Inczédy-Farkas G - Search Results

1

[SCHIZOBANK - The Hungarian national schizophrenia biobank and its role in schizophrenia research and in personalized medicine].

Inczédy-Farkas G, Benkovits J, Balogh N, Almos P, Scholtz B, Zahuczky G, Török Z, Nagy K, Réthelyi J, Makkos Z, Kassai-Farkas A, Egerházy A, Tuzko J, Janka Z, Bitter I, Németh G, Nagy L, Molnár MJ. Inczédy-Farkas G, et al. Orv Hetil. 2010 Aug 29;151(35):1403-8. doi: 10.1556/OH.2010.28943. Orv Hetil. 2010. PMID: 20719713 Hungarian.

2

[Clinical characteristics of cannabis-induced schizophrenia spectrum disorder].

Makkos Z, Fejes L, Inczédy-Farkas G, Kassai-Farkas A, Faludi G, Lazáry J. Makkos Z, et al. Among authors: inczedy farkas g. Neuropsychopharmacol Hung. 2011 Sep;13(3):127-38. doi: 10.5706/nph201109001. Neuropsychopharmacol Hung. 2011. PMID: 21876221 Free article. Hungarian.

3

Psychopharmacological comparison of schizophrenia spectrum disorder with and without cannabis dependency.

Makkos Z, Fejes L, Inczédy-Farkas G, Kassai-Farkas A, Faludi G, Lazary J. Makkos Z, et al. Among authors: inczedy farkas g. Prog Neuropsychopharmacol Biol Psychiatry. 2011 Jan 15;35(1):212-7. doi: 10.1016/j.pnpbp.2010.11.007. Epub 2010 Nov 16. Prog Neuropsychopharmacol Biol Psychiatry. 2011. PMID: 21087649

4

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

5

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

6

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

7

Wernicke-Korsakoff syndrome associated with mtDNA disease.

Jimoh IJ, Sebe B, Balicza P, Fedor M, Pataky I, Rudas G, Gal A, Inczedy-Farkas G, Nemeth G, Molnar MJ. Jimoh IJ, et al. Among authors: inczedy farkas g. Ther Adv Neurol Disord. 2020 Jul 30;13:1756286420938972. doi: 10.1177/1756286420938972. eCollection 2020. Ther Adv Neurol Disord. 2020. PMID: 32821290 Free PMC article.

8

Mitochondrial DNA mutations and cognition: a case-series report.

Inczedy-Farkas G, Trampush JW, Perczel Forintos D, Beech D, Andrejkovics M, Varga Z, Remenyi V, Bereznai B, Gal A, Molnar MJ. Inczedy-Farkas G, et al. Arch Clin Neuropsychol. 2014 Jun;29(4):315-21. doi: 10.1093/arclin/acu016. Epub 2014 Apr 28. Arch Clin Neuropsychol. 2014. PMID: 24777554

9

The coexistence of dynamin 2 mutation and multiple mitochondrial DNA (mtDNA) deletions in the background of severe cardiomyopathy and centronuclear myopathy.

Gal A, Inczedy-Farkas G, Pal E, Remenyi V, Bereznai B, Geller L, Szelid Z, Merkely B, Molnar MJ. Gal A, et al. Among authors: inczedy farkas g. Clin Neuropathol. 2015 Mar-Apr;34(2):89-95. doi: 10.5414/NP300789. Clin Neuropathol. 2015. PMID: 25492887 Free article.

10

The modifying effect a PMP22 deletion in a family with Charcot-Marie-Tooth type 1 neuropathy due to an EGR2 mutation.

Reményi V, Inczédy-Farkas G, Gál A, Bereznai B, Pál Z, Karcagi V, Mechler F, Molnár MJ. Reményi V, et al. Among authors: inczedy farkas g. Ideggyogy Sz. 2014 Nov 30;67(11-12):420-5. Ideggyogy Sz. 2014. PMID: 25720245

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