Molnar MJ - Search Results

1

A heterozygous truncating mutation in RRM2B causes autosomal-dominant progressive external ophthalmoplegia with multiple mtDNA deletions.

Tyynismaa H, Ylikallio E, Patel M, Molnar MJ, Haller RG, Suomalainen A. Tyynismaa H, et al. Among authors: molnar mj. Am J Hum Genet. 2009 Aug;85(2):290-5. doi: 10.1016/j.ajhg.2009.07.009. Epub 2009 Aug 6. Am J Hum Genet. 2009. PMID: 19664747 Free PMC article.

2

[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.

3

Interleukin-4 receptor alpha polymorphisms in autoimmune myasthenia gravis in a Caucasian population.

Pál Z, Varga Z, Semsei Á, Reményi V, Rózsa C, Falus A, Illes Z, Buzás EI, Molnar MJ. Pál Z, et al. Among authors: molnar mj. Hum Immunol. 2012 Feb;73(2):193-5. doi: 10.1016/j.humimm.2011.11.001. Epub 2011 Nov 12. Hum Immunol. 2012. PMID: 22119518

4

Mitochondrial diseases.

Molnar MJ, Kovacs GG. Molnar MJ, et al. Handb Clin Neurol. 2017;145:147-155. doi: 10.1016/B978-0-12-802395-2.00010-9. Handb Clin Neurol. 2017. PMID: 28987165 Review.

5

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

6

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

7

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.

8

[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.

9

Marked phenotypic variation in a family with a new myelin protein zero mutation.

Szabo A, Züchner S, Siska E, Mechler F, Molnar MJ. Szabo A, et al. Among authors: molnar mj. Neuromuscul Disord. 2005 Nov;15(11):760-3. doi: 10.1016/j.nmd.2005.07.006. Epub 2005 Sep 28. Neuromuscul Disord. 2005. PMID: 16198109

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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