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Childhood epilepsy, familial hemiplegic migraine, cerebellar ataxia, and a new CACNA1A mutation. [electronic resource] by
- Kors, E E
- Melberg, A
- Vanmolkot, K R J
- Kumlien, E
- Haan, J
- Raininko, R
- Flink, R
- Ginjaar, H B
- Frants, R R
- Ferrari, M D
- van den Maagdenberg, A M J M
Producer: 20050518
In:
Neurology vol. 63
Availability: No items available.
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16.
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Animal models of migraine: looking at the component parts of a complex disorder. [electronic resource] by
- Bergerot, A
- Holland, P R
- Akerman, S
- Bartsch, T
- Ahn, A H
- MaassenVanDenBrink, A
- Reuter, U
- Tassorelli, C
- Schoenen, J
- Mitsikostas, D D
- van den Maagdenberg, A M J M
- Goadsby, P J
Producer: 20070105
In:
The European journal of neuroscience vol. 24
Availability: No items available.
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Expanding the phenotypic spectrum of the CACNA1A gene T666M mutation: a description of 5 families with familial hemiplegic migraine. [electronic resource] 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
Producer: 20030612
In:
Archives of neurology vol. 60
Availability: No items available.
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19.
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A novel missense ATP1A2 mutation in a Finnish family with familial hemiplegic migraine type 2. [electronic resource] by
- Kaunisto, M A
- Harno, H
- Vanmolkot, K R J
- Gargus, J J
- Sun, G
- Hämäläinen, E
- Liukkonen, E
- Kallela, M
- van den Maagdenberg, A M J M
- Frants, R R
- Färkkilä, M
- Palotie, A
- Wessman, M
Producer: 20040924
In:
Neurogenetics vol. 5
Availability: No items available.
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20.
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Alternating hemiplegia of childhood: no mutations in the glutamate transporter EAAT1. [electronic resource] by
- de Vries, B
- Haan, J
- Stam, A H
- Vanmolkot, K R J
- Stroink, H
- Laan, L A E M
- Gill, D S
- Pascual, J
- Frants, R R
- van den Maagdenberg, A M J M
- Ferrari, M D
Producer: 20070321
In:
Neuropediatrics vol. 37
Availability: No items available.
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