Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Karin J. Naarding"'
Autor:
Karin J. Naarding, Kevin R. Keene, Aashley S.D. Sardjoe Mishre, Thom T.J. Veeger, Nienke M. van deVelde, Arina J. Prins, Jedrzej Burakiewicz, Jan J.G.M. Verschuuren, Menno van derHolst, Erik H. Niks, Hermien E. Kan
Publikováno v:
Journal of Cachexia, Sarcopenia and Muscle, Vol 12, Iss 3, Pp 694-703 (2021)
Abstract Background Clinical trials in Duchenne muscular dystrophy (DMD) focus primarily on ambulant patients. Results cannot be extrapolated to later disease stages due to a decline in targeted muscle tissue. In non‐ambulant DMD patients, hand fun
Externí odkaz:
https://doaj.org/article/26d2999fe15a4b3dac887ede12e33b30
Autor:
Erik H. Niks, Hermien E. Kan, Erik W. van Zwet, Jan J.G.M. Verschuuren, Karin J. Naarding, Imelda J. M. de Groot, Menno van der Holst, Nienke M van de Velde
Publikováno v:
Neurology, 97, E1737-E1742
Neurology, 97, 17, pp. E1737-E1742
Neurology, 97(17), E1737-E1742. LIPPINCOTT WILLIAMS & WILKINS
Neurology
article-version (Version of Record) 3
Neurology, 97, 17, pp. E1737-E1742
Neurology, 97(17), E1737-E1742. LIPPINCOTT WILLIAMS & WILKINS
Neurology
article-version (Version of Record) 3
Background and ObjectivesTo study the potential of quantitative MRI (qMRI) fat fraction (FF) as a biomarker in nonambulant patients with Duchenne muscular dystrophy (DMD), we assessed the additive predictive value of elbow flexor FF to age at loss of
Autor:
Karin J. Naarding, Mariska M.H.P. Janssen, Ruben D. Boon, Paulina J.M. Bank, Robert P. Matthew, Gregorij Kurillo, Jay J. Han, Jan J.G.M. Verschuuren, Imelda J.M. de Groot, Menno van der Holst, Hermien E. Kan, Erik H. Niks
Publikováno v:
Journal of Neuromuscular Diseases, 9(4), 555-569. IOS PRESS
Journal of Neuromuscular Diseases, 9, 555-569
Journal of Neuromuscular Diseases, 9, 4, pp. 555-569
Journal of Neuromuscular Diseases, 9, 555-569
Journal of Neuromuscular Diseases, 9, 4, pp. 555-569
Background: Outcome measures for non-ambulant Duchenne muscular dystrophy (DMD) patients are limited, with only the Performance of the Upper Limb (PUL) approved as endpoint for clinical trials. Objective: We assessed four outcome measures based on de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b12063cc64a27c4994b9d6ba9b7331e3
http://hdl.handle.net/1887/3497478
http://hdl.handle.net/1887/3497478
Autor:
Erik W. van Zwet, Hermien E. Kan, Melissa T. Hooijmans, Karin J. Naarding, Andrew G. Webb, Jurriaan H. de Groot, Erik H. Niks, Diaa Al Mohamad, Thom T.J. Veeger, Nienke M van de Velde
Publikováno v:
Muscle & Nerve, 64(5), 576-584. WILEY
Muscle & nerve, 64(5), 576-584. John Wiley and Sons Inc.
Muscle & nerve, 64(5), 576-584. John Wiley and Sons Inc.
Introduction/aims Duchenne and Becker muscular dystrophies (DMD and BMD, respectively) are characterized by fat replacement of different skeletal muscles in a specific temporal order. Given the structural role of dystrophin in skeletal muscle mechani
Autor:
Aashley S D Sardjoe Mishre, Jedrzej Burakiewicz, Jan J.G.M. Verschuuren, Kevin R Keene, Nienke M van de Velde, Thom T J Veeger, Karin J. Naarding, Erik H. Niks, Arina J Prins, Hermien E. Kan, Menno van der Holst
Publikováno v:
Journal of Cachexia, Sarcopenia and Muscle, 12(3), 694-703. WILEY
Journal of Cachexia, Sarcopenia and Muscle
Journal of Cachexia, Sarcopenia and Muscle, Vol 12, Iss 3, Pp 694-703 (2021)
Journal of Cachexia, Sarcopenia and Muscle
Journal of Cachexia, Sarcopenia and Muscle, Vol 12, Iss 3, Pp 694-703 (2021)
Background Clinical trials in Duchenne muscular dystrophy (DMD) focus primarily on ambulant patients. Results cannot be extrapolated to later disease stages due to a decline in targeted muscle tissue. In non-ambulant DMD patients, hand function is re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60162bdefeb1ce0431f95c58467ad319
https://doi.org/10.1002/jcsm.12711
https://doi.org/10.1002/jcsm.12711
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
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
http://hdl.handle.net/1887/3245883
Autor:
Martijn R. Tannemaat, Kevin R Keene, W. Ludo van der Pol, Martijn Froeling, Karin J. Naarding, Jan-Willem M Beenakker, Melissa T. Hooijmans, Erik H. Niks, Hermien E. Kan, Louise A.M. Otto
Publikováno v:
Magnetic Resonance in Medicine
Magnetic resonance in medicine, 84(5), 2656-2670. John Wiley and Sons Inc.
Magnetic Resonance in Medicine, 84(5), 2656-2670. WILEY
Magnetic resonance in medicine, 84(5), 2656-2670. John Wiley and Sons Inc.
Magnetic Resonance in Medicine, 84(5), 2656-2670. WILEY
Purpose Multi-echo spin-echo (MSE) transverse relaxometry mapping using multi-component models is used to study disease activity in neuromuscular disease by assessing the T-2 of the myocytic component (T-2water). Current extended phase graph algorith
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1643262f9b3dc9d8c48e12a1e0310851
https://doi.org/10.1002/mrm.28290
https://doi.org/10.1002/mrm.28290
Autor:
I. Rybalsky, Julien Le Louër, Karin J. Naarding, Harmen Reyngoudt, Erik W. van Zwet, Pierre G. Carlier, K. Shellenbarger, Melissa T. Hooijmans, Cuixia Tian, Brenda Wong, Hermien E. Kan, Erik H. Niks
Publikováno v:
Neurology, 94(13), e1386-e1394. Lippincott, Williams & Wilkins
Neurology, 94(13), E1386-E1394. LIPPINCOTT WILLIAMS & WILKINS
Neurology
Neurology, 94(13), E1386-E1394. LIPPINCOTT WILLIAMS & WILKINS
Neurology
ObjectiveWe studied the potential of quantitative MRI (qMRI) as a surrogate endpoint in Duchenne muscular dystrophy by assessing the additive predictive value of vastus lateralis (VL) fat fraction (FF) to age on loss of ambulation (LoA).MethodsVL FFs
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e2c55ecfa62673714a7e3c763830248
https://n.neurology.org/content/94/13/e1386
https://n.neurology.org/content/94/13/e1386
Autor:
Maria Fiorella Contarino, J.J. van Hilten, N.A. van der Gaag, Johan Marinus, Carel F.E. Hoffmann, Victor J. Geraedts, Arne Mosch, Karin J. Naarding
Publikováno v:
Parkinsonism and Related Disorders, 69, 30-33
Parkinsonism and Related Disorders
Parkinsonism and Related Disorders
Objective Although subthalamic Deep Brain Stimulation (STN DBS) is proven effective in improving symptoms of Parkinson's Disease (PD), previous literature demonstrates a discrepancy between objective improvement and patients' perception thereof. We a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::972a465747b40847ed9ef8b156ed5992
https://hdl.handle.net/1887/120804
https://hdl.handle.net/1887/120804
Autor:
Hermien E. Kan, J. Verschuuren, Karin J. Naarding, Thom T.J. Veeger, A. Sardjoe Mishre, Erik H. Niks, M. van der Holst, N. van de Velde
Publikováno v:
Neuromuscular Disorders. 29:S156