Genotype and corticosteroid treatment are distinctively associated with gray matter characteristics in patients with Duchenne muscular dystrophy

Authors: Geuens, Sam, Van Dessel, Jeroen, Kan, Hermien E., Govaarts, Rosanne, Niks, Erik H., Goemans, Nathalie, Lemiere, Jurgen, Doorenweerd, Nathalie, De Waele, Liesbeth

Source: In Neuromuscular Disorders December 2024 45

Probing diffusion of water and metabolites to assess white matter microstructure in Duchenne muscular dystrophy.

Authors: Govaarts, Rosanne, Doorenweerd, Nathalie, Najac, Chloé F., Broek, Emma M., Tamsma, Maud E., Hollingsworth, Kieren G., Niks, Erik H., Ronen, Itamar, Straub, Volker, Kan, Hermien E.

Source: NMR in Biomedicine; Nov2024, Vol. 37 Issue 11, p1-11, 11p

Subject Terms: DIFFUSION tensor imaging, DUCHENNE muscular dystrophy, WHITE matter (Nerve tissue), NEUROGLIA, NEUROMUSCULAR diseases

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

Authors: Doorenweerd, Nathalie

Source: In Neuromuscular Disorders June 2020 30(6):437-442

Longitudinal follow-up of verbal span and processing speed in Duchenne muscular dystrophy

Authors: Hellebrekers, Danique M.J., Doorenweerd, Nathalie, Sweere, Dirk J.J., van Kuijk, Sander M.J., Aartsma-Rus, Annemieke M., Klinkenberg, Sylvia, Vles, Johan S.H., Hendriksen, Jos G.M.

Source: In European Journal of Paediatric Neurology March 2020 25:120-126

Development and Pilot Validation of the DuMAND Checklist to Screen for Duchenne Muscular Dystrophy-Associated Neurobehavioral Difficulties (DuMAND).

Authors: Geuens, Sam, Goemans, Nathalie, Lemiere, Jurgen, Doorenweerd, Nathalie, De Waele, Liesbeth

Source: Journal of Neuromuscular Diseases; 2024, Vol. 11 Issue 4, p801-814, 14p

Duchenne Muscular Dystrophy-Associated Neurobehavioral Difficulties: Insights from Clinical Practice.

Authors: Geuens, Sam, Goemans, Nathalie, Lemiere, Jurgen, Doorenweerd, Nathalie, De Waele, Liesbeth

Source: Journal of Neuromuscular Diseases; 2024, Vol. 11 Issue 4, p791-799, 9p

Continuous infusion of manganese improves contrast and reduces side effects in manganese-enhanced magnetic resonance imaging studies

Authors: Poole, Dana S., Doorenweerd, Nathalie, Plomp, Jaap J., Mahfouz, Ahmed, Reinders, Marcel J.T., van der Weerd, Louise

Source: In NeuroImage 15 February 2017 147:1-9

Decreased cerebral perfusion in Duchenne muscular dystrophy patients

Authors: Doorenweerd, Nathalie ^*, Dumas, Eve M., Ghariq, Eidrees, Schmid, Sophie, Straathof, Chiara S.M., Roest, Arno A.W., Wokke, Beatrijs H., van Zwet, Erik W., Webb, Andrew G., Hendriksen, Jos G.M., van Buchem, Mark A., Verschuuren, Jan J.G.M., Asllani, Iris, Niks, Erik H., van Osch, Matthias J.P., Kan, Hermien E.

Source: In Neuromuscular Disorders January 2017 27(1):29-37

Timing and localization of human dystrophin isoform expression provide insights into the cognitive phenotype of Duchenne muscular dystrophy

Authors: Doorenweerd, Nathalie, Mahfouz, Ahmed, van Putten, Maaike, Kaliyaperumal, Rajaram, t' Hoen, Peter, Hendriksen, Jos, Aartsma-Rus, Annemieke, Verschuuren, Jan, Niks, Erik, Reinders, Marcel, Kan, Hermien, Lelieveldt, Boudewijn

Source: Scientific reports. 7(1):1-12

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100184102625.0x000001&indx=1&recIds=ETOCvdc_100184102625.0x000001

Comparison of two corticosteroid regimens on brain volumetrics in patients with Duchenne muscular dystrophy.

Authors: Geuens, Sam, Van Dessel, Jeroen, Govaarts, Rosanne, Ikelaar, Nadine A., Meijer, Onno C., Kan, Hermien E., Niks, Erik H., Goemans, Nathalie, Lemiere, Jurgen, Doorenweerd, Nathalie, De Waele, Liesbeth

Source: Annals of Clinical & Translational Neurology; Dec2023, Vol. 10 Issue 12, p2324-2333, 10p

Subject Terms: DUCHENNE muscular dystrophy, GRAY matter (Nerve tissue), WHITE matter (Nerve tissue), MAGNETIC resonance imaging, VOXEL-based morphometry

Geographic Terms: LEIDEN (Netherlands)

Author Correction: Timing and localization of human dystrophin isoform expression provide insights into the cognitive phenotype of Duchenne muscular dystrophy

Authors: Doorenweerd, Nathalie, Mahfouz, Ahmed, van Putten, Maaike, Kaliyaperumal, Rajaram, t' Hoen, Peter A. C., Hendriksen, Jos G. M., Aartsma-Rus, Annemieke M., Verschuuren, Jan J. G. M., Niks, Erik H., Reinders, Marcel J. T., Kan, Hermien E., Lelieveldt, Boudewijn P. F.

Source: Scientific reports. 8(1)

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100131349953.0x000001&indx=1&recIds=ETOCvdc_100131349953.0x000001

Resting-state functional MRI shows altered default-mode network functional connectivity in Duchenne muscular dystrophy patients.

Authors: Doorenweerd, Nathalie, de Rover, Mischa, Marini-Bettolo, Chiara, Hollingsworth, Kieren G., Niks, Erik H., Hendriksen, Jos G. M., Kan, Hermien E., Straub, Volker

Source: Brain Imaging & Behavior; Oct2021, Vol. 15 Issue 5, p2297-2307, 11p

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

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

Source: Brain Imaging & Behavior; Apr2021, Vol. 15 Issue 2, p748-757, 10p

Decision-Making And Selection Bias in Four Observational Studies on Duchenne and Becker Muscular Dystrophy

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

Source: Journal of Neuromuscular Diseases; September 2020, Vol. 7 Issue: 4 p433-442, 10p

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Proton Magnetic Resonance Spectroscopy Indicates Preserved Cerebral Biochemical Composition in Duchenne Muscular Dystrophy Patients

Authors: Doorenweerd, Nathalie, Hooijmans, Melissa, Schubert, Stephanie A., Webb, Andrew G., Straathof, Chiara S.M., van Zwet, Erik W., van Buchem, Mark A., Verschuuren, Jan J.G.M., Hendriksen, Jos G.M., Niks, Erik H., Kan, Hermien E.

Source: Journal of Neuromuscular Diseases; October 2017, Vol. 4 Issue: 1 p53-58, 6p

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