نتائج البحث - Ann‐Kathrin Hauser

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  1. 1
    Dissecting genetic architecture of rare dystonia: genetic, molecular and clinical insights

    Dissecting genetic architecture of rare dystonia: genetic, molecular and clinical insights حسب Burcu Atasu, Javier Simón‐Sánchez, Haşmet Hanağası, Başar Bılgıç, Ann‐Kathrin Hauser, Gamze Güven, Peter Heutink, Thomas Gasser, Ebba Lohmann

    منشور في 2024
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  2. 2
    Plasma Ceramide and Glucosylceramide Metabolism Is Altered in Sporadic Parkinson's Disease and Associated with Cognitive Impairment: A Pilot Study

    Plasma Ceramide and Glucosylceramide Metabolism Is Altered in Sporadic Parkinson's Disease and Associated with Cognitive Impairment: A Pilot Study حسب Michelle M. Mielke, Walter Maetzler, Norman J. Haughey, Veera Venkata Ratnam Bandaru, Rodolfo Savica, Christian Deuschle, Thomas Gasser, Ann-Kathrin Hauser, Susanne Gräber‐Sultan, Erwin Schleicher, Daniela Berg, Inga Liepelt‐Scarfone

    منشور في 2013
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  3. 3
    CSF α-synuclein seed amplification kinetic profiles are associated with cognitive decline in Parkinson’s disease

    CSF α-synuclein seed amplification kinetic profiles are associated with cognitive decline in Parkinson’s disease حسب Kathrin Brockmann, Stefanie Lerche, Simone Baiardi, Marcello Rossi, Isabel Wurster, Corinne Quadalti, Benjamin Röeben, Angela Mammana, Milan Zimmermann, Ann‐Kathrin Hauser, Christian Deuschle, Claudia Schulte, Inga Liepelt‐Scarfone, Thomas Gasser, Piero Parchi

    منشور في 2024
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  4. 4
    A Novel SNCA A30G Mutation Causes Familial Parkinsonʼs Disease

    A Novel SNCA A30G Mutation Causes Familial Parkinsonʼs Disease حسب Hui Liu, Christos Koros, Timo Strohäker, Claudia Schulte, Maria Bozi, Stefanos Varvaresos, Alain Ibáñez de Opakua, Athina Maria Simitsi, Anastasia Bougea, Konstantinos Voumvourakis, Matina Maniati, Sokratis G. Papageorgiou, Ann‐Kathrin Hauser, Stefan Becker, Markus Zweckstetter, Leonidas Stefanis, Thomas Gasser

    منشور في 2021
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  5. 5
    Association between CSF alpha-synuclein seeding activity and genetic status in Parkinson’s disease and dementia with Lewy bodies

    Association between CSF alpha-synuclein seeding activity and genetic status in Parkinson’s disease and dementia with Lewy bodies حسب Kathrin Brockmann, Corinne Quadalti, Stefanie Lerche, Marcello Rossi, Isabel Wurster, Simone Baiardi, Benjamin Röeben, Angela Mammana, Milan Zimmermann, Ann‐Kathrin Hauser, Christian Deuschle, Claudia Schulte, Katharina Waniek, Ingolf Lachmann, Simon Sjödin, Ann Brinkmalm, Kaj Blennow, Henrik Zetterberg, Thomas Gasser, Piero Parchi

    منشور في 2021
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  6. 6
    Phenylalanine Effects on Brain Function in Adult Phenylketonuria

    Phenylalanine Effects on Brain Function in Adult Phenylketonuria حسب Andrea Pilotto, Carl Moritz Zipser, Edytha Leks, Dorothea Haas, Gwendolyn Gramer, Peter Freisinger, Eva Schaeffer, Inga Liepelt‐Scarfone, Kathrin Brockmann, Walter Maetzler, Claudia Schulte, Christian Deuschle, Ann Kathrin Hauser, Georg F. Hoffmann, Klaus Scheffler, Francjan J. van Spronsen, Alessandro Padovani, Friedrich K. Trefz, Daniela Berg

    منشور في 2020
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  7. 7
    The novel p.<scp>A30G <i>SNCA</i></scp> pathogenic variant in Greek patients with familial and sporadic Parkinson's disease

    The novel p.<scp>A30G <i>SNCA</i></scp> pathogenic variant in Greek patients with familial and sporadic Parkinson's disease حسب Ioanna Alefanti, Christos Koros, Viktoria Tsami, Athina Maria Simitsi, Chrisoula Kartanou, Nikolaos Papagiannakis, Maria Bozi, Roubina Antonelou, Matina Maniati, Ann‐Kathrin Hauser, Stefanos Varvaressos, Anastasios Bonakis, Konstantinos Lourentzos, Periklis Makrythanasis, Sokratis G. Papageorgiou, Christos Proukakis, Constantin Potagas, Thomas Gasser, Georgios Koutsis, Georgia Karadima, Leonidas Stefanis

    منشور في 2025
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  8. 8
    The Mutation Matters: <scp>CSF</scp> Profiles of <scp>GCase</scp> , Sphingolipids, α‐Synuclein in <scp> PD <sub>GBA</sub> </scp>

    The Mutation Matters: <scp>CSF</scp> Profiles of <scp>GCase</scp> , Sphingolipids, α‐Synuclein in <scp> PD <sub>GBA</sub> </scp> حسب Stefanie Lerche, Claudia Schulte, Isabel Wurster, Gerrit Machetanz, Benjamin Röeben, Milan Zimmermann, Christian Deuschle, Ann‐Kathrin Hauser, Judith Böhringer, Ingeborg Krägeloh‐Mann, Katharina Waniek, Ingolf Lachmann, Xuan-Mai Petterson, Ruby W. Chiang, Hye Jung Park, Bing Wang, Inga Liepelt‐Scarfone, Walter Maetzler, Douglas Galasko, Clemens R. Scherzer, Thomas Gasser, Michelle M. Mielke, Samantha J. Hutten, Brit Mollenhauer, S. Pablo Sardi, Daniela Berg, Kathrin Brockmann

    منشور في 2021
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  9. 9
    A Missense Mutation in KCTD17 Causes Autosomal Dominant Myoclonus-Dystonia

    A Missense Mutation in KCTD17 Causes Autosomal Dominant Myoclonus-Dystonia حسب Niccolò E. Mencacci, Ignacio Rubio‐Agusti, Anselm A. Zdebik, Friedrich Asmus, Marthe H. R. Ludtmann, Mina Ryten, Vincent Plagnol, Ann‐Kathrin Hauser, Sara Bandrés‐Ciga, Conceição Bettencourt, Paola Forabosco, Deborah Hughes, Marc P. M. Soutar, Kathryn J. Peall, Huw R. Morris, Daniah Trabzuni, Mehmet Tekman, Horia Stanescu, Robert Kleta, Miryam Carecchio, Giovanna Zorzi, Nardo Nardocci, Barbara Garavaglia, Ebba Lohmann, Anne Weißbach, Christine Klein, John Hardy, Alan Pittman, Thomas Foltynie, Andrey Y. Abramov, Thomas Gasser, Kailash P. Bhatia, Nicholas Wood

    منشور في 2015
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  10. 10
    Accurate long-read sequencing identified GBA1 as major risk factor in the Luxembourgish Parkinson’s study

    Accurate long-read sequencing identified GBA1 as major risk factor in the Luxembourgish Parkinson’s study حسب Sinthuja Pachchek, Zied Landoulsi, Lukas Pavelka, Claudia Schulte, Elena Buena‐Atienza, Caspar Groß, Ann‐Kathrin Hauser, Dheeraj Reddy Bobbili, Nicolas Casadei, Patrick May, Rejko Krüger, Geeta Acharya, Gloria Aguayo, Myriam Alexandre, Muhammad Ali, Wim Ammerlann, Giuseppe Arena, Rudi Balling, Michele Bassis, Roxane Batutu, Katy Beaumont, Regina Becker, Camille Bellora, Guy Berchem, Daniela Berg, Alexandre Bisdorff, Ibrahim Boussaad, David Bouvier, Kathrin Brockmann, Jessica Calmes, Lorieza Castillo, Gessica Contesotto, Nancy De Bremaeker, Nico J. Diederich, Rene Dondelinger, Nancy E. Ramia, Daniela Esteves, Guy Fagherazzi, Jean-Yves Ferrand, Katrin Frauenknecht, Manon Gantenbein, Thomas Gasser, Piotr Gawron, Soumyabrata Ghosh, Marijus Giraitis, Enrico Glaab, Martine Goergen, Elisa Gómez De Lope, Jérôme Graas, Mariella Graziano, Valentin Grouès, Anne Grünewald, Wei Gu, Gaël Hammot, Anne-Marie Hanff, Linda Hansen, Michael T. Heneka, Estelle Henry, Sylvia Herbrink, Sascha Herzinger, Michaël Heymann, Joshua Shulman, Alexander Hundt, Nadine Jacoby, Jacek Jaroslaw Lebioda, Yohan Jarosz, Sonja Jónsdóttir, Quentin Klopfenstein, Jochen Klucken, Rejko Krüger, Pauline Lambert, Roseline Lentz, Inga Liepelt, Robert Liszka, Laura Longhino, Victoria Lorentz, Paula Cristina Lupu, Tainá M. Marques, Clare E. Mackay, Walter Maetzler, Katrin Marcus, Guilherme Fernandes Marques, Patricia Martins Conde, Deborah McIntyre, Chouaib Mediouni, Françoise Meisch, Myriam Menster, Maura Minelli, Michel Mittelbronn, Brit Mollenhauer, Friedrich Mühlschlegel, Romain Nati, Ulf Nehrbass, Sarah Nickels, Béatrice Nicolai, Jean-Paul Nicolay, Noor Fatima, Marek Ostaszewski, Clarissa P. C. Gomes, Claire Pauly

    منشور في 2023
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