Search Results - "Vandereyken, W"

A Novel Splicing Mutation in KCNQ2 in a Multigenerational Family with BFNC Followed for 25 Years by De Haan, Gerrit‐Jan, Pinto, Dalila, Carton, Dietbrandt, Bader, Adri, Witte, Jorien, Peters, Edith, Van Erp, Gerard, Vandereyken, Willem, Boezeman, Eduard, Wapenaar, Martin C., Boon, Paul, Halley, Dicky, Koeleman, Bobby P. C., Lindhout, Dick

“…Purpose: A large multigenerational family with benign familial neonatal convulsions (BFNC) was revisited to identify the disease‐causing mutation and to assess…”
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Gene symbol: KCNQ2. Disease: Benign neonatal familial convulsion by Pinto, D, de Haan, G-J, Carton, D, Bader, A, Witte, J, Peters, E, van Erp, M G, Vandereyken, W, Boezeman, E H J F, Boon, P, Halley, D J J, Koeleman, B P C, Lindhout, D

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Radiological work-up of primary malignant bone tumours by Taconis, W K, van der Eyken, J W

“…2 cases with primary malignant bone tumour - 1 with osteosarcoma in the distal femur and 1 with chondrosarcoma in the proximal humerus - are described in which…”
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