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Author/Creator Lemmers, Richard

1. Deep characterization of a common D4Z4 variant identifies biallelic DUX4 expression as a modifier for disease penetrance in FSHD2. (January 2018)

Authors:
Lemmers, Richard; Vliet, Patrick; Balog, Judit; Goeman, Jelle; Arindrarto, Wibowo; Krom, Yvonne; Straasheijm, Kirsten; Debipersad, Rashmie; Özel, Gizem; Sowden, Janet; Snider, Lauren; Mul, Karlien; Sacconi, Sabrina; Engelen, Baziel; Tapscott, Stephen; Tawil, Rabi; Maarel, Silvère
Journal:
European journal of human genetics
Issue:
Volume 26:Number 1(2018)
Page Start:
94
Record Type:
Journal Article
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2. Facioscapulohumeral dystrophy in children: design of a prospective, observational study on natural history, predictors and clinical impact (iFocus FSHD). Issue 1 (December 2016)

Authors:
Goselink, Rianne; Schreuder, Tim; Mul, Karlien; Voermans, Nicol; Pelsma, Maaike; de Groot, Imelda; van Alfen, Nens; Franck, Bas; Theelen, Thomas; Lemmers, Richard; Mah, Jean; van der Maarel, Silvère; van Engelen, Baziel; Erasmus, Corrie
Journal:
BMC neurology
Issue:
Volume 16:Issue 1(2016)
Page Start:
1
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

3. Magnetic resonance imaging correlates with electrical impedance myography in facioscapulohumeral muscular dystrophy. Issue 5 (22nd January 2020)

Authors:
Hamel, Johanna; Lee, Phil; Glenn, Melanie D.; Burka, Tekalign; Choi, In‐Young; Friedman, Seth D.; Shaw, Dennis W. W.; McCalley, Ayla; Herbelin, Laura; Dimachkie, Mazen M.; Lemmers, Richard; van der Maarel, Silvère M.; Barohn, Richard J.; Tawil, Rabi; Statland, Jeffrey M.
Journal:
Muscle & nerve
Issue:
Volume 61:Issue 5(2020)
Page Start:
644
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗