Výsledky vyhledávání - "N. Doorenweerd"

Akademický článek

Spatially localized phosphorous metabolism of skeletal muscle in Duchenne muscular dystrophy patients: 24-month follow-up.

Autor: M T Hooijmans, N Doorenweerd, C Baligand, J J G M Verschuuren, I Ronen, E H Niks, A G Webb, H E Kan

Publikováno v: PLoS ONE, Vol 12, Iss 8, p e0182086 (2017)

To assess the changes in phosphodiester (PDE)-levels, detected by 31P magnetic resonance spectroscopy (MRS), over 24-months to determine the potential of PDE as marker for muscle tissue changes in Duchenne Muscular Dystrophy (DMD) patients.Spatially

Externí odkaz: https://doaj.org/article/ad08d6eda20f466ab91105c46a92fd2c

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Akademický článek

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Akademický článek

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249th ENMC International Workshop: The role of brain dystrophin in muscular dystrophy: Implications for clinical care and translational research, Hoofddorp, The Netherlands, November 29th–December 1st 2019

Publikováno v: Neuromuscular Disorders
Neuromuscular Disorders, Elsevier, 2020, 30 (9), pp.782-794. ⟨10.1016/j.nmd.2020.08.357⟩
Neuromuscular Disorders, 30(9), 782-794. PERGAMON-ELSEVIER SCIENCE LTD

International audience; The role of brain dystrophin in muscular dystrophy: Implications for clinical care and translational research, Hoofddorp, the Netherlands, November 29 th-December 1 st 2019

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::575f77fed85a047101751fd1582bb226
https://doi.org/10.1016/j.nmd.2020.08.357

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Functional and structural impairment of transcallosal motor fibres in ALS: a study using transcranial magnetic stimulation, diffusion tensor imaging, and diffusion weighted spectroscopy

Autor: N. Doorenweerd, Dorothée Lulé, Bastian Böckler, Ece Ercan, Volker Rasche, Thomas Kammer, Hans-Peter Müller, Annemarie Hübers, Jan Kassubek, Jens Dreyhaupt, Alireza Abaei, Itamar Ronen, Albert C. Ludolph

Publikováno v: Brain Imaging and Behavior. SPRINGER
Brain Imaging and Behavior

Imaging studies showed that the structure of the corpus callosum (CC) is affected in amyotrophic lateral sclerosis (ALS). Some clinical studies also suggest that interhemispheric connectivity is altered, since mirror movements seem to occur in ALS. F

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd9e949216c11728799e4d0142b60c7c
https://doi.org/10.1007/s11682-020-00282-x

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P.63 Comparison of brain volume reduction in boys with Duchenne muscular dystrophy treated with different corticosteroid regimes

Autor: S. Geuens, J. Van Dessel, J. Lemiere, E. Niks, N. Goemans, H. Kan, L. De Waele, N. Doorenweerd

Publikováno v: Neuromuscular Disorders. 32:S68

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::b1fffea8aa3cc0424e94defd4af15c4f
https://doi.org/10.1016/j.nmd.2022.07.111

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IMAGING

Autor: S. Geuens, C. Sleurs, J. Lemiere, M. Verly, E. Niks, N. Goemans, H. Kan, L. De Waele, N. Doorenweerd

Publikováno v: Neuromuscular Disorders. 31:S149-S150

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::d9f3830edc52a2f0b7978ea3cdbd977b
https://doi.org/10.1016/j.nmd.2021.07.353

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Decision-making and selection bias in four observational studies on Duchenne and Becker muscular dystrophy

Autor: Ruben G.F. Hendriksen, Chiara S. M. Straathof, N. Doorenweerd, Karin J. Naarding, Erik H. Niks, Kinita A. Chotkan, Imelda J. M. de Groot, Hermien E. Kan, Yvonne D. Krom, Zaïda Koeks

Publikováno v: Journal of Neuromuscular Diseases, 7(4), 433-442. IOS Press
Journal of Neuromuscular Diseases, 7, 4, pp. 433-442
Journal of Neuromuscular Diseases
Journal of Neuromuscular Diseases, 7, 433-442

Contains fulltext : 225944.pdf (Publisher’s version ) (Open Access) BACKGROUND: Natural history data are essential for trial design in Duchenne (DMD) and Becker muscular dystrophy (BMD), but recruitment for observational studies can be challenging.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f60671a3f391d2b60faa3338fd8fe46
http://hdl.handle.net/1887/3245883

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Combining genetics, neuropsychology and neuroimaging to improve understanding of brain involvement in Duchenne muscular dystrophy - a narrative review

Autor: N. Doorenweerd

Publikováno v: Neuromuscular Disorders, 30(6), 437-442. PERGAMON-ELSEVIER SCIENCE LTD

Duchenne muscular dystrophy is a multifactorial disease including a cognitive phenotype. It is caused by mutations in the X-chromosomal DMD gene from which dystrophin is synthesized. Multiple isoforms of dystrophin have been identified. The full leng

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::918979a47673db32a5226b03cc27d61c
https://hdl.handle.net/1887/3184242

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