Search Results - "Bereznai, B"

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

“…Parkinson's disease (PD) is a common degenerative neurologic disorder, which is pathologically characterized by a selective degeneration of dopaminergic…”
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Phenotypic expression of the DYT1 mutation: a family with writer's cramp of juvenile onset by Gasser, T, Windgassen, K, Bereznai, B, Kabus, C, Ludolph, A C

“…Recently, the mutation causing early-onset generalized torsion dystonia has been identified as a GAG deletion in the gene for an adenosine triphosphate-binding…”
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Genetic complexity and Parkinson's disease by 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 by 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.

“…The apparent chromosome locus identified in a study of Parkinson's disease (PD) may not be responsible for the majority of inherited idiopathic PD cases. Other…”
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Linkage studies in alcohol-responsive myoclonic dystonia by Gasser, T, Bereznai, B, Müller, B, Pruszak-Seel, R, Damrich, R, Deuschl, G, Oertel, W H

“…A large German family with "myoclonic dystonia with lightning jerks responsive to alcohol" was identified. Eleven affected pedigree members and six obligate…”
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A novel SOD1 mutation in an Austrian family with amyotrophic lateral sclerosis by Bereznai, Benjamin, Winkler, Andrea, Borasio, Gian Domenico, Gasser, Thomas

“…We report on an Austrian pedigree with autosomal dominant amyotrophic lateral sclerosis (ALS), diagnosed in six patients from two generations. The only…”
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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, and generalized dystonia by Bereznai, Benjamin, Steude, Ulrich, Seelos, Klaus, Bötzel, Kai

“…The results of deep brain stimulation (DBS) of the globus pallidus internus (Gpi) in six patients with generalized, focal, and segmental dystonia are…”
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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 by 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.

“…Recently an Ile93Met mutation in the ubiquitin-carboxy-terminal-hydrolase-L1 gene (UCH-L1) has been described in a German family with Parkinson's disease (PD)…”
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Point mutations in exon 1 of the NR4A2 gene are not a major cause of familial Parkinson's disease by 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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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 Parkinson's Disease by 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

“…We report the results of a screen of 230 European familial index cases of Parkinson's disease for the recently described Ala53Thr mutation in the…”
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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 study by Ries, Vincent, Selzer, Roland, Eichhorn, Tobias, Oertel, Wolfgang H, Eggert, Karla

“…This study investigated the feasibility, safety, and potential benefit in motor symptom control when switching from a dopamine agonist to tolcapone as an…”
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Nimodipine inhibits [3H]nitrobenzylthioinosine binding to the adenosine transporter in human brain by Deckert, J, Bereznai, B, Hennemann, A, Gsell, W, Götz, M, Fritze, J, Riederer, P

“…The inhibition of [3H]nitrobenzylthioinosine ([3H]NBI) binding to human parietal cortex membranes by adenosine transport inhibitors, adenosine receptor…”
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(3H)dipyridamole and (3H)nitrobenzylthioinosine binding sites at the human parietal cortex and erythrocyte adenosine transporter: a comparison by Deckert, J, Hennemann, A, Bereznai, B, Fritze, J, Vock, R, Marangos, P J, Riederer, P

“…We compared the binding sites of the adenosine transport inhibitors (3H)dipyridamole (DPR) and (3H)nitrobenzylthioinosine (NBI) in human parietal cortex and…”
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Therapy of multiple sclerosis by Bereznai, B, Goebels, N, Dang, T, Voltz, R, Walther, E, Zimmermann, C, Hohlfeld, R

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