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Results: 1-14 |
Results: 14
VARIABLE CLINICAL EXPRESSION OF MUTATIONS IN THE P Q-TYPE CALCIUM-CHANNEL GENE IN FAMILIAL HEMIPLEGIC MIGRAINE/
Authors: TERWINDT GM OPHOFF RA HAAN J VERGOUWE MN VANEIJK R FRANTS RR FERRARI MD
Citation: Gm. Terwindt et al., VARIABLE CLINICAL EXPRESSION OF MUTATIONS IN THE P Q-TYPE CALCIUM-CHANNEL GENE IN FAMILIAL HEMIPLEGIC MIGRAINE/, Neurology, 50(4), 1998, pp. 1105-1111
BRCA1 GENOMIC DELETIONS ARE MAJOR FOUNDER MUTATIONS IN DUTCH BREAST-CANCER PATIENTS (VOL 17, PG 341, 1997)
Authors: PETRIJBOSCH A PEELEN T VANVLIET M VANEIJK R OLMER R DRUSEDAU M HOGERVORST FBL HAGEMAN S ARTS PJW LIGTENBERG MJL MEIJERSHEIJBOER H KLIJN JGM VASEN HFA CORNELISSE CJ VANTVEER LJ BAKKER E VANOMMEN GJ DEVILEE P
Citation: A. Petrijbosch et al., BRCA1 GENOMIC DELETIONS ARE MAJOR FOUNDER MUTATIONS IN DUTCH BREAST-CANCER PATIENTS (VOL 17, PG 341, 1997), Nature genetics, 17(4), 1997, pp. 503-503
BRCA1 GENOMIC DELETIONS ARE MAJOR FOUNDER MUTATIONS IN DUTCH BREAST-CANCER PATIENTS
Authors: PETRIJBOSCH A PEELEN T VANVLIET M VANEIJK R OLMER R DRUSEDAU M HOGERVORST FBL HAGEMAN S ARTS PJW LIGTENBERG MJL MEIJERSHEIJBOER H KLIJN JGM VASEN HFA CORNELISSE CJ VANTVEER LJ BAKKER E VANOMMEN GJB DEVILEE P
Citation: A. Petrijbosch et al., BRCA1 GENOMIC DELETIONS ARE MAJOR FOUNDER MUTATIONS IN DUTCH BREAST-CANCER PATIENTS, Nature genetics, 17(3), 1997, pp. 341-345
LARGE GENOMIC DELETIONS IN BRCA1 AS MAJOR FOUNDER MUTATIONS AMONG DUTCH BREAST-CANCER FAMILIES
Authors: PEELEN T PETRIJBOSCH A VANVIET M VANEIJK R HOGERVORST F LIGTENBERG M MEIJERSHEIJBOER H KLIJN JGM VASEN HFA VANVEER L BAKKER E VANOMMEN GJB DEVILEE P
Citation: T. Peelen et al., LARGE GENOMIC DELETIONS IN BRCA1 AS MAJOR FOUNDER MUTATIONS AMONG DUTCH BREAST-CANCER FAMILIES, American journal of human genetics, 61(4), 1997, pp. 65-65
A 3-MB REGION FOR THE FAMILIAL HEMIPLEGIC MIGRAINE LOCUS ON 19P13.1-P13.2 - EXCLUSION OF PRKCSH AS A CANDIDATE GENE
Authors: OPHOFF RA TERWINDT GM VERGOUWE MN VANEIJK R MOHRENWEISER H LITT M HOFKER MH HAAN J FERRARI MD FRANTS RR
Citation: Ra. Ophoff et al., A 3-MB REGION FOR THE FAMILIAL HEMIPLEGIC MIGRAINE LOCUS ON 19P13.1-P13.2 - EXCLUSION OF PRKCSH AS A CANDIDATE GENE, European journal of human genetics, 4(6), 1996, pp. 321-328
DOES CONTEXT DISCRIMINATE RECOLLECTION FROM FAMILIARITY IN RECOGNITION MEMORY
Authors: PERFECT TJ MAYES AR DOWNES JJ VANEIJK R
Citation: Tj. Perfect et al., DOES CONTEXT DISCRIMINATE RECOLLECTION FROM FAMILIARITY IN RECOGNITION MEMORY, The Quarterly journal of experimental psychology. A, Human experimental psychology, 49(3), 1996, pp. 797-813
ACCURACY AND QUANTITY ARE POOR MEASURES OF RECALL AND RECOGNITION
Authors: MAYES AR VANEIJK R GOODING PL
Citation: Ar. Mayes et al., ACCURACY AND QUANTITY ARE POOR MEASURES OF RECALL AND RECOGNITION, Behavioral and brain sciences, 19(2), 1996, pp. 201-202
FAMILIAL HEMIPLEGIC MIGRAINE AND EPISODIC ATAXIA TYPE-2 ARE CAUSED BYMUTATIONS IN THE CA2+ CHANNEL GENE CACNL1A4
Authors: OPHOFF RA TERWINDT GM VERGOUWE MN VANEIJK R OEFNER PJ HOFFMAN SMG LAMERDIN JE MOHRENWEISER HW BULMAN DE FERRARI M HAAN J LINDHOUT D VANOMMEN GJB HOFKER MH FERRARI MD FRANTS RR
Citation: Ra. Ophoff et al., FAMILIAL HEMIPLEGIC MIGRAINE AND EPISODIC ATAXIA TYPE-2 ARE CAUSED BYMUTATIONS IN THE CA2+ CHANNEL GENE CACNL1A4, Cell, 87(3), 1996, pp. 543-552
FAMILIAL HEMIPLEGIC MIGRAINE LOCUS ON 19P13 IS INVOLVED IN THE COMMONFORMS OF MIGRAINE WITH AND WITHOUT AURA
Authors: MAY A OPHOFF RA TERWINDT GM URBAN C VANEIJK R HAAN J DIENER HC LINDHOUT D FRANTS RR SANDKUIJL LA FERRARI MD
Citation: A. May et al., FAMILIAL HEMIPLEGIC MIGRAINE LOCUS ON 19P13 IS INVOLVED IN THE COMMONFORMS OF MIGRAINE WITH AND WITHOUT AURA, Human genetics, 96(5), 1995, pp. 604-608
MUTATION IN DHP RECEPTOR ALPHA-1 SUBUNIT (CACLN1A3) GENE IN A DUTCH FAMILY WITH HYPOKALEMIC PERIODIC PARALYSIS
Authors: BOERMAN RH OPHOFF RA LINKS TP VANEIJK R SANDKUIJL LA ELBAZ A VALESANTOS JE WINTZEN AR VANDEUTEKOM JC ISLES DE FONTAINE B PADBERG GW FRANTS RR
Citation: Rh. Boerman et al., MUTATION IN DHP RECEPTOR ALPHA-1 SUBUNIT (CACLN1A3) GENE IN A DUTCH FAMILY WITH HYPOKALEMIC PERIODIC PARALYSIS, Journal of Medical Genetics, 32(1), 1995, pp. 44-47
GENE FOR FAMILIAL HEMIPLEGIC MIGRAINE ON CHROMOSOME 19P13
Authors: OPHOFF RA TERWINDT GM VANEIJK R VERGOUWE M HOFKER MH HAAN J HOFFMAN S MOHRENWEISER H FERRARI MD FRANTS RR
Citation: Ra. Ophoff et al., GENE FOR FAMILIAL HEMIPLEGIC MIGRAINE ON CHROMOSOME 19P13, American journal of human genetics, 57(4), 1995, pp. 1284-1284
GENETIC-HETEROGENEITY OF FAMILIAL HEMIPLEGIC MIGRAINE
Authors: OPHOFF RA VANEIJK R SANDKUIJL LA TERWINDT GM GRUBBEN CPM HAAN J LINDHOUT D FERRARI MD FRANTS RR
Citation: Ra. Ophoff et al., GENETIC-HETEROGENEITY OF FAMILIAL HEMIPLEGIC MIGRAINE, Genomics, 22(1), 1994, pp. 21-26
CHROMOSOME 4 LOCALIZATION OF A 2ND GENE FOR AUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY-DISEASE
Authors: PETERS DJM SPRUIT L SARIS JJ RAVINE D SANDKUIJL LA FOSSDAL R BOERSMA J VANEIJK R NORBY S CONSTANTINOUDELTAS CD PIERIDES A BRISSENDEN JE FRANTS RR VANOMMEN GJB BREUNING MH
Citation: Djm. Peters et al., CHROMOSOME 4 LOCALIZATION OF A 2ND GENE FOR AUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY-DISEASE, Nature genetics, 5(4), 1993, pp. 359-362
PRESERVED PATTERN COMPLETION PRIMING FOR NOVEL, ABSTRACT GEOMETRIC SHAPES IN AMNESICS OF SEVERAL ETIOLOGIES
Authors: GOODING PA VANEIJK R MAYES AR MEUDELL P
Citation: Pa. Gooding et al., PRESERVED PATTERN COMPLETION PRIMING FOR NOVEL, ABSTRACT GEOMETRIC SHAPES IN AMNESICS OF SEVERAL ETIOLOGIES, Neuropsychologia, 31(8), 1993, pp. 789-810
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