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Results: 1-8 |
Results: 8
Petrology of the plutonic suites from the Chalkidiki ophiolites,northern Greece. Implications for parental magma characteristics and tectonic provenance
Authors: CHRISTODOULOU C MICHAELIDES K
Citation: C. Christodoulou et K. Michaelides, Petrology of the plutonic suites from the Chalkidiki ophiolites,northern Greece. Implications for parental magma characteristics and tectonic provenance, Ofioliti (Bologna) Bollettino del gruppo di lavoro sulle ofioliti mediterranee , 15(1), 1990, pp. 17-44
FACTOR-VIII GENE-MUTATIONS FOUND BY A COMPARATIVE-STUDY OF SSCP, DGGEAND CMC AND THEIR ANALYSIS ON A MOLECULAR-MODEL OF FACTOR-VIII PROTEIN
Authors: SCHWAAB R OLDENBURG J LALLOZ MRA SCHWAAB U PEMBERTON S HANFLAND P BRACKMANN HH TUDDENHAM EGD MICHAELIDES K
Citation: R. Schwaab et al., FACTOR-VIII GENE-MUTATIONS FOUND BY A COMPARATIVE-STUDY OF SSCP, DGGEAND CMC AND THEIR ANALYSIS ON A MOLECULAR-MODEL OF FACTOR-VIII PROTEIN, Human genetics, 101(3), 1997, pp. 323-332
HOMOZYGOUS LEU-105 PRO MUTATION IN PLATELET MEMBRANE GP1B-ALPHA CAUSING BERNARD-SOULIER-SYNDROME AND ITS ANALYSIS ON A STRUCTURE MODEL OF THE LRG DOMAIN
Authors: MICHAELIDES K PEMBERTON S TUDDENHAM EGD
Citation: K. Michaelides et al., HOMOZYGOUS LEU-105 PRO MUTATION IN PLATELET MEMBRANE GP1B-ALPHA CAUSING BERNARD-SOULIER-SYNDROME AND ITS ANALYSIS ON A STRUCTURE MODEL OF THE LRG DOMAIN, Thrombosis and haemostasis, 1997, pp. 277-277
AN UNUSUAL CASE OF BERNARD-SOULIER-SYNDROME DUE TO A NOVEL HOMOZYGOUSSINGLE-BASE SUBSTITUTION IN THE PLATELET MEMBRANE GLYCOPROTEIN-IX (GPIX) GENE, CYS8-]ARG
Authors: MICHAELIDES K TUDDENHAM EGD
Citation: K. Michaelides et Egd. Tuddenham, AN UNUSUAL CASE OF BERNARD-SOULIER-SYNDROME DUE TO A NOVEL HOMOZYGOUSSINGLE-BASE SUBSTITUTION IN THE PLATELET MEMBRANE GLYCOPROTEIN-IX (GPIX) GENE, CYS8-]ARG, British Journal of Haematology, 93, 1996, pp. 24-24
MODERATION OF HEMOPHILIA-A PHENOTYPE BY THE FACTOR-V R506Q MUTATION
Authors: NICHOLS WC AMANO K CACHERIS PM FIGUEIREDO MS MICHAELIDES K SCHWAAB R HOYER L KAUFMAN RJ GINSBURG D
Citation: Wc. Nichols et al., MODERATION OF HEMOPHILIA-A PHENOTYPE BY THE FACTOR-V R506Q MUTATION, Blood, 88(4), 1996, pp. 1183-1187
HEMOPHILIA-A DIAGNOSIS BY SIMULTANEOUS ANALYSIS OF 2 VARIABLE DINUCLEOTIDE TANDEM REPEATS WITHIN THE FACTOR-VIII GENE
Authors: LALLOZ MRA SCHWAAB R MCVEY JH MICHAELIDES K TUDDENHAM EGD
Citation: Mra. Lalloz et al., HEMOPHILIA-A DIAGNOSIS BY SIMULTANEOUS ANALYSIS OF 2 VARIABLE DINUCLEOTIDE TANDEM REPEATS WITHIN THE FACTOR-VIII GENE, British Journal of Haematology, 86(4), 1994, pp. 804-809
RAPID SCREENING OF THE FACTOR-VIII GENE BY MULTIPLEXED SSCP - APPLICATION TO PATIENTS DEVELOPING INHIBITORS DURING TREATMENT WITH RECOMBINANT FACTOR-VIII
Authors: TUDDENHAM EGD LALLOZ MRA MICHAELIDES K ESMON PC HURST D
Citation: Egd. Tuddenham et al., RAPID SCREENING OF THE FACTOR-VIII GENE BY MULTIPLEXED SSCP - APPLICATION TO PATIENTS DEVELOPING INHIBITORS DURING TREATMENT WITH RECOMBINANT FACTOR-VIII, Blood, 82(10), 1993, pp. 10000446-10000446
DOUBLE HETEROZYGOSITY FOR MUTATIONS IN THE PLATELET GLYCOPROTEIN-IX GENE IN 3 SIBLINGS WITH BERNARD-SOULIER SYNDROME
Authors: WRIGHT SD MICHAELIDES K JOHNSON DJD WEST NC TUDDENHAM EGD
Citation: Sd. Wright et al., DOUBLE HETEROZYGOSITY FOR MUTATIONS IN THE PLATELET GLYCOPROTEIN-IX GENE IN 3 SIBLINGS WITH BERNARD-SOULIER SYNDROME, Blood, 81(9), 1993, pp. 2339-2347
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