Search Results - "Vermeulen, M. F. J."

Expanding the phenotypic spectrum of the CACNA1A gene T666M mutation: a description of 5 families with familial hemiplegic migraine by Kors, E E, Haan, J, Giffin, N J, Pazdera, L, Schnittger, C, Lennox, G G, Terwindt, G M, Vermeulen, F L M J, Van den Maagdenberg, A M J M, Frants, R R, Ferrari, M D

“…Familial hemiplegic migraine (FHM) is a rare autosomal dominant subtype of migraine with aura. Missense mutations in the chromosome 19 CACNA1A calcium channel…”
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Interceptive treatment of maxillary hypoplasia with the use of bone anchors. A review of the literature by Vermeulen, F M J, De Clerck, H J, van Beek, H, Becking, A G

“…A Class III malocclusion is mainly caused by a hypoplastic maxilla and therefore the treatment is principally aimed at stimulating the growth of the maxilla…”
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Parallel plate Transmission Line Transformer by Voeten, S. J., Vermeulen, M. F. J., Brussaard, G. J. H., Pemen, A. J. M.

“…A Transmission Line Transformer (TLT) can be used to transform high-voltage nanosecond pulses. These transformers rely on the fact that the length of the pulse…”
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Awake daytime oximetry measurements in the management of infants with chronic lung disease by Weening, MJ VERMEULEN, FT, Battistutta, D, Masters, IB

“…Objective: To assess the value of 1‐h daytime awake oximetry as a means of weaning oxygen flows in infants with oxygen dependent chronic lung disease. Methods:…”
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