Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Elisabeth A. Cats"'
Autor:
Kevin Budding, Jeroen W. Bos, Kim Dijkxhoorn, Elisabeth de Zeeuw, Lauri M. Bloemenkamp, Eva M. Zekveld, Ewout J.N. Groen, Bart C. Jacobs, Ruth Huizinga, H. Stephan Goedee, Elisabeth A. Cats, Jeanette H.W. Leusen, Leonard H. van den Berg, C. Erik Hack, W. Ludo van der Pol
Publikováno v:
Journal of Neuroinflammation, Vol 21, Iss 1, Pp 1-14 (2024)
Abstract Background Multifocal motor neuropathy (MMN) is a rare, chronic immune-mediated polyneuropathy characterized by asymmetric distal limb weakness. An important feature of MMN is the presence of IgM antibodies against gangliosides, in particula
Externí odkaz:
https://doaj.org/article/6a575bd7333941c8bd8c09e509cbb6f7
Autor:
Leonard H. van den Berg, Talitha A. de Hoop, Jeroen W. Bos, Henny G. Otten, H. Stephan Goedee, Ingrid J.T. Herraets, W. Ludo van der Pol, Willem Verduijn, Elisabeth A. Cats
Publikováno v:
Neurobiology of Aging. 101:79-84
To gain further insight in the immunopathology underlying multifocal motor neuropathy (MMN) by exploring the association between MMN and the human leukocyte antigen (HLA) class II DRB1, DQB1, and DQA loci in depth and by correlating associated haplot
Autor:
Elisabeth A. Cats, W-Ludo van der Pol, Abraham C. J. Stork, Nicolette C. Notermans, Jan H. Veldink, Ruth D E Fritsch-Stork, Ben A.W. de Jong, Lotte Vlam, Ger T. Rijkers, Leonard H. van den Berg
Publikováno v:
Muscle & Nerve, 59(6), 694-698. John Wiley & Sons Inc.
Muscle & Nerve, 59(6), 694. John Wiley and Sons Inc.
Muscle & Nerve, 59(6), 694. John Wiley and Sons Inc.
Introduction Polyneuropathy with immunoglobulin M monoclonal gammopathy (IgM-PNP) is associated with the presence of IgM antibodies against nerve constituents such as myelin associated glycoprotein (MAG) and gangliosides. Methods To test whether B-ce
Autor:
Bart van den Munckhof, Nico W. Teunissen, Elisabeth A. Cats, Karin Geleijns, Anouk van Westrhenen, Sandra M. A. van der Salm, Cyrille H. Ferrier, Frans S. S. Leijten
Publikováno v:
Clinical Neurophysiology, 129(10), 2127. Elsevier Ireland Ltd
Objective To examine whether rhythmic high-amplitude delta with superimposed (poly)spikes (RHADS) in EEG allow a reliable early diagnosis of Alpers-Huttenlocher syndrome (AHS) and contribute to recognition of this disease. Methods EEGs of nine patien
Autor:
W. Ludo van der Pol, Kenneth C. Gorson, David R. Cornblath, Pieter A. van Doorn, Elisabeth A. Cats, Ingemar S. J. Merkies, Catharina G. Faber, Leonard H. van den Berg, Els K. Vanhoutte, Sonja I. van Nes
Publikováno v:
Journal of the Peripheral Nervous System. 20:296-305
Clinical trials in multifocal motor neuropathy (MMN) have often used ordinal-based measures that may not accurately capture changes. We aimed to construct a disability interval outcome measure specifically for MMN using the Rasch model and to examine
Autor:
Bjorn L. Herpers, Jos A. G. van Strijp, Ben A.W. de Jong, Lotte Vlam, Erik C. Heezius, Abraham C. J. Stork, W-Ludo van der Pol, Nicolette C. Notermans, Leonard H. van den Berg, Suzan H.M. Rooijakkers, Elisabeth A. Cats, Ger T. Rijkers
Publikováno v:
Journal of Neuroimmunology, 290, 76. Elsevier
Journal of Neuroimmunology, 290, pp. 76-9
Journal of Neuroimmunology, 290, 76-9
Journal of Neuroimmunology, 290, pp. 76-9
Journal of Neuroimmunology, 290, 76-9
Item does not contain fulltext Polyneuropathy associated with IgM monoclonal gammopathy (IgM-PNP) is a slowly progressive, sensorimotor neuropathy. It is assumed that complement activation contributes to IgM-PNP pathogenesis. We investigated whether
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f532de31fadc7188ece737e13684de0b
https://doi.org/10.1016/j.jneuroim.2015.11.010
https://doi.org/10.1016/j.jneuroim.2015.11.010
Publikováno v:
International Journal of Pediatric Otorhinolaryngology. 99:152-153
Autor:
Lotte Vlam, Leonard H. van den Berg, Elisabeth A. Cats, W-Ludo van der Pol, Meinie Seelen, Paul W.J. van Vught
Publikováno v:
Journal of the Peripheral Nervous System. 16:175-179
The contribution of genetic heterogeneity to the pathogenesis of multifocal motor neuropathy (MMN) has not been elucidated. We investigated frequencies of single nucleotide polymorphisms (SNPs) in the candidate genes protein tyrosine phosphatase, non
Publikováno v:
Journal of the Peripheral Nervous System. 15:113-119
Patients with multifocal motor neuropathy (MMN) have slowly progressive, predominantly distal asymmetric limb weakness without sensory loss. While previous studies have investigated the impact of MMN on body functions and structures, relatively littl
Publikováno v:
Journal of Clinical Immunology
Introduction Multifocal motor neuropathy (MMN) is characterized by asymmetric weakness of limbs and the electrophysiological finding of conduction block in motor nerves. Conduction block is the inability of nerves to propagate action potentials and i