Zobrazeno 1 - 10
of 35
pro vyhledávání: '"F. Hendriksen"'
Autor:
Catharina G. Faber, Gommert van Koeveringe, Johan S.H. Vles, Ruben G. F. Hendriksen, Danique M. J. Hellebrekers, Judith M. Lionarons, Sandra Schipper, Govert Hoogland
Publikováno v:
Muscle & Nerve
Muscle & Nerve, 60(2), 202-210. Wiley
Muscle & Nerve, 60(2), 202-210. Wiley
Introduction With increasing life expectancy, comorbidities become overt in Duchenne muscular dystrophy (DMD). Although micturition problems are common, bladder function is poorly understood in DMD. We studied dystrophin expression and multiple isofo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b27183a019384eed235262f3263a454f
https://doi.org/10.1002/mus.26518
https://doi.org/10.1002/mus.26518
Autor:
Jos G.M. Hendriksen, Marlien W. Aalbers, Richard F.M. Chin, Johan S.H. Vles, Ruben G. F. Hendriksen
Publikováno v:
European Journal of Paediatric Neurology, 22(3), 488-497. ELSEVIER SCI LTD
Hendriksen, R G F, Vles, J S H, Aalbers, M W, Chin, R F M & Hendriksen, J G M 2017, ' Brain-related comorbidities in boys and men with Duchenne Muscular Dystrophy : A descriptive study ', European Journal of Paediatric Neurology . https://doi.org/10.1016/j.ejpn.2017.12.004
Hendriksen, R G F, Vles, J S H, Aalbers, M W, Chin, R F M & Hendriksen, J G M 2017, ' Brain-related comorbidities in boys and men with Duchenne Muscular Dystrophy : A descriptive study ', European Journal of Paediatric Neurology . https://doi.org/10.1016/j.ejpn.2017.12.004
Aim: Duchenne Muscular Dystrophy (DMD) is more than a muscle disease since there is a higher prevalence of neuropsychological comorbidities. Similarly, the prevalence of epilepsy is increased. Given the nowadays-increasing interest in brain-related c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c4dea38a5bb164713948e49bfcd4cd5
https://research.rug.nl/en/publications/5fdcfab9-3c22-43e4-92dc-2d26f6fe3d7f
https://research.rug.nl/en/publications/5fdcfab9-3c22-43e4-92dc-2d26f6fe3d7f
Autor:
Olaf E. M. G. Schijns, Marlien W. Aalbers, Marc P. H. Hendriks, Govert Hoogland, Johan S.H. Vles, Ruben G. F. Hendriksen, Rutger J. Slegers
Publikováno v:
Hippocampus, 29, 102-110
Hippocampus, 29(2), 102-110. Wiley
Hippocampus, 29(2), 102-110. WILEY-LISS
Hippocampus, 29, 2, pp. 102-110
Hippocampus, 29(2), 102-110. Wiley
Hippocampus, 29(2), 102-110. WILEY-LISS
Hippocampus, 29, 2, pp. 102-110
Item does not contain fulltext Dystrophin is an important protein within the central nervous system. The absence of dystrophin, characterizing Duchenne Muscular Dystrophy (DMD), is associated with brain related comorbidities such as neurodevelopmenta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec47037727b1c9727227cb968ce15d9a
http://hdl.handle.net/2066/200761
http://hdl.handle.net/2066/200761
Autor:
Jos G.M. Hendriksen, Marlien W. Aalbers, Ruben G. F. Hendriksen, Johan S.H. Vles, Govert Hoogland, Sandra Schipper
Publikováno v:
Neuroscience and Biobehavioral Reviews, 51, 255-262. Elsevier Science
Duchenne muscular dystrophy (DMD) is a recessive hereditary form of muscular dystrophy caused by a mutation in the dystrophin gene on the X chromosome. Clinical observations show that in addition to progressive muscular degeneration, DMD is more ofte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc89d9b8eee37f33cf1d71634d9cd541
https://doi.org/10.1016/j.neubiorev.2015.01.023
https://doi.org/10.1016/j.neubiorev.2015.01.023
Autor:
Johan S.H. Vles, George F. Vles, Jose G.M. Hendriksen, Antonio W. D. Gavilanes, Elisabeth P.M. van Raak, Ruben G. F. Hendriksen, Dan L.H.M. Soudant
Publikováno v:
ResearcherID
Cns & Neurological Disorders-Drug Targets, 14(1), 102-109. Bentham Science Publishers
Cns & Neurological Disorders-Drug Targets, 14(1), 102-109. Bentham Science Publishers
Objective: To compare the quality of life (QoL) of 8-18 year old children with cerebral palsy (CP) in the Southern part of The Netherlands to a sample of European children from the general population and to investigate factors associated with possibl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0c5b725992d92a91c26e5a168bd7982
https://doi.org/10.2174/1871527314666150116123045
https://doi.org/10.2174/1871527314666150116123045
Autor:
Johan S.H. Vles, Jos G.M. Hendriksen, Christine E. M. de Die-Smulders, Marlien W. Aalbers, Govert Hoogland, Ruben G. F. Hendriksen
Publikováno v:
Child neurology open, 3
Child neurology open
Child neurology open
We present a case of an unusual triad in pediatric neurology: a currently 12-year-old boy with cerebral palsy and epilepsy who was later also diagnosed with Duchenne muscular dystrophy. We describe the clinical path that resulted in this exceptional
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::514d62c15de51496b96cb8c8c12c06bb
https://research.rug.nl/en/publications/709dcb99-17c9-4fb9-aa7c-823d1dfcbf8e
https://research.rug.nl/en/publications/709dcb99-17c9-4fb9-aa7c-823d1dfcbf8e
Autor:
Sandra Schipper, Olaf E. M. G. Schijns, Jim Dings, Marlien W. Aalbers, Johan S.H. Vles, Govert Hoogland, Ruben G. F. Hendriksen
Publikováno v:
Frontiers in Cellular Neuroscience, 10:174. Frontiers Media S.A.
Frontiers in cellular neuroscience, 10:174. Frontiers Media SA
Frontiers in Cellular Neuroscience
Frontiers in cellular neuroscience, 10:174. Frontiers Media SA
Frontiers in Cellular Neuroscience
Objective: Dystrophin is part of a protein complex that connects the cytoskeleton to the extracellular matrix. In addition to its role in muscle tissue, it functions as an anchoring protein within the central nervous system such as in hippocampus and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::221e32978395f97bace00a65c3076f4a
https://hdl.handle.net/11370/772ce428-1dfd-41ce-81a6-9c7e33daec47
https://hdl.handle.net/11370/772ce428-1dfd-41ce-81a6-9c7e33daec47
Autor:
Ruben G. F. Hendriksen BSc, Marlien W. Aalbers MD, PhD, Jos G. M. Hendriksen PhD, Christine E. M. de Die-Smulders MD, PhD, Govert Hoogland PhD, Johan S. H. Vles MD, PhD
Publikováno v:
Child Neurology Open, Vol 3 (2016)
We present a case of an unusual triad in pediatric neurology: a currently 12-year-old boy with cerebral palsy and epilepsy who was later also diagnosed with Duchenne muscular dystrophy. We describe the clinical path that resulted in this exceptional
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::5065495017bee68d5a0e7a34739d921a
https://doaj.org/article/9b4ca3244ba8426ba68f9f8a08485712
https://doaj.org/article/9b4ca3244ba8426ba68f9f8a08485712
Autor:
E. Santegoeds, Johan Arends, B. Aldenkamp, Ruben G. F. Hendriksen, van der E. Horst, Saskia C.M. Ebus, Paul Boon, Jos G.M. Hendriksen, de la N. Parra
Publikováno v:
European Journal of Paediatric Neurology, 16(6), 697-706. ELSEVIER SCI LTD
European Journal of Paediatric Neurology, 16(6), 697-706. W.B. Saunders Ltd
European Journal of Paediatric Neurology, 16(6), 697-706. W.B. Saunders Ltd
Frequent interictal epileptiform discharges (IEDs) may have effects on cognition. We analysed a group of 182 children with different epilepsy syndromes as well as children with IEDs without observed seizures [corrected], with 24-h ambulatory EEG and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee9ccf6bc7a5355207f892f2d73f7a4f
https://doi.org/10.1016/j.ejpn.2012.05.010
https://doi.org/10.1016/j.ejpn.2012.05.010
Autor:
George F. Vles, Jos G.M. Hendriksen, Johan S.H. Vles, Alfons G. H. Kessels, Ruben G. F. Hendriksen
Publikováno v:
European Journal of Paediatric Neurology, 16(4), 365-372. ELSEVIER SCI LTD
Background Over the last couple of years, there has been increasing interest for QoL in children with CP. Psychosocial adjustment in these children remains underrepresented in current literature. Aims To describe psychosocial adjustment in children w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4989a531ca8bd7ac253ef39109a0d1f2
https://doi.org/10.1016/j.ejpn.2011.12.002
https://doi.org/10.1016/j.ejpn.2011.12.002