Temperature measuring analysis of the nuclear reactor fuel assembly von Urban, F, Kučák, Ľ, Bereznai, J, Závodný, Z, Muškát, P

Volltext

The calibration of five-hole pressure probe von Bereznai, J., Mlynár, P.

Volltext

Results of the non-nulling calibration of five-hole pressure probe von Bereznai, J., Mlynár, P., Masaryk, M.

Volltext

Heat plant as a heat source of the centralized heat supply with high efficiency von Urban, F., Muškát, P., Bereznai, J.

Volltext

Analysis of the water flow through the simplified central tube of the VVER 440 nuclear reactor fuel assembly von Závodný, Z., Bereznai, J., Urban, F.

Volltext

Psychiatric symptoms of patients with primary mitochondrial DNA disorders von Inczedy-Farkas, Gabriella, Remenyi, Viktoria, Gal, Aniko, Varga, Zsofia, Balla, Petra, Udvardy-Meszaros, Agnes, Bereznai, Benjamin, Molnar, Maria Judit

Volltext

Rare variants in PLXNA4 and Parkinson's disease von Schulte, Eva C, Stahl, Immanuel, Czamara, Darina, Ellwanger, Daniel C, Eck, Sebastian, Graf, Elisabeth, Mollenhauer, Brit, Zimprich, Alexander, Lichtner, Peter, Haubenberger, Dietrich, Pirker, Walter, Brücke, Thomas, Bereznai, Benjamin, Molnar, Maria J, Peters, Annette, Gieger, Christian, Müller-Myhsok, Bertram, Trenkwalder, Claudia, Winkelmann, Juliane

Volltext

Rare variants in β-Amyloid precursor protein (APP) and Parkinson's disease von Schulte, Eva C, Fukumori, Akio, Mollenhauer, Brit, Hor, Hyun, Arzberger, Thomas, Perneczky, Robert, Kurz, Alexander, Diehl-Schmid, Janine, Hüll, Michael, Lichtner, Peter, Eckstein, Gertrud, Zimprich, Alexander, Haubenberger, Dietrich, Pirker, Walter, Brücke, Thomas, Bereznai, Benjamin, Molnar, Maria J, Lorenzo-Betancor, Oswaldo, Pastor, Pau, Peters, Annette, Gieger, Christian, Estivill, Xavier, Meitinger, Thomas, Kretzschmar, Hans A, Trenkwalder, Claudia, Haass, Christian, Winkelmann, Juliane

Volltext

Ellipsometric study of nanostructured carbon films deposited by pulsed laser deposition von Bereznai, M., Budai, J., Hanyecz, I., Kopniczky, J., Veres, M., Koós, M., Toth, Z.

Volltext

Variants in eukaryotic translation initiation factor 4G1 in sporadic Parkinson’s disease von Schulte, Eva C., Mollenhauer, Brit, Zimprich, Alexander, Bereznai, Benjamin, Lichtner, Peter, Haubenberger, Dietrich, Pirker, Walter, Brücke, Thomas, Molnar, Maria J., Peters, Annette, Gieger, Christian, Trenkwalder, Claudia, Winkelmann, Juliane

Volltext

Rare variants in [beta]-Amyloid precursor protein (APP) and Parkinson's disease von Schulte, Eva C, Fukumori, Akio, Mollenhauer, Brit, Hor, Hyun, Arzberger, Thomas, Perneczky, Robert, Kurz, Alexander, Diehl-schmid, Janine, Hüll, Michael, Lichtner, Peter, Eckstein, Gertrud, Zimprich, Alexander, Haubenberger, Dietrich, Pirker, Walter, Brücke, Thomas, Bereznai, Benjamin, Molnar, Maria J, Lorenzo-betancor, Oswaldo, Pastor, Pau, Peters, Annette, Gieger, Christian, Estivill, Xavier, Meitinger, Thomas, Kretzschmar, Hans A, Trenkwalder, Claudia, Haass, Christian, Winkelmann, Juliane

Volltext

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.

Volltext

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.

Volltext

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

Volltext

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

Volltext

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.

Volltext

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

Volltext

( 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

Volltext

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

Volltext

( 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

Volltext