Результати пошуку - Peter Van den Bergh
- Показ 1 - 20 результатів із 40
- На наступну сторінку
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Tibial muscular dystrophy in a Belgian family за авторством Peter Van den Bergh, Olivier Bouquiaux, Christine Verellen, Sylvie Marchand, Isabelle Richard, Peter Hackman, Bjarne Udd
Опубліковано 2003Artigo -
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Impact of Very Early Physical Therapy During Septic Shock on Skeletal Muscle: A Randomized Controlled Trial за авторством Cheryl Hickmann, Diego Castanares‐Zapatero, Louise Deldicque, Peter Van den Bergh, Gilles Caty, Annie Robert, Jean Roeseler, Marc Francaux, Pierre‐François Laterre
Опубліковано 2018Artigo -
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Efficacy and Safety of Rozanolixizumab in Moderate to Severe Generalized Myasthenia Gravis за авторством Vera Bril, Michael Benatar, Henning Andersen, John Vissing, Melissa Brock, Bernhard Greve, Peter Kießling, Franz Woltering, Laura E. Griffin, Peter Van den Bergh
Опубліковано 2020Artigo -
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New <i>POMT2</i> mutations causing congenital muscular dystrophy за авторством Akiko Yanagisawa, C Bouchet, Peter Van den Bergh, Jean‐Marie Cuisset, Louis Viollet, France Leturcq, Norma B. Romero, Susana Quijano‐Roy, Michel Fardeau, Nathalie Seta, Pascale Guicheney
Опубліковано 2007Artigo -
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Randomized controlled trial of intravenous immunoglobulin versus oral prednisolone in chronic inflammatory demyelinating polyradiculoneuropathy за авторством Richard AC Hughes, S. Bensa, Hugh J. Willison, Peter Van den Bergh, Gıancarlo Comı, Isabel Illa, Eduardo Nobile‐Orazio, P. van Doorn, Marinos C. Dalakas, Martin Bojar, A V Swan
Опубліковано 2001Artigo -
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Identification of 45 novel mutations in the nebulin gene associated with autosomal recessive nemaline myopathy за авторством Vilma‐Lotta Lehtokari, Katarina Pelin, Maria Sandbacka, Salla Ranta, Kati Donner, Francesco Muntoni, Caroline A. Sewry, C. Angelini, Kate Bushby, Peter Van den Bergh, Susan T. Iannaccone, Nigel G. Laing, Carina Wallgren‐Pettersson
Опубліковано 2006Artigo -
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A new muscle glycogen storage disease associated with glycogenin‐1 deficiency за авторством Edoardo Malfatti, Johanna Nilsson, Carola Hedberg‐Oldfors, Aurelio Hernández‐Laín, Fabrice Michel, Cristina Domínguez‐González, G. Viennet, Hasan O. Akman, Cornelia Kornblum, Peter Van den Bergh, Norma B. Romero, Andrew G. Engel, Salvatore DiMauro, Anders Oldfors
Опубліковано 2014Artigo -
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European consensus for starting and stopping enzyme replacement therapy in adult patients with Pompe disease: a 10‐year experience за авторством Ans T. van der Ploeg, Michelle E. Kruijshaar, António Toscano, Pascal Laforêt, C. Angelini, Robin Lachmann, Samuel Ignacio Pascual Pascual, Mark Roberts, Kai M. Rösler, Thomas M. Stulnig, Pieter A. van Doorn, Peter Van den Bergh, John Vissing, Benedikt Schoser
Опубліковано 2017Revisão -
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European Federation of Neurological Societies/Peripheral Nerve Society guideline on management of multifocal motor neuropathy* за авторством Ivo N. van Schaik, P. Bouché, Isabel Illa, J.M. Léger, Peter Van den Bergh, David R. Cornblath, E. Evers, Robert D. M. Hadden, R. A. C. Hughes, Carol Lee Koski, Eduardo Nobile‐Orazio, J. Pollard, Claudia Sommer, Pieter A. van Doorn
Опубліковано 2006Artigo -
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European Federation of Neurological Societies/Peripheral Nerve Society guideline on management of chronic inflammatory demyelinating polyradiculoneuropathy: report of a joint task... за авторством Richard AC Hughes, P. Bouché, David R. Cornblath, E. Evers, Robert D. M. Hadden, Andreas Hahn, Isabel Illa, Carol Lee Koski, J.‐M. Léger, Eduardo Nobile‐Orazio, John D. Pollard, Claudia Sommer, Peter Van den Bergh, Pieter A. van Doorn, Ivo N. van Schaik
Опубліковано 2006Artigo -
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Sporadic late-onset nemaline myopathy with MGUS за авторством Nicol C. Voermans, Olivier Benvéniste, Monique C. Minnema, Henk M. Lokhorst, Martin Lammens, Wouter Meersseman, Michel Delforge, Thierry Küntzer, Jan Nový, Thomas Pabst, Françoise Bouhour, Norma B. Romero, Véronique Leblond, Peter Van den Bergh, Marie‐Christiane Vekemans, Baziel G.M. van Engelen, B. Eymard
Опубліковано 2014Artigo -
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Human light meromyosin mutations linked to skeletal myopathies disrupt the coiled coil structure and myosin head sequestration за авторством Glenn Carrington, Abbi Hau, Sarah Kosta, Hannah F. Dugdale, Francesco Muntoni, Adele D’Amico, Peter Van den Bergh, Norma B. Romero, Edoardo Malfatti, Juan J. Vílchez, Anders Oldfors, Sander Pajusalu, Katrin Õunap, Marta Giralt‐Pujol, Edmar Zanoteli, Kenneth S. Campbell, Hiroyuki Iwamoto, Michelle Peckham, Julien Ochala
Опубліковано 2023Pré-impressão -
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Human skeletal myopathy myosin mutations disrupt myosin head sequestration за авторством Glenn Carrington, Abbi Hau, Sarah Kosta, Hannah F. Dugdale, Francesco Muntoni, Adele D’Amico, Peter Van den Bergh, Norma B. Romero, Edoardo Malfatti, Juan J. Vílchez, Anders Oldfors, Sander Pajusalu, Katrin Õunap, Marta Giralt‐Pujol, Edmar Zanoteli, Kenneth S. Campbell, Hiroyuki Iwamoto, Michelle Peckham, Julien Ochala
Опубліковано 2023Artigo -
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Heterozygous missense mutations in BSCL2 are associated with distal hereditary motor neuropathy and Silver syndrome за авторством Christian Windpassinger, Michaela Auer‐Grumbach, Joy Irobi, Heema Patel, Erwin Petek, Gerd Hörl, Roland Malli, Johanna A. Reed, Ines Dierick, Nathalie Verpoorten, Thomas T. Warner, Christos Proukakis, Peter Van den Bergh, Christine Verellen, Lionel Van Maldergem, Luciano Merlini, Peter De Jonghe, Vincent Timmerman, Andrew H. Crosby, Klaus Wagner
Опубліковано 2004Artigo -
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Unusual multisystemic involvement and a novel BAG3 mutation revealed by NGS screening in a large cohort of myofibrillar myopathies за авторством Anna-Lena Semmler, Sabrina Sacconi, J Elisa Bach, Claus Liebe, J. Bürmann, Rudolf A. Kley, A. Ferbert, Roland Anderheiden, Peter Van den Bergh, Jean‐Jacques Martin, Peter De Jonghe, Eva Neuen-Jacob, Oliver J. Müller, Marcus Deschauer, Markus Bergmann, J. M. Schröder, Matthias Vorgerd, Jörg B. Schulz, Joachim Weis, Wolfram Kreß, Kristl G. Claeys
Опубліковано 2014Artigo -
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Original research: Second IVIg course in Guillain-Barré syndrome with poor prognosis: the non-randomised ISID study за авторством Christine Verboon, Bianca van den Berg, David R. Cornblath, Esmée Venema, Kenneth C. Gorson, Michael P. Lunn, Hester F. Lingsma, Peter Van den Bergh, Thomas Harbo, Kathleen Bateman, Yann Péréon, Søren H. Sindrup, Susumu Kusunoki, James Miller, Zhahirul Islam, Hans-Peter Hartung, Govindsinh Chavada, Bart C. Jacobs, Richard AC Hughes, Pieter A. van Doorn
Опубліковано 2019Artigo -
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European Academy of Neurology/Peripheral Nerve Society guideline on diagnosis and treatment of chronic inflammatory demyelinating polyradiculoneuropathy: Report of a joint Task For... за авторством Peter Van den Bergh, Pieter A. van Doorn, Robert D. M. Hadden, Bert Avau, Patrik Vankrunkelsven, Jeffrey A. Allen, Shahram Attarian, Patricia H. Blomkwist‐Markens, David R. Cornblath, Filip Eftimov, H. Stephan Goedee, Thomas Harbo, Satoshi Kuwabara, Richard A. Lewis, Michael P. Lunn, Eduardo Nobile‐Orazio, Luís Querol, Yusuf A. Rajabally, Claudia Sommer, Haluk Topaloğlu
Опубліковано 2021Artigo -
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European Academy of Neurology/Peripheral Nerve Society guideline on diagnosis and treatment of chronic inflammatory demyelinating polyradiculoneuropathy: Report of a joint Task For... за авторством Peter Van den Bergh, Pieter A. van Doorn, Robert D. M. Hadden, Bert Avau, Patrik Vankrunkelsven, Jeffrey A. Allen, Shahram Attarian, Patricia H. Blomkwist‐Markens, David R. Cornblath, Filip Eftimov, H. Stephan Goedee, Thomas Harbo, Satoshi Kuwabara, Richard A. Lewis, Michael P. Lunn, Eduardo Nobile‐Orazio, Luís Querol, Yusuf A. Rajabally, Claudia Sommer, Haluk Topaloğlu
Опубліковано 2021Artigo -
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European Academy of Neurology/Peripheral Nerve Society Guideline on diagnosis and treatment of <scp>Guillain–Barré</scp> syndrome за авторством Pieter A. van Doorn, Peter Van den Bergh, Robert D. M. Hadden, Bert Avau, Patrik Vankrunkelsven, Shahram Attarian, Patricia H. Blomkwist‐Markens, David R. Cornblath, H. Stephan Goedee, Thomas Harbo, Bart C. Jacobs, Susumu Kusunoki, Helmar C. Lehmann, Richard A. Lewis, Michael P. Lunn, Eduardo Nobile‐Orazio, Luís Querol, Yusuf A. Rajabally, Thirugnanam Umapathi, Haluk Topaloğlu, Hugh J. Willison
Опубліковано 2023Revisão
Інструменти для пошуку:
Пов'язані теми
Medicine
Biology
Internal medicine
Pathology
Genetics
Gene
Pediatrics
Guillain-Barre syndrome
Mutation
Phenotype
Anatomy
Disease
Cell biology
Physical therapy
Guideline
Neurology
Psychiatry
Skeletal muscle
Biopsy
Muscle biopsy
Myopathy
Physical medicine and rehabilitation
Randomized controlled trial
Antibody
Endocrinology
Immunology
Myocyte
Neuroscience
Polyradiculoneuropathy
Weakness