A family-based study into penetrance in facioscapulohumeral muscular dystrophy type 1
Wohlgemuth, Mariëlle, Lemmers, Richard J, Jonker, Marianne, van der Kooi, Elly, Horlings, Corinne G, van Engelen, Baziel G, van der Maarel, Silvere M, Padberg, George W, Voermans, Nicol C
Published in Neurology (31.07.2018)
Published in Neurology (31.07.2018)
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Journal Article
Specific Sequence Variations within the 4q35 Region Are Associated with Facioscapulohumeral Muscular Dystrophy
Lemmers, Richard J.L.F., Wohlgemuth, Mariëlle, van der Gaag, Kristiaan J., van der Vliet, Patrick J., van Teijlingen, Corrie M.M., de Knijff, Peter, Padberg, George W., Frants, Rune R., van der Maarel, Silvère M.
Published in American journal of human genetics (01.11.2007)
Published in American journal of human genetics (01.11.2007)
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Journal Article
Quantitative MR imaging of individual muscle involvement in facioscapulohumeral muscular dystrophy
Kan, Hermien E, Scheenen, Tom W.J, Wohlgemuth, Marielle, Klomp, Dennis W.J, van Loosbroek-Wagenmans, Ivonne, Padberg, George W, Heerschap, Arend
Published in Neuromuscular disorders : NMD (01.05.2009)
Published in Neuromuscular disorders : NMD (01.05.2009)
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Journal Article
Acupuncture for psychogenic movement disorders: Treatment or diagnostic tool?
Van Nuenen, Bart F. L., Wohlgemuth, Marielle, Wong Chung, Rudi E., Abdo, Wilson F., Bloem, Bas R.
Published in Movement disorders (15.07.2007)
Published in Movement disorders (15.07.2007)
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Journal Article
Movement disorder of the lower lip
Wohlgemuth, Marielle, Pasman, Jaco W., de Swart, Bert J.M., Horstink, Martin W.I.M.
Published in Movement disorders (01.08.2005)
Published in Movement disorders (01.08.2005)
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Journal Article
Contractions of D4Z4 on 4qB Subtelomeres Do Not Cause Facioscapulohumeral Muscular Dystrophy
Lemmers, Richard J. F.L., Wohlgemuth, Mariëlle, Frants, Rune R., Padberg, George W., Morava, Eva, van der Maarel, Silvère M.
Published in American journal of human genetics (01.12.2004)
Published in American journal of human genetics (01.12.2004)
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Journal Article
Possible phenotypic dosage effect in patients compound heterozygous for FSHD-sized 4q35 alleles
Wohlgemuth, M, Lemmers, R J, van der Kooi, E L, van der Wielen, M J, van Overveld, P G, Dauwerse, H, Bakker, E, Frants, R R, Padberg, G W, van der Maarel, S M
Published in Neurology (14.10.2003)
Published in Neurology (14.10.2003)
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Journal Article
Ocular myasthenia gravis: diagnosis often delayed
van den Berg, Bianca, Wohlgemuth, Mariëlle, Tijssen, Cees C
Published in Nederlands tijdschrift voor geneeskunde (2011)
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Published in Nederlands tijdschrift voor geneeskunde (2011)
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