Search Results - Bart P. van de Warrenburg

  • Showing 1 - 13 results of 13
Refine Results
  1. 1
    Effects of acetyl-dl-leucine in patients with cerebellar ataxia: a case series

    Effects of acetyl-dl-leucine in patients with cerebellar ataxia: a case series by Michael Strupp, Julian Teufel, M. Habs, Regina Feuerecker, Carolin Muth, Bart P. van de Warrenburg, Thomas Klopstock, Katharina Feil

    Published 2013
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  2. 2
    Cerebellar theta burst stimulation impairs eyeblink classical conditioning

    Cerebellar theta burst stimulation impairs eyeblink classical conditioning by Britt S. Hoffland, Matteo Bologna, Panagiotis Kassavetis, James Teo, John C. Rothwell, Christopher H. Yeo, Bart P. van de Warrenburg, Mark J. Edwards

    Published 2011
    Get full text
    Artigo
    Save to List
    Saved in:
  3. 3
    Mutations in SLC30A10 Cause Parkinsonism and Dystonia with Hypermanganesemia, Polycythemia, and Chronic Liver Disease

    Mutations in SLC30A10 Cause Parkinsonism and Dystonia with Hypermanganesemia, Polycythemia, and Chronic Liver Disease by Marialuisa Quadri, Antonio Federico, Tianna Zhao, Guido J. Breedveld, Carla Battisti, Cathérine C.S. Delnooz, Lies-Anne Severijnen, Lara Di Toro Mammarella, Andrea Mignarri, Lucia Monti, Antioco Sanna, Peng Lü, Francesca Punzo, Giovanni Cossu, Rob Willemsen, Fabrizio Rasi, Ben A. Oostra, Bart P. van de Warrenburg, Vincenzo Bonifati

    Published 2012
    Get full text
    Artigo
    Save to List
    Saved in:
  4. 4
    Genotype–phenotype correlations in spastic paraplegia type 7: a study in a large Dutch cohort

    Genotype–phenotype correlations in spastic paraplegia type 7: a study in a large Dutch cohort by Koen L.I. van Gassen, Charlotte D.C.C. van der Heijden, Susanne T. de Bot, Wilfred F.A. den Dunnen, Leonard H. van den Berg, Corien C. Verschuuren‐Bemelmans, H.P.H. Kremer, Jan H. Veldink, Erik‐Jan Kamsteeg, Hans Scheffer, Bart P. van de Warrenburg

    Published 2012
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  5. 5
    Autosomal Recessive Spinocerebellar Ataxia 7 (SCAR7) is Caused by Variants in<i>TPP1</i>, The Gene Involved in Classic Late-Infantile Neuronal Ceroid Lipofuscinosis 2 Disease (CLN2 Disease)

    Autosomal Recessive Spinocerebellar Ataxia 7 (SCAR7) is Caused by Variants in<i>TPP1</i>, The Gene Involved in Classic Late-Infantile Neuronal Ceroid Lipofuscinosis 2 Disease (CLN2... by Yu Sun, Rowida Almomani, Guido J. Breedveld, Gijs W.E. Santen, Emmelien Aten, Dirk J. Lefeber, Jorrit I. Hoff, Esther Brusse, Frans W. Verheijen, Robert M. Verdijk, Marjolein Kriek, Ben A. Oostra, Martijn H. Breuning, Monique Losekoot, Johan T. den Dunnen, Bart P. van de Warrenburg, Anneke Maat‐Kievit

    Published 2013
    Get full text
    Artigo
    Save to List
    Saved in:
  6. 6
    The Personalized Parkinson Project: examining disease progression through broad biomarkers in early Parkinson’s disease

    The Personalized Parkinson Project: examining disease progression through broad biomarkers in early Parkinson’s disease by Bastiaan R. Bloem, William J. Marks, Ana Lígia Silva de Lima, Mark L. Kuijf, Teus van Laar, Bram Jacobs, Marcel M. Verbeek, Rick C. Helmich, Bart P. van de Warrenburg, Luc J. W. Evers, Joanna IntHout, T. van de Zande, Thomas M. Snyder, Ritu Kapur, Marjan J. Meinders

    Published 2019
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  7. 7
    Prediction of the age at onset in spinocerebellar ataxia type 1, 2, 3 and 6

    Prediction of the age at onset in spinocerebellar ataxia type 1, 2, 3 and 6 by Sophie Tézenas du Montcel, Alexandra Dürr, Maria Rakowicz, Lorenzo Nanetti, Perrine Charles, Anna Sułek, Caterina Mariotti, Rafał Rola, Lüdger Schöls, Peter Bauer, I. Dufaure-Garé, Heike Jacobi, Sylvie Forlani, Tanja Schmitz‐Hübsch, Alessandro Filla, Dagmar Timmann, Bart P. van de Warrenburg, Cecila Marelli, Jun-Suk Kang, Paola Giunti, Arron Cook, László Balikó, Béla Melegh, Sylvia Boesch, Sandra Szymanski, José Berciano, Jon Infante, Katrin Buerk, Marcella Masciullo, Roberto Di Fabio, Chantal Depondt, Susanne Ratka, Giovanni Stévanin, Thomas Klockgether, Alexis Brice, Jean-Louis Golmard

    Published 2014
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  8. 8
    Genetic risk of Parkinson disease and progression:

    Genetic risk of Parkinson disease and progression: by Hirotaka Iwaki, Cornelis Blauwendraat, Hampton L. Leonard, Ganqiang Liu, Jodi Maple‐Grødem, Jean‐Christophe Corvol, Lasse Pihlstrøm, Marlies van Nimwegen, Samantha J. Hutten, Khanh‐Dung H. Nguyen, Jacqueline Rick, Shirley Eberly, Faraz Faghri, Peggy Auinger, Kirsten M. Scott, Ruwani Wijeyekoon, Vivianna M. Van Deerlin, Dena Hernández, Aaron Day-Williams, Alexis Brice, Guido Alves, Alastair Noyce, Ole‐Bjørn Tysnes, Jonathan Evans, David P. Breen, Karol Estrada, Claire Wegel, Fabrice Danjou, David K. Simon, Bernard Ravina, Mathias Toft, Peter Heutink, Bastiaan R. Bloem, Daniel Weintraub, Roger A. Barker, Caroline H. Williams‐Gray, Bart P. van de Warrenburg, Jacobus J. van Hilten, Clemens R. Scherzer, Andrew Singleton, Mike A. Nalls

    Published 2019
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  9. 9
    Genomewide association study of Parkinson's disease clinical biomarkers in 12 longitudinal patients' cohorts

    Genomewide association study of Parkinson's disease clinical biomarkers in 12 longitudinal patients' cohorts by Hirotaka Iwaki, Cornelis Blauwendraat, Hampton L. Leonard, Jonggeol J. Kim, Ganqiang Liu, Jodi Maple‐Grødem, Jean‐Christophe Corvol, Lasse Pihlstrøm, Marlies van Nimwegen, Samantha J. Hutten, Khanh‐Dung H. Nguyen, Jacqueline Rick, Shirley Eberly, Faraz Faghri, Peggy Auinger, Kirsten M. Scott, Ruwani Wijeyekoon, Vivianna M. Van Deerlin, Dena G. Hernandez, J. Raphael Gibbs, Kumaraswamy Naidu Chitrala, Aaron Day-Williams, Alexis Brice, Guido Alves, Alastair Noyce, Ole‐Bjørn Tysnes, Jonathan Evans, David P. Breen, Karol Estrada, Claire Wegel, Fabrice Danjou, David K. Simon, Ole A. Andreassen, Bernard Ravina, Mathias Toft, Peter Heutink, Bastiaan R. Bloem, Daniel Weintraub, Roger A. Barker, Caroline H. Williams‐Gray, Bart P. van de Warrenburg, Jacobus J. van Hilten, Clemens R. Scherzer, Andrew Singleton, Mike A. Nalls

    Published 2019
    Get full text
    Artigo
    Save to List
    Saved in:
  10. 10
    Differences in the Presentation and Progression of Parkinson's Disease by Sex

    Differences in the Presentation and Progression of Parkinson's Disease by Sex by Hirotaka Iwaki, Cornelis Blauwendraat, Hampton L. Leonard, Mary B. Makarious, Jonggeol J. Kim, Ganqiang Liu, Jodi Maple‐Grødem, Jean‐Christophe Corvol, Lasse Pihlstrøm, Marlies van Nimwegen, Luba Smolensky, Ninad Amondikar, Samantha J. Hutten, Mark Frasier, Khanh‐Dung H. Nguyen, Jacqueline Rick, Shirley Eberly, Faraz Faghri, Peggy Auinger, Kirsten M. Scott, Ruwani Wijeyekoon, Vivianna M. Van Deerlin, Dena G. Hernandez, J. Raphael Gibbs, Aaron Day-Williams, Alexis Brice, Guido Alves, Alastair Noyce, Ole‐Bjørn Tysnes, Jonathan Evans, David P. Breen, Karol Estrada, Claire Wegel, Fabrice Danjou, David K. Simon, Ole A. Andreassen, Bernard Ravina, Mathias Toft, Peter Heutink, Bastiaan R. Bloem, Daniel Weintraub, Roger A. Barker, Caroline H. Williams‐Gray, Bart P. van de Warrenburg, Jacobus J. van Hilten, Clemens R. Scherzer, Andrew B. Singleton, Mike A. Nalls

    Published 2020
    Get full text
    Artigo
    Save to List
    Saved in:
  11. 11
    Mutations in DDHD2, Encoding an Intracellular Phospholipase A1, Cause a Recessive Form of Complex Hereditary Spastic Paraplegia

    Mutations in DDHD2, Encoding an Intracellular Phospholipase A1, Cause a Recessive Form of Complex Hereditary Spastic Paraplegia by Janneke Schuurs-Hoeijmakers, Michael T. Geraghty, Erik‐Jan Kamsteeg, Salma Ben‐Salem, Susanne T. de Bot, Bonnie Nijhof, Ilse I.G.M. van de Vondervoort, Marinette van der Graaf, Anna Castells‐Nobau, Irene Otte‐Höller, Sascha Vermeer, Amanda Smith, Peter Humphreys, Jeremy Schwartzentruber, Bassam R. Ali, Saeed Al‐Yahyaee, Said Tariq, Thachillath Pramathan, Riad Bayoumi, H.P.H. Kremer, Bart P. van de Warrenburg, Willem M.R. van den Akker, Christian Gilissen, Joris A. Veltman, Irene M. Janssen, Anneke T. Vulto-van Silfhout, Saskia van der Velde-Visser, Dirk Lefeber, Adinda Diekstra, Corrie E. Erasmus, Michèl A.A.P. Willemsen, Lisenka E.L.M. Vissers, Martin Lammens, Hans van Bokhoven, Han G. Brunner, Ron A. Wevers, Annette Schenck, Lihadh Al‐Gazali, Bert B.A. de Vries, Arjan P.M. de Brouwer

    Published 2012
    Get full text
    Artigo
    Save to List
    Saved in:
  12. 12
    Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis

    Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis by Michael A. van Es, Helenius J. Schelhaas, Paul W.J. van Vught, Nicola Ticozzi, Peter M. Andersen, Ewout J. N. Groen, Claudia Schulte, Hylke M. Blauw, Max Koppers, Frank P. Diekstra, Katsumi Fumoto, Ashley LeClerc, Pamela Keagle, Bastiaan R. Bloem, Hans Scheffer, Bart F.L. van Nuenen, Marka van Blitterswijk, Wouter van Rheenen, Anne‐Marie Wills, Patrick Lowe, Guo‐fu Hu, Wenhao Yu, Hiroko Kishikawa, David M. Wu, Rebecca D. Folkerth, Claudio Mariani, Stefano Goldwurm, Gianni Pezzoli, Philip Van Damme, Robin Lemmens, Caroline Dahlberg, Anna Birve, Rubén Fernández‐Santiago, Stefan Waibel, Christine Klein, Markus Weber, Anneke J. van der Kooi, Marianne de Visser, Dagmar Verbaan, Jacobus J. van Hilten, Peter Heutink, Eric A. M. Hennekam, Edwin Cuppen, Daniela Berg, Robert H. Brown, Vincenzo Silani, Thomas Gasser, Albert C. Ludolph, Wim Robberecht, Roel A. Ophoff, Jan H. Veldink, R. Jeroen Pasterkamp, Paul I. W. de Bakker, John E. Landers, Bart P. van de Warrenburg, Leonard H. van den Berg

    Published 2011
    Get full text
    Revisão
    Save to List
    Saved in:
  13. 13
    Mendelian Randomisation Study of Smoking, Alcohol, and Coffee Drinking in Relation to Parkinson’s Disease

    Mendelian Randomisation Study of Smoking, Alcohol, and Coffee Drinking in Relation to Parkinson’s Disease by Cloé Domenighetti, Pierre‐Emmanuel Sugier, Ashwin Ashok Kumar Sreelatha, Claudia Schulte, Sandeep Grover, Océane Mohamed, Berta Portugal, Patrick May, Dheeraj Reddy Bobbili, Milena Radivojkov‐Blagojevic, Peter Lichtner, Andrew Singleton, Dena G. Hernandez, Connor Edsall, George D. Mellick, Alexander Zimprich, Walter Pirker, Ekaterina Rogaeva, Anthony E. Lang, Sulev Kõks, Pille Taba, Suzanne Lesage, Alexis Brice, Jean‐Christophe Corvol, Marie‐Christine Chartier‐Harlin, Eugénie Mutez, Kathrin Brockmann, Angela Deutschländer, G. Hadjigeorgiou, Efthimos Dardiotis, Leonidas Stefanis, Athina Maria Simitsi, Enza Maria Valente, Simona Petrucci, Stefano Duga, Letizia Straniero, Anna Zecchinelli, Gianni Pezzoli, Laura Brighina, Carlo Ferrarese, Grazia Annesi, Andrea Quattrone, Monica Gagliardi, Hirotaka Matsuo, Yusuke Kawamura, Nobutaka Hattori, Kenya Nishioka, Sun Ju Chung, Yun Joong Kim, Pierre Kolber, Bart P. van de Warrenburg, Bastiaan R. Bloem, Jan Aasly, Mathias Toft, Lasse Pihlstrøm, Leonor Correia Guedes, Joaquim J. Ferreira, Soraya Bardien, Jonathan Carr, Eduardo Tolosa, Mario Ezquerra, Pau Pástor, Mónica Díez-Fairén, Karin Wirdefeldt, Nancy L. Pedersen, Caroline Ran, Andrea Carmine Belin, Andreas Puschmann, Clara Hellberg, Carl E Clarke, Karen Morrison, Manuela Tan, Dimitri Krainc, Lena F. Burbulla, Matthew J. Farrer, Rejko Krüger, Thomas Gasser, Manu Sharma, Alexis Elbaz

    Published 2021
    Get full text
    Artigo
    Save to List
    Saved in:

Search Tools: