Zobrazeno 1 - 10
of 177
pro vyhledávání: '"Oebele F Brouwer"'
Autor:
Jelte Helfferich, Rinze F. Neuteboom, Marit M.A. de Lange, Kimberley S.M. Benschop, Coretta C. Van Leer-Buter, Adam Meijer, Dewi P. Bakker, Eva de Bie, Hilde M.H. Braakman, Rick Brandsma, Erik H. Niks, Jikke-Mien Niermeijer, Vincent Roelfsema, Niels Schoenmaker, Lilian T. Sie, Hubert G. Niesters, Margreet J.M. te Wierik, Bart C. Jacobs, Oebele F. Brouwer
Publikováno v:
Helfferich, J, Neuteboom, R F, de Lange, M M A, Benschop, K S M, van Leer-Buter, C C, Meijer, A, Bakker, D P, de Bie, E, Braakman, H M H, Brandsma, R, Niks, E H, Niermeijer, J-M, Roelfsema, V, Schoenmaker, N, Sie, L T, Niesters, H G, te Wierik, M J M, Jacobs, B C & Brouwer, O F 2023, ' Pediatric acute flaccid myelitis : Evaluation of diagnostic criteria and differentiation from other causes of acute flaccid paralysis ', European Journal of Paediatric Neurology, vol. 44, pp. 28-36 . https://doi.org/10.1016/j.ejpn.2023.03.002
European Journal of Paediatric Neurology, 44, 28-36. W.B. Saunders
European Journal of Paediatric Neurology, 44, 28-36. W.B. Saunders Ltd
European Journal of Paediatric Neurology, 44, pp. 28-36
European Journal of Paediatric Neurology, 44, 28-36
European Journal of Paediatric Neurology, 44, 28-36. ELSEVIER SCI LTD
European Journal of Paediatric Neurology, 44, 28-36. W.B. Saunders
European Journal of Paediatric Neurology, 44, 28-36. W.B. Saunders Ltd
European Journal of Paediatric Neurology, 44, pp. 28-36
European Journal of Paediatric Neurology, 44, 28-36
European Journal of Paediatric Neurology, 44, 28-36. ELSEVIER SCI LTD
Background: Acute flaccid paralysis (AFP) is characterized by rapidly progressive limb weakness with low muscle tone. It has a broad differential diagnosis, which includes acute flaccid myelitis (AFM), a rare polio-like condition that mainly affects
Autor:
Jelte Helfferich, Marit MA de Lange, Kimberley SM Benschop, Bart C Jacobs, Coretta C Van Leer-Buter, Adam Meijer, Dewi P Bakker, Eva de Bie, Hilde MH Braakman, Rick Brandsma, Rinze F Neuteboom, Erik H Niks, Jikke-Mien Niermeijer, Vincent Roelfsema, Niels Schoenmaker, Lilian T Sie, Hubert G Niesters, Oebele F Brouwer, Margreet JM te Wierik
Publikováno v:
Eurosurveillance, 27(42). EUR CENTRE DIS PREVENTION & CONTROL
Eurosurveillance, 27(42). Centre Europeen pour la Surveillance Epidemiologique du SIDA
Helfferich, J, de Lange, M M A, Benschop, K S M, Jacobs, B C, van Leer-Buter, C C, Meijer, A, Bakker, D P, de Bie, E, Braakman, H M H, Brandsma, R, Neuteboom, R F, Niks, E H, Niermeijer, J-M, Roelfsema, V, Schoenmaker, N, Sie, L T, Niesters, H G, Brouwer, O F & te Wierik, M J M 2022, ' Epidemiology of acute flaccid myelitis in children in the Netherlands, 2014 to 2019 ', Eurosurveillance, vol. 27, no. 42 . https://doi.org/10.2807/1560-7917.ES.2022.27.42.2200157
Eurosurveillance, 27(42). Centre Europeen pour la Surveillance Epidemiologique du SIDA
Helfferich, J, de Lange, M M A, Benschop, K S M, Jacobs, B C, van Leer-Buter, C C, Meijer, A, Bakker, D P, de Bie, E, Braakman, H M H, Brandsma, R, Neuteboom, R F, Niks, E H, Niermeijer, J-M, Roelfsema, V, Schoenmaker, N, Sie, L T, Niesters, H G, Brouwer, O F & te Wierik, M J M 2022, ' Epidemiology of acute flaccid myelitis in children in the Netherlands, 2014 to 2019 ', Eurosurveillance, vol. 27, no. 42 . https://doi.org/10.2807/1560-7917.ES.2022.27.42.2200157
Background Acute flaccid myelitis (AFM) is a polio-like condition affecting mainly children and involving the central nervous system (CNS). AFM has been associated with different non-polio-enteroviruses (EVs), in particular EV-D68 and EV-A71. Reliabl
Autor:
Patrick Rump, Oebele F. Brouwer, Adelita V. Ranchor, Eva H. Brilstra, Petra M.C. Callenbach, Danique R.M. Vlaskamp, Conny M. A. van Ravenswaaij-Arts, Mary E. Velthuizen
Publikováno v:
European Journal of Paediatric Neurology, 32, 128-135. ELSEVIER SCI LTD
Genetic testing and counselling are increasingly important in epilepsy care, aiming at finding a diagnosis, understanding aetiology and improving treatment and outcome. The psychological impact of genetic counselling from patients' or parents' perspe
Publikováno v:
European Journal of Paediatric Neurology, 25, 172-180. ELSEVIER SCI LTD
Background Melatonin may offer a safe and cheap alternative to general anaesthesia and sedatives in neuropaediatric MRI. The purpose of our study was to evaluate its efficacy during a daily scanning programme and to assess its financial benefit. Meth
Publikováno v:
Seizure-European Journal of Epilepsy, 69, 298-303. W.B. Saunders Ltd
Purpose Studies in adults with epilepsy, mainly in specialized epilepsy clinics, have shown that sleep disturbances were twice as prevalent in people with epilepsy as in healthy controls. Our aim was to determine the prevalence of sleep disturbances
Autor:
Kathryn J. Peall, Michèl A.A.P. Willemsen, Nicole I. Wolf, Oebele F. Brouwer, Coen H. A. Lugtenberg, Marina A. J. Tijssen, Emmanuel Roze, Martje E. van Egmond, Tom J. de Koning, Victor S.C. Fung, Roy E. Stewart, Maria Fiorella Contarino
Publikováno v:
Movement Disorders, 34(3), 317-320. John Wiley and Sons Inc.
Movement disorders, 34(3), 317-320. John Wiley and Sons Inc.
Movement Disorders, 34(3), 317-320. Wiley
Movement Disorders, 34, 3, pp. 317-320
van Egmond, M E, Contarino, M F, Lugtenberg, C H A, Peall, K J, Brouwer, O F, Fung, V S C, Roze, E, Stewart, R E, Willemsen, M A, Wolf, N I, de Koning, T J & Tijssen, M A 2019, ' Variable Interpretation of the Dystonia Consensus Classification Items Compromises Its Solidity ', Movement Disorders, vol. 34, no. 3, pp. 317-320 . https://doi.org/10.1002/mds.27627
Movement Disorders, 34, 317-320
Movement disorders, 34(3), 317-320. John Wiley and Sons Inc.
Movement Disorders, 34(3), 317-320. Wiley
Movement Disorders, 34, 3, pp. 317-320
van Egmond, M E, Contarino, M F, Lugtenberg, C H A, Peall, K J, Brouwer, O F, Fung, V S C, Roze, E, Stewart, R E, Willemsen, M A, Wolf, N I, de Koning, T J & Tijssen, M A 2019, ' Variable Interpretation of the Dystonia Consensus Classification Items Compromises Its Solidity ', Movement Disorders, vol. 34, no. 3, pp. 317-320 . https://doi.org/10.1002/mds.27627
Movement Disorders, 34, 317-320
Item does not contain fulltext
Autor:
Seth I. Berger, Maximilian Muenke, Omkar Hajirnis, Paul Kruszka, David R. Murdock, Raymond J. Louie, Joshua L. Everson, Luis F. Escobar, Chitra Prasad, Maria Iascone, Hülya Kayserili, Raymond A. Poot, Valentina Casa, Nancy J. Clegg, Evelien Zonneveld-Huijssoon, Anna Cereda, Jenna Gaesser, Meena Balasubramanian, Nicole Corsten-Janssen, Mike R. Dekker, Jacob Hogue, Mark J. Stephan, Mauricio R. Delgado, Ariel F. Martinez, Oebele F. Brouwer, Allison Schreiber, Ping Hu, Angie W Lichty, Vickie Zurcher, Kerstin S. Wendt, Karin Weiss, Eloise J. Prijoles, Robert J. Lipinski, Momoko Tanima-Nagai, Matthew A. Deardorff
Publikováno v:
Brain
Paediatrics Publications
Brain, 142, 2631-2643. Oxford University Press
Paediatrics Publications
Brain, 142, 2631-2643. Oxford University Press
Marked by incomplete division of the embryonic forebrain, holoprosencephaly is one of the most common human developmental disorders. Despite decades of phenotype-driven research, 80-90% of aneuploidy-negative holoprosencephaly individuals with a prob
Autor:
Oebele F. Brouwer, Coretta Van Leer-Buter, Linda C. Meiners, Rinze F. Neuteboom, Jelte Helfferich, Hubert G. M. Niesters, Marjolein Knoester
Publikováno v:
European Journal of Pediatrics
European Journal of Pediatrics, 178(9), 1305-1315. Springer-Verlag
European Journal of Pediatrics, 178(9), 1305-1315. Springer-Verlag
Acute flaccid myelitis is characterized by the combination of acute flaccid paralysis and a spinal cord lesion largely restricted to the gray matter on magnetic resonance imaging. The term acute flaccid myelitis was introduced in 2014 after the upsur
Autor:
Jeroen J de Vries, E. Brusse, Gea Drost, Michèl A.A.P. Willemsen, Hubertus P. H. Kremer, Martje E. van Egmond, Sjoukje S Polet, Oebele F. Brouwer, Marina A. J. Tijssen, Lisette H. Koens, Tom J. de Koning, David G. Anderson, Deborah A Sival
Publikováno v:
Parkinsonism & Related Disorders, 72, pp. 44-48
Parkinsonism and Related Disorders, 72, 44-48. Elsevier
Parkinsonism & Related Disorders, 72, 44-48
Parkinsonism & Related Disorders, 72, 44-48. Elsevier
Parkinsonism and Related Disorders, 72, 44-48. Elsevier
Parkinsonism & Related Disorders, 72, 44-48
Parkinsonism & Related Disorders, 72, 44-48. Elsevier
INTRODUCTION: In 2011, a homozygous mutation in GOSR2 (c.430G > T; p. Gly144Trp) was reported as a novel cause of Progressive Myoclonus Epilepsy (PME) with early-onset ataxia. Interestingly, the ancestors of patients originate from countries bound to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c14856971225a9a8268139c20bd4b23
https://hdl.handle.net/2066/218550
https://hdl.handle.net/2066/218550
A 22-year follow-up reveals a variable disease severity in early-onset facioscapulohumeral dystrophy
Autor:
Richard J.L.F. Lemmers, Oebele F. Brouwer, Nicol C. Voermans, Baziel G.M. van Engelen, George W. Padberg, Corrie E. Erasmus, Karlien Mul, Caroline R. van Kernebeek, Rianne J.M. Goselink, Silvère M. van der Maarel
Publikováno v:
European Journal of Paediatric Neurology, 22(5), 782-785. ELSEVIER SCI LTD
European Journal of Paediatric Neurology, 22, 5, pp. 782-785
European Journal of Paediatric Neurology, 22, 782-785
European Journal of Paediatric Neurology, 22, 5, pp. 782-785
European Journal of Paediatric Neurology, 22, 782-785
Aim: To assess the long-term natural course of early-onset facioscapulohumeral dystrophy (FSHD), which is important for patient management and trial-readiness, and is currently lacking.Methods: We had the unique opportunity to evaluate 10 patients wi