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Neurology|August 28, 2002
Clinical and genetic heterogeneity in benign hereditary choreaG J Breedveld, A K Percy, M E MacDonald, et al.
Neurology|April 28, 2012
Cognitive outcome of patients with classic infantile Pompe disease receiving enzyme therapyB J Ebbink, F K Aarsen, C M van Gelder, et al.
Clinical and Experimental Immunology|March 26, 2003
Immunoglobulins in children with epilepsy: the Dutch Study of Epilepsy in ChildhoodP M C Callenbach, C M Jol-Van Der Zijde, A T Geerts, et al.
Neuromuscular Disorders : NMD|May 30, 2008
Eight years experience with enzyme replacement therapy in two children and one adult with Pompe diseaseC I van Capelle, L P F Winkel, M L C Hagemans, et al.
Neurology|October 22, 2008
Cerebellar leukoencephalopathy: most likely histiocytosis-relatedM S van der Knaap, W F M Arts, J Y Garbern, et al.
Neuromuscular Disorders : NMD|September 7, 2010
Effect of enzyme therapy in juvenile patients with Pompe disease: a three-year open-label studyC I van Capelle, N A M E van der Beek, M L C Hagemans, et al.
Neurogenetics|January 22, 2013
Clinical and genetic aspects of PCDH19-related epilepsy syndromes and the possible role of PCDH19 mutations in males with autism spectrum disordersJ J T van Harssel, S Weckhuysen, M J A van Kempen, et al.
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