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Results: 1-10 |
Results: 10

Authors: DHERMY D GALAND C BOURNIER O CYNOBER T MECHINAUD F TCHEMIA G GARBARZ M
Citation: D. Dhermy et al., HEREDITARY SPHEROCYTOSIS WITH SPECTRIN DEFICIENCY RELATED TO NULL MUTATIONS OF THE BETA-SPECTRIN GENE, Blood cells, molecules, & diseases (Print), 24(12), 1998, pp. 251-261

Authors: GARBARZ M GALAND C BIBAS D BOURNIER O DEVAUX I HAROUSSEAU JL GRANDCHAMP B DHERMY D
Citation: M. Garbarz et al., A 5'-SPLICE REGION G-]C MUTATION IN EXON-3 OF THE HUMAN BETA-SPECTRINGENE LEADS TO DECREASED LEVELS OF BETA-SPECTRIN MESSENGER-RNA AND IS RESPONSIBLE FOR DOMINANT HEREDITARY SPHEROCYTOSIS (SPECTRIN GUEMENE-PENFAO), British Journal of Haematology, 100(1), 1998, pp. 90-98

Authors: DHERMY D GALAND C BOURNIER O KING MJ CYNOBER T ROBERTS I KANYIKE F ADEKILE A
Citation: D. Dhermy et al., COINHERITANCE OF ALPHA-SPECTRIN AND BETA-SPECTRIN GENE-MUTATIONS IN ACASE OF HEREDITARY ELLIPTOCYTOSIS, Blood, 92(11), 1998, pp. 4481-4482

Authors: DHERMY D GALAND C BOURNIER O BOULANGER L CYNOBER T SCHISMANOFF PO BURSAUX E TCHERNIA G BOIVIN P GARBARZ M
Citation: D. Dhermy et al., HETEROGENOUS BAND-3 DEFICIENCY IN HEREDITARY SPHEROCYTOSIS RELATED TODIFFERENT BAND-3 GENE DEFECTS. (VOL 98, PG 32, 1997), British Journal of Haematology, 99(2), 1997, pp. 474-474

Authors: DHERMY D GALAND C BOURNIER O BOULANGER L CYNOBER T SCHISMANOFF PO BURSAUX E TCHERNIA G BOIVIN P GARBARZ M
Citation: D. Dhermy et al., HETEROGENOUS BAND-3 DEFICIENCY IN HEREDITARY SPHEROCYTOSIS RELATED TODIFFERENT BAND-3 GENE DEFECTS, British Journal of Haematology, 98(1), 1997, pp. 32-40

Authors: GARBARZ M BIBAS D CYNOBER T GALAND C BOURNIER O DEVAUX I TCHERNIA G DHERMY D
Citation: M. Garbarz et al., SEARCH FOR THE CANDIDATE GENES IN DOMINANT HEREDITARY SPHEROCYTOSIS USING LINKAGE ANALYSIS, Comptes rendus de l'Academie des sciences. Serie 3, Sciences de la vie, 319(10), 1996, pp. 913-919

Authors: GLELEKAKAI C GARBARZ M LECOMTE MC LEBORGNE S GALAND C BOURNIER O DEVAUX I GAUTERO H ZOHOUN I GALLAGHER PG FORGET BG DHERMY D
Citation: C. Glelekakai et al., EPIDEMIOLOGIC STUDIES OF SPECTRIN MUTATIONS RELATED TO HEREDITARY ELLIPTOCYTOSIS AND SPECTRIN POLYMORPHISMS IN BENIN, British Journal of Haematology, 95(1), 1996, pp. 57-66

Authors: GARBARZ M DEVAUX I BOURNIER O GRANDCHAMP B DHERMY D
Citation: M. Garbarz et al., PROTEIN-4.1-LILLE, A NOVEL MUTATION IN THE DOWNSTREAM INITIATION CODON OF PROTEIN-4.1 GENE ASSOCIATED WITH HETEROZYGOUS-4,1(-) HEREDITARY ELLIPTOCYTOSIS, Human mutation, 5(4), 1995, pp. 339-340

Authors: NAVARROPRIGENT MJ RABETAFIKA E BOURNIER O BOIVIN P DHERMY D
Citation: Mj. Navarroprigent et al., EFFECT OF OKADAIC ACID ON THE RHEOLOGICAL PROPERTIES OF HUMAN ERYTHROCYTE-MEMBRANES, Clinical hemorheology, 14(6), 1994, pp. 819-830

Authors: LECOMTE MC GARBARZ M GAUTERO H BOURNIER O GALAND C BOIVIN P DHERMY D
Citation: Mc. Lecomte et al., MOLECULAR-BASIS OF CLINICAL AND MORPHOLOGICAL HETEROGENEITY IN HEREDITARY ELLIPTOCYTOSIS (HE) WITH SPECTRIN ALPHA-I VARIANTS, British Journal of Haematology, 85(3), 1993, pp. 584-595
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