Molnar MJ - Search Results

1

Correlation of GAA Genotype and Acid-α-Glucosidase Enzyme Activity in Hungarian Patients with Pompe Disease.

Gal A, Grosz Z, Borsos B, Szatmari I, Sebők A, Jávor L, Harmath V, Szakszon K, Dezsi L, Balku E, Jobbagy Z, Herczegfalvi A, Almássy Z, Kerényi L, Molnar MJ. Gal A, et al. Among authors: molnar mj. Life (Basel). 2021 May 31;11(6):507. doi: 10.3390/life11060507. Life (Basel). 2021. PMID: 34072668 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

Genetically determined neuropathy (CMT 1A) accompanied by immune dysfunction: a case report.

Pál Z, Kiss E, Gál A, Csépány T, Lengyel A, Molnar MJ. Pál Z, et al. Among authors: molnar mj. Inflamm Res. 2009 Jul;58(7):359-61. doi: 10.1007/s00011-009-0025-7. Epub 2009 Mar 10. Inflamm Res. 2009. PMID: 19274435

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

[Clinical manifestations, course and outcome of enzyme replacement therapy in Hungarian patients with Pompe's disease].

Bereznai B, Trauninger A, György I, Szakszon K, Almássy Z, Pál E, Herczegfalvi A, Várdi Visy K, Illés Z, Molnár MJ. Bereznai B, et al. Among authors: molnar mj. Orv Hetil. 2011 Sep 25;152(39):1569-75. doi: 10.1556/OH.2011.29184. Orv Hetil. 2011. PMID: 21920843 Hungarian.

7

[Role of associated alleles and hypomethylation status in the clinical expression of facioscapulohumeral muscular dystrophy].

Pikó H, Molnár MJ, Herczegfalvi A, Mayer P, Karcagi V. Pikó H, et al. Among authors: molnar mj. Orv Hetil. 2011 Sep 25;152(39):1576-85. doi: 10.1556/OH.2011.29179. Orv Hetil. 2011. PMID: 21920844 Hungarian.

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: 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.

9

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

10

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

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