• 1170 Citations
  • 15 h-Index
19932018

Research output per year

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Research Output

  • 1170 Citations
  • 15 h-Index
  • 26 Article
  • 3 Review article
  • 2 Letter
  • 1 Comment/debate
2018

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, M. J., Nagy, N. & Széll, M., 2018, In : Parkinson's Disease. 2018, 9351598.

Research output: Article

6 Citations (Scopus)
2015

Rare variants in β-Amyloid precursor protein (APP) and Parkinson's disease

Schulte, E. C., Fukumori, A., Mollenhauer, B., Hor, H., Arzberger, T., Perneczky, R., Kurz, A., Diehl-Schmid, J., Hüll, M., Lichtner, P., Eckstein, G., Zimprich, A., Haubenberger, D., Pirker, W., Brücke, T., Bereznai, B., Molnar, M. J., Lorenzo-Betancor, O., Pastor, P., Peters, A. & 7 others, Gieger, C., Estivill, X., Meitinger, T., Kretzschmar, H. A., Trenkwalder, C., Haass, C. & Winkelmann, J., okt. 22 2015, In : European Journal of Human Genetics. 23, 10, p. 1328-1333 6 p.

Research output: Article

21 Citations (Scopus)

The coexistence of dynamin 2 mutation and multiple mitochondrial DNA (mtDNA) deletions in the background of severe cardiomyopathy and centronuclear myopathy

Gal, A., Inczedy-Farkas, G., Pal, E., Remenyi, V., Bereznai, B., Geller, L., Szelid, Z., Merkely, B. & Molnar, M. J., jan. 1 2015, In : Clinical Neuropathology. 34, 2, p. 89-95 7 p.

Research output: Article

8 Citations (Scopus)
2014
22 Citations (Scopus)

Mitochondrial DNA mutations and cognition: A case-series report

Inczedy-Farkas, G., Trampush, J. W., Perczel Forintos, D., Beech, D., Andrejkovics, M., Varga, Z., Remenyi, V., Bereznai, B., Gal, A. & Molnar, M. J., jún. 2014, In : Archives of Clinical Neuropsychology. 29, 4, p. 315-321 7 p.

Research output: Article

9 Citations (Scopus)

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, M. J., nov. 30 2014, In : Ideggyogyaszati szemle. 67, 11-12, p. 420-425 6 p.

Research output: Article

1 Citation (Scopus)
2013

Rare variants in PLXNA4 and Parkinson's disease

Schulte, E. C., Stahl, I., Czamara, D., Ellwanger, D. C., Eck, S., Graf, E., Mollenhauer, B., Zimprich, A., Lichtner, P., Haubenberger, D., Pirker, W., Brücke, T., Bereznai, B., Molnar, M. J., Peters, A., Gieger, C., Müller-Myhsok, B., Trenkwalder, C. & Winkelmann, J., nov. 11 2013, In : PloS one. 8, 11, e79145.

Research output: Article

6 Citations (Scopus)

The role of SCARB2 as susceptibility factor in Parkinson's disease

Hopfner, F., Schulte, E. C., Mollenhauer, B., Bereznai, B., Knauf, F., Lichtner, P., Zimprich, A., Haubenberger, D., Pirker, W., Brücke, T., Peters, A., Gieger, C., Kuhlenbäumer, G., Trenkwalder, C. & Winkelmann, J., ápr. 1 2013, In : Movement Disorders. 28, 4, p. 538-540 3 p.

Research output: Article

25 Citations (Scopus)
2012

Az LRRK2 gyakori G2019S-mutációjának hiánya 120, korai kezdetu magyar Parkinson-beteg esetében

Balicza, P., Bereznai, B., Takáts, A., Klivényi, P., Dibó, G., Hidasi, E., Balogh, I. & Molnár, M. J., júl. 30 2012, In : Ideggyogyaszati szemle. 65, 7-8, p. 239-242 4 p.

Research output: Article

2 Citations (Scopus)

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, M. J., febr. 13 2012, In : Behavioral and Brain Functions. 8, 9.

Research output: Article

38 Citations (Scopus)
62 Citations (Scopus)

Variants in eukaryotic translation initiation factor 4G1 in sporadic Parkinson's disease

Schulte, E. C., Mollenhauer, B., Zimprich, A., Bereznai, B., Lichtner, P., Haubenberger, D., Pirker, W., Brücke, T., Molnar, M. J., Peters, A., Gieger, C., Trenkwalder, C. & Winkelmann, J., aug. 1 2012, In : Neurogenetics. 13, 3, p. 281-285 5 p.

Research output: Article

22 Citations (Scopus)
2011

A MuSK-ellenes antitest pozitív myasthenia gravis kezelése

Pál, Z., Boczán, J., Bereznai, B., Lovas, G. & Molnár, M. J., szept. 1 2011, In : Orvosi hetilap. 152, 39, p. 1586-1589 4 p.

Research output: Article

1 Citation (Scopus)

MELAS syndrome mimicking somatoform disorder

Inczedy-Farkas, G., Remenyi, V., Meszaros, A., Gal, A., Blasko, G., Bereznai, B. & Molnar, M. J., dec. 1 2011, In : Central European Journal of Medicine. 6, 6, p. 758-761 4 p.

Research output: Article

2 Citations (Scopus)

Pompe-kór fenotípusvariációi, kórlefolyása és az enzimpótló kezelés eredményei: Hazai tapasztalatok

Bereznai, B., Trauninger, A., György, I., Szakszon, K., Almássy, Z., Pál, E., Herczegfalvi, Á., Várdi Visy, K., Illés, Z. & Molnár, M. J., szept. 1 2011, In : Orvosi hetilap. 152, 39, p. 1569-1575 7 p.

Research output: Article

2010

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

Bereznai, B., Lovas, G., Pentelenyi, K., Rudas, G. & Molnar, M. J., jún. 15 2010, In : Journal of the Neurological Sciences. 293, 1-2, p. 116-118 3 p.

Research output: Article

3 Citations (Scopus)
2009

A parkinson-kór genetikája és aktuális terápiás lehetocombining double acute accentségei

Bereznai, B. & Molnár, M. J., máj. 30 2009, In : Ideggyogyaszati szemle. 62, 5-6, p. 155-163 9 p.

Research output: Review article

3 Citations (Scopus)
2007

DYT1-pozitív generalizált dystonia: egy testvérpár esettanulmánya.

Bereznai, B., Baraczka, K., Nagy, Z. & Molnár, M. J., júl. 30 2007, In : Ideggyógyászati szemle. 60, 7-8, p. 342-347 6 p.

Research output: Article

1 Citation (Scopus)
2003

Point mutations in exon 1 of the NR4A2 gene are not a major cause of familial Parkinson's disease [1]

Zimprich, A., Asmus, F., Leitner, P., Castro, M., Bereznai, B., Homann, N., Ott, E., Wijnand, A., Rutgers, F., Wieditz, G., Trenkwalder, C. & Gasser, T., aug. 1 2003, In : Neurogenetics. 4, 4, p. 219-220 2 p.

Research output: Letter

26 Citations (Scopus)
2002
137 Citations (Scopus)
1999

Auftreten von immunthyreopathien unter β-interferontherapie der multiplen sklerose

Buchinger, W., Niederwieser, G., Rainer, F., Hohlfeld, R. & Bereznai, B., dec. 3 1999, In : Deutsche Medizinische Wochenschrift. 124, 48, 1 p.

Research output: Letter

2 Citations (Scopus)

Immunmodulierende therapie der multiplen sklerose mit betainterferon

Bereznai, B. & Hohlfeld, R., márc. 12 1999, In : Munchener Medizinische Wochenschrift. 141, 10, p. 115-117 3 p.

Research output: Review article

1 Citation (Scopus)

The Ile93Met mutation in the ubiquitin carboxy-terminal-hydrolase-L1 gene is not observed in European cases with familial Parkinson's disease

Harhangi, B. S., Farrer, M. J., Lincoln, S., Bonifati, V., Meco, G., De Michele, G., Brice, A., Dürr, A., Martinez, M., Gasser, T., Bereznai, B., Vaughan, J. R., Wood, N. W., Hardy, J., Oostra, B. A. & Breteler, M. M. B., júl. 23 1999, In : Neuroscience Letters. 270, 1, p. 1-4 4 p.

Research output: Article

61 Citations (Scopus)

Therapie der multiplen sklerose

Bereznai, B., Goebels, N., Dang, T., Voltz, R., Walther, E., Zimmermann, C. & Hohlfeld, R., máj. 14 1999, In : Deutsche Medizinische Wochenschrift. 124, 19, p. 595-599 5 p.

Research output: Review article

2 Citations (Scopus)
1998

A susceptibility locus for Parkinson's disease maps to chromosome 2p13

Gasser, T., Muller-Myhsok, B., Wszolek, Z. K., Oehlmann, R., Calne, D. B., Bonifati, V., Bereznai, B., Fabrizio, E., Vieregge, P. & Horstmann, R. D., márc. 26 1998, In : Nature genetics. 18, 3, p. 262-265 4 p.

Research output: Article

431 Citations (Scopus)

Phenotypic expression of the DYT1 mutation: A family with writer's cramp of juvenile onset

Gasser, T., Windgassen, K., Bereznai, B., Kabus, C. & Ludolph, A. C., júl. 1 1998, In : Annals of Neurology. 44, 1, p. 126-128 3 p.

Research output: Article

84 Citations (Scopus)

The α-synuclein Ala53Thr mutation is not a common cause of familial Parkinson's disease: A study of 230 European cases

Vaughan, J., Durr, A., Tassin, J., Bereznai, B., Gasser, T., Bonifati, V., De Michele, G., Fabrizio, E., Volpe, G., Bandmann, O., Johnson, W. G., Golbe, L. I., Breteler, M., Meco, G., Agid, Y., Brice, A., Marsden, C. D. & Wood, N. W., aug. 1 1998, In : Annals of Neurology. 44, 2, p. 270-273 4 p.

Research output: Article

79 Citations (Scopus)
1997

A novel SOD1 mutation in an Austrian family with amyotrophic lateral sclerosis

Bereznai, B., Winkler, A., Borasio, G. D. & Gasser, T., márc. 1 1997, In : Neuromuscular Disorders. 7, 2, p. 113-116 4 p.

Research output: Article

14 Citations (Scopus)

Genetic complexity and Parkinson's disease.

Gasser, T., Müller-Myhsok, B., Wszolek, Z. K., Dürr, A., Vaughan, J. R., Bonifati, V., Meco, G., Bereznai, B., Oehlmann, R., Agid, Y., Brice, A. & Wood, N., júl. 18 1997, In : Science. 277, 5324, p. 388-389; author reply 389

Research output: Comment/debate

50 Citations (Scopus)
1996

Linkage studies in alcohol-responsive myoclonic dystonia

Gasser, T., Bereznai, B., Müller, B., Pruszak-Seel, R., Damrich, R., Deuschl, G. & Oertel, W. H., júl. 29 1996, In : Movement Disorders. 11, 4, p. 363-370 8 p.

Research output: Article

24 Citations (Scopus)
1994

(3H)dipyridamole and (3H)nitrobenzylthioinosine binding sites at the human parietal cortex and erythrocyte adenosine transporter: A comparison

Deckert, J., Hennemann, A., Bereznai, B., Fritze, J., Vock, R., Marangos, P. J. & Riederer, P., 1994, In : Life Sciences. 55, 21, p. 1675-1682 8 p.

Research output: Article

9 Citations (Scopus)
1993

Nimodipine inhibits [3H]nitrobenzylthioinosine binding to the adenosine transporter in human brain

Deckert, J., Bereznai, B., Hennemann, A., Gsell, W., Götz, M., Fritze, J. & Riederer, P., júl. 6 1993, In : European Journal of Pharmacology. 238, 1, p. 131-133 3 p.

Research output: Article

18 Citations (Scopus)