Molnár MJ - Search Results

1

[Laboratory diagnosis of a rare congenital neurodegenerative disease: cerebrotendinous xanthomatosis].

Varga VE, Katkó M, Harangi J, Balogh I, Kapás I, Madar L, Seres I, Molnár MJ, Paragh G, Kovács GG, Harangi M. Varga VE, et al. Among authors: molnar mj. Orv Hetil. 2014 May 25;155(21):811-6. doi: 10.1556/OH.2014.29887. Orv Hetil. 2014. PMID: 24836315 Review. Hungarian.

2

[Muscle involvement in Crohn disease].

Diószeghy P, Molnár M, Mechler F. Diószeghy P, et al. Orv Hetil. 1994 Jun 5;135(23):1259-61. Orv Hetil. 1994. PMID: 8015822 Hungarian.

3

TARDBP variation associated with frontotemporal dementia, supranuclear gaze palsy, and chorea.

Kovacs GG, Murrell JR, Horvath S, Haraszti L, Majtenyi K, Molnar MJ, Budka H, Ghetti B, Spina S. Kovacs GG, et al. Among authors: molnar mj. Mov Disord. 2009 Sep 15;24(12):1843-7. doi: 10.1002/mds.22697. Mov Disord. 2009. PMID: 19609911

4

Clinicopathological variability in neurodegeneration with brain iron accumulation.

Vincze A, Kapás I, Molnar MJ, Kovács GG. Vincze A, et al. Among authors: molnar mj. Ideggyogy Sz. 2010 Mar 30;63(3-4):129-35. Ideggyogy Sz. 2010. PMID: 20405671

5

[SCHIZOBANK - The Hungarian national schizophrenia biobank and its role in schizophrenia research and in personalized medicine].

Inczédy-Farkas G, Benkovits J, Balogh N, Almos P, Scholtz B, Zahuczky G, Török Z, Nagy K, Réthelyi J, Makkos Z, Kassai-Farkas A, Egerházy A, Tuzko J, Janka Z, Bitter I, Németh G, Nagy L, Molnár MJ. Inczédy-Farkas G, et al. Among authors: molnar mj. Orv Hetil. 2010 Aug 29;151(35):1403-8. doi: 10.1556/OH.2010.28943. Orv Hetil. 2010. PMID: 20719713 Hungarian.

6

[Editorial comment. Neuromuscular diseases].

Molnár MJ. Molnár MJ. Orv Hetil. 2011 Sep 25;152(39):1551. doi: 10.1556/OH.2011.29183. Orv Hetil. 2011. PMID: 21920840 Hungarian. No abstract available.

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

[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.

10

Cerebrotendinous xanthomatosis with the c.379C>T (p.R127W) mutation in the CYP27A1 gene associated with premature age-associated limbic tauopathy.

Kapás I, Katkó M, Harangi M, Paragh G, Balogh I, Kóczi Z, Regelsberger G, Molnár MJ, Kovacs GG. Kapás I, et al. Among authors: molnar mj. Neuropathol Appl Neurobiol. 2014 Apr;40(3):345-50. doi: 10.1111/nan.12058. Neuropathol Appl Neurobiol. 2014. PMID: 23659550 No abstract available.

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