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Annals of Neurology|April 14, 2016
Mutation-specific effects on thin filament length in thin filament myopathyJosine M de Winter, Barbara Joureau, Eun-Jeong Lee, et al.
British Journal of Cancer|June 26, 2018
Ovarian stimulation for IVF and risk of primary breast cancer in BRCA1/2 mutation carriersInge A P Derks-Smeets, Lieske H Schrijver, Christine E M de Die-Smulders, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|August 3, 2024
Development of thresholds and a visualization tool for use of a blood test in routine clinical dementia practiceInge M W Verberk, Jolien Jutte, Maurice Y Kingma, et al.
Contact Dermatitis|February 21, 2013
Results of a cosmetovigilance survey in The NetherlandsJoanne G W Salverda, Peter J C Bragt, Lianne de Wit-Bos, et al.
Orphanet Journal of Rare Diseases|November 14, 2012
Clinical features and predictors for disease natural progression in adults with Pompe disease: a nationwide prospective observational studyNadine A M E van der Beek, Juna M de Vries, Marloes L C Hagemans, et al.
Human Molecular Genetics|September 27, 2014
Inter-individual differences in CpG methylation at D4Z4 correlate with clinical variability in FSHD1 and FSHD2Richard J L F Lemmers, Jelle J Goeman, Patrick J van der Vliet, et al.
Neurology|July 8, 2018
FSHD type 2 and Bosma arhinia microphthalmia syndrome: Two faces of the same mutationKarlien Mul, Richard J L F Lemmers, Marjolein Kriek, et al.
Brain : a Journal of Neurology|September 13, 2023
Autosomal dominant in cis D4Z4 repeat array duplication alleles in facioscapulohumeral dystrophyRichard J L F Lemmers, Russell Butterfield, Patrick J van der Vliet, et al.
Brain Communications|June 9, 2025
Differentiating sporadic frontotemporal dementia from late-onset primary psychiatric disordersSterre C M de Boer, Lina Riedl, Simon Braak, et al.
Journal of Hepatology|July 24, 2017
Hepatitis E virus infection and acute non-traumatic neurological injury: A prospective multicentre studyHarry R Dalton, Jeroen J J van Eijk, Pascal Cintas, et al.
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