 8;10:434. doi: 10.3389/fgene.2019.00434. eCollection 2019. Front Genet. 2019. PMID: 31134136 Free PMC article.

8

Genetic background of the hereditary spastic paraplegia phenotypes in Hungary - An analysis of 58 probands.

Balicza P, Grosz Z, Gonzalez MA, Bencsik R, Pentelenyi K, Gal A, Varga E, Klivenyi P, Koller J, Züchner S, Molnar JM. Balicza P, et al. Among authors: pentelenyi k. J Neurol Sci. 2016 May 15;364:116-21. doi: 10.1016/j.jns.2016.03.018. Epub 2016 Mar 12. J Neurol Sci. 2016. PMID: 27084228

9

Broadening the phenotype of the TWNK gene associated Perrault syndrome.

Fekete B, Pentelényi K, Rudas G, Gál A, Grosz Z, Illés A, Idris J, Csukly G, Domonkos A, Molnar MJ. Fekete B, et al. Among authors: pentelenyi k. BMC Med Genet. 2019 Dec 18;20(1):198. doi: 10.1186/s12881-019-0934-4. BMC Med Genet. 2019. PMID: 31852434 Free PMC article.

10

[Hereditary Parkinson’s disease as a new clinical manifestation of the damaged POLG gene].

Illés A, Balicza P, Gál A, Pentelényi K, Csabán D, Gézsi A, Molnár V, Molnár MJ. Illés A, et al. Among authors: pentelenyi k. Orv Hetil. 2020 May 1;161(20):821-828. doi: 10.1556/650.2020.31724. Orv Hetil. 2020. PMID: 32364361 Hungarian.

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