Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4 von Ophoff, R A, Terwindt, G M, Vergouwe, M N, van Eijk, R, Oefner, P J, Hoffman, S M, Lamerdin, J E, Mohrenweiser, H W, Bulman, D E, Ferrari, M, Haan, J, Lindhout, D, van Ommen, G J, Hofker, M H, Ferrari, M D, Frants, R R

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Involvement of the CACNA1A gene containing region on 19p13 in migraine with and without aura von TERWINDT, G. M, OPHOFF, R. A, VAN EIJK, R, VERGOUWE, M. N, HAAN, J, FRANTS, R. R, SANDKUIJL, L. A, FERRARI, M. D

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Hyperekplexia phenotype due to compound heterozygosity for GLRA1 gene mutations von Vergouwe, M. N., Tijssen, M. A. J., Peters, A. C. B., Wielaard, R., Frants, R. R.

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Variable clinical expression of mutations in the P/Q-type calcium channel gene in familial hemiplegic migraine von TERWINDT, G. M, OPHOFF, R. A, HAAN, J, VERGOUWE, M. N, VAN EIJK, R, FRANTS, R. R, FERRARI, M. D

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5-HT1B Receptor Polymorphism and Clinical Response to Sumatriptan von MaassenVanDenBrink, Antoinette, Vergouwe, Monique N., Ophoff, Roel A., Saxena, Pramod R., Ferrari, Michel D., Frants, Rune R.

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Assignment of the porcine loci for MYOD1 to chromosome 2 and MYF5 to chromosome 5 von Soumillion, A, Vergouwe, M N, Erkens, J H F, Te Pas, M F W, Rettenberger, G, Lenstra, J A

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Hyperekplexia-like syndromes without mutations in the GLRA1 gene von Vergouwe, M.N., Tijssen, M.A.J., Shiang, R., van Dijk, J.G., Shahwan, Saad Al, Ophoff, R.A., Frants, R.R.

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Hematopoietic NF-κB1 deficiency results in small atherosclerotic lesions with an inflammatory phenotype von Kanters, Edwin, Gijbels, Marion J.J., van der Made, Ingeborg, Vergouwe, Monique N., Heeringa, Peter, Kraal, Georg, Hofker, Marten H., de Winther, Menno P.J.

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Abnormal transmitter release at neuromuscular junctions of mice carrying the tottering alpha(1A) Ca(2+) channel mutation von Plomp, J J, Vergouwe, M N, Van den Maagdenberg, A M, Ferrari, M D, Frants, R R, Molenaar, P C

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Involvement of a Ca2+ channel gene in familial hemiplegic migraine and migraine with and without aura von OPHOFF, R. A, TERWINDT, G. M, VERGOUWE, M. N, FRANTS, R. R, FERRARI, M. D

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Health outcomes and cost-effectiveness of monoclonal SARS-CoV-2 antibodies as pre-exposure prophylaxis von Popping, S., Nichols, B.E., Appelman, B., Biemond, J.J., Vergouwe, M., Rosendaal, F.R., Valk, M. van der, Bree, G.J. de, Wiersinga, W.J., Birnie, E.

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Major and minor form of hereditary hyperekplexia von Tijssen, Marina A.J., Vergouwe, Monique N., van Dijk, J. Gert, Rees, Michelle, Frants, Rune R., Brown, Peter

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Alternating Hemiplegia of Childhood: No Mutations in the Familial Hemiplegic Migraine CACNA1A Gene von Haan, J, Kors, EE, Terwindt, GM, Vermeulen, FLMG, Vergouwe, MN, van den Maagdenberg, AMJM, Gill, DS, Pascual, J, Ophoff, RA, Frants, RR, Ferrari, MD

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Abnormal transmitter release at neuromuscular junctions of mice carrying the tottering α1A Ca2+ channel mutation von Plomp, Jaap J., Vergouwe, Monique N., Van den Maagdenberg, Arn M., Ferrari, Michel D., Frants, Rune R., Molenaar, Peter C.

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Chromosomal localization of the 5-HT1F receptor gene: No evidence for involvement in response to sumatriptan in migraine patients von VanDenBrink, Antoinette Maassen, Vergouwe, Monique N., Ophoff, Roel A., Naylor, Susan L., Dauwerse, Hans G., Saxena, Pramod R., Ferrari, Michel D., Frants, Rune R.

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Abnormal transmitter release at neuromuscular junctions of mice carrying the tottering alpha sub(1A) Ca super(2+) channel mutation von Plomp, J J, Vergouwe, M N, Van den Maagdenberg, AM, Ferrari, MD, Frants, R R, Molenaar, P C

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Variable clinical expression of mutations in the P/Q-type calcium channel gene in familial hemiplegic migraine. Dutch Migraine Genetics Research Group von Terwindt, G M, Ophoff, R A, Haan, J, Vergouwe, M N, van Eijk, R, Frants, R R, Ferrari, M D

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Wolff Award 1997. Involvement of a Ca2+ channel gene in familial hemiplegic migraine and migraine with and without aura. Dutch Migraine Genetics Research Group von Ophoff, R A, Terwindt, G M, Vergouwe, M N, Frants, R R, Ferrari, M D

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Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca super(2+) channel gene CACNL1A4 von Ophoff, R A, Terwindt, G M, Vergouwe, M N, Van Eijk, R, Oefner, P J, Hoffman, SMG, Lamerdin, JE, Mohrenweiser, H W

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A 3-Mb region for the familial hemiplegic migraine locus on 19p13.1-p13.2: exclusion of PRKCSH as a candidate gene. Dutch Migraine Genetic Research Group von Ophoff, R A, Terwindt, G M, Vergouwe, M N, van Eijk, R, Mohrenweiser, H, Litt, M, Hofker, M H, Haan, J, Ferrari, M D, Frants, R R

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