ACNP - Italian Periodicals Catalogue

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Results: 1-25 |

Results: 25

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

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

THE IMPACT OF MIGRAINE ON QUALITY-OF-LIFE IN THE GENERAL-POPULATION -THE GEM STUDY

Authors: TERWINDT GM LAUNER LJ FERRARI MD

Citation: Gm. Terwindt et al., THE IMPACT OF MIGRAINE ON QUALITY-OF-LIFE IN THE GENERAL-POPULATION -THE GEM STUDY, Neurology, 50(4), 1998, pp. 68002-68002

WHO RECEIVES A PHYSICIANS DIAGNOSIS OF MIGRAINE - THE CEM STUDY

Authors: LAUNER LJ TERWINDT GM FERRARI MD

Citation: Lj. Launer et al., WHO RECEIVES A PHYSICIANS DIAGNOSIS OF MIGRAINE - THE CEM STUDY, Neurology, 50(4), 1998, pp. 68006-68006

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

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

GENETICS OF MIGRAINE

Authors: HAAN J TERWINDT GM FERRARI MD

Citation: J. Haan et al., GENETICS OF MIGRAINE, Neurologic clinics, 15(1), 1997, pp. 43

SUBTYPES OF MIGRAINE IN A POPULATION-BASED SAMPLE - THE GEM STUDY

Authors: TERWINDT GM LAUNER LJ GROENEN SM FERRARI MD

Citation: Gm. Terwindt et al., SUBTYPES OF MIGRAINE IN A POPULATION-BASED SAMPLE - THE GEM STUDY, Neurology, 48(3), 1997, pp. 2096-2096

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

RIZATRIPTAN VS SUMATRIPTAN IN THE ACUTE TREATMENT OF MIGRAINE - A PLACEBO-CONTROLLED, DOSE-RANGING STUDY

Authors: VISSER WH TERWINDT GM REINES SA JIANG K LINES CR FERRARI MD

Citation: Wh. Visser et al., RIZATRIPTAN VS SUMATRIPTAN IN THE ACUTE TREATMENT OF MIGRAINE - A PLACEBO-CONTROLLED, DOSE-RANGING STUDY, Archives of neurology, 53(11), 1996, pp. 1132-1137

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

ASSOCIATION STUDY IN MIGRAINE

Authors: TERWINDT GM FERRARI MD

Citation: Gm. Terwindt et Md. Ferrari, ASSOCIATION STUDY IN MIGRAINE, Cephalalgia, 15(3), 1995, pp. 163-163

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

A POLYMORPHIC STS IN INTRON-44 OF THE DYSTROPHIN GENE

Authors: BLONDEN LAJ TERWINDT GM DENDUNNEN JT VANOMMEN GJB

Citation: Laj. Blonden et al., A POLYMORPHIC STS IN INTRON-44 OF THE DYSTROPHIN GENE, Human genetics, 93(4), 1994, pp. 479-480

FAMILIAL HEMIPLEGIC MIGRAINE IN THE NETHERLANDS

Authors: HAAN J TERWINDT GM BOS PLJM OPHOFF RA FRANTS RR FERRARI MD LINDHOUT DL SANDKUYL LA VANEYK R

Citation: J. Haan et al., FAMILIAL HEMIPLEGIC MIGRAINE IN THE NETHERLANDS, Clinical neurology and neurosurgery, 96(3), 1994, pp. 244-249

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