Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Marlies van Nimwegen"'
Autor:
Nienke M. de Vries, Ana Lígia Silva de Lima, Marlies van Nimwegen, Danique L.M. Radder, Samyra H.J. Keus, Bastiaan R. Bloem, Josefa Domingos
Publikováno v:
Neurorehabilitation and Neural Repair
Neurorehabilitation and Neural Repair, 34, 871-880
Neurorehabilitation and Neural Repair, 34, 10, pp. 871-880
Neurorehabilitation and Neural Repair, 34, 871-880
Neurorehabilitation and Neural Repair, 34, 10, pp. 871-880
Background Physiotherapy is a commonly prescribed intervention for people with Parkinson’s disease (PD). Conventional types of physiotherapy have been studied extensively, while novel modalities are being developed and evaluated. Objective To evalu
Autor:
Tamine T.C. Capato, Bastiaan R. Bloem, Catarina Godinho, Lorena R S Almeida, Nienke M. de Vries, Marlies van Nimwegen, Maarten J. Nijkrake, Josefa Domingos
Publikováno v:
Journal of Neurology, 268, 1, pp. 214-218
Journal of Neurology, 268, 214-218
Journal of Neurology, 268, 214-218
Contains fulltext : 235690.pdf (Publisher’s version ) (Open Access) BACKGROUND: The use of the European Physiotherapy Guideline for Parkinson's Disease is limited in countries where the official language is not English. OBJECTIVE: To provide practi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::793ad9c7c4dd9186259ec00ba0c7a58c
https://hdl.handle.net/10400.26/40477
https://hdl.handle.net/10400.26/40477
Autor:
Baziel G.M. van Engelen, Marlies van Nimwegen, Linda Heskamp, Kees Okkersen, Marieke J. Ploegmakers, Jean-François Deux, Guillaume Bassez, Arend Heerschap
Publikováno v:
Radiology, 297, 132-142
Radiology, 297, 1, pp. 132-142
Radiology, 297, 1, pp. 132-142
Item does not contain fulltext Background Patients with myotonic dystrophy type 1 (DM1) increased their physical activity and exercise capacity following a behavioral intervention. However, it is unknown what is altered in muscles of patients with DM
Autor:
Josefa M M, Domingos, Tamine T C, Capato, Lorena R S, Almeida, Catarina, Godinho, Marlies, van Nimwegen, Maarten, Nijkrake, Nienke M, de Vries, Bastiaan R, Bloem
Publikováno v:
Journal of neurology. 268(1)
The use of the European Physiotherapy Guideline for Parkinson's Disease is limited in countries where the official language is not English.To provide practical steps on how to translate the European Physiotherapy Guideline for Parkinson's Disease.We
Recommendations for the Organization of Multidisciplinary Clinical Care Teams in Parkinson's Disease
Autor:
Joaquim J. Ferreira, Michael S. Okun, Nir Giladi, Jochen Klucken, Giuseppe Frazzitta, Marten Munneke, Anne Louise Lafontaine, Carsten Eggers, Jori Fleisher, Nina Browner, Peter Fletcher, John Nutt, Connie Marras, Marlies van Nimwegen, Mark Guttman, Robert Iansek, Sotirios A. Parashos, Danique L.M. Radder, Guido Alves, Georg Ebersbach, Jorik Nonnekes, Suketu M. Khandhar, Bastiaan R. Bloem, K. Ray Chaudhuri, Giovanni Abbruzzese
Publikováno v:
Journal of Parkinson's Disease, 10, 1087-1098
Journal of Parkinson's disease
Journal of Parkinson's Disease, 10, 3, pp. 1087-1098
Journal of Parkinson's disease
Journal of Parkinson's Disease, 10, 3, pp. 1087-1098
Background Optimal management in expert centers for Parkinson's disease (PD) usually involves pharmacological and non-pharmacological interventions, delivered by a multidisciplinary approach. However, there is no guideline specifying how this model s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c3e9a6aa59f880c59e40e46b7e8d15f9
http://hdl.handle.net/2066/221564
http://hdl.handle.net/2066/221564
Autor:
Ole A. Andreassen, Vivianna M. Van Deerlin, David Simon, Claire E. Wegel, Guido Alves, Ruwani Wijeyekoon, Jodi Maple-Grødem, Alastair J. Noyce, Roger A. Barker, Bart P.C. van de Warrenburg, Peter Heutink, Shirley Eberly, J. Raphael Gibbs, Alexis Brice, Kumaraswamy Naidu Chitrala, Lasse Pihlstrøm, Marlies van Nimwegen, Khanh-Dung H. Nguyen, Ganqiang Liu, Bernard Ravina, Clemens R. Scherzer, Jean-Christophe Corvol, Bastiaan R. Bloem, Jacobus J. van Hilten, Karol Estrada, Faraz Faghri, Jonathan R. Evans, Daniel Weintraub, Ole-Bjørn Tysnes, Aaron G. Day-Williams, Hampton L. Leonard, Jonggeol J. Kim, Fabrice Danjou, David P. Breen, Samantha J. Hutten, Andrew B. Singleton, Hirotaka Iwaki, Peggy Auinger, Mike A. Nalls, Kirsten M. Scott, Dena G. Hernandez, Mathias Toft, Jacqueline Rick, Caroline H. Williams-Gray, Cornelis Blauwendraat
Publikováno v:
2019, ' Genomewide association study of Parkinson's disease clinical biomarkers in 12 longitudinal patients' cohorts ', Movement Disorders, vol. 34, no. 12 . https://doi.org/10.1002/mds.27845
Movement Disorders, 34, 1839-1850
Movement disorders 34(12), 1839-1850 (2019). doi:10.1002/mds.27845
Mov Disord
Movement Disorders
Movement Disorders, 34, 12, pp. 1839-1850
Movement Disorders, 34, 1839-1850
Movement disorders 34(12), 1839-1850 (2019). doi:10.1002/mds.27845
Mov Disord
Movement Disorders
Movement Disorders, 34, 12, pp. 1839-1850
Item does not contain fulltext BACKGROUND: Several reports have identified different patterns of Parkinson's disease progression in individuals carrying missense variants in GBA or LRRK2 genes. The overall contribution of genetic factors to the sever
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d75d743e4735219496720da03a92501
https://www.pure.ed.ac.uk/ws/files/112990604/Breen_GWAS_MovtDisorders.pdf
https://www.pure.ed.ac.uk/ws/files/112990604/Breen_GWAS_MovtDisorders.pdf
Autor:
Jean-François Deux, Arend Heerschap, Guillaume Bassez, Marlies van Nimwegen, Baziel G.M. van Engelen, Linda Heskamp, Darren G. Monckton, Marieke J. Ploegmakers, Sarah A. Cumming
Publikováno v:
Neurology
Neurology, 2019, 92, pp.e2803-e2814. ⟨10.1212/wnl.0000000000007648⟩
Neurology, 92, e2803-e2814
Neurology, American Academy of Neurology, 2019, 92, pp.e2803-e2814. ⟨10.1212/wnl.0000000000007648⟩
Neurology, 92, 24, pp. e2803-e2814
Neurology, 2019, 92, pp.e2803-e2814. ⟨10.1212/wnl.0000000000007648⟩
Neurology, 92, e2803-e2814
Neurology, American Academy of Neurology, 2019, 92, pp.e2803-e2814. ⟨10.1212/wnl.0000000000007648⟩
Neurology, 92, 24, pp. e2803-e2814
ObjectiveTo determine the value of quantitative MRI in providing imaging biomarkers for disease in 20 different upper and lower leg muscles of patients with myotonic dystrophy type 1 (DM1).MethodsWe acquired images covering these muscles in 33 geneti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::91a3c34f4048e9263fb07273c830f5d8
https://hal.sorbonne-universite.fr/hal-03463112/document
https://hal.sorbonne-universite.fr/hal-03463112/document
Autor:
David P. Breen, Samantha J. Hutten, Alastair J. Noyce, Dena G. Hernandez, Kumaraswamy Naidu Chitrala, Lasse Pihlstrøm, Jacqueline Rick, Mathias Toft, Mike A. Nalls, Ganqiang Liu, Karol Estrada, Jean-Christophe Corvol, Marlies van Nimwegen, Bernard Ravina, Shirley Eberly, Aaron G. Day-Williams, Jonathan R. Evans, Peter Heutink, Claire E. Wegel, Ole-Bjørn Tysnes, J. Raphael Gibbs, Bart P.C. van de Warrenburg, Peggy Auinger, Alexis Brice, Hirotaka Iwaki, Clemens R. Scherzer, Jonggeol J. Kim, Jodi Maple-Grødem, Kirsten M. Scott, Fabrice Danjou, Daniel Weintraub, H. Nguyen Khanh-Dung, Jacobus J. van Hilten, Roger A. Barker, Caroline H. Williams-Gray, Hampton L. Leonard, Cornelis Blauwendraat, David Simon, Andrew B. Singleton, Faraz Faghri, Guido Alves, Ruwani Wijeyekoon, Ole A. Andreassen, Vivianna M. Van Deerlin, Bastiaan R. Bloem
BackgroundSeveral reports have identified different patterns of Parkinson’s disease progression in individuals carrying missense variants in theGBAorLRRK2genes. The overall contribution of genetic factors to the severity and progression of Parkinso
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::63e500b2bfcbaa1c99a721afb2cb6777
Autor:
Peggy Auinger, David Simon, Ganqiang Liu, Daniel Weintraub, Alexis Brice, Bart P.C. van de Warrenburg, Jacqueline Rick, Bernard Ravina, Kirsten M. Scott, Hampton L. Leonard, Fabrice Danjou, Caroline H. Williams-Gray, Faraz Faghri, Hirotaka Iwaki, Ole-Bjørn Tysnes, Cornelis Blauwendraat, Lasse Pihlstrøm, Clemens R. Scherzer, Marlies van Nimwegen, Jacobus J. van Hilten, Alastair J. Noyce, Samantha J. Hutten, Mike A. Nalls, Vivianna M. van Deerlin, Peter Heutink, Roger A. Barker, Karol Estrada, Jonathan R. Evans, Aaron G. Day-Williams, Shirley Eberly, Andrew B. Singleton, Jean-Christophe Corvol, David P. Breen, Dena G. Hernandez, Khanh-Dung H. Nguyen, Bastiaan R. Bloem, Claire E. Wegel, Jodi Maple-Grødem, Mathias Toft, Guido Alves, Ruwani Wijeyekoon
Publikováno v:
Neurology: Genetics
Neurology. Genetics, 5, 4
Neurology. Genetics, 5
Iwaki, H, Blauwendraat, C, Leonard, H L, Liu, G, Maple-grødem, J, Corvol, J, Pihlstrøm, L, Van Nimwegen, M, Hutten, S J, Nguyen, K H, Rick, J, Eberly, S, Faghri, F, Auinger, P, Scott, K M, Wijeyekoon, R, Van Deerlin, V M, Hernandez, D G, Day-williams, A G, Brice, A, Alves, G, Noyce, A J, Tysnes, O, Evans, J R, Breen, D P, Estrada, K, Wegel, C E, Danjou, F, Simon, D K, Ravina, B, Toft, M, Heutink, P, Bloem, B R, Weintraub, D, Barker, R A, Williams-gray, C H, Van De Warrenburg, B P, Van Hilten, J J, Scherzer, C R, Singleton, A B & Nalls, M A 2019, ' Genetic risk of Parkinson disease and progression: An analysis of 13 longitudinal cohorts ', Neurology Genetics, vol. 5, no. 4, pp. e348 . https://doi.org/10.1212/NXG.0000000000000348
Neurology / Genetics 5(4), e348 (2019). doi:10.1212/NXG.0000000000000348
Neurology Genetics, 5(4)
Neurology. Genetics, 5, 4
Neurology. Genetics, 5
Iwaki, H, Blauwendraat, C, Leonard, H L, Liu, G, Maple-grødem, J, Corvol, J, Pihlstrøm, L, Van Nimwegen, M, Hutten, S J, Nguyen, K H, Rick, J, Eberly, S, Faghri, F, Auinger, P, Scott, K M, Wijeyekoon, R, Van Deerlin, V M, Hernandez, D G, Day-williams, A G, Brice, A, Alves, G, Noyce, A J, Tysnes, O, Evans, J R, Breen, D P, Estrada, K, Wegel, C E, Danjou, F, Simon, D K, Ravina, B, Toft, M, Heutink, P, Bloem, B R, Weintraub, D, Barker, R A, Williams-gray, C H, Van De Warrenburg, B P, Van Hilten, J J, Scherzer, C R, Singleton, A B & Nalls, M A 2019, ' Genetic risk of Parkinson disease and progression: An analysis of 13 longitudinal cohorts ', Neurology Genetics, vol. 5, no. 4, pp. e348 . https://doi.org/10.1212/NXG.0000000000000348
Neurology / Genetics 5(4), e348 (2019). doi:10.1212/NXG.0000000000000348
Neurology Genetics, 5(4)
ObjectiveTo determine if any association between previously identified alleles that confer risk for Parkinson disease and variables measuring disease progression.MethodsWe evaluated the association between 31 risk variants and variables measuring dis
Autor:
Kees Okkersen, Cecilia Jimenez-Moreno, Stephan Wenninger, Ferroudja Daidj, Jeffrey Glennon, Sarah Cumming, Roberta Littleford, Darren G Monckton, Hanns Lochmüller, Michael Catt, Catharina G Faber, Adrian Hapca, Peter T Donnan, Gráinne Gorman, Guillaume Bassez, Benedikt Schoser, Hans Knoop, Shaun Treweek, Baziel G M van Engelen, Marie Kierkegaard, Darren Monckton, Catharina Faber, Peter Donnan, Baziel van Engelen, Daphne Maas, Stephanie Nikolaus, Yvonne Cornelissen, Marlies van Nimwegen, Ellen Klerks, Sacha Bouman, Linda Heskamp, Arend Heerschap, Ridho Rahmadi, Perry Groot, Tom Heskes, Katarzyna Kapusta, Shaghayegh Abghari, Armaz Aschrafi, Geert Poelmans, Joost Raaphorst, Michael Trenell, Sandra van Laar, Libby Wood, Sophie Cassidy, Jane Newman, Sarah Charman, Renae Steffaneti, Louise Taylor, Allan Brownrigg, Sharon Day, Antonio Atalaya, Fiona Hogarth, Angela Schüller, Kristina Stahl, Heike Künzel, Martin Wolf, Anna Jelinek, Baptiste Lignier, Florence Couppey, Stéphanie Delmas, Jean-François Deux, Karolina Hankiewicz, Celine Dogan, Lisa Minier, Pascale Chevalier, Amira Hamadouche, Berit Adam, Michael Hannah, Emma McKenzie, Petra Rauchhaus, Vincent Van Hees, Sharon Catt, Ameli Schwalber, Ingemar Merkies, Juliane Dittrich
Publikováno v:
Lancet Neurology, 17, 671-680
Lancet neurology, 17(8), 671-680. Lancet Publishing Group
Lancet Neurology, 17, 8, pp. 671-680
Lancet Neurology, 17(8), 671-680. Elsevier Science
Lancet neurology, 17(8), 671-680. Lancet Publishing Group
Lancet Neurology, 17, 8, pp. 671-680
Lancet Neurology, 17(8), 671-680. Elsevier Science
Background: \ud Myotonic dystrophy type 1 is the most common form of muscular dystrophy in adults and leads to severe fatigue, substantial physical functional impairment, and restricted social participation. In this study, we aimed to determine wheth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::44d6c0dd11bb724ca61b2edfa09e7325
https://doi.org/10.1016/S1474-4422(18)30203-5
https://doi.org/10.1016/S1474-4422(18)30203-5