Molnar MJ - Search Results

1

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: molnar v, molnar mj. 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.

2

Challenges for the genetic screening in dysferlin deficiency--report of an instructive case and review of the literature.

Gal A, Siska E, Nagy Z, Karpati G, Molnar MJ. Gal A, et al. Among authors: molnar mj. Clin Neuropathol. 2008 Sep-Oct;27(5):289-94. doi: 10.5414/npp27289. Clin Neuropathol. 2008. PMID: 18808059

3

Cathepsin D (C224T) polymorphism in sporadic and genetic Creutzfeldt-Jakob disease.

Kovacs GG, Sanchez-Juan P, Ströbel T, Schuur M, Poleggi A, Nocentini S, Giannattasio C, Belay G, Bishop M, Capellari S, Parchi P, Gelpi E, Gal A, Bakos A, Molnar MJ, Heinemann U, Zerr I, Knight RS, Mitrova E, van Duijn C, Budka H. Kovacs GG, et al. Among authors: molnar mj. Alzheimer Dis Assoc Disord. 2010 Jan-Mar;24(1):104-7. doi: 10.1097/WAD.0b013e3181ad378c. Alzheimer Dis Assoc Disord. 2010. PMID: 19571726

4

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: molnar mj. 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

5

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: molnar mj. 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

6

Coexisting huntingtin and SCA8 repeat expansion: case report of a severe complex neurodegenerative syndrome.

Bereznai B, Lovas G, Pentelenyi K, Rudas G, Molnar MJ. Bereznai B, et al. Among authors: molnar mj. J Neurol Sci. 2010 Jun 15;293(1-2):116-8. doi: 10.1016/j.jns.2010.03.006. Epub 2010 Apr 18. J Neurol Sci. 2010. PMID: 20403608

7

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: molnar mj. Behav Brain Funct. 2012 Feb 13;8:9. doi: 10.1186/1744-9081-8-9. Behav Brain Funct. 2012. PMID: 22329956 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: molnar mj. 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: molnar mj. Ideggyogy Sz. 2011 Nov 30;64(11-12):399-403. Ideggyogy Sz. 2011. PMID: 22611618

10

[The absence of the common LRRK2 G2019S mutation in 120 young onset Hungarian Parkinon's disease patients].

Balicza P, Bereznai B, Takáts A, Klivényi P, Dibó G, Hidasi E, Balogh I, Molnár MJ. Balicza P, et al. Among authors: molnar mj. Ideggyogy Sz. 2012 Jul 30;65(7-8):239-42. Ideggyogy Sz. 2012. PMID: 23074843 Hungarian.

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