Bereznai B - 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. Among authors: bereznai b. Ideggyogy Sz. 2012 Jul 30;65(7-8):239-42. Ideggyogy Sz. 2012. PMID: 23074843 Hungarian.

2

[Genetics and present therapy options in Parkinson's disease: a review].

Bereznai B, Molnar MJ. Bereznai B, et al. Ideggyogy Sz. 2009 May 30;62(5-6):155-63. Ideggyogy Sz. 2009. PMID: 19579663 Review. Hungarian.

3

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

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

4

[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. Orv Hetil. 2011 Sep 25;152(39):1569-75. doi: 10.1556/OH.2011.29184. Orv Hetil. 2011. PMID: 21920843 Hungarian.

5

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: bereznai b. Parkinsons Dis. 2018 Apr 3;2018:9351598. doi: 10.1155/2018/9351598. eCollection 2018. Parkinsons Dis. 2018. PMID: 29850016 Free PMC article.

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: bereznai b. 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

[Therapy for anti-MuSK antibody positive myasthenia gravis].

Pál Z, Boczán J, Bereznai B, Lovas G, Molnár MJ. Pál Z, et al. Among authors: bereznai b. Orv Hetil. 2011 Sep 25;152(39):1586-9. doi: 10.1556/OH.2011.29177. Orv Hetil. 2011. PMID: 21920845 Hungarian.

8

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

9

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: bereznai b. Behav Brain Funct. 2012 Feb 13;8:9. doi: 10.1186/1744-9081-8-9. Behav Brain Funct. 2012. PMID: 22329956 Free PMC article.

10

Coexisting huntingtin and SCA8 repeat expansion: case report of a severe complex neurodegenerative syndrome.

Bereznai B, Lovas G, Pentelenyi K, Rudas G, Molnar MJ. Bereznai B, et al. J Neurol Sci. 2010 Jun 15;293(1-2):116-8. doi: 10.1016/j.jns.2010.03.006. Epub 2010 Apr 18. J Neurol Sci. 2010. PMID: 20403608

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