Search Results - Kristl G. Claeys

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  1. 1
    Color Discrimination Involves Ventral and Dorsal Stream Visual Areas

    Color Discrimination Involves Ventral and Dorsal Stream Visual Areas by Kristl G. Claeys

    Published 2004
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  2. 2
    Congenital myopathies: an update

    Congenital myopathies: an update by Kristl G. Claeys

    Published 2019
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  3. 3
    A Higher Order Motion Region in Human Inferior Parietal Lobule

    A Higher Order Motion Region in Human Inferior Parietal Lobule by Kristl G. Claeys, Delwin T. Lindsey, Erik De Schutter, Guy A. Orban

    Published 2003
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  4. 4
    Biochemical and clinical biomarkers in adult <scp>SMA</scp> 3–4 patients treated with nusinersen for 22 months

    Biochemical and clinical biomarkers in adult <scp>SMA</scp> 3–4 patients treated with nusinersen for 22 months by Bram De Wel, Maxim De Schaepdryver, Koen Poesen, Kristl G. Claeys

    Published 2022
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  5. 5
    Diagnostic Challenges and Clinical Characteristics of Hepatitis E Virus–Associated Guillain-Barré Syndrome

    Diagnostic Challenges and Clinical Characteristics of Hepatitis E Virus–Associated Guillain-Barré Syndrome by Olivier Stevens, Kristl G. Claeys, Koen Poesen, Veroniek Saegeman, Philip Van Damme

    Published 2016
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  6. 6
    Charcot‐Marie‐Tooth Disease: A Clinico‐genetic Confrontation

    Charcot‐Marie‐Tooth Disease: A Clinico‐genetic Confrontation by Nina Barišić, Kristl G. Claeys, Maja Sirotković-Skerlev, A. Löfgren, Eva Nelis, Peter De Jonghe, Vincent Timmerman

    Published 2008
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  7. 7
    Phenotype variability and therapeutic response to Patisiran in patients with hereditary transthyretin amyloidosis: a Belgian real-world experience

    Phenotype variability and therapeutic response to Patisiran in patients with hereditary transthyretin amyloidosis: a Belgian real-world experience by Stéphanie Delstanche, Kristl G. Claeys, Jan De Bleecker, Gauthier Remiche, Pierre Troisfontaines, Vinciane Van Parys, Antoine Bondue

    Published 2025
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  8. 8
    Recommendations for the management of myasthenia gravis in Belgium

    Recommendations for the management of myasthenia gravis in Belgium by Jan De Bleecker, Gauthier Remiche, Alicia Alonso‐Jiménez, Vinciane Van Parys, Véronique Bissay, Stéphanie Delstanche, Kristl G. Claeys

    Published 2024
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  9. 9
    Muscle Glycogenosis Due to Phosphoglucomutase 1 Deficiency

    Muscle Glycogenosis Due to Phosphoglucomutase 1 Deficiency by Tanya Stojkovic, John Vissing, François Petit, Monique Piraud, Mette Cathrine Ørngreen, Grete Andersen, Kristl G. Claeys, Claire Wary, Jean‐Yves Hogrel, Pascal Laforêt

    Published 2009
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  10. 10
    Clinical and biometrical 12-month follow-up in patients after reconstruction of the sural nerve biopsy defect by the collagen-based nerve guide Neuromaix

    Clinical and biometrical 12-month follow-up in patients after reconstruction of the sural nerve biopsy defect by the collagen-based nerve guide Neuromaix by Ahmet Bozkurt, Kristl G. Claeys, Simone Schrading, Jana Vienna Rödler, Haktan Altinova, Jörg B. Schulz, Joachim Weis, Norbert Pallua, Sabien Geraldine Antonia van Neerven

    Published 2017
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  11. 11
    Detection of myositis-specific antibodies

    Detection of myositis-specific antibodies by Jean‐Baptiste Vulsteke, Ellen De Langhe, Kristl G. Claeys, Doreen Dillaerts, Koen Poesen, Jan Lenaerts, René Westhovens, Philip Van Damme, Daniël Blockmans, Petra De Haes, Xavier Bossuyt

    Published 2018
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  12. 12
    Serum neurofilament heavy chains as early marker of motor neuron degeneration

    Serum neurofilament heavy chains as early marker of motor neuron degeneration by Maxim De Schaepdryver, Janne Goossens, Steffi De Meyer, Andreas Jeromin, Pegah Masrori, Britta Brix, Kristl G. Claeys, Jolien Schaeverbeke, Katarzyna Adamczuk, Rik Vandenberghe, Philip Van Damme, Koen Poesen

    Published 2019
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  13. 13
    Serum neurofilament light chain levels as a marker of upper motor neuron degeneration in patients with Amyotrophic Lateral Sclerosis

    Serum neurofilament light chain levels as a marker of upper motor neuron degeneration in patients with Amyotrophic Lateral Sclerosis by Benjamin Gille, Maxim De Schaepdryver, Janne Goossens, Lieselot Dedeene, Joke De Vocht, Emanuela Oldoni, An Goris, Ludo Van Den Bosch, Bart Depreitere, Kristl G. Claeys, Jos Tournoy, Philip Van Damme, Koen Poesen

    Published 2018
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  14. 14
    Recessive RYR1 mutations cause unusual congenital myopathy with prominent nuclear internalization and large areas of myofibrillar disorganization

    Recessive RYR1 mutations cause unusual congenital myopathy with prominent nuclear internalization and large areas of myofibrillar disorganization by Jorge A. Bevilacqua, Nicole Monnier, Marc Bitoun, B. Eymard, Ana Ferreiro, Soledad Monges, F. Lubieniecki, Analía Taratuto, A. Laquérrière, Kristl G. Claeys, Isabelle Marty, Michel Fardeau, Pascale Guicheney, Joël Lunardi, Norma B. Romero

    Published 2010
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  15. 15
    The Latin American experience with a next generation sequencing genetic panel for recessive limb-girdle muscular weakness and Pompe disease

    The Latin American experience with a next generation sequencing genetic panel for recessive limb-girdle muscular weakness and Pompe disease by Jorge A. Bevilacqua, Maria del Rosario Guecaimburu Ehuletche, Abayubá Perna, Alberto Dubrovsky, Marcondes C. França, Steven Vargas, Madhuri Hegde, Kristl G. Claeys, Volker Straub, Nadia Daba, Roberta Faria, Magali Periquet, Susan Sparks, Nathan Thibault, Roberto Araujo

    Published 2020
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  16. 16
    Patient-reported burden of myasthenia gravis: baseline results of the international prospective, observational, longitudinal real-world digital study MyRealWorld-MG

    Patient-reported burden of myasthenia gravis: baseline results of the international prospective, observational, longitudinal real-world digital study MyRealWorld-MG by Sarah Dewilde, Glenn Philips, Sandra Paci, Jon Beauchamp, Silvia Chiroli, Casey Quinn, Laura Day, Mark Larkin, Jacqueline Palace, Sonia Berrih‐Aknin, Kristl G. Claeys, Srikanth Muppidi, Renato Mantegazza, Francesco Saccà, Andreas Meisel, Guillaume Bassez, Hiroyuki Murai, M.H.M. Janssen

    Published 2023
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  17. 17
    Switching Enzyme Replacement Therapy for Late‐Onset Pompe Disease From Alglucosidase Alfa to Cipaglucosidase Alfa Plus Miglustat: Post Hoc Effect Size Analysis of <scp>PROPEL</scp>

    Switching Enzyme Replacement Therapy for Late‐Onset Pompe Disease From Alglucosidase Alfa to Cipaglucosidase Alfa Plus Miglustat: Post Hoc Effect Size Analysis of <scp>PROPEL</scp>... by Hani Kushlaf, Jordi Díaz‐Manera, Drago Bratkovic, Barry J. Byrne, Kristl G. Claeys, Paula R. Clemens, Mazen M. Dimachkie, Priya S. Kishnani, Pascal Laforêt, Mark Roberts, Benedikt Schoser, António Toscano, Jeff Castelli, Fred Holdbrook, Sheela Sitaraman Das, Mitchell H. Goldman, Tahseen Mozaffar

    Published 2025
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  18. 18
    Anti-Ku + myositis: an acquired inflammatory protein-aggregate myopathy

    Anti-Ku + myositis: an acquired inflammatory protein-aggregate myopathy by Marie‐Therese Holzer, Akinori Uruha, Andreas Roos, Andreas Hentschel, Anne Schänzer, Joachim Weis, Kristl G. Claeys, Benedikt Schoser, Federica Montagnese, Hans-Hilmar Goebel, Melanie Huber, Sarah Léonard-Louis, Ina Kötter, Nathalie Streichenberger, Laure Gallay, Olivier Benvéniste, Udo Schneider, Corinna Preuße, Martin Krusche, Werner Stenzel

    Published 2024
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  19. 19
    Microdeletions involving theSCN1A gene may be common inSCN1A-mutation-negative SMEI patients

    Microdeletions involving theSCN1A gene may be common inSCN1A-mutation-negative SMEI patients by Arvid Suls, Kristl G. Claeys, D. Goossens, B Harding, Rob van Luijk, Stefaan Scheers, Liesbet Deprez, Dominique Audenaert, Tine Van Dyck, Sabine Beeckmans, Iris Smouts, Berten Ceulemans, Lieven Lagae, Gunnar Buyse, Nina Barišić, Jean‐Paul Misson, J. Wauters, Jurgen Del‐Favero, Peter De Jonghe, Lieve Claes

    Published 2006
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  20. 20
    Phenotypic spectrum of dynamin 2 mutations in Charcot-Marie-Tooth neuropathy

    Phenotypic spectrum of dynamin 2 mutations in Charcot-Marie-Tooth neuropathy by Kristl G. Claeys, Stephan Züchner, Marina Kennerson, José Berciano, Abel Garcı́a Garcı́a, K. Verhoeven, Elsdon Storey, John Merory, H.M.E. Bienfait, Martin Lammens, Eva Nelis, Jonathan Baets, Els De Vriendt, Zwi Berneman, Ilse De Veuster, Jeffery M. Vance, Garth A. Nicholson, Vincent Timmerman, Peter De Jonghe

    Published 2009
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