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Results: 1-8 |
Results: 8
Delayed cerebral edema and fatal coma after minor head trauma: Role of theCACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraine
Authors: Kors, EE Terwindt, GM Vermeulen, FLMG Fitzsimons, RB Jardine, PE Heywood, P Love, S van den Maagdenberg, AMJM Haan, J Frants, RR Ferrari, MD
Citation: Ee. Kors et al., Delayed cerebral edema and fatal coma after minor head trauma: Role of theCACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraine, ANN NEUROL, 49(6), 2001, pp. 753-760
Involvement of the CACNA1A gene containing region on 19p13 in migraine with and without aura
Authors: Terwindt, GM Ophoff, RA van Eijk, R Vergouwe, MN Haan, J Frants, RR Sandkuijl, LA Ferrari, MD
Citation: Gm. Terwindt et al., Involvement of the CACNA1A gene containing region on 19p13 in migraine with and without aura, NEUROLOGY, 56(8), 2001, pp. 1028-1032
Hereditary vascular retinopathy, cerebroretinal vasculopathy, and hereditary endotheliopathy with retinopathy, nephropathy, and stroke map to a single locus on chromosome 3p21.1-p21.3
Authors: Ophoff, RA DeYoung, J Service, SK Joose, M Caffo, NA Sandkuijl, LA Terwindt, GM Haan, J van den Maagdenberg, AMJM Jen, J Baloh, RW Barilla-LaBarca, ML Saccone, NL Atkinson, JP Ferrari, MD Freimer, NB Frants, RR
Citation: Ra. Ophoff et al., Hereditary vascular retinopathy, cerebroretinal vasculopathy, and hereditary endotheliopathy with retinopathy, nephropathy, and stroke map to a single locus on chromosome 3p21.1-p21.3, AM J HU GEN, 69(2), 2001, pp. 447-453
Alternating hemiplegia of childhood: no mutations in the familial hemiplegic migraine CACNA1A gene
Authors: Haan, J Kors, EE Terwindt, GM Vermeulen, FLMG Vergouwe, MN van den Maagdenberg, AMJM Gill, DS Pascual, J Ophoff, RA Frants, RR Ferrari, MD
Citation: J. Haan et al., Alternating hemiplegia of childhood: no mutations in the familial hemiplegic migraine CACNA1A gene, CEPHALALGIA, 20(8), 2000, pp. 696-700
The impact of migraine on quality of life in the general population - The GEM study
Authors: Terwindt, GM Ferrari, MD Tijhuis, M Groenen, SMA Picavet, HSJ Launer, LJ
Citation: Gm. Terwindt et al., The impact of migraine on quality of life in the general population - The GEM study, NEUROLOGY, 55(5), 2000, pp. 624-629
Search for mitochondrial DNA mutations in migraine subgroups
Authors: Haan, J Terwindt, GM Maassen, JA 't Hart, LM Frants, RR Ferrari, MD
Citation: J. Haan et al., Search for mitochondrial DNA mutations in migraine subgroups, CEPHALALGIA, 19(1), 1999, pp. 20-22
The prevalence and characteristics of migraine in a population-based cohort - The GEM Study
Authors: Launer, LJ Terwindt, GM Ferrari, MD
Citation: Lj. Launer et al., The prevalence and characteristics of migraine in a population-based cohort - The GEM Study, NEUROLOGY, 53(3), 1999, pp. 537-542
Prothrombotic mutations and ischaemic stroke at a young age in two sisters
Authors: Haan, J Schoonman, GG Terwindt, GM Ferrari, MD Bertina, RM Kappelle, LJ Haan, J
Citation: J. Haan et al., Prothrombotic mutations and ischaemic stroke at a young age in two sisters, J NE NE PSY, 65(6), 1998, pp. 958-959
Risultati: 1-8 |