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Results: 1-19 |
Results: 19
Incidental pregnancy in trauma patients
Authors: Bochicchio, GV Napolitano, LM Haan, J Champion, H Scalea, T
Citation: Gv. Bochicchio et al., Incidental pregnancy in trauma patients, J AM COLL S, 192(5), 2001, pp. 566-569
Dementia in hereditary cerebral hemorrhage with amyloidosis-Dutch type is associated with cerebral amyloid angiopathy but is independent of plaques and neurofibrillary tangles
Authors: Natte, R Maat-Schieman, MLC Haan, J Bornebroek, M Roos, RAC van Duinen, SG
Citation: R. Natte et al., Dementia in hereditary cerebral hemorrhage with amyloidosis-Dutch type is associated with cerebral amyloid angiopathy but is independent of plaques and neurofibrillary tangles, ANN NEUROL, 50(6), 2001, pp. 765-772
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
Cerebral microbleeds in CADASIL
Authors: Oberstein, SAJL van den Boom, R van Buchem, MA van Houwelingen, HC Bakker, E Vollebregt, E Ferrari, MD Breuning, MH Haan, J
Citation: Sajl. Oberstein et al., Cerebral microbleeds in CADASIL, NEUROLOGY, 57(6), 2001, pp. 1066-1070
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
Migraine aura, illusory vertical splitting, and Picasso
Authors: Ferrari, MD Haan, J
Citation: Md. Ferrari et J. Haan, Migraine aura, illusory vertical splitting, and Picasso, CEPHALALGIA, 20(8), 2000, pp. 686-686
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
Mahler's migraine
Authors: Haan, J Ferrari, MD
Citation: J. Haan et Md. Ferrari, Mahler's migraine, CEPHALALGIA, 20(4), 2000, pp. 254-254
Acetazolamide treatment for migraine aura status
Authors: Haan, J Sluis, P Sluis, LH Ferrari, MD
Citation: J. Haan et al., Acetazolamide treatment for migraine aura status, NEUROLOGY, 55(10), 2000, pp. 1588-1589
Idiopathic senile gait disorders are signs of subclinical disease
Authors: Bloem, BR Gussekloo, J Lagaay, AM Remarque, EJ Haan, J Westendorp, RGJ
Citation: Br. Bloem et al., Idiopathic senile gait disorders are signs of subclinical disease, J AM GER SO, 48(9), 2000, pp. 1098-1101
Genetics of primary headaches
Authors: Kors, EE Haan, J Ferrari, MD
Citation: Ee. Kors et al., Genetics of primary headaches, CURR OP NEU, 12(3), 1999, pp. 249-254
Hereditary cerebral hemorrhage with amyloidosis - Dutch type (HCHWA-D): a review of the variety in phenotypic expression
Authors: Bornebroek, M Haan, J Roos, RAC
Citation: M. Bornebroek et al., Hereditary cerebral hemorrhage with amyloidosis - Dutch type (HCHWA-D): a review of the variety in phenotypic expression, AMYLOID, 6(3), 1999, pp. 215-224
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
Blood damage, platelet and clotting activation during application of radiofrequency or cryoablation catheters: A comparative in vitro study
Authors: van Oeveren, W Crijns, HJGM Korteling, BJ Wegereef, EW Haan, J Tigchelaar, I Hoekstra, A
Citation: W. Van Oeveren et al., Blood damage, platelet and clotting activation during application of radiofrequency or cryoablation catheters: A comparative in vitro study, J MED EN TE, 23(1), 1999, pp. 20-25
Fluorescence labeling to study platelet and leucocyte deposition onto vascular grafts in vitro
Authors: Toes, GJ van den Dungen, JJAM Haan, J Hermens, RAEC van Oeveren, W
Citation: Gj. Toes et al., Fluorescence labeling to study platelet and leucocyte deposition onto vascular grafts in vitro, BIOMATERIAL, 20(20), 1999, pp. 1951-1958
Diagnostic Notch3 sequence analysis in CADASIL: Three new mutations in Dutch patients
Authors: Oberstein, SAJL Ferrari, MD Bakker, E van Gestel, J Kneppers, ALJ Frants, RR Breuning, MH Haan, J
Citation: Sajl. Oberstein et al., Diagnostic Notch3 sequence analysis in CADASIL: Three new mutations in Dutch patients, NEUROLOGY, 52(9), 1999, pp. 1913-1915
Sleep disturbance in spinocerebellar ataxias - Is the SCA3 mutation a cause of restless legs syndrome?
Authors: Schols, L Haan, J Riess, O Amoiridis, G Przuntek, H
Citation: L. Schols et al., Sleep disturbance in spinocerebellar ataxias - Is the SCA3 mutation a cause of restless legs syndrome?, NEUROLOGY, 51(6), 1998, pp. 1603-1607
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: 1-19 |