Molnár MJ - Search Results

1

Beyond C9orf72: repeat expansions and copy number variations as risk factors of amyotrophic lateral sclerosis across various populations.

Nagy ZF, Pál M, Engelhardt JI, Molnár MJ, Klivényi P, Széll M. Nagy ZF, et al. Among authors: molnar mj. BMC Med Genomics. 2024 Jan 22;17(1):30. doi: 10.1186/s12920-024-01807-9. BMC Med Genomics. 2024. PMID: 38254109 Free PMC article. Review.

2

Probing the biological consequences of a previously undescribed de novo mutation of ZMYND11 in a schizophrenia patient by CRISPR genome editing and induced pluripotent stem cell based in vitro disease-modeling.

Tordai C, Hathy E, Gyergyák H, Vincze K, Baradits M, Koller J, Póti Á, Jezsó B, Homolya L, Molnár MJ, Nagy L, Szüts D, Apáti Á, Réthelyi JM. Tordai C, et al. Among authors: molnar mj. Schizophr Res. 2024 Jan 29:S0920-9964(24)00024-0. doi: 10.1016/j.schres.2024.01.024. Online ahead of print. Schizophr Res. 2024. PMID: 38290943 Free article.

3

Compound heterozygous variants in MAPK8IP3 were detected in severe congenital hypotonia mimicking lethal spinal muscular atrophy.

Kárteszi J, Ziegler A, Tihanyi M, Elmont B, Zhang Y, Patócs B, Molnár MJ, Méhes G, Wells K, Jakus R, Bessenyei B, Ranatunga W, Morava É. Kárteszi J, et al. Among authors: molnar mj. Am J Med Genet A. 2023 Sep;191(9):2428-2432. doi: 10.1002/ajmg.a.63340. Epub 2023 Jul 18. Am J Med Genet A. 2023. PMID: 37462082

4

A new family with transportinopathy: increased clinical heterogeneity.

Angelini C, Marozzo R, Pinzan E, Pegoraro V, Molnar MJ, Torella A, Nigro V. Angelini C, et al. Among authors: molnar mj. Ther Adv Neurol Disord. 2019 Jun 9;12:1756286419850433. doi: 10.1177/1756286419850433. eCollection 2019. Ther Adv Neurol Disord. 2019. PMID: 31217819 Free PMC article.

5

Polymyositis and rhabdomyolysis caused by hepatocellular carcinoma - Case report and literature review.

Bárdos D, Molnár MJ, Dudás I, Tuza S, Szijártó A, Hahn O. Bárdos D, et al. Among authors: molnar mj. Ann Med Surg (Lond). 2021 Apr 4;65:102269. doi: 10.1016/j.amsu.2021.102269. eCollection 2021 May. Ann Med Surg (Lond). 2021. PMID: 33912342 Free PMC article.

6

Factors influencing the efficacy, longevity, and safety of electroporation-assisted plasmid-based gene transfer into mouse muscles.

Molnar MJ, Gilbert R, Lu Y, Liu AB, Guo A, Larochelle N, Orlopp K, Lochmuller H, Petrof BJ, Nalbantoglu J, Karpati G. Molnar MJ, et al. Mol Ther. 2004 Sep;10(3):447-55. doi: 10.1016/j.ymthe.2004.06.642. Mol Ther. 2004. PMID: 15336645 Free article.

7

Systematic review on the evaluation criteria of orphan medicines in Central and Eastern European countries.

Zelei T, Molnár MJ, Szegedi M, Kaló Z. Zelei T, et al. Among authors: molnar mj. Orphanet J Rare Dis. 2016 Jun 4;11(1):72. doi: 10.1186/s13023-016-0455-6. Orphanet J Rare Dis. 2016. PMID: 27259284 Free PMC article. Review.

8

Mitochondrial Ca2+ uptake correlates with the severity of the symptoms in autosomal dominant optic atrophy.

Fülöp L, Rajki A, Maka E, Molnár MJ, Spät A. Fülöp L, et al. Among authors: molnar mj. Cell Calcium. 2015 Jan;57(1):49-55. doi: 10.1016/j.ceca.2014.11.008. Epub 2014 Dec 9. Cell Calcium. 2015. PMID: 25533789

9

Chloroquine cardiotoxicity mimicking connective tissue disease heart involvement.

Vereckei A, Fazakas A, Baló T, Fekete B, Molnár MJ, Karádi I. Vereckei A, et al. Among authors: molnar mj. Immunopharmacol Immunotoxicol. 2013 Apr;35(2):304-6. doi: 10.3109/08923973.2013.766801. Epub 2013 Feb 15. Immunopharmacol Immunotoxicol. 2013. PMID: 23409733

10

Management of seizures in patients with primary mitochondrial diseases: consensus statement from the InterERNs Mitochondrial Working Group.

Mancuso M, Papadopoulou MT, Ng YS, Ardissone A, Bellusci M, Bertini E, Di Vito L, Evangelista T, Fons C, Hikmat O, Horvath R, Klopstock T, Kornblum C, Lamperti C, Licchetta L, Molnar MJ, Varhaug KN, O'Callaghan M, Pressler RM, Schiff M, Servidei S, Szabo N, Gorman GS, Cross JH, Rahman S. Mancuso M, et al. Among authors: molnar mj. Eur J Neurol. 2024 Apr 4:e16275. doi: 10.1111/ene.16275. Online ahead of print. Eur J Neurol. 2024. PMID: 38576261

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