Thomas Harbo

ORCID: 0000-0003-2178-6076
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Research Areas
  • Peripheral Neuropathies and Disorders
  • Hereditary Neurological Disorders
  • Long-Term Effects of COVID-19
  • Peripheral Nerve Disorders
  • Myasthenia Gravis and Thymoma
  • Acute Ischemic Stroke Management
  • Stroke Rehabilitation and Recovery
  • Cerebrovascular and Carotid Artery Diseases
  • Nerve injury and regeneration
  • Multiple Sclerosis Research Studies
  • Parkinson's Disease and Spinal Disorders
  • Venous Thromboembolism Diagnosis and Management
  • Fibromyalgia and Chronic Fatigue Syndrome Research
  • Autoimmune Neurological Disorders and Treatments
  • Monoclonal and Polyclonal Antibodies Research
  • COVID-19 and Mental Health
  • Muscle and Compartmental Disorders
  • Psychosomatic Disorders and Their Treatments
  • Botulinum Toxin and Related Neurological Disorders
  • Neurobiology of Language and Bilingualism
  • Antifungal resistance and susceptibility
  • Intensive Care Unit Cognitive Disorders
  • Myofascial pain diagnosis and treatment
  • Protein Tyrosine Phosphatases
  • Sports Performance and Training

Aarhus University Hospital
2016-2025

Aarhus University
2012-2025

Erasmus MC
2018-2023

Health and Education Research Management and Epidemiologic Services (United States)
2023

University of Michigan
2023

Capital Region of Denmark
2023

Columbia University
2022

University of Milano-Bicocca
2022

Aalborg University
2021

Rigshospitalet
2021

To revise the 2010 consensus guideline on chronic inflammatory demyelinating polyradiculoneuropathy (CIDP). Seventeen disease experts, a patient representative, and two Cochrane methodologists constructed 12 Population/Intervention/Comparison/Outcome (PICO) questions regarding diagnosis treatment to guide literature search. Data were extracted summarized in GRADE summary of findings (for PICOs) or evidence tables diagnostic PICOs). Statements prepared according Evidence-to-Decision...

10.1111/jns.12455 article EN Journal of the Peripheral Nervous System 2021-06-04

To revise the 2010 consensus guideline on chronic inflammatory demyelinating polyradiculoneuropathy (CIDP).Seventeen disease experts, a patient representative, and two Cochrane methodologists constructed 12 Population/Intervention/Comparison/Outcome (PICO) questions regarding diagnosis treatment to guide literature search. Data were extracted summarized in GRADE summary of findings (for PICOs) or evidence tables diagnostic PICOs).Statements prepared according Evidence-to-Decision frameworks....

10.1111/ene.14959 article EN European Journal of Neurology 2021-07-30
Alex Y. Doets Christine Verboon Bianca van den Berg Thomas Harbo David R. Cornblath and 95 more Hugh J. Willison Zhahirul Islam Shahram Attarian Fábio Barroso Kathleen Bateman Luana Benedetti Peter Van den Bergh Carlos Casasnovas Guido Cavaletti Govindsinh Chavada Kristl G. Claeys Efthimios Dardiotis Amy Davidson Pieter A. van Doorn T E Feasby Giuliana Galassi Kenneth C. Gorson Hans-Peter Hartung Sung‐Tsang Hsieh Richard AC Hughes Isabel Illa Badrul Islam Susumu Kusunoki Satoshi Kuwabara Helmar C. Lehmann James Miller Quazi Deen Mohammad Soledad Monges Eduardo Nobile‐Orazio Julio Pardo Yann Péréon Simon Rinaldi Luís Querol Stephen Reddel Ricardo Reisin Nortina Shahrizaila Søren H. Sindrup Waqar Waheed Bart C. Jacobs Bart C. Jacobs Richard AC Hughes David R. Cornblath Kenneth C. Gorson H.‐P. Hartung Susumu Kusunoki Pieter A. van Doorn Hugh J. Willison M. van Woerkom Benno van den Berg Christine Verboon Alex Y. Doets Joyce Roodbol Bart C. Jacobs Ricardo Reisin Stephen Reddel Zhahirul Islam Badrul Islam Quazi Deen Mohammad P. van den Bergh T E Feasby Thomas Harbo Yann Péréon H.‐P. Hartung Helmar C. Lehmann Efthimios Dardiotis Eduardo Nobile‐Orazio Susumu Kusunoki Nortina Shahrizaila Bart C. Jacobs Benno van den Berg Christine Verboon Alex Y. Doets Kathleen Bateman Isabel Illa Luís Querol Sung‐Tsang Hsieh Hugh J. Willison Govindsinh Chavada Amy Davidson Kenneth C. Gorson Jean Addington Senda Ajroud‐Driss Henning Andersen Giovanni Antonini Alessandra Ariatti Shahram Attarian Umesh A. Badrising Fábio Barroso Luana Benedetti Alessandro Beronio Marcelle Martim Bianco Delphine Binda Chiara Briani Carina Bunschoten Jan Bürmann

Guillain-Barré syndrome is a heterogeneous disorder regarding the clinical presentation, electrophysiological subtype and outcome. Previous single country reports indicate that may differ among regions, but no systematic comparative studies have been conducted. Comparative are required to identify factors determining disease susceptibility, variation prognosis, improve diagnostic criteria. The International Syndrome Outcome Study prospective, observational cohort study including all patients...

10.1093/brain/awy232 article EN Brain 2018-08-10

Abstract Background and purpose Among post‐COVID‐19 symptoms, fatigue is reported as one of the most common, even after mild acute infection, cause fatigue, myopathy diagnosed by electromyography has been proposed in previous reports. This study aimed to explore histopathological changes patients with fatigue. Methods Sixteen (mean age = 46 years) complaints myalgia, or weakness persisting for up 14 months were included. In all patients, quantitative muscle biopsies analyzed light electron...

10.1111/ene.15435 article EN European Journal of Neurology 2022-06-06

Guillain-Barré syndrome (GBS) is an acute polyradiculoneuropathy. Symptoms may vary greatly in presentation and severity. Besides weakness sensory disturbances, patients have cranial nerve involvement, respiratory insufficiency, autonomic dysfunction pain. To develop evidence-based guideline for the diagnosis treatment of GBS, using Grading Recommendations, Assessment, Development Evaluation (GRADE) methodology a Task Force (TF) European Academy Neurology (EAN) Peripheral Nerve Society (PNS)...

10.1111/ene.16073 article EN cc-by-nc-nd European Journal of Neurology 2023-10-10

Background and purpose: For treatment of multifocal motor neuropathy (MMN), we hypothesized that (i) infusion equivalent dosages subcutaneous immunoglobulin (SCIG) is as effective intravenous (IVIG) (ii) at home associated with a better quality life. Methods: In randomized single‐blinded cross‐over study, nine IVIG responsive patients were allocated to receive either SCIG or for period three intervals and, subsequently, crossed over the other treatment. Primary end‐points dynamometric...

10.1111/j.1468-1331.2009.02568.x article EN European Journal of Neurology 2009-02-19

We hypothesized that subcutaneous administration of immunoglobulins (SCIG) in chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) is feasible, safe and superior to treatment with saline for the performance muscle strength.Thirty patients motor involvement maintenance therapy intravenous immunoglobulin (IVIG) fulfilling EFNS/PNS criteria CIDP, aged 18-80 years, were randomized either SCIG at a dose corresponding their pre-study IVIG or given twice thrice weekly 12 weeks home. At...

10.1111/ene.12080 article EN European Journal of Neurology 2013-01-07

Abstract Guillain‐Barré syndrome (GBS) is an acute polyradiculoneuropathy with a highly variable clinical presentation, course, and outcome. The factors that determine the variation of GBS are poorly understood which complicates care treatment individual patients. protocol ongoing International Outcome Study (IGOS), prospective, observational, multicenter cohort study aims to identify biological determinants predictors disease onset, subtype, course outcome presented here. Patients...

10.1111/jns.12209 article EN Journal of the Peripheral Nervous System 2017-04-13

To investigate the peripheral nerve and muscle function electrophysiologically in patients with persistent neuromuscular symptoms following Coronavirus disease 2019 (COVID-19).Twenty consecutive from a Long-term COVID-19 Clinic referred to electrophysiological examination suspicion of mono- or polyneuropathy were included. Examinations performed 77 255 (median: 216) days after acute COVID-19. None had received treatment at intensive care unit. Of these, 10 not even hospitalized. Conventional...

10.1016/j.clinph.2021.04.009 article EN cc-by Clinical Neurophysiology 2021-05-07
Linda W.G. Luijten Sonja E. Leonhard Annemiek A. van der Eijk Alex Y. Doets Luise Appeltshauser and 95 more Samuel Arends Shahram Attarian Luana Benedetti Chiara Briani Carlos Casasnovas Francesca Castellani Efthimios Dardiotis Andoni Echaniz‐Laguna Marcel P.J. Garssen Thomas Harbo Ruth Huizinga Andrea M. Humm Korné Jellema Anneke J. van der Kooi Krista Kuitwaard Thierry Küntzer Susumu Kusunoki Agustina M. Lascano Eugenia Martínez‐Hernández Simon Rinaldi Johnny P.A. Samijn Olivier Scheidegger Pinelopi Tsouni Alex Vicino Leo H. Visser Christa Walgaard Yuzhong Wang Paul W. Wirtz Paolo Ripellino Bart C. Jacobs Bart C. Jacobs Richard AC Hughes David R. Cornblath Kenneth C. Gorson Hans‐Peter Hartung Susumu Kusunoki Pieter A. van Doorn Hugh J. Willison Bianca van den Berg Christine Verboon Joyce Roodbol Alex Y. Doets Sonja E. Leonhard Linda W.G. Luijten L.C. de Koning Melissa R. Mandarakas M. van Woerkom Samuel Arends Ricardo Reisin Stephen Reddel Zhahirul Islam Quazi Deen Mohammad Peter Van den Bergh T E Feasby Yuzhong Wang Thomas Harbo Yann Péréon Helmar C. Lehmann Efthimios Dardiotis Eduardo Nobile‐Orazio Nortina Shahrizaila Kathleen Bateman Isabel Illa Luís Querol Paolo Ripellino Sung‐Tsang Hsieh Govindsinh Chavada Amy Davidson James M Addington Henning Andersen Giovanni Antonini Senda Ajroud‐Driss Shahram Attarian Umesh A. Badrising Claudia Balducci Fábio Barroso I.R. Bella Luana Benedetti Tulio E. Bertorini Ratna Bhavaraju‐Sanka Thomas H. Brannagan Chiara Briani Jan Bürmann Mark Busby Stephen Butterworth Carlos Casasnovas Francesca Castellani Guido Cavaletti Chi‐Chao Chao Shan Chen Kristl G. Claeys M E Conti Jeremy Cosgrove Marinos C. Dalakas Miroslawa A Derejko

In the wake of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic, an increasing number patients with neurological disorders, including Guillain-Barré (GBS), have been reported following this infection. It remains unclear, however, if these cases are coincidental or not, as most publications were case reports small regional retrospective cohort studies. The International GBS Outcome Study is ongoing prospective observational study enrolling within weeks from onset...

10.1093/brain/awab279 article EN cc-by-nc Brain 2021-07-20
Sonja E. Leonhard Annemiek A. van der Eijk Henning Andersen Giovanni Antonini Samuel Arends and 95 more Shahram Attarian Fábio Barroso Kathleen Bateman Manou R. Batstra Luana Benedetti Bianca van den Berg Peter Van den Bergh Jan Bürmann Mark Busby Carlos Casasnovas David R. Cornblath Amy Davidson Alex Y. Doets Pieter A. van Doorn Charlotte Dornonville de la Cour Thomas E. Feasby Janev Fehmi Tania García‐Sobrino Jonathan Goldstein Kenneth C. Gorson Volkan Granit Robert D. M. Hadden Thomas Harbo Hans‐Peter Hartung Imran Hasan Jakob Vormstrup Holbech James K. L. Holt Israt Jahan Zhahirul Islam Summer Karafiath Hans Katzberg R. P. Kleyweg Noah Kolb Krista Kuitwaard Motoi Kuwahara Susumu Kusunoki Linda W.G. Luijten Satoshi Kuwabara Edward Pan Helmar C. Lehmann Marijke Maas L. Aguilar James Miller Quazi Deen Mohammad Soledad Monges Velina Nedkova-Hristova Eduardo Nobile‐Orazio J. Marín Pardo Yann Péréon Luís Querol Ricardo Reisin Wouter van Rijs Simon Rinaldi Rhys Roberts Joyce Roodbol Nortina Shahrizaila Søren H. Sindrup Beth Stein Tan Cheng-Yin Hatice Tankişi Anne P. Tio‐Gillen María J. Sedano Tous Christine Verboon Frédérique H Vermeij Leo H. Visser Ruth Huizinga Hugh J. Willison Bart C. Jacobs Richard AC Hughes L.C. de Koning Melissa R. Mandarakas M. van Woerkom Stephen Reddel Isabel Illa Yuzhong Wang Efthimios Dardiotis Sung‐Tsang Hsieh Christa Walgaard Waqar Waheed Mazen M. Dimachkie Badrul Islam J.M. Addington Senda Ajroud‐Driss Umesh A. Badrising I.R. Bella T. E. Bertoríni R. Bhavaraju-Sanka Thomas H. Brannagan Chiara Briani S. Butterworth Guido Cavaletti Chi‐Chao Chao Kristl G. Claeys M.E. Conti Jeremy Cosgrove

<h3>Background and Objectives</h3> Infections play a key role in the development of Guillain-Barré syndrome (GBS) have been associated with specific clinical features disease severity. The variation GBS across geographical regions has suggested to be related differences distribution preceding infections, but this not studied on large scale. <h3>Methods</h3> We analyzed first 1,000 patients included International Outcome Study available biosamples (n = 768) for presence recent infection...

10.1212/wnl.0000000000200885 article EN Neurology 2022-08-18
Robin C.M. Thomma Susan K. Halstead L.C. de Koning Evelin E J A Wiegers Dawn Gourlay and 95 more Anne P. Tio‐Gillen Wouter van Rijs Henning Andersen Giovanni Antonini Samuel Arends Shahram Attarian Fábio Barroso Kathleen Bateman Luana Benedetti Peter Van den Bergh Jan Bürmann Mark Busby Carlos Casasnovas Efthimios Dardiotis Amy Davidson Thomas E. Feasby Janev Fehmi Giuliana Galassi Tania García‐Sobrino Volkan Granit Gerardo Gutiérrez‐Gutiérrez Robert D. M. Hadden Thomas Harbo Hans‐Peter Hartung Imran Hasan James Holt Zhahirul Islam Summer Karafiath Hans Katzberg Noah Kolb Susumu Kusunoki Satoshi Kuwabara Motoi Kuwahara Helmar C. Lehmann Sonja E. Leonhard L. Aguilar Soledad Monges Eduardo Nobile‐Orazio Julio Pardo Yann Péréon Luís Querol Ricardo Reisin Simon Rinaldi Paolo Ripellino Rhys Roberts Olivier Scheidegger Nortina Shahrizaila Kazim A. Sheikh Nicholas J. Silvestri Søren H. Sindrup Beth Stein Cheng‐Yin Tan Hatice Tankişi Leo H. Visser Waqar Waheed Ruth Huizinga Olivier Scheidegger Hugh J. Willison Jean Addington Senda Ajroud‐Driss Henning Andersen Giovanni Antonini Suzanne Arends S. Attarian Umesh A. Badrising Claudia Balducci Fábio Barroso Kevin P. Bateman I.R. Bella Luana Benedetti Benno van den Berg Peter Van den Bergh T. E. Bertoríni Ratna Bhavaraju‐Sanka Federica Bozzano Thomas H. Brannagan Chiara Briani J. Bürmann Mark Busby S. Butterworth Giovanna Capodivento Carlos Casasnovas Guido Cavaletti Chi‐Chao Chao Shiping Chen Elisa Cisneros Kristl G. Claeys M E Conti David R. Cornblath Jeremy Cosgrove M. C. Dalakas Philip Van Damme Efthimios Dardiotis Andrew R. Davidson Gert W. van Dijk

Abstract Guillain-Barré syndrome is an acute polyradiculoneuropathy in which preceding infections often elicit the production of antibodies that target peripheral nerve antigens, principally gangliosides. Anti-ganglioside are thought to play a key role clinical diversity disease and can be helpful practice. Extensive research into associations individual anti-ganglioside antibody specificities has been performed. Recent highlighted glycolipid complexes, combinations may alter binding, as...

10.1093/brain/awaf102 article EN cc-by-nc Brain 2025-03-17

<h3>Background:</h3> In multifocal motor neuropathy (MMN), high dose of IV immunoglobulin (IVIg) is the only established treatment. Subcutaneous self-infusion with G (IgG) (SCIG) increases patient autonomy and treatment flexibility, might be associated fewer side effects due to lower peak IgG levels. a recent study 9 patients MMN, we reported that SCIG preserves muscle strength for few months Five preferred continue after trial another chose apply SCIG. <h3>Methods:</h3> this case series 6...

10.1212/wnl.0b013e3181f735ce article EN Neurology 2010-10-11
Christine Verboon Alex Y. Doets Giuliana Galassi Amy Davidson Waqar Waheed and 95 more Yann Péréon Nortina Shahrizaila Susumu Kusunoki Helmar C. Lehmann Thomas Harbo Soledad Monges Peter Van den Bergh Hugh J. Willison David R. Cornblath Bart C. Jacobs Richard AC Hughes Kenneth C. Gorson H.‐P. Hartung Pieter A. van Doorn Benno van den Berg Joyce Roodbol M. van Woerkom Ricardo Reisin Stephen Reddel Zhahirul Islam Badrul Islam Quazi Deen Mohammad Thomas E. Feasby Efthimios Dardiotis Eduardo Nobile‐Orazio Kathleen Bateman Isabel Illa Luís Querol Sung‐Tsang Hsieh Govindsinh Chavada Jean Addington Senda Ajroud‐Driss Henning Andersen Giovanni Antonini Alessandra Ariatti S. Attarian Umesh A. Badrising Fábio Barroso Luana Benedetti Alessandro Beronio Marcelle Martim Bianco Davide Binda Chiara Briani Carina Bunschoten Jan Bürmann I.R. Bella T. E. Bertoríni R. Bhavaraju-Sanka Thomas H. Brannagan Mark Busby S. Butterworth Carlos Casasnovas Guido Cavaletti Chi‐Chao Chao Shiping Chen S Chetty Kristl G. Claeys M.E. Conti Jeremy Cosgrove Marinos C. Dalakas Chiara Demichelis Miroslawa A Derejko Ulrich Dillmann Mazen M. Dimachkie Kathrin Doppler Charlotta Dornonville de la Cour Andoni Echaniz‐Laguna Filip Eftimov Catharina G. Faber Raffaella Fazio C. Fokke T. Fujioka E. Fulgenzi Tania García‐Sobrino Marcel P.J. Garssen H.M. Georgios C.J. Gijsbers James M. Gilchrist Job Gilhuis Elisa Giorli Jonathan Goldstein Namita Goyal Volkan Granit Aude‐Marie Grapperon Gerardo Gutiérrez‐Gutiérrez Robert D. M. Hadden Jakob Vormstrup Holbech James K. L. Holt Christian Homedes Pedret M. Htut Korné Jellema I. Jericó Pascual María Concepción Jimeno-Montero Kenichi Kaida Summer Karafiath

<h3>Objective</h3> To define the current treatment practice of Guillain-Barré syndrome (GBS). <h3>Methods</h3> The study was based on prospective observational data from first 1,300 patients included in International GBS Outcome Study. We described general, and for (1) severe forms (unable to walk independently), (2) no recovery after initial treatment, (3) treatment-related fluctuations, (4) mild (able (5) variant including Miller Fisher syndrome, taking patient characteristics hospital...

10.1212/wnl.0000000000007719 article EN Neurology 2019-06-08
Helle Al-Hakem Alex Y. Doets Amro Stino Sasha Živković Henning Andersen and 95 more Hugh J. Willison David R. Cornblath Kenneth C. Gorson Zhahirul Islam Quazi Deen Mohammad Søren H. Sindrup Susumu Kusunoki Amy Davidson Carlos Casasnovas Kathleen Bateman James Miller Bianca van den Berg Christine Verboon Joyce Roodbol Sonja E. Leonhard Samuel Arends Linda W.G. Luijten Luana Benedetti Satoshi Kuwabara Peter Van den Bergh Soledad Monges Girolama Alessandra Marfia Nortina Shahrizaila Giuliana Galassi Yann Péréon J. Bürmann Krista Kuitwaard R. P. Kleyweg Cintia Marchesoni María J. Sedano Tous Luís Querol L. Aguilar Yuzhong Wang Eduardo Nobile‐Orazio Simon Rinaldi Angelo Schenone J. Marín Pardo Frédérique H Vermeij Waqar Waheed Helmar C. Lehmann Volkan Granit Beth Stein Guido Cavaletti Gerardo Gutiérrez‐Gutiérrez Fábio Barroso Leo H. Visser Hans Katzberg Efthimios Dardiotis Shahram Attarian Anneke J. van der Kooi Filip Eftimov Paul W. Wirtz Johnny P.A. Samijn H. Jacobus Gilhuis Robert D. M. Hadden James Holt Kazim A. Sheikh Noah Kolb Summer Karafiath Michal Vytopil Giovanni Antonini Thomas E. Feasby Catharina G. Faber H. A. Kramers Mark Busby Rhys Roberts Nicholas J. Silvestri Raffaella Fazio Gert W. van Dijk Marcel P.J. Garssen Jan J.G.M. Verschuuren Thomas Harbo Bart C. Jacobs Richard AC Hughes H.‐P. Hartung L.C. de Koning Melissa R. Mandarakas M. van Woerkom Ricardo Reisin Stephen Reddel Sung‐Tsang Hsieh Jean Addington Senda Ajroud‐Driss Lucas Alessandro Umesh A. Badrising G. Balloy I.R. Bella T. E. Bertoríni R. Bhavaraju-Sanka Mariangela Bianco Thomas H. Brannagan Kirsty Brennan Chiara Briani S. Butterworth Chi‐Chao Chao

To investigate CSF findings in relation to clinical and electrodiagnostic subtypes, severity, outcome of Guillain-Barré syndrome (GBS) based on 1,500 patients the International GBS Outcome Study.

10.1212/wnl.0000000000207282 article EN Neurology 2023-04-19

To describe neurophysiological abnormalities in Long COVID and correlate quantitative electromyography (qEMG) single fiber EMG (sfEMG) results to clinical scores histopathology. 84 patients with non-improving musculoskeletal symptoms were examined qEMG sfEMG. Muscle biopsies taken a subgroup. Mean motor unit potential (MUP) duration was decreased ≥ 1 muscles 52 % of the patients. jitter increased 17 tibialis anterior 25 extensor digitorum communis. Increased seen or without myopathic qEMG....

10.1016/j.clinph.2023.01.010 article EN cc-by Clinical Neurophysiology 2023-02-01

Background and purpose Subcutaneous immunoglobulin ( SCIG ) is superior to placebo treatment for maintenance of muscle strength during 12 weeks in patients with chronic inflammatory demyelinating polyneuropathy CIDP ). The present study evaluated whether preserves 1 year an open‐label follow‐up study. Methods Seventeen responders intravenous IVIG who had participated the previous versus were included. After one infusion 2 prior baseline, all continued on at weekly equal dosage after 3, 6...

10.1111/ene.12513 article EN European Journal of Neurology 2014-07-07

To compare disease course in patients with Guillain-Barré syndrome (GBS) a poor prognosis who were treated one or two intravenous immunoglobulin (IVIg) courses.From the International GBS Outcome Study, we selected whose modified Erasmus Score at week 1 predicted prognosis. We compared those IVIg to courses. The primary endpoint, disability scale 4 weeks, was assessed multivariable ordinal regression.Of 237 eligible patients, 199 received single course. Twenty an 'early' second (1-2 weeks...

10.1136/jnnp-2019-321496 article EN Journal of Neurology Neurosurgery & Psychiatry 2019-10-05
Alex Y. Doets Hester F. Lingsma Christa Walgaard Badrul Islam Nowshin Papri and 95 more Amy Davidson Yuko Yamagishi Susumu Kusunoki Mazen M. Dimachkie Waqar Waheed Noah Kolb Zhahirul Islam Quazi Deen Mohammad Thomas Harbo Søren H. Sindrup Govindsinh Chavada Hugh J. Willison Carlos Casasnovas Kathleen Bateman James Miller Bianca van den Berg Christine Verboon Joyce Roodbol Sonja E. Leonhard Luana Benedetti Satoshi Kuwabara Peter Van den Bergh Soledad Monges Girolama Alessandra Marfia Nortina Shahrizaila Giuliana Galassi Yann Péréon J. Bürmann Krista Kuitwaard R. P. Kleyweg Cintia Marchesoni María J. Sedano Tous Luís Querol Isabel Illa Yuzhong Wang Eduardo Nobile‐Orazio Simon Rinaldi Angelo Schenone J. Marín Pardo Frédérique H Vermeij Helmar C. Lehmann Volkan Granit Guido Cavaletti Gerardo Gutiérrez‐Gutiérrez Fábio Barroso Leo H. Visser Hans Katzberg Efthimios Dardiotis Shahram Attarian Anneke J. van der Kooi Filip Eftimov Paul W. Wirtz Johnny P.A. Samijn H. Jacobus Gilhuis Robert D. M. Hadden James K. L. Holt Kazim A. Sheikh Summer Karafiath Michal Vytopil Giovanni Antonini Thomas E. Feasby Catharina G. Faber C.J. Gijsbers Mark Busby Rhys Roberts Nicholas J. Silvestri Raffaella Fazio Gert W. van Dijk Marcel P.J. Garssen C.S.M. Straathof Kenneth C. Gorson Bart C. Jacobs Richard AC Hughes David R. Cornblath H.‐P. Hartung Pieter A. van Doorn L.C. de Koning M. van Woerkom Melissa R. Mandarakas BHIthSci MPhty Ricardo Reisin Stephen Reddel Paolo Ripellino Sung‐Tsang Hsieh Jean Addington Senda Ajroud‐Driss Henning Andersen Umesh A. Badrising I.R. Bella T. E. Bertoríni R. Bhavaraju-Sanka Mariangela Bianco Thomas H. Brannagan Chiara Briani S. Butterworth

<h3>Background and Objectives</h3> The clinical course outcome of the Guillain-Barré syndrome (GBS) are diverse vary among regions. modified Erasmus GBS Outcome Score (mEGOS), developed with data from Dutch patients, is a model that predicts risk walking inability in patients GBS. study objective was to validate mEGOS International Study (IGOS) cohort improve its performance region specificity. <h3>Methods</h3> We used prospective first 1,500 included IGOS, aged ≥6 years unable walk...

10.1212/wnl.0000000000013139 article EN Neurology 2021-12-22

Abstract Background Current proposed criteria for functional cognitive disorder (FCD) have not been externally validated. We sought to analyse the current perspectives of specialists in diagnosis and management FCD comparison with neurodegenerative conditions. Methods International experts disorders were invited assess seven illustrative clinical vignettes containing history bedside characteristics alone. Participants assigned a probable selected appropriate investigation treatment....

10.1111/ene.16318 article EN cc-by-nc-nd European Journal of Neurology 2024-05-03

Abstract Background and purpose Various electrodiagnostic criteria have been developed in Guillain–Barré syndrome (GBS). Their performance a broad representation of GBS patients has not evaluated. Motor conduction data from the International Outcome Study (IGOS) cohort were used to compare two widely criterion sets relate these diagnostic amyotrophic lateral sclerosis criteria. Methods From first 1500 IGOS, nerve studies 1137 (75.8%) available for current study. These classified according...

10.1111/ene.16335 article EN cc-by-nc-nd European Journal of Neurology 2024-07-04

High dose intravenous immunoglobulin (IVIG) is an established treatment for various neuromuscular disorders. Recently, cases of hemolytic anemia following IVIG have been observed. The objective this study was to determine the extent and hemolysis after its relationship AB0 blood type system.In a prospective 34 de novo treated patients were given 2.0 g/kg bodyweight Privigen 50 received either [n = 28; 1.53 ± 0.4 (mean SD)] or Kiovig (n 22; 1.7 g/kg) as maintenance therapy. all had post-polio...

10.1111/ene.12287 article EN European Journal of Neurology 2013-11-04
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