Follow up of patients with signs and symptoms of polyneuropathy not confirmed by electrophysiological studies

di Rosenberg, N, Slotema, C, Hoogendijk, J, Vermeulen, M
Pubblicazione 2005

Isolation and nucleotide sequence of the methanol dehydrogenase structural gene from Paracoccus denitrificans.

di Harms, N, de Vries, G E, Maurer, K, Hoogendijk, J, Stouthamer, A H
Pubblicazione 1987

Absence of characteristic features in two patients with inclusion body myositis

di van der Meulen, M F G, Hoogendijk, J, Jansen, G, Veldman, H, Wokke, J
Pubblicazione 1998

Late onset axonal Charcot‐Marie‐Tooth phenotype caused by a novel myelin protein zero mutation

di Bienfait, H M E, Faber, C G, Baas, F, Gabreëls‐Festen, A A W M, Koelman, J H T M, Hoogendijk, J E, Verschuuren, J J, Wokke, J H J, de Visser, M
Pubblicazione 2006

Long‐term outcome in polymyositis and dermatomyositis

di Bronner, I M, van der Meulen, M F G, de Visser, M, Kalmijn, S, van Venrooij, W J, Voskuyl, A E, Dinant, H J, Linssen, W H J P, Wokke, J H J, Hoogendijk, J E
Pubblicazione 2006

Recurrent and founder mutations in the Netherlands: the cardiac phenotype of DES founder mutations p.S13F and p.N342D

di van Spaendonck-Zwarts, K. Y., van der Kooi, A. J., van den Berg, M. P., Ippel, E. F., Boven, L. G., Yee, W.-C., van den Wijngaard, A., Brusse, E., Hoogendijk, J. E., Doevendans, P. A., de Visser, M., Jongbloed, J. D. H., van Tintelen, J. P.
Pubblicazione 2012