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Results: 1-25 | 26-28
Results: 1-25/28
P Q-TYPE CA2+ CHANNEL DEFECTS IN MIGRAINE, ATAXIA AND EPILEPSY/
Authors: OPHOFF RA TERWINDT GM FRANTS RR FERRARI MD
Citation: Ra. Ophoff et al., P Q-TYPE CA2+ CHANNEL DEFECTS IN MIGRAINE, ATAXIA AND EPILEPSY/, Trends in pharmacological sciences, 19(4), 1998, pp. 121-127
MIGRAINE, ATAXIA AND EPILEPSY - A CHALLENGING SPECTRUM OF GENETICALLY-DETERMINED CALCIUM CHANNELOPATHIES
Authors: TERWINDT GM OPHOFF RA HAAN J SANDKUIJL LA FRANTS RR FERRARI MD
Citation: Gm. Terwindt et al., MIGRAINE, ATAXIA AND EPILEPSY - A CHALLENGING SPECTRUM OF GENETICALLY-DETERMINED CALCIUM CHANNELOPATHIES, European journal of human genetics, 6(4), 1998, pp. 297-307
MOLECULAR ANALYSIS OF THE GENE CACNA1A - REFINED MAPPING OF THE CONTAINING REGION AND SCREENING FOR MUTATIONS IN EA2
Authors: TRETTEL F MANTUANO E VENEZIANO L SABBADINI G OLSEN A OPHOFF RA FRANTS RR JODICE C FRONTALI M
Citation: F. Trettel et al., MOLECULAR ANALYSIS OF THE GENE CACNA1A - REFINED MAPPING OF THE CONTAINING REGION AND SCREENING FOR MUTATIONS IN EA2, European journal of human genetics, 6, 1998, pp. 4186-4186
MIGRAINE ATAXIA, AND EPILEPSY - A CHALLENGING SPECTRUM OF GENETIC DETERMINED CALCIUM CHANNELOPATHIES
Authors: TERWINDT GM OPHOFF RA HAAN J SANDKUIJL LA FRANTS RR FERRARI MD
Citation: Gm. Terwindt et al., MIGRAINE ATAXIA, AND EPILEPSY - A CHALLENGING SPECTRUM OF GENETIC DETERMINED CALCIUM CHANNELOPATHIES, European journal of neuroscience, 10, 1998, pp. 19704-19704
GENETICS AND PATHOLOGY OF VOLTAGE-GATED CA2+ CHANNELS
Authors: OPHOFF RA TERWINDT GM FERRARI MD FRANTS RR
Citation: Ra. Ophoff et al., GENETICS AND PATHOLOGY OF VOLTAGE-GATED CA2+ CHANNELS, Histology and histopathology, 13(3), 1998, pp. 827-836
CHROMOSOMAL LOCALIZATION OF THE 5-HT1F RECEPTOR GENE - NO EVIDENCE FOR INVOLVEMENT IN RESPONSE TO SUMATRIPTAN IN MIGRAINE PATIENTS
Authors: VANDENBRINK AM VERGOUWE MN OPHOFF RA NAYLOR SL DAUWERSE HG SAXENA PR FERRARI MD FRANTS RR
Citation: Am. Vandenbrink et al., CHROMOSOMAL LOCALIZATION OF THE 5-HT1F RECEPTOR GENE - NO EVIDENCE FOR INVOLVEMENT IN RESPONSE TO SUMATRIPTAN IN MIGRAINE PATIENTS, American journal of medical genetics, 77(5), 1998, pp. 415-420
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
5-HT1B RECEPTOR POLYMORPHISM AND CLINICAL-RESPONSE TO SUMATRIPTAN
Authors: MASSENVANDENBRINK A VERGOUWE MN OPHOFF RA SAXENA PR FERRARI MD FRANTS RR
Citation: A. Massenvandenbrink et al., 5-HT1B RECEPTOR POLYMORPHISM AND CLINICAL-RESPONSE TO SUMATRIPTAN, Headache, 38(4), 1998, pp. 288-291
CLINICAL AND GENETIC-ANALYSIS OF A LARGE DUTCH FAMILY WITH AUTOSOMAL-DOMINANT VASCULAR RETINOPATHY, MIGRAINE AND RAYNAUD PHENOMENON
Authors: TERWINDT GM HAAN J OPHOFF RA GROENEN SMA STORIMANS CWJM LANSER JBK ROOS RAC BLEEKERWAGEMAKERS EM FRANTS RR FERRARI MD
Citation: Gm. Terwindt et al., CLINICAL AND GENETIC-ANALYSIS OF A LARGE DUTCH FAMILY WITH AUTOSOMAL-DOMINANT VASCULAR RETINOPATHY, MIGRAINE AND RAYNAUD PHENOMENON, Brain, 121, 1998, pp. 303-316
THE QUEST FOR MIGRAINE GENES
Authors: TERWINDT GM HAAN J OPHOFF RA FRANTS RR FERRARI MD
Citation: Gm. Terwindt et al., THE QUEST FOR MIGRAINE GENES, Current opinion in neurology, 10(3), 1997, pp. 221-225
EPISODIC ATAXIA TYPE-2 (EA2) AND SPINOCEREBELLAR ATAXIA TYPE-6 (SCA6)DUE TO CAG REPEAT EXPANSION IN THE CACNA1A GENE ON CHROMOSOME 19P
Authors: JODICE C MANTUANO E VENEZIANO L TRETTEL F SABBADINI G CALANDRIELLO L FRANCIA A SPADARO M PIERELLI F SALVI F OPHOFF RA FRANTS RR FRONTALI M
Citation: C. Jodice et al., EPISODIC ATAXIA TYPE-2 (EA2) AND SPINOCEREBELLAR ATAXIA TYPE-6 (SCA6)DUE TO CAG REPEAT EXPANSION IN THE CACNA1A GENE ON CHROMOSOME 19P, Human molecular genetics, 6(11), 1997, pp. 1973-1978
TOWARDS A UNIFIED NOMENCLATURE DESCRIBING VOLTAGE-GATED CALCIUM-CHANNEL GENES
Authors: LORY P OPHOFF RA NAHMIAS J
Citation: P. Lory et al., TOWARDS A UNIFIED NOMENCLATURE DESCRIBING VOLTAGE-GATED CALCIUM-CHANNEL GENES, Human genetics, 100(2), 1997, pp. 149-150
HYPEREKPLEXIA-LIKE SYNDROMES WITHOUT MUTATIONS IN THE GLRA1 GENE
Authors: VERGOUWE MN TIJSSEN MAJ SHIANG R VANDIJK JG ALSHAHWAN S OPHOFF RA FRANTS RR
Citation: Mn. Vergouwe et al., HYPEREKPLEXIA-LIKE SYNDROMES WITHOUT MUTATIONS IN THE GLRA1 GENE, Clinical neurology and neurosurgery, 99(3), 1997, pp. 172-178
INVOLVEMENT OF A CA2+ CHANNEL GENE IN FAMILIAL HEMIPLEGIC MIGRAINE AND MIGRAINE WITH AND WITHOUT AURA
Authors: OPHOFF RA TERWINDT GM VERGOUWE MN FRANTS RR FERRARI MD
Citation: Ra. Ophoff et al., INVOLVEMENT OF A CA2+ CHANNEL GENE IN FAMILIAL HEMIPLEGIC MIGRAINE AND MIGRAINE WITH AND WITHOUT AURA, Headache, 37(8), 1997, pp. 479-485
PARTIAL COSEGREGATION OF FAMILIAL HEMIPLEGIC MIGRAINE AND A BENIGN FAMILIAL INFANTILE EPILEPTIC SYNDROME
Authors: TERWINDT GM OPHOFF RA LINDHOUT D HAAN J HALLEY DJJ SANDKUIJL LA BROUWER OF FRANTS RR FERRARI MD
Citation: Gm. Terwindt et al., PARTIAL COSEGREGATION OF FAMILIAL HEMIPLEGIC MIGRAINE AND A BENIGN FAMILIAL INFANTILE EPILEPTIC SYNDROME, Epilepsia, 38(8), 1997, pp. 915-921
INVOLVEMENT OF THE P Q-TYPE CA2+ CHANNEL ALPHA(1A) SUBUNIT (CACNA1A) GENE REGION ON 19P13 IN MIGRAINE WITH AND WITHOUT AURA/
Authors: OPHOFF RA TERWINDT GM FERRARI MD SANDKUIJL LA FRANTS RR
Citation: Ra. Ophoff et al., INVOLVEMENT OF THE P Q-TYPE CA2+ CHANNEL ALPHA(1A) SUBUNIT (CACNA1A) GENE REGION ON 19P13 IN MIGRAINE WITH AND WITHOUT AURA/, American journal of human genetics, 61(4), 1997, pp. 1851-1851
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
FAMILIAL HEMIPLEGIC MIGRAINE - A CLINICAL COMPARISON OF FAMILIES LINKED AND UNLINKED TO CHROMOSOME-19
Authors: TERWINDT GM OPHOFF RA HAAN J FRANTS RR FERRARI MD
Citation: Gm. Terwindt et al., FAMILIAL HEMIPLEGIC MIGRAINE - A CLINICAL COMPARISON OF FAMILIES LINKED AND UNLINKED TO CHROMOSOME-19, Cephalalgia, 16(3), 1996, pp. 153-155
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
IS FAMILIAL HEMIPLEGIC MIGRAINE A HEREDITARY FORM OF BASILAR MIGRAINE
Authors: HAAN J TERWINDT GM OPHOFF RA BOS PLJM FRANTS RR FERRARI MD
Citation: J. Haan et al., IS FAMILIAL HEMIPLEGIC MIGRAINE A HEREDITARY FORM OF BASILAR MIGRAINE, Cephalalgia, 15(6), 1995, pp. 477-481
A 4-GENERATION DUTCH FAMILY WITH CEREBRAL AUTOSOMAL-DOMINANT ARTERIOPATHY WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY (CADASIL), LINKED TO CHROMOSOME 19P13
Authors: WIELAARD R BORNEBROEK M OPHOFF RA WINTERWARNARS HAO SCHELTENS P FRANTS RR FERRARI MD HAAN J
Citation: R. Wielaard et al., A 4-GENERATION DUTCH FAMILY WITH CEREBRAL AUTOSOMAL-DOMINANT ARTERIOPATHY WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY (CADASIL), LINKED TO CHROMOSOME 19P13, Clinical neurology and neurosurgery, 97(4), 1995, pp. 307-313
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
HYPOKALEMIC PERIODIC PARALYSIS AND THE DIHYDROPYRIDINE RECEPTOR (CACNLIA3) - GENOTYPE-PHENOTYPE CORRELATIONS FOR 2 PREDOMINANT MUTATIONS AND EVIDENCE FOR THE ABSENCE OF A FOUNDER EFFECT IN 16 CAUCASIAN FAMILIES
Authors: ELBAZ A VALESANTOS J JURKATROTT K LAPIE P OPHOFF RA BADY B LINKS TP PIUSSAN C VILA A MONNIER N PADBERG GW ABE K FEINGOLD N GUIMARAES J WINTZEN AR VANDERHOEVEN JH SAUDUBRAY JM GRUNFELD JP LENOIR G NIVET H ECHENNE B FRANTS RR FARDEAU M LEHMANNHORN F FONTAINE B
Citation: A. Elbaz et al., HYPOKALEMIC PERIODIC PARALYSIS AND THE DIHYDROPYRIDINE RECEPTOR (CACNLIA3) - GENOTYPE-PHENOTYPE CORRELATIONS FOR 2 PREDOMINANT MUTATIONS AND EVIDENCE FOR THE ABSENCE OF A FOUNDER EFFECT IN 16 CAUCASIAN FAMILIES, American journal of human genetics, 56(2), 1995, pp. 374-380
Risultati: 1-25 | 26-28