Αποτελέσματα αναζήτησης - Peter Van den Bergh

Περιορισμός αποτελεσμάτων
  1. 1
    Validity of diagnostic criteria for chronic inflammatory demyelinating polyneuropathy: a multicentre European study

    Validity of diagnostic criteria for chronic inflammatory demyelinating polyneuropathy: a multicentre European study από Yusuf A. Rajabally, Guillaume Nicolas, Françoise Piéret, P. Bouché, Peter Van den Bergh

    Έκδοση 2009
    Λήψη πλήρους κειμένου
    Artigo
    Προσθήκη στα αγαπημένα
    Αποθηκεύτηκε σε:
  2. 2
    Tibial muscular dystrophy in a Belgian family

    Tibial muscular dystrophy in a Belgian family από Peter Van den Bergh, Olivier Bouquiaux, Christine Verellen, Sylvie Marchand, Isabelle Richard, Peter Hackman, Bjarne Udd

    Έκδοση 2003
    Λήψη πλήρους κειμένου Λήψη πλήρους κειμένου
    Artigo
    Προσθήκη στα αγαπημένα
    Αποθηκεύτηκε σε:
  3. 3
    Impact of Very Early Physical Therapy During Septic Shock on Skeletal Muscle: A Randomized Controlled Trial

    Impact of Very Early Physical Therapy During Septic Shock on Skeletal Muscle: A Randomized Controlled Trial από Cheryl Hickmann, Diego Castanares‐Zapatero, Louise Deldicque, Peter Van den Bergh, Gilles Caty, Annie Robert, Jean Roeseler, Marc Francaux, Pierre‐François Laterre

    Έκδοση 2018
    Λήψη πλήρους κειμένου
    Artigo
    Προσθήκη στα αγαπημένα
    Αποθηκεύτηκε σε:
  4. 4
    Efficacy and Safety of Rozanolixizumab in Moderate to Severe Generalized Myasthenia Gravis

    Efficacy and Safety of Rozanolixizumab in Moderate to Severe Generalized Myasthenia Gravis από Vera Bril, Michael Benatar, Henning Andersen, John Vissing, Melissa Brock, Bernhard Greve, Peter Kießling, Franz Woltering, Laura E. Griffin, Peter Van den Bergh

    Έκδοση 2020
    Λήψη πλήρους κειμένου Λήψη πλήρους κειμένου
    Artigo
    Προσθήκη στα αγαπημένα
    Αποθηκεύτηκε σε:
  5. 5
    New <i>POMT2</i> mutations causing congenital muscular dystrophy

    New <i>POMT2</i> mutations causing congenital muscular dystrophy από 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

    Έκδοση 2007
    Λήψη πλήρους κειμένου
    Artigo
    Προσθήκη στα αγαπημένα
    Αποθηκεύτηκε σε:
  6. 6
    Randomized controlled trial of intravenous immunoglobulin versus oral prednisolone in chronic inflammatory demyelinating polyradiculoneuropathy

    Randomized controlled trial of intravenous immunoglobulin versus oral prednisolone in chronic inflammatory demyelinating polyradiculoneuropathy από 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

    Έκδοση 2001
    Λήψη πλήρους κειμένου Λήψη πλήρους κειμένου
    Artigo
    Προσθήκη στα αγαπημένα
    Αποθηκεύτηκε σε:
  7. 7
    Identification of 45 novel mutations in the nebulin gene associated with autosomal recessive nemaline myopathy

    Identification of 45 novel mutations in the nebulin gene associated with autosomal recessive nemaline myopathy από 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

    Έκδοση 2006
    Λήψη πλήρους κειμένου
    Artigo
    Προσθήκη στα αγαπημένα
    Αποθηκεύτηκε σε:
  8. 8
    A new muscle glycogen storage disease associated with glycogenin‐1 deficiency

    A new muscle glycogen storage disease associated with glycogenin‐1 deficiency από 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

    Έκδοση 2014
    Λήψη πλήρους κειμένου
    Artigo
    Προσθήκη στα αγαπημένα
    Αποθηκεύτηκε σε:
  9. 9
    European consensus for starting and stopping enzyme replacement therapy in adult patients with Pompe disease: a 10‐year experience

    European consensus for starting and stopping enzyme replacement therapy in adult patients with Pompe disease: a 10‐year experience από 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

    Έκδοση 2017
    Λήψη πλήρους κειμένου
    Revisão
    Προσθήκη στα αγαπημένα
    Αποθηκεύτηκε σε:
  10. 10
    European Federation of Neurological Societies/Peripheral Nerve Society guideline on management of multifocal motor neuropathy*

    European Federation of Neurological Societies/Peripheral Nerve Society guideline on management of multifocal motor neuropathy* από 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

    Έκδοση 2006
    Λήψη πλήρους κειμένου Λήψη πλήρους κειμένου
    Artigo
    Προσθήκη στα αγαπημένα
    Αποθηκεύτηκε σε:
  11. 11
    European Federation of Neurological Societies/Peripheral Nerve Society guideline on management of chronic inflammatory demyelinating polyradiculoneuropathy: report of a joint task force of the European Federation of Neurological Societies and the Peripheral Nerve Society

    European Federation of Neurological Societies/Peripheral Nerve Society guideline on management of chronic inflammatory demyelinating polyradiculoneuropathy: report of a joint task... από 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

    Έκδοση 2006
    Λήψη πλήρους κειμένου Λήψη πλήρους κειμένου
    Artigo
    Προσθήκη στα αγαπημένα
    Αποθηκεύτηκε σε:
  12. 12
    Sporadic late-onset nemaline myopathy with MGUS

    Sporadic late-onset nemaline myopathy with MGUS από 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

    Έκδοση 2014
    Λήψη πλήρους κειμένου
    Artigo
    Προσθήκη στα αγαπημένα
    Αποθηκεύτηκε σε:
  13. 13
    Human light meromyosin mutations linked to skeletal myopathies disrupt the coiled coil structure and myosin head sequestration

    Human light meromyosin mutations linked to skeletal myopathies disrupt the coiled coil structure and myosin head sequestration από 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

    Έκδοση 2023
    Λήψη πλήρους κειμένου Λήψη πλήρους κειμένου
    Pré-impressão
    Προσθήκη στα αγαπημένα
    Αποθηκεύτηκε σε:
  14. 14
    Human skeletal myopathy myosin mutations disrupt myosin head sequestration

    Human skeletal myopathy myosin mutations disrupt myosin head sequestration από 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

    Έκδοση 2023
    Λήψη πλήρους κειμένου Λήψη πλήρους κειμένου
    Artigo
    Προσθήκη στα αγαπημένα
    Αποθηκεύτηκε σε:
  15. 15
    Heterozygous missense mutations in BSCL2 are associated with distal hereditary motor neuropathy and Silver syndrome

    Heterozygous missense mutations in BSCL2 are associated with distal hereditary motor neuropathy and Silver syndrome από 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

    Έκδοση 2004
    Λήψη πλήρους κειμένου Λήψη πλήρους κειμένου
    Artigo
    Προσθήκη στα αγαπημένα
    Αποθηκεύτηκε σε:
  16. 16
    Unusual multisystemic involvement and a novel BAG3 mutation revealed by NGS screening in a large cohort of myofibrillar myopathies

    Unusual multisystemic involvement and a novel BAG3 mutation revealed by NGS screening in a large cohort of myofibrillar myopathies από 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

    Έκδοση 2014
    Λήψη πλήρους κειμένου Λήψη πλήρους κειμένου
    Artigo
    Προσθήκη στα αγαπημένα
    Αποθηκεύτηκε σε:
  17. 17
    Original research: Second IVIg course in Guillain-Barré syndrome with poor prognosis: the non-randomised ISID study

    Original research: Second IVIg course in Guillain-Barré syndrome with poor prognosis: the non-randomised ISID study από 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

    Έκδοση 2019
    Λήψη πλήρους κειμένου Λήψη πλήρους κειμένου
    Artigo
    Προσθήκη στα αγαπημένα
    Αποθηκεύτηκε σε:
  18. 18
    European Academy of Neurology/Peripheral Nerve Society guideline on diagnosis and treatment of chronic inflammatory demyelinating polyradiculoneuropathy: Report of a joint Task Force—Second revision

    European Academy of Neurology/Peripheral Nerve Society guideline on diagnosis and treatment of chronic inflammatory demyelinating polyradiculoneuropathy: Report of a joint Task For... από 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

    Έκδοση 2021
    Λήψη πλήρους κειμένου Λήψη πλήρους κειμένου
    Artigo
    Προσθήκη στα αγαπημένα
    Αποθηκεύτηκε σε:
  19. 19
    European Academy of Neurology/Peripheral Nerve Society guideline on diagnosis and treatment of chronic inflammatory demyelinating polyradiculoneuropathy: Report of a joint Task Force—Second revision

    European Academy of Neurology/Peripheral Nerve Society guideline on diagnosis and treatment of chronic inflammatory demyelinating polyradiculoneuropathy: Report of a joint Task For... από 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

    Έκδοση 2021
    Λήψη πλήρους κειμένου
    Artigo
    Προσθήκη στα αγαπημένα
    Αποθηκεύτηκε σε:
  20. 20
    European Academy of Neurology/Peripheral Nerve Society Guideline on diagnosis and treatment of <scp>Guillain–Barré</scp> syndrome

    European Academy of Neurology/Peripheral Nerve Society Guideline on diagnosis and treatment of <scp>Guillain–Barré</scp> syndrome από 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

    Έκδοση 2023
    Λήψη πλήρους κειμένου Λήψη πλήρους κειμένου
    Revisão
    Προσθήκη στα αγαπημένα
    Αποθηκεύτηκε σε:

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