Hereditary spastic paraplegia caused by compound heterozygous mutations outside the motor domain of the KIF1A gene von Krenn, M., Zulehner, G., Hotzy, C., Rath, J., Stogmann, E., Wagner, M., Haack, T. B., Strom, T. M., Zimprich, A., Zimprich, F.

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A splice site variant in the sodium channel gene SCN1A confers risk of febrile seizures von SCHLACHTER, K, GRUBER-SEDLMAYR, U, WICHMANN, H. E, LICHTNER, P, MEITINGER, T, STROM, T. M, ZIMPRICH, A, ZIMPRICH, F, STOGMANN, E, LAUSECKER, M, HOTZY, C, BALZAR, J, SCHUH, E, BAUMGARTNER, C, MUELLER, J. C, ILLIG, T

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Idiopathic generalized epilepsy phenotypes associated with different EFHC1 mutations von STOGMANN, E, LICHTNER, P, ZIMPRICH, F, ZIMPRICH, A, BAUMGARTNER, C, BONELLI, S, ASSEM-HILGER, E, LEUTMEZER, F, SCHMIED, M, HOTZY, C, STROM, T. M, MEITINGER, T

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Evidence that the N-terminal part of the S-layer protein from Bacillus stearothermophilus PV72/p2 recognizes a secondary cell wall polymer von Ries, W, Hotzy, C, Schocher, I, Sleytr, U B, Sára, M

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Mutations in the CLCN2 gene are a rare cause of idiopathic generalized epilepsy syndromes von STOGMANN, E, LICHTNER, P, HATALA, K, STROM, T. M, MEITINGER, T, ZIMPRICH, F, ZIMPRICH, A, BAUMGARTNER, C, SCHMIED, M, HOTZY, C, ASMUS, F, LEUTMEZER, F, BONELLI, S, ASSEM-HILGER, E, VASS, K

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Mutations in the gene tripeptidyl peptidase II (TPP2) and multiple sclerosis von Reinthaler, E. M., Graf, E., Zrzavy, T., Wieland, T., Hotzy, C., Kopecky, C., Schmied, C., Leutmezer, F., Keilani, M., Lill, C. M., Hoffjan, S., Epplen, J. T., Zettl, U. K., Hecker, M., Deutschlaender, A., Ahram, M., Mustafa, B., El-Khateeb, M., Vilarino-Guell, C., Sadovnick, D. A., Zimprich, F., Tomkinson, B, Strom, T. M., Kristoferitsch, W., Lassmann, H., Zimprich, A.

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The S-Layer Proteins of Two Bacillus stearothermophilus Wild-Type Strains Are Bound via Their N-Terminal Region to a Secondary Cell Wall Polymer of Identical Chemical Composition von Egelseer, E M, Leitner, K, Jarosch, M, Hotzy, C, Zayni, S, Sleytr, U B, Sára, M

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A recombinant bacterial cell surface (S-layer)-major birch pollen allergen-fusion protein (rSbsC/Bet v1) maintains the ability to self-assemble into regularly structured monomolecu... von Breitwieser, Andreas, Egelseer, Eva M., Moll, Dieter, Ilk, Nicola, Hotzy, Christoph, Bohle, Barbara, Ebner, Christof, Sleytr, Uwe B., Sára, Margit

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Characterization of an S-layer glycoprotein produced in the course of S-layer variation of Bacillus stearothermophilus ATCC 12980 and sequencing and cloning of the sbsD gene encodi... von EGELSEER, Eva M, DANHORN, Thomas, PLESCHBERGER, Magdalena, HOTZY, Christoph, SLEYTR, Uwe B, SARA, Margit

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Regulation of S-layer protein synthesis of Bacillus stearothermophilus PV72 through variation of continuous cultivation conditions von Pink, Tomas, Langer, Klemens, Hotzy, Christoph, Sara, Margit

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Evidence that the N-terminal part of the S-layer protein from Bacillus stearothermophilus PV72/p27 recognizes a secondary cell wall polymer von Ries, W, Hotzy, C, Schocher, I, Sleytr, U B, Sara, M

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A Mutation in VPS35, Encoding a Subunit of the Retromer Complex, Causes Late-Onset Parkinson Disease von Zimprich, Alexander, Benet-Pagès, Anna, Struhal, Walter, Graf, Elisabeth, Eck, Sebastian H., Offman, Marc N., Haubenberger, Dietrich, Spielberger, Sabine, Schulte, Eva C., Lichtner, Peter, Rossle, Shaila C., Klopp, Norman, Wolf, Elisabeth, Seppi, Klaus, Pirker, Walter, Presslauer, Stefan, Mollenhauer, Brit, Katzenschlager, Regina, Foki, Thomas, Hotzy, Christoph, Reinthaler, Eva, Harutyunyan, Ashot, Kralovics, Robert, Peters, Annette, Zimprich, Fritz, Brücke, Thomas, Poewe, Werner, Auff, Eduard, Trenkwalder, Claudia, Rost, Burkhard, Ransmayr, Gerhard, Winkelmann, Juliane, Meitinger, Thomas, Strom, Tim M.

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Rare variants in γ-aminobutyric acid type A receptor genes in rolandic epilepsy and related syndromes von Reinthaler, Eva M., Dejanovic, Borislav, Lal, Dennis, Semtner, Marcus, Merkler, Yvonne, Reinhold, Annika, Pittrich, Dorothea A., Hotzy, Christoph, Feucht, Martha, Steinböck, Hannelore, Gruber-Sedlmayr, Ursula, Ronen, Gabriel M., Neophytou, Birgit, Geldner, Julia, Haberlandt, Edda, Muhle, Hiltrud, Ikram, M. Arfan, van Duijn, Cornelia M., Uitterlinden, Andre G., Hofman, Albert, Altmüller, Janine, Kawalia, Amit, Toliat, Mohammad R., Nürnberg, Peter, Lerche, Holger, Nothnagel, Michael, Thiele, Holger, Sander, Thomas, Meier, Jochen C., Schwarz, Günter, Neubauer, Bernd A., Zimprich, Fritz

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Rare variants in [gamma]-aminobutyric acid type A receptor genes in rolandic epilepsy and related syndromes von Reinthaler, Eva M, Dejanovic, Borislav, Lal, Dennis, Semtner, Marcus, Merkler, Yvonne, Reinhold, Annika, Pittrich, Dorothea A, Hotzy, Christoph, Feucht, Martha, Steinbock, Hannelore, Gruber-Sedlmayr, Ursula, Ronen, Gabriel M, Neophytou, Birgit, Geldner, Julia, Haberlandt, Edda, Muhle, Hiltrud, Ikram, M Arfan, van Duijn, Cornelia M, Uitterlinden, Andre G, Hofman, Albert, Altmuller, Janine, Kawalia, Amit, Toliat, Mohammad R, Nurnberg, Peter, Lerche, Holger, Nothnagel, Michael, Thiele, Holger, Sander, Thomas, Meier, Jochen C, Schwarz, Gunter, Neubauer, Bernd A, Zimprich, Fritz

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Replication study of multiple sclerosis (MS) susceptibility alleles and correlation of DNA-variants with disease features in a cohort of Austrian MS patients von Schmied, Mascha C., Zehetmayer, Sonja, Reindl, Markus, Ehling, Rainer, Bajer-Kornek, Barbara, Leutmezer, Fritz, Zebenholzer, Karin, Hotzy, Christoph, Lichtner, Peter, Meitinger, Thomas, Wichmann, H-Erich, Illig, Thomas, Gieger, Christian, Huber, Klaus, Khalil, Michael, Fuchs, Sigrid, Schmidt, Helena, Auff, Eduard, Kristoferitsch, Wolfgang, Fazekas, Franz, Berger, Thomas, Vass, Karl, Zimprich, Alexander

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