Molnár MJ - Search Results

1

[Retinal ganglion cell layer and visual function in patients with progressive external ophthalmoplegia caused by common mtDNA deletion].

Naghizadeh F, Varga ET, Molnár MJ, Holló G. Naghizadeh F, et al. Among authors: molnar mj. Ideggyogy Sz. 2014 Sep 30;67(9-10):335-41. Ideggyogy Sz. 2014. PMID: 25518262 Hungarian.

2

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: molnar mj. 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

3

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: molnar mj. 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

4

New Insights of Phospholipase A2 Associated Neurodegeneration Phenotype Based on the Long-Term Follow-Up of a Large Hungarian Family.

Toth-Bencsik R, Balicza P, Varga ET, Lengyel A, Rudas G, Gal A, Molnar MJ. Toth-Bencsik R, et al. Among authors: molnar mj. Front Genet. 2021 Jun 8;12:628904. doi: 10.3389/fgene.2021.628904. eCollection 2021. Front Genet. 2021. PMID: 34168672 Free PMC article.

5

[DYT1 positive generalised dystonia: a case study of two siblings].

Bereznai B, Baraczka K, Nagy Z, Molnár MJ. Bereznai B, et al. Among authors: molnar mj. Ideggyogy Sz. 2007 Jul 30;60(7-8):342-7. Ideggyogy Sz. 2007. PMID: 17713116 Hungarian.

6

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

7

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: molnar mj. Ideggyogy Sz. 2014 Nov 30;67(11-12):420-5. Ideggyogy Sz. 2014. PMID: 25720245

8

[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.

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: molnar mj. 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

[DISEASE BURDEN OP DUCHENNE MUSCULAR DYSTROPHY PATIENTS AND THEIR CAREGIVERS].

Péntek M, Herczegfalvi Á, Molnár MJ, Szőnyi LP, Kosztolányi G, Pfliegler G, Melegh B, Boncz I, Brodszky V, Baji P, Szegedi M, Pogány G, Gulácsi L. Péntek M, et al. Among authors: molnar mj. Ideggyogy Sz. 2016 Mar 30;69(5-6):183-93. doi: 10.18071/isz.69.0183. Ideggyogy Sz. 2016. PMID: 27468608 Free article. Hungarian.

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