Molnár MJ - 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: molnar mj. Ideggyogy Sz. 2012 Jul 30;65(7-8):239-42. Ideggyogy Sz. 2012. PMID: 23074843 Hungarian.

2

[Hereditary motor and sensory Lom-neuropathy--first Hungarian case report].

Szabó A, Siska E, Molnár MJ. Szabó A, et al. Among authors: molnar mj. Ideggyogy Sz. 2007 Jan 20;60(1-2):51-5. Ideggyogy Sz. 2007. PMID: 17432095 Hungarian.

3

[Congenital cataracts facial dysmorphism neuropathy syndrome--first Hungarian case report].

Siska E, Neuwirth M, Rebecca G, Molnár MJ. Siska E, et al. Among authors: molnar mj. Ideggyogy Sz. 2007 May 30;60(5-6):257-62. Ideggyogy Sz. 2007. PMID: 17578274 Hungarian.

4

[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.

5

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

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

6

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. Among authors: molnar mj. 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

7

[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.

8

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

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

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: 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.

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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