Balicza P - Search Results

1

[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. Ideggyogy Sz. 2012 Jul 30;65(7-8):239-42. Ideggyogy Sz. 2012. PMID: 23074843 Hungarian.

2

Genetic background of the hereditary spastic paraplegia phenotypes in Hungary - An analysis of 58 probands.

Balicza P, Grosz Z, Gonzalez MA, Bencsik R, Pentelenyi K, Gal A, Varga E, Klivenyi P, Koller J, Züchner S, Molnar JM. Balicza P, et al. J Neurol Sci. 2016 May 15;364:116-21. doi: 10.1016/j.jns.2016.03.018. Epub 2016 Mar 12. J Neurol Sci. 2016. PMID: 27084228

3

Targeted next generation sequencing of a panel of autism-related genes identifies an EHMT1 mutation in a Kleefstra syndrome patient with autism and normal intellectual performance.

Bock I, Németh K, Pentelényi K, Balicza P, Balázs A, Molnár MJ, Román V, Nagy J, Lévay G, Kobolák J, Dinnyés A. Bock I, et al. Among authors: balicza p. Gene. 2016 Dec 31;595(2):131-141. doi: 10.1016/j.gene.2016.09.027. Epub 2016 Sep 17. Gene. 2016. PMID: 27651234

4

MSTO1 is a cytoplasmic pro-mitochondrial fusion protein, whose mutation induces myopathy and ataxia in humans.

Gal A, Balicza P, Weaver D, Naghdi S, Joseph SK, Várnai P, Gyuris T, Horváth A, Nagy L, Seifert EL, Molnar MJ, Hajnóczky G. Gal A, et al. Among authors: balicza p. EMBO Mol Med. 2017 Jul;9(7):967-984. doi: 10.15252/emmm.201607058. EMBO Mol Med. 2017. PMID: 28554942 Free PMC article.

5

The Panomics Approach in Neurodegenerative Disorders.

Szatmari B, Balicza P, Nemeth G, Molnar MJ. Szatmari B, et al. Among authors: balicza p. Curr Med Chem. 2019;26(10):1712-1720. doi: 10.2174/0929867324666170705120038. Curr Med Chem. 2019. PMID: 28685677 Review.

6

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: balicza p. 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.

7

Implementation of personalized medicine in Central-Eastern Europe: pitfalls and potentials based on citizen's attitude.

Balicza P, Terebessy A, Grosz Z, Varga NA, Gal A, Fekete BA, Molnar MJ. Balicza P, et al. EPMA J. 2018 Feb 9;9(1):103-112. doi: 10.1007/s13167-017-0125-3. eCollection 2018 Mar. EPMA J. 2018. PMID: 29515690 Free PMC article.

8

The rs13388259 Intergenic Polymorphism in the Genomic Context of the BCYRN1 Gene Is Associated with Parkinson's Disease in the Hungarian Population.

Márki S, Göblös A, Szlávicz E, Török N, Balicza P, Bereznai B, Takáts A, Engelhardt J, Klivényi P, Vécsei L, Molnár MJ, Nagy N, Széll M. Márki S, et al. Among authors: balicza p. Parkinsons Dis. 2018 Apr 3;2018:9351598. doi: 10.1155/2018/9351598. eCollection 2018. Parkinsons Dis. 2018. PMID: 29850016 Free PMC article.

9

[Significance of whole exome sequencing in the diagnostics of rare neurological diseases - own experiences through a case presenting with ataxia].

Balicza P, Grosz Z, Bencsik R, Illés A, Gál A, Gézsi A, Molnár MJ. Balicza P, et al. Orv Hetil. 2018 Jul;159(28):1163-1169. doi: 10.1556/650.2018.31049. Orv Hetil. 2018. PMID: 29983107 Hungarian.

10

NKX2-1 New Mutation Associated With Myoclonus, Dystonia, and Pituitary Involvement.

Balicza P, Grosz Z, Molnár V, Illés A, Csabán D, Gézsi A, Dézsi L, Zádori D, Vécsei L, Molnár MJ. Balicza P, et al. Front Genet. 2018 Aug 22;9:335. doi: 10.3389/fgene.2018.00335. eCollection 2018. Front Genet. 2018. PMID: 30186310 Free PMC article.

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