Christopher Lindberg

• Rituximab in New-Onset Generalized Myasthenia Gravis: Long-Term Follow-Up of the RINOMAX Clinical Trial

  Jing Wu, Ann Eriksson-Dufva, Anna Budzianowska, Amalia Feresiadou, William Hansson, Max Albert Hietala, Irene Håkansson, Rune Johansson, Daniel Jons, Ivan Kmezic, Christopher Lindberg, Jonas Lindh, Fredrik Lundin, Ingela Nygren, Anna Rostedt Punga, Rayomand Press, Kristin Samuelsson, Peter Sundström, Oskar Wickberg, Thomas Frisell, Susanna Brauner, Fredrik Piehl
  European Journal of Neurology - 2025
• Neurocognitive disorder in Myotonic dystrophy type 1.

  Stefan Winblad, Olöf Eliasdottir, Sara Nordström, Christopher Lindberg
  Heliyon - 2024
• Self-perceived cognitive failures in patients with Myotonic dystrophy type 1 (DM1)

  Stefan Winblad, Olöf Eliasdottir, Sara Nordström, Christopher Lindberg
  "Conferenece proceeding IDMC 14" - 2024
• Clinical stage and plasma neurofilament concentration in adults with Friedreich ataxia

  Magnus Johnsson, Henrik Zetterberg, Kaj Blennow, Christopher Lindberg
  Heliyon - 2023
• Efficacy and Safety of Rituximab for New-Onset Generalized Myasthenia Gravis The RINOMAX Randomized Clinical Trial

  F. Piehl, A. Eriksson-Dufva, A. Budzianowska, A. Feresiadou, W. Hansson, M. A. Hietala, I. Hakansson, R. Johansson, Daniel Jons, I. Kmezic, Christopher Lindberg, J. Lindh, F. Lundin, I. Nygren, A. R. Punga, R. Press, K. Samuelsson, P. Sundstrom, O. Wickberg, S. Brauner, T. Frisell
  Jama Neurology - 2022
• Proteomic characterisation of polyglucosan bodies in skeletal muscle in RBCK1 deficiency

  Christer Thomsen, E. Malfatti, A. Jovanovic, M. Roberts, O. Kalev, Christopher Lindberg, Anders Oldfors
  Neuropathology and Applied Neurobiology - 2022
• Phenotypic spectrum and clinical course of single large-scale mitochondrial DNA deletion disease in the paediatric population: a multicentre study.

  Kristoffer Björkman, John Vissing, Elsebet Østergaard, Laurence A Bindoff, Irenaeus F M de Coo, Martin Engvall, Omar Hikmat, Pirjo Isohanni, Gittan Kollberg, Christopher Lindberg, Kari Majamaa, Karin Naess, Johanna Uusimaa, Mar Tulinius, Niklas Darin
  Journal of Medical Genetics - 2021
• Mitochondrial DNA variants in inclusion body myositis characterized by deep sequencing

  Carola Oldfors Hedberg, Ulrika Lindgren, Swaraj Basu, Kittichate Visuttijai, Christopher Lindberg, Maria Falkenberg, Erik Larsson Lekholm, Anders Oldfors
  Brain Pathology - 2021
• Deep sequencing of mitochondrial DNA and characterization of a novel POLG mutation in a patient with arPEO.

  Carola Oldfors Hedberg, Bertil Macao, Swaraj Basu, Christopher Lindberg, Bradley Peter, Jay (Jennifer) Uhler, Erik Larsson, Maria Falkenberg, Anders Oldfors
  Neurology. Genetics - 2020
• Perceived fatigue in myotonic dystrophy type 1: a case-control study.

  Stefan Winblad, Christopher Lindberg
  BMC Neurology - 2019
• A SCA7 premutation may be a novel Mendelian modifier of MS course: A case report

  Christina Sundal, Markus Axelsson, L. Wiklund, Christopher Lindberg, Oluf Andersen
  Multiple Sclerosis and Related Disorders - 2019
• Cerebral palsy and bruxism: Effects of botulinum toxin injections—A randomized controlled trial

  Birgitta Johansson Cahlin, Christopher Lindberg, Lars Dahlström
  Clinical and Experimental Dental Research - 2019
• Cerebrospinal Fluid Biomarkers in DM1: a 14-year Follow Up Study.

  Magnus Rudenholm, Stefan Winblad, Henrik Zetterberg, Radu Constantinescu, Christopher Lindberg
  IDMC-12, Göteborg 2019, Konferensprogram - 2019
• Cognitive Decline in DM1: a 14-year Longitudinal Study.

  Stefan Winblad, Magnus Rudenholm, Iraj Abedini, Christopher Lindberg
  IDMC-12 2019, Göteborg, Konferensprogram - 2019
• Association between muscle strength, histopathology, and magnetic resonance imaging in sporadic inclusion body myositis.

  Kathe Dahlbom, Mats Geijer, Anders Oldfors, Christopher Lindberg
  Acta neurologica Scandinavica - 2019
• Carey-Fineman-Ziter syndrome with mutations in the myomaker gene and muscle fiber hypertrophy

  Carola Oldfors Hedberg, Christopher Lindberg, Anders Oldfors
  Neurology-Genetics - 2018
• Prevalence of myotonic dystrophy type 1 in adults in western Sweden.

  Christopher Lindberg, Fredrik Bjerkne
  Neuromuscular disorders : NMD - 2017
• Skeletal muscle metabolism during prolonged exercise in Pompe disease.

  Nicolai Preisler, Pascal Laforêt, Karen Lindhardt Madsen, Edith Husu, Christoffer Rasmus Vissing, Gitte Hedermann, Henrik Galbo, Christopher Lindberg, John Vissing
  Endocrine connections - 2017
• Reduced renal function in patients with Myotonic Dystrophy type 1 and the association to CTG expansion and other potential risk factors for chronic kidney disease.

  Annika Aldenbratt, Christopher Lindberg, Maria K Svensson
  Neuromuscular disorders : NMD - 2017
• The Reliability and Validity of the Swedish Version of the Fatigue and Daytime Sleepiness Scale (FDSS)

  Ulrika Edofsson, Stefan Winblad, Christopher Lindberg
  Conference book for IDMC-11. San Fransisco, California, Usa: 5-9 September - 2017
• Cognition in myotonic dystrophy type 1: a 5-year follow-up study.

  Stefan Winblad, Lena Samuelsson, Christopher Lindberg, Giovanni Meola
  European Journal of Neurology - 2016
• Search for Pompe disease among patients with undetermined myopathies

  Christopher Lindberg, B. Anderson, M. Engvall, M. Hult, Anders Oldfors
  Acta Neurologica Scandinavica - 2016
• Effects of a balance exercise programme in Myotonic Dystrophy type 1: A pilot study.

  Elisabet Hammarén, Christopher Lindberg, Gunilla Kjellby-Wendt
  European Journal of Physiotherapy - 2015
• Surgical treatment of obesity in DM1--a case report and a review of the literature.

  K Håkansson, Srdjan Kostic, Christopher Lindberg
  Neuromuscular disorders : NMD - 2015
• Executive cognitive dysfunction in adult onset Myotonic Dystrophy type 1

  Stefan Winblad, Marita Hällgren, Christopher Lindberg
  Abstract booklet: 10th International Myotonic Dystrophy Consortium Meeting (IDMC-10), Paris, France - 2015
• Mitochondrial pathology in inclusion body myositis

  Ulrika Lindgren, Sara Roos, Carola Oldfors Hedberg, Ali-Reza Moslemi, Christopher Lindberg, Anders Oldfors
  Neuromuscular Disorders - 2015
• Muscle force, balance and falls in muscular impaired individuals with myotonic dystrophy type 1: A five-year prospective cohort study

  Elisabet Hammarén, Gunilla Kjellby-Wendt, Christopher Lindberg
  Neuromuscular Disorders - 2015
• Factors of importance for dynamic balance impairment and frequency of falls in individuals with myotonic dystrophy type 1 - A cross-sectional study - Including reference values of Timed Up & Go, 10m walk and step test

  Elisabet Hammarén, Gunilla Kjellby-Wendt, Jan Kowalski, Christopher Lindberg
  Neuromuscular Disorders - 2014
• Late-onset spinal motor neuronopathy - A common form of dominant SMA

  S. Penttilä, M. Jokela, S. Huovinen, A. M. Saukkonen, J. Toivanen, Christopher Lindberg, P. Baumann, B. Udd
  Neuromuscular Disorders - 2014
• Facial memory deficits in myotonic dystrophy type 1.

  Johan Lundin Kleberg, Christopher Lindberg, Stefan Winblad
  Acta Neurologica Scandinavica - 2014
• Recessive myosin myopathy with external ophthalmoplegia associated with MYH2 mutations.

  Homa Tajsharghi, Simon Hammans, Christopher Lindberg, Alexander Lossos, Nigel F Clarke, Ingrid Mazanti, Leigh B Waddell, Yakov Fellig, Nicola Foulds, Haider Katifi, Richard Webster, Olayinka Raheem, Bjarne Udd, Zohar Argov, Anders Oldfors
  European journal of human genetics : EJHG - 2014
• Polyglucosan body myopathy caused by defective ubiquitin ligase RBCK1.

  Johanna Nilsson, Benedikt Schoser, Pascal Laforet, Ognian Kalev, Christopher Lindberg, Norma B Romero, Marcela Davila Lopez, Hasan O Akman, Karim Wahbi, Stephan Iglseder, Christian Eggers, Andrew G Engel, Salvatore DiMauro, Anders Oldfors
  Annals of neurology - 2013
• Subnormal levels of POLgA cause inefficient initiation of light-strand DNA synthesis and lead to mitochondrial DNA deletions and progressive external ophthalmoplegia

  Sara Roos, Bertil Macao, Javier Miralles Fusté, Christopher Lindberg, Elisabeth Jemt, Elisabeth Holme, Ali-Reza Moslemi, Anders Oldfors, Maria Falkenberg
  Human Molecular Genetics - 2013
• Experienced fatigue in myotonic dystrophy type 1 (DM1) is associated with muscle impairment and depression

  Stefan Winblad, Christopher Lindberg
  IDMC-9 International Myotonic Dystrophy Consortium Meeting, October 2013, Program - 2013
• On parole: The natural history of recovery from fibromyalgia in women: A grounded theory study

  Kerstin Wentz, Christopher Lindberg, Lillemor R-M Hallberg
  Journal of Pain Management - 2012
• Prognosis and prognostic factors in sporadic inclusion body myositis.

  Christopher Lindberg, Anders Oldfors
  Acta neurologica Scandinavica - 2012
• Episodes of exercise-induced dark urine and myalgia in LGMD 2I.

  Christopher Lindberg, C Sixt, Anders Oldfors
  Acta neurologica Scandinavica - 2012
• Hereditary myopathy with early respiratory failure associated with a mutation in A-band titin

  Monica Ohlsson, Carola Hedberg, B. Bradvik, Christopher Lindberg, Homa Tajsharghi, O. Danielsson, A. Melberg, B. Udd, Tommy Martinsson, Anders Oldfors
  Brain - 2012
• Myopathy in a woman and her daughter associated with a novel splice site MTM1 mutation.

  Carola Hedberg, Christopher Lindberg, Gyöngyvér Máthé, Ali-Reza Moslemi, Anders Oldfors
  Neuromuscular disorders : NMD - 2012
• Reliability of static and dynamic balance tests in subjects with myotonic dystrophy type 1

  Elisabet Hammarén, Jennie Ann Ohlsson, Christopher Lindberg, Gunilla Kjellby-Wendt
  Advances in Physiotherapy - 2012
• Hand Function in 45 Patients with Sporadic Inclusion Body Myositis

  Marianne Eriksson, Christopher Lindberg
  Occupational Therapy International - 2012
• Depression in Myotonic Dystrophy type 1: clinical and neuronal correlates.

  Stefan Winblad, Christer Jensen, Jan-Eric Månsson, Lena Samuelsson, Christopher Lindberg
  Behavioral and brain functions : BBF - 2010
• Glycogenin-1 deficiency and inactivated priming of glycogen synthesis.

  Ali-Reza Moslemi, Christopher Lindberg, Johanna Nilsson, Homa Tajsharghi, Bert Andersson, Anders Oldfors
  The New England journal of medicine - 2010
• Subtle cognitive decline in Myotonic dystrophy type 1: a five-year follow up study

  Stefan Winblad, Christopher Lindberg
  Medizinische genetik - 2009
• Ephedrine therapy in eight patients with congenital myasthenic syndrome due to DOK7 mutations.

  U Schara, N Barisic, M Deschauer, Christopher Lindberg, V Straub, N Strigl-Pill, M Wendt, A Abicht, J S Müller, H Lochmüller
  Neuromuscular disorders : NMD - 2009
• Qualitatively and quantitatively identified dissociative and self-loading self-regulation in women developing and maintaining fibromyalgia.

  Kerstin Wentz, Christopher Lindberg, Annika Dahlgren Sandberg
  Pain Research Progress: Migraine, Fibromyalgia and Related Pain" - 2008
• Cerebrospinal fluid tau and amyloid beta42 protein in patients with myotonic dystrophy type 1.

  S Winblad, Jan-Eric Månsson, Kaj Blennow, C Jensen, L Samuelsson, Christopher Lindberg
  European journal of neurology : the official journal of the European Federation of Neurological Societies - 2008
• MELAS syndrome in a patient with a point mutation in MTTS1.

  Christopher Lindberg, Ali-Reza Moslemi, Anders Oldfors
  Acta neurologica Scandinavica - 2008
• Congenital myopathy with nemaline rods and cap structures caused by a mutation in the beta-tropomyosin gene (TPM2)

  Homa Tajsharghi, Monica Ohlsson, Christopher Lindberg, Anders Oldfors
  Arch Neurol - 2007
• Facial emotion recognition in myotonic dystrophy type 1 correlates with CTG repeat expansion

  Stefan Winblad, Per Hellström, Christopher Lindberg, Stefan Hansen
  Journal of Neurology, Neurosurgery and Psychiatry - 2006

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