Risultati della ricerca - Christiaan G. J. Saris

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  1. 1
    Association of diaphragm thickness and echogenicity with age, sex, and <scp>body mass index</scp> in healthy subjects

    Association of diaphragm thickness and echogenicity with age, sex, and <scp>body mass index</scp> in healthy subjects di Jeroen L. M. van Doorn, Juerd Wijntjes, Christiaan G. J. Saris, Coen A. C. Ottenheijm, Nens van Alfen, Jonne Doorduin

    Pubblicazione 2022
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  2. 2
    Seronegative patients form a distinctive subgroup of immune-mediated necrotizing myopathy

    Seronegative patients form a distinctive subgroup of immune-mediated necrotizing myopathy di Johan Lim, Anke Rietveld, Jan De Bleecker, Umesh A. Badrising, Christiaan G. J. Saris, Anneke J. van der Kooi, Marjolein Visser

    Pubblicazione 2018
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  3. 3
    Weighted gene co-expression network analysis of the peripheral blood from Amyotrophic Lateral Sclerosis patients

    Weighted gene co-expression network analysis of the peripheral blood from Amyotrophic Lateral Sclerosis patients di Christiaan G. J. Saris, Steve Horvath, Paul W.J. van Vught, Michael A. van Es, Hylke M. Blauw, Tova F Fuller, Peter Langfelder, Joseph DeYoung, John H. J. Wokke, Jan H. Veldink, Leonard H. van den Berg, Roel A. Ophoff

    Pubblicazione 2009
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  4. 4
    Whole blood transcriptome analysis in amyotrophic lateral sclerosis: A biomarker study

    Whole blood transcriptome analysis in amyotrophic lateral sclerosis: A biomarker study di Wouter van Rheenen, Frank P. Diekstra, Oliver Harschnitz, Henk-Jan Westeneng, Kristel R. van Eijk, Christiaan G. J. Saris, Ewout J. N. Groen, Michael A. van Es, Hylke M. Blauw, Paul W.J. van Vught, Jan H. Veldink, Leonard H. van den Berg

    Pubblicazione 2018
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  5. 5
    Effect of Mexiletine on Muscle Stiffness in Patients With Nondystrophic Myotonia Evaluated Using Aggregated N-of-1 Trials

    Effect of Mexiletine on Muscle Stiffness in Patients With Nondystrophic Myotonia Evaluated Using Aggregated N-of-1 Trials di Bas C. Stunnenberg, Joost Raaphorst, Hans Groenewoud, Jeffrey Statland, Robert C. Griggs, Willem Woertman, Dick F. Stegeman, Janneke Timmermans, Jaya Trivedi, Emma Matthews, Christiaan G. J. Saris, B.J.J.W. Schouwenberg, Gea Drost, Baziel G.M. van Engelen, Gert Jan van der Wilt

    Pubblicazione 2018
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  6. 6
    Frequencies and clinical associations of myositis-related antibodies in The Netherlands: A one-year survey of all Dutch patients

    Frequencies and clinical associations of myositis-related antibodies in The Netherlands: A one-year survey of all Dutch patients di Anouk C. M. Platteel, Brigitte A. Wevers, Johan Lim, Jaap Bakker, Hetty J. Bontkes, Joyce Curvers, Jan Damoiseaux, Michiel Heron, G. de Kort, Maarten Limper, Ellen G. van Lochem, A. H. L. Mulder, Christiaan G. J. Saris, Hester van der Valk, Anneke J. van der Kooi, Ester M. M. van Leeuwen, Marcel Veltkamp, Marco W.J. Schreurs, Bob Meek, Dörte Hamann

    Pubblicazione 2019
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  7. 7
    Cytosolic 5′-nucleotidase 1A autoantibody profile and clinical characteristics in inclusion body myositis

    Cytosolic 5′-nucleotidase 1A autoantibody profile and clinical characteristics in inclusion body myositis di James B Lilleker, Anke Rietveld, Stephen R. Pye, K. Mariampillai, Olivier Benvéniste, Maikel Peeters, James Miller, Michael G. Hanna, Pedro Machado, Matt Parton, Karina Gheorghe, Umesh A. Badrising, Ingrid E. Lundberg, Sabrina Sacconi, Megan K. Herbert, Neil McHugh, Bryan Lecky, Charlotte Brierley, David Hilton‐Jones, Janine A. Lamb, Marc Roberts, Robert G. Cooper, Christiaan G. J. Saris, Ger J.M. Pruijn, Hector Chinoy, Baziel G.M. van Engelen

    Pubblicazione 2017
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  8. 8
    KIF1A variants are a frequent cause of autosomal dominant hereditary spastic paraplegia

    KIF1A variants are a frequent cause of autosomal dominant hereditary spastic paraplegia di Maartje Pennings, Meyke Schouten, Judith van Gaalen, Rowdy Meijer, Susanne T. de Bot, Marjolein Kriek, Christiaan G. J. Saris, Leonard H. van den Berg, Michael A. van Es, Dick M. H. Zuidgeest, Mariet W. Elting, Jiddeke M. van de Kamp, Karin Y. van Spaendonck‐Zwarts, Christine de Die‐Smulders, Eva H. Brilstra, Corien Verschuuren, Bert B.A. de Vries, Jacques Bruijn, Kalliopi Sofou, Floor A.M. Duijkers, Bregje Jaeger, Jolanda Schieving, Bart P.C. van de Warrenburg, Erik-Jan Kamsteeg

    Pubblicazione 2019
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  9. 9
    Trans-eQTLs Reveal That Independent Genetic Variants Associated with a Complex Phenotype Converge on Intermediate Genes, with a Major Role for the HLA

    Trans-eQTLs Reveal That Independent Genetic Variants Associated with a Complex Phenotype Converge on Intermediate Genes, with a Major Role for the HLA di Rudolf S.N. Fehrmann, Ritsert C. Jansen, Jan H. Veldink, Harm-Jan Westra, Danny Arends, Marc Jan Bonder, Jingyuan Fu, Patrick Deelen, Harry J.M. Groen, Asia Smolonska, Rinse K. Weersma, Robert M.W. Hofstra, Wim A. Buurman, Sander S. Rensen, Marcel G. M. Wolfs, Mathieu Platteel, Alexandra Zhernakova, Clara C. Elbers, Eleonora A. Festen, Gosia Trynka, Marten H. Hofker, Christiaan G. J. Saris, Roel A. Ophoff, Leonard H. van den Berg, David A. van Heel, Cisca Wijmenga, Gerard J. te Meerman, Lude Franke

    Pubblicazione 2011
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  10. 10
    Mapping of Gene Expression Reveals CYP27A1 as a Susceptibility Gene for Sporadic ALS

    Mapping of Gene Expression Reveals CYP27A1 as a Susceptibility Gene for Sporadic ALS di Frank P. Diekstra, Christiaan G. J. Saris, Wouter van Rheenen, Lude Franke, Ritsert C. Jansen, Michael A. van Es, Paul W.J. van Vught, Hylke M. Blauw, Ewout J. N. Groen, Steve Horvath, Karol Estrada, Fernando Rivadeneira, Albert Hofman, André G. Uitterlinden, Wim Robberecht, Peter M. Andersen, Judith Melki, Vincent Meininger, Orla Hardiman, John E. Landers, Robert H. Brown, Aleksey Shatunov, Christopher E. Shaw, P. Nigel Leigh, Ammar Al‐Chalabi, Roel A. Ophoff, Leonard H. van den Berg, Jan H. Veldink

    Pubblicazione 2012
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  11. 11
    MT-ND5 Mutation Exhibits Highly Variable Neurological Manifestations at Low Mutant Load

    MT-ND5 Mutation Exhibits Highly Variable Neurological Manifestations at Low Mutant Load di Yi Shiau Ng, Nichola Z. Lax, Paul Maddison, Charlotte L. Alston, Emma L. Blakely, Philippa D. Hepplewhite, Gillian Riordan, Surita Meldau, Patrick F. Chinnery, Germaine Pierre, Efstathia Chronopoulou, Ailian Du, Imelda Hughes, Andrew A. M. Morris, Smaragda Kamakari, Georgia Antonakou Chrousos, Richard J. Rodenburg, Christiaan G. J. Saris, Catherine Feeney, Steven Hardy, Takafumi Sakakibara, Akira Sudo, Yasushi Okazaki, Kei Murayama, Helen Mundy, Michael G. Hanna, Akira Ohtake, Andrew M. Schaefer, Mike Champion, Douglass M. Turnbull, Robert W. Taylor, Robert D. S. Pitceathly, Robert McFarland, Gráinne S. Gorman

    Pubblicazione 2018
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  12. 12
    A large genome scan for rare CNVs in amyotrophic lateral sclerosis

    A large genome scan for rare CNVs in amyotrophic lateral sclerosis di Hylke M. Blauw, Ammar Al‐Chalabi, Peter M. Andersen, Paul W.J. van Vught, Frank P. Diekstra, Michael A. van Es, Christiaan G. J. Saris, Ewout J. N. Groen, Wouter van Rheenen, Max Koppers, Ruben van't Slot, Eric Strengman, Karol Estrada, Fernando Rivadeneira, Albert Hofman, André G. Uitterlinden, Lambertus A. Kiemeney, Sita H. Vermeulen, Anna Birve, Stefan Waibel, Thomas Meyer, Simon Cronin, Russell L. McLaughlin, Orla Hardiman, Peter C. Sapp, Martin D. Tobin, Louise V. Wain, Barbara Tomik, Agnieszka Słowik, Robin Lemmens, Dan Rujescu, Claudia Schulte, Thomas Gasser, Robert H. Brown, John E. Landers, Wim Robberecht, Albert C. Ludolph, Roel A. Ophoff, Jan H. Veldink, Leonard H. van den Berg

    Pubblicazione 2010
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  13. 13
    Reduced expression of the <i>Kinesin-Associated Protein 3</i> ( <i>KIFAP3</i> ) gene increases survival in sporadic amyotrophic lateral sclerosis

    Reduced expression of the <i>Kinesin-Associated Protein 3</i> ( <i>KIFAP3</i> ) gene increases survival in sporadic amyotrophic lateral sclerosis di John E. Landers, Judith Melki, Vincent Meininger, Jonathan D. Glass, Leonard H. van den Berg, Michael A. van Es, Peter C. Sapp, Paul W.J. van Vught, Diane McKenna‐Yasek, Hylke M. Blauw, Ting-Jan Cho, Meraida Polak, Lijia Shi, Anne‐Marie Wills, Wendy Broom, Nicola Ticozzi, Vincenzo Silani, Aslıhan Özoğuz, Ildefonso Rodríguez‐Leyva, Jan H. Veldink, Adrian J. Ivinson, Christiaan G. J. Saris, Betsy A. Hosler, Alayna Barnes-Nessa, Nicole Couture, John H. J. Wokke, Thomas J. Kwiatkowski, Roel A. Ophoff, Simon Cronin, Orla Hardiman, Frank P. Diekstra, P. Nigel Leigh, Christopher E. Shaw, Claire L. Simpson, Valerie K. Hansen, John Powell, Philippe Corcia, François Salachas, Simon Heath, Pilar Galán, Georges Franck, H. Robert Horvitz, Mark Lathrop, Shaun Purcell, Ammar Al‐Chalabi, Robert H. Brown

    Pubblicazione 2009
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  14. 14
    Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1

    Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1 di Kreshnik Ahmeti, Senda Ajroud‐Driss, Ammar Al‐Chalabi, Peter M. Andersen, Jennifer A. Armstrong, A. Birve, Hylke M. Blauw, Robert H. Brown, Lucie Bruijn, Wenjie Chen, Adriano Chió, Mary C. Comeau, Simon Cronin, Frank P. Diekstra, Athina Soraya Gkazi, Jonathan D. Glass, Josh D Grab, Ewout J. N. Groen, Jonathan L. Haines, Orla Hardiman, Scott Heller, Jie Huang, Wu-Yen Hung, James Jaworski, Ashley Jones, Humaira Majeed Khan, John E. Landers, Carl D. Langefeld, P. Nigel Leigh, Miranda C. Marion, Russell L. McLaughlin, Vincent Meininger, Judith Melki, Jack W. Miller, Gabriele Mora, Margaret A. Pericak‐Vance, Evadnie Rampersaud, Wim Robberecht, Laurie Russell, François Salachas, Christiaan G. J. Saris, Aleksey Shatunov, Christopher E. Shaw, Nailah Siddique, Teepu Siddique, Bradley Smith, Robert Sufit, Simon Topp, Bryan J. Traynor, Caroline Vance, Philip Van Damme, Leonard H. van den Berg, Michael A van Es, Paul W van Vught, Jan H. Veldink, Yi Yang, Jingang Zheng

    Pubblicazione 2012
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