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41.
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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
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42.
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44.
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Plasma lipoproteins in familial dysbetalipoproteinemia associated with apolipoproteins E2(Arg158-->Cys), E3-Leiden, and E2(Lys146-->Gln), and effects of treatment with simvastatin. [electronic resource] by
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- Smelt, A H
- Van den Maagdenberg, A M
- Van Tol, A
- Vroom, T F
- Gevers Leuven, J A
- Frants, R R
- Havekes, L M
- Van der Laarse, A
- Van 't Hooft, F M
Producer: 19941220
In:
Arteriosclerosis and thrombosis : a journal of vascular biology vol. 14
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45.
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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
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46.
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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
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47.
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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
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48.
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The 3p21.1-p21.3 hereditary vascular retinopathy locus increases the risk for Raynaud's phenomenon and migraine. [electronic resource] by
- Hottenga, J J
- Vanmolkot, K R J
- Kors, E E
- Kheradmand Kia, S
- de Jong, P T V M
- Haan, J
- Terwindt, G M
- Frants, R R
- Ferrari, M D
- van den Maagdenberg, A M J M
Producer: 20060123
In:
Cephalalgia : an international journal of headache vol. 25
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49.
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Alternating hemiplegia of childhood: no mutations in the second familial hemiplegic migraine gene ATP1A2. [electronic resource] by
- Kors, E E
- Vanmolkot, K R J
- Haan, J
- Kheradmand Kia, S
- Stroink, H
- Laan, L A E M
- Gill, D S
- Pascual, J
- van den Maagdenberg, A M J M
- Frants, R R
- Ferrari, M D
Producer: 20050210
In:
Neuropediatrics vol. 35
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50.
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Increased noise level of purkinje cell activities minimizes impact of their modulation during sensorimotor control. [electronic resource] by
- Hoebeek, F E
- Stahl, J S
- van Alphen, A M
- Schonewille, M
- Luo, C
- Rutteman, M
- van den Maagdenberg, A M J M
- Molenaar, P C
- Goossens, H H L M
- Frens, M A
- De Zeeuw, C I
Producer: 20050519
In:
Neuron vol. 45
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51.
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TREX1 gene variant in neuropsychiatric systemic lupus erythematosus. [electronic resource] by
- de Vries, B
- Steup-Beekman, G M
- Haan, J
- Bollen, E L
- Luyendijk, J
- Frants, R R
- Terwindt, G M
- van Buchem, M A
- Huizinga, T W J
- van den Maagdenberg, A M J M
- Ferrari, M D
Producer: 20101015
In:
Annals of the rheumatic diseases vol. 69
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52.
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Gene dosage-dependent transmitter release changes at neuromuscular synapses of CACNA1A R192Q knockin mice are non-progressive and do not lead to morphological changes or muscle weakness. [electronic resource] by
- Kaja, S
- van de Ven, R C G
- Broos, L A M
- Veldman, H
- van Dijk, J G
- Verschuuren, J J G M
- Frants, R R
- Ferrari, M D
- van den Maagdenberg, A M J M
- Plomp, J J
Producer: 20051201
In:
Neuroscience vol. 135
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53.
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First mutation in the voltage-gated Nav1.1 subunit gene SCN1A with co-occurring familial hemiplegic migraine and epilepsy. [electronic resource] by
- Castro, M-J
- Stam, A H
- Lemos, C
- de Vries, B
- Vanmolkot, K R J
- Barros, J
- Terwindt, G M
- Frants, R R
- Sequeiros, J
- Ferrari, M D
- Pereira-Monteiro, J M
- van den Maagdenberg, A M J M
Producer: 20090430
In:
Cephalalgia : an international journal of headache vol. 29
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54.
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CACNA1A mutation linking hemiplegic migraine and alternating hemiplegia of childhood. [electronic resource] by
- de Vries, B
- Stam, A H
- Beker, F
- van den Maagdenberg, A M J M
- Vanmolkot, K R J
- Laan, Laem
- Ginjaar, I B
- Frants, R R
- Lauffer, H
- Haan, J
- Haas, J P
- Terwindt, G M
- Ferrari, M D
Producer: 20080916
In:
Cephalalgia : an international journal of headache vol. 28
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55.
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Episodic ataxia type 2. Three novel truncating mutations and one novel missense mutation in the CACNA1A gene. [electronic resource] by
- van den Maagdenberg, A M J M
- Kors, E E
- Brunt, E R
- van Paesschen, W
- Pascual, J
- Ravine, D
- Keeling, S
- Vanmolkot, K R J
- Vermeulen, F L M G
- Terwindt, G M
- Haan, J
- Frants, R R
- Ferrari, M D
Producer: 20030410
In:
Journal of neurology vol. 249
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56.
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Shared genetic factors in migraine and depression: evidence from a genetic isolate. [electronic resource] by
- Stam, A H
- de Vries, B
- Janssens, A C J W
- Vanmolkot, K R J
- Aulchenko, Y S
- Henneman, P
- Oostra, B A
- Frants, R R
- van den Maagdenberg, A M J M
- Ferrari, M D
- van Duijn, C M
- Terwindt, G M
Producer: 20100219
In:
Neurology vol. 74
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57.
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Two novel functional mutations in the Na+,K+-ATPase alpha2-subunit ATP1A2 gene in patients with familial hemiplegic migraine and associated neurological phenotypes. [electronic resource] by
- Castro, M-J
- Nunes, B
- de Vries, B
- Lemos, C
- Vanmolkot, K R J
- van den Heuvel, J J M W
- Temudo, T
- Barros, J
- Sequeiros, J
- Frants, R R
- Koenderink, J B
- Pereira-Monteiro, J M
- van den Maagdenberg, A M J M
Producer: 20080229
In:
Clinical genetics vol. 73
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58.
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Systemic features of retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations: a monogenic small vessel disease. [electronic resource] by
- Pelzer, N
- Hoogeveen, E S
- Haan, J
- Bunnik, R
- Poot, C C
- van Zwet, E W
- Inderson, A
- Fogteloo, A J
- Reinders, M E J
- Middelkoop, H A M
- Kruit, M C
- van den Maagdenberg, A M J M
- Ferrari, M D
- Terwindt, G M
Producer: 20200316
In:
Journal of internal medicine vol. 285
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59.
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CACNA1A R1347Q: a frequent recurrent mutation in hemiplegic migraine. [electronic resource] by
- Stam, A H
- Vanmolkot, K R J
- Kremer, H P H
- Gärtner, J
- Brown, J
- Leshinsky-Silver, E
- Gilad, R
- Kors, E E
- Frankhuizen, W S
- Ginjaar, H B
- Haan, J
- Frants, R R
- Ferrari, M D
- van den Maagdenberg, A M J M
- Terwindt, G M
Producer: 20081215
In:
Clinical genetics vol. 74
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60.
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Systematic analysis of three FHM genes in 39 sporadic patients with hemiplegic migraine. [electronic resource] by
- de Vries, B
- Freilinger, T
- Vanmolkot, K R J
- Koenderink, J B
- Stam, A H
- Terwindt, G M
- Babini, E
- van den Boogerd, E H
- van den Heuvel, J J M W
- Frants, R R
- Haan, J
- Pusch, M
- van den Maagdenberg, A M J M
- Ferrari, M D
- Dichgans, M
Producer: 20071214
In:
Neurology vol. 69
Availability: No items available.
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