A susceptibility locus for Parkinson's disease maps to chromosome 2p13 von Gasser, Thomas, Müller-Myhsok, Bertram, Wszolek, Zbigniew K., Oehlmann, Ralph, Calne, Donald B., Bonifati, Vincenzo, Bereznai, Benjamin, Fabrizio, Edito, Vieregge, Peter, Horstmann, Rolf D.

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Phenotypic expression of the DYT1 mutation: A family with writer's cramp of juvenile onset von Gasser, T., Windgassen, K., Bereznai, B., Kabus, C., Ludolph, A. C.

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Chronic high-frequency globus pallidus internus stimulation in different types of dystonia: A clinical, video, and MRI report of six patients presenting with segmental, cervical, a... von Bereznai, Benjamin, Steude, Ulrich, Seelos, Klaus, Bötzel, Kai

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Genetic complexity and Parkinson's disease von 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

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Genetic Complexity and Parkinson's Disease von Scott, William K., Stajich, Jeffrey M., Yamaoka, Larry H., Speer, Marcy C., Vance, Jeffery M., Roses, Allen D., Pericak-Vance, Margaret A., 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., Polymeropoulos, Michael H.

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A novel SOD1 mutation in an Austrian family with amyotrophic lateral sclerosis von Bereznai, Benjamin, Winkler, Andrea, Borasio, Gian Domenico, Gasser, Thomas

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Linkage studies in alcohol-responsive myoclonic dystonia von Gasser, T., Bereznai, B., Müller, B., Pruszak-Seel, R., Damrich, R., Deuschl, G., Oertel, W. H.

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The α-synuclein Ala53Thr mutation is not a common cause of familial Parkinson's disease: A study of 230 European cases von Vaughan, Jenny, Durr, Alexandra, Tassin, Johann, Bereznai, Benjamin, Gasser, Thomas, Bonifati, Vincenzo, De Michele, Giuseppe, Fabrizio, Edito, Volpe, Gianpiero, Bandmann, O., Johnson, William G., Golbe, Lawrence I., Breteler, Monique, Meco, Giuseppe, Agid, Yves, Brice, Alexis, Marsden, C. David, Wood, Nicholas W.

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The Ile93Met mutation in the ubiquitin carboxy-terminal-hydrolase-L1 gene is not observed in European cases with familial Parkinson's disease von Harhangi, B.Sanjay, Farrer, Matthew J., Lincoln, Sarah, Bonifati, Vincenzo, Meco, Giuseppe, De Michele, Giuseppe, Brice, Alexis, Dürr, Alexandra, Martinez, Maria, Gasser, Thomas, Bereznai, Benjamin, Vaughan, Jenny R., Wood, Nicholas W., Hardy, John, Oostra, Ben A., Breteler, Monique M.B.

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Point mutations in exon 1 of the NR4A2 gene are not a major cause of familial Parkinson's disease von Zimprich, Alexander, Asmus, Friedrich, Leitner, Petra, Castro, Mirna, Bereznai, Benjamin, Homann, Nikolaus, Ott, Erwin, Rutgers, A Wijnand F, Wieditz, Gyri, Trenkwalder, Claudia, Gasser, Thomas

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Replacing a dopamine agonist by the COMT-inhibitor tolcapone as an adjunct to L-dopa in the treatment of Parkinson's disease: a randomized, multicenter, open-label, parallel-group... von Ries, Vincent, Selzer, Roland, Eichhorn, Tobias, Oertel, Wolfgang H, Eggert, Karla

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Nimodipine inhibits [ 3H]nitrobenzylthioinosine binding to the adenosine transporter in human brain von Deckert, Jürgen, Bereznai, Benjamin, Hennemann, Anja, Gsell, Wieland, Götz, Mario, Fritze, Jürgen, Riederer, Peter

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The alpha-synuclein Ala53Thr mutation is not a common cause of familial Parkinson's disease: a study of 230 European cases. European Consortium on Genetic Susceptibility in Parkins... von 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

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( 3H)dipyridamole and ( 3H)nitrobenzylthioinosine binding sites at the human parietal cortex and erythrocyte adenosine transporter: A comparison von Deckert, Jürgen, Hennemann, Anja, Bereznai, Benjamin, Fritze, Jürgen, Vock, Reinhard, Marangos, Paul J., Riederer, Peter

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( super(3)H)Dipyridamole and ( super(3)H)nitrobenzylthioinosine binding sites at the human parietal cortex and erythrocyte adenosine transporter: A comparison von Deckert, J, Hennemann, A, Bereznai, B, Fritze, J, Vock, R, Marangos, P J, Riederer, P

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Nimodipine inhibits [ super(3)H]nitrobenzyl-thioinosine binding to the adenosine transporter in human brain von Deckert, J, Bereznai, B, Hennemann, A, Gsell, W, Goetz, M, Fritze, J, Riederer, P

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DIHYDROPYRIDINE CALCIUM CHANNEL ANTAGONISTS: INTERACTION WITH ADENOSINE UPTAKE SITES IN HUMAN BRAIN von Deckert, J., Bereznai, B., Hennemann, A., Gsell, W., Götz, M., Fritze, J., Beckmann, H., Riederer, P.

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Therapie der multiplen Sklerose von Bereznai, B., Goebels, N., Dang, T., Voltz, R., Walther, E., Zimmermann, C., Hohlfeld, R.

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Therapy of multiple sclerosis von Bereznai, B, Goebels, N, Dang, T, Voltz, R, Walther, E, Zimmermann, C, Hohlfeld, R

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Processing of transparent materials using visible nanosecond laser pulses von HOPP, B, SMAUSZ, T, BEREZNAI, M

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