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Results: 1-9 |
Results: 9
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
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
ASSIGNMENT OF THE PORCINE LOCI FOR MYOD1 TO CHROMOSOME-2 AND MYF5 TO CHROMOSOME-5
Authors: SOUMILLION A RETTENBERGER G VERGOUWE MN ERKENS JHF LENSTRA JA PAS MFWT
Citation: A. Soumillion et al., ASSIGNMENT OF THE PORCINE LOCI FOR MYOD1 TO CHROMOSOME-2 AND MYF5 TO CHROMOSOME-5, Animal genetics, 28(1), 1997, pp. 37-38
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
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 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
ISOLATION AND CHARACTERIZATION OF PORCINE MYF GENES
Authors: SOUMILLION A ERKENS JHF VERGOUWE MN LENSTRA JA TEPAS MFW
Citation: A. Soumillion et al., ISOLATION AND CHARACTERIZATION OF PORCINE MYF GENES, Journal of cellular biochemistry, 1994, pp. 522-522
Risultati: 1-9 |