Resultats de la cerca - Judit Horváth

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  1. 1
    Microbiological Oxidation of Cholesterol with Azotobacter

    Microbiological Oxidation of Cholesterol with Azotobacter per Judit Horváth, A Krámli

    Publicat 1947
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  2. 2
    Opsoclonus-Myoclonus Syndrome in Anti-N-Methyl-D-Aspartate Receptor Encephalitis

    Opsoclonus-Myoclonus Syndrome in Anti-N-Methyl-D-Aspartate Receptor Encephalitis per Manju A. Kurian, Patrice H. Lalive, Josep Dalmau, Judit Horváth

    Publicat 2010
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  3. 3
    Neuropathology of dementia in a large cohort of patients with Parkinson's disease

    Neuropathology of dementia in a large cohort of patients with Parkinson's disease per Judit Horváth, François R. Herrmann, Pierre R. Burkhard, Constantin Bouras, Enikò Kövari

    Publicat 2013
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  4. 4
    Analysis of complement and plasma cells in the brain of patients with anti-NMDAR encephalitis

    Analysis of complement and plasma cells in the brain of patients with anti-NMDAR encephalitis per Eugenia Martínez‐Hernández, Judit Horváth, Y. Shiloh-Malawsky, N. Sangha, Maria Martinez‐Lage, Josep Dalmau

    Publicat 2011
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  5. 5
    Synthesis and biological activities of highly potent antagonists of growth hormone-releasing hormone.

    Synthesis and biological activities of highly potent antagonists of growth hormone-releasing hormone. per M. Zarándi, Judit Horváth, György B. Halmos, J. Pinski, Attila Nagy, Kate Groot, Zoltán Rékási, Andrew V. Schally

    Publicat 1994
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  6. 6
    Mislocalization of DNAH5 and DNAH9 in Respiratory Cells from Patients with Primary Ciliary Dyskinesia

    Mislocalization of DNAH5 and DNAH9 in Respiratory Cells from Patients with Primary Ciliary Dyskinesia per Manfred Fliegauf, Heike Olbrich, Judit Horváth, Johannes H. Wildhaber, Maimoona A. Zariwala, Marcus P. Kennedy, Michael R. Knowles, Heymut Omran

    Publicat 2005
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  7. 7
    The Port Delivery System with ranibizumab: a new paradigm for long-acting retinal drug delivery

    The Port Delivery System with ranibizumab: a new paradigm for long-acting retinal drug delivery per Shrirang V. Ranade, Mark R. Wieland, Tammy Tam, Jennifer C. Rea, Judit Horvath, Aaron R. Hieb, Weitao Jia, Lori Grace, Giulio Barteselli, Jay M. Stewart

    Publicat 2022
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  8. 8
    Nephrocystin Specifically Localizes to the Transition Zone of Renal and Respiratory Cilia and Photoreceptor Connecting Cilia

    Nephrocystin Specifically Localizes to the Transition Zone of Renal and Respiratory Cilia and Photoreceptor Connecting Cilia per Manfred Fliegauf, Judit Horváth, Christian von Schnakenburg, Heike Olbrich, Dominik N. Müller, Julia Thumfart, Bernhard Schermer, Gregory J. Pazour, Hartmut P.H. Neumann, Hanswalter Zentgraf, Thomas Benzing, Heymut Omran

    Publicat 2006
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  9. 9
    The expression of the pituitary growth hormone-releasing hormone receptor and its splice variants in normal and neoplastic human tissues

    The expression of the pituitary growth hormone-releasing hormone receptor and its splice variants in normal and neoplastic human tissues per Alexandre Havt, Andrew V. Schally, Gábor Halmos, József L. Varga, Gabor L. Toller, Judit Horváth, Károly Szepesházi, Frank Köster, Kevin L. Kovitz, Kate Groot, Márta Zarándi, Célia A. Kanashiro

    Publicat 2005
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  10. 10
    Defects in the cytoplasmic assembly of axonemal dynein arms cause morphological abnormalities and dysmotility in sperm cells leading to male infertility

    Defects in the cytoplasmic assembly of axonemal dynein arms cause morphological abnormalities and dysmotility in sperm cells leading to male infertility per Isabella Aprea, Johanna Raidt, Inga M. Höben, Niki T. Loges, Tabea Nöthe-Menchen, Petra Pennekamp, Heike Olbrich, Thomas Kaiser, Luisa Biebach, Frank Tüttelmann, Judit Horváth, Maria Schubert, Claudia Krallmann, Sabine Kliesch, Heymut Omran

    Publicat 2021
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  11. 11
    Mutations in ACY1, the Gene Encoding Aminoacylase 1, Cause a Novel Inborn Error of Metabolism

    Mutations in ACY1, the Gene Encoding Aminoacylase 1, Cause a Novel Inborn Error of Metabolism per Jörn Oliver Sass, Verena Mohr, Heike Olbrich, Udo F. H. Engelke, Judit Horváth, Manfred Fliegauf, Niki T. Loges, Susanne Schweitzer‐Krantz, Ralf Moebus, Polly Weiler, Andreas Kispert, Andrea Superti‐Furga, Ron A. Wevers, Heymut Omran

    Publicat 2006
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  12. 12
    Phosphorylation by casein kinase 2 induces PACS-1 binding of nephrocystin and targeting to cilia

    Phosphorylation by casein kinase 2 induces PACS-1 binding of nephrocystin and targeting to cilia per Bernhard Schermer, Katja Höpker, Heymut Omran, Cristina Ghenoiu, Manfred Fliegauf, Andrea Fekete, Judit Horváth, Michael Köttgen, Matthias J. Hackl, Stefan Zschiedrich, Tobias B. Huber, Albrecht Kramer-Zucker, Hanswalter Zentgraf, Andree Blaukat, Gerd Walz, Thomas Benzing

    Publicat 2005
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  13. 13
    <i>DNAH5</i> Mutations Are a Common Cause of Primary Ciliary Dyskinesia with Outer Dynein Arm Defects

    <i>DNAH5</i> Mutations Are a Common Cause of Primary Ciliary Dyskinesia with Outer Dynein Arm Defects per Nada Hornef, Heike Olbrich, Judit Horváth, Maimoona A. Zariwala, Manfred Fliegauf, Niki T. Loges, Johannes H. Wildhaber, Peadar G. Noone, Marcus P. Kennedy, Stylianos E. Antonarakis, Jean-Louis Blouin, Lucia Bartoloni, Thomas Nüßlein, Peter Ahrens, Matthias Griese, Heiner Kuhl, Ralf Sudbrak, Michael R. Knowles, Richard Reinhardt, Heymut Omran

    Publicat 2006
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  14. 14
    DNAI2 Mutations Cause Primary Ciliary Dyskinesia with Defects in the Outer Dynein Arm

    DNAI2 Mutations Cause Primary Ciliary Dyskinesia with Defects in the Outer Dynein Arm per Niki T. Loges, Heike Olbrich, Lale Fenske, Huda Mussaffi, Judit Horváth, Manfred Fliegauf, Heiner Kuhl, G Baktai, Erzsebet Peterffy, Rahul Chodhari, Eddie M.K. Chung, Andrew Rutman, Christopher O’Callaghan, Hannah Blau, László Tiszlavicz, Katarzyna Voelkel, Michał Witt, Ewa Ziętkiewicz, Jürgen Neesen, Richard Reinhardt, Hannah M. Mitchison, Heymut Omran

    Publicat 2008
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  15. 15
    Robot-induced hallucinations in Parkinson’s disease depend on altered sensorimotor processing in fronto-temporal network

    Robot-induced hallucinations in Parkinson’s disease depend on altered sensorimotor processing in fronto-temporal network per Fosco Bernasconi, Eva Blondiaux, Jevita Potheegadoo, Giedre Stripeikyte, Javier Pagonabarraga, Helena Bejr‐Kasem, Michela Bassolino, Michel Akselrod, Saül Martínez‐Horta, Frederic Sampedro, Masayuki Hara, Judit Horváth, Matteo Franza, Stéphanie Konik, Matthieu Béreau, Joseph-André Ghika, Pierre R. Burkhard, Dimitri Van De Ville, Nathan Faivre, Giulio Rognini, Paul Krack, Jaime Kulisevsky, Olaf Blanke

    Publicat 2021
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  16. 16
    Mutations of<b><i>DNAI1</i></b>in Primary Ciliary Dyskinesia

    Mutations of<b><i>DNAI1</i></b>in Primary Ciliary Dyskinesia per Maimoona A. Zariwala, Margaret W. Leigh, Franck Ceppa, Marcus P. Kennedy, Peadar G. Noone, Johnny L. Carson, Milan J. Hazucha, Adriana Lori, Judit Horváth, Heike Olbrich, Niki T. Loges, Anne-Marie Bridoux, Gaëlle Pennarun, Bénédicte Duriez, Estelle Escudier, Hannah M. Mitchison, Rahul Chodhari, Eddie M.K. Chung, Lucy Morgan, Robb U. de Iongh, Jonathan Rutland, Ugo Pradal, Heymut Omran, Serge Amselem, Michael R. Knowles

    Publicat 2006
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  17. 17
    Germline loss-of-function variants in the BARD1 gene are associated with early-onset familial breast cancer but not ovarian cancer

    Germline loss-of-function variants in the BARD1 gene are associated with early-onset familial breast cancer but not ovarian cancer per Nana Weber‐Lassalle, Julika Borde, Konstantin Weber‐Lassalle, Judit Horváth, Dieter Niederacher, Norbert Arnold, Silke Kaulfuß, Corinna Ernst, Victoria Paul, Ellen Honisch, Kristina Klaschik, Alexander E. Volk, Christian Kubisch, Steffen Rapp, Nadine Lichey, Janine Altmüller, Louisa Lepkes, Esther Pohl‐Rescigno, Hölger Thiele, Peter Nürnberg, Mirjam Larsen, Lisa Richters, Kerstin Rhiem, Barbara Wappenschmidt, Christoph Engel, Alfons Meindl, Rita K. Schmutzler, Eric Hahnen, Jan Hauke

    Publicat 2019
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  18. 18
    Prevalence of<i>BRCA1/2</i>germline mutations in 21 401 families with breast and ovarian cancer

    Prevalence of<i>BRCA1/2</i>germline mutations in 21 401 families with breast and ovarian cancer per Karin Kast, Kerstin Rhiem, Barbara Wappenschmidt, Eric Hahnen, Jan Hauke, Britta Bluemcke, V Zarghooni, N Herold, Nina Ditsch, Marion Kiechle, Michael Braun, Christine Fischer, Nicola Dikow, Sarah Schott, Nils Rahner, Dieter Niederacher, Tanja Fehm, Andrea Gehrig, Clemens Mueller-Reible, Norbert Arnold, Nicolaì Maass, Guntram Borck, Nikolaus de Gregorio, Caroline Scholz, Bernd Auber, Raymonda Varon-Manteeva, Dorothee Speiser, Judit Horváth, Nadine Lichey, Pauline Wimberger, Sylvia Stark, Ulrike Faust, Bernhard H. F. Weber, Günter Emons, Silke Zachariae, Alfons Meindl, Rita K. Schmutzler, Christoph Engel

    Publicat 2016
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  19. 19
    BRIP1 loss-of-function mutations confer high risk for familial ovarian cancer, but not familial breast cancer

    BRIP1 loss-of-function mutations confer high risk for familial ovarian cancer, but not familial breast cancer per Nana Weber‐Lassalle, Jan Hauke, Juliane Ramser, Lisa Richters, Eva Groß, Britta Blümcke, Andrea Gehrig, Anne-Karin Kahlert, Clemens R. Müller, Karl Hackmann, Ellen Honisch, Konstantin Weber‐Lassalle, Dieter Niederacher, Julika Borde, Hölger Thiele, Corinna Ernst, Janine Altmüller, Guido Neidhardt, Peter Nürnberg, Kristina Klaschik, Christopher Schroeder, Konrad Platzer, Alexander E. Volk, Shan Wang‐Gohrke, Walter Just, Bernd Auber, Christian Kubisch, Gunnar Schmidt, Judit Horváth, Barbara Wappenschmidt, Christoph Engel, Norbert Arnold, Bernd Dworniczak, Kerstin Rhiem, Alfons Meindl, Rita K. Schmutzler, Eric Hahnen

    Publicat 2018
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  20. 20
    Gene panel testing of 5589 <i><scp>BRCA</scp>1/2</i>‐negative index patients with breast cancer in a routine diagnostic setting: results of the German Consortium for Hereditary Breast and Ovarian Cancer

    Gene panel testing of 5589 <i><scp>BRCA</scp>1/2</i>‐negative index patients with breast cancer in a routine diagnostic setting: results of the German Consortium for Hereditary Bre... per Jan Hauke, Judit Horváth, Eva Groß, Andrea Gehrig, Ellen Honisch, Karl Hackmann, Gunnar Schmidt, Norbert Arnold, Ulrike Faust, Christian Sutter, Julia Hentschel, Shan Wang‐Gohrke, Mateja Smogavec, Bernhard H. F. Weber, Nana Weber‐Lassalle, Konstantin Weber‐Lassalle, Julika Borde, Corinna Ernst, Janine Altmüller, Alexander E. Volk, Hölger Thiele, Verena Hübbel, Peter Nürnberg, Katharina Keupp, Beatrix Versmold, Esther Pohl, Christian Kubisch, Sabine Grill, Victoria Paul, N Herold, Nadine Lichey, Kerstin Rhiem, Nina Ditsch, Christian Rückert, Barbara Wappenschmidt, Bernd Auber, Andreas Rump, Dieter Niederacher, Thomas Haaf, Juliane Ramser, Bernd Dworniczak, Christoph Engel, Alfons Meindl, Rita K. Schmutzler, Eric Hahnen

    Publicat 2018
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