Feo C - Search Results

1

Point mutation in the beta-spectrin gene associated with alpha I/74 hereditary elliptocytosis. Implications for the mechanism of spectrin dimer self-association.

Tse WT, Lecomte MC, Costa FF, Garbarz M, Feo C, Boivin P, Dhermy D, Forget BG. Tse WT, et al. Among authors: feo c. J Clin Invest. 1990 Sep;86(3):909-16. doi: 10.1172/JCI114792. J Clin Invest. 1990. PMID: 1975598 Free PMC article.

2

Spectrin beta-chain variant associated with hereditary elliptocytosis.

Dhermy D, Lecomte MC, Garbarz M, Bournier O, Galand C, Gautero H, Feo C, Alloisio N, Delaunay J, Boivin P. Dhermy D, et al. Among authors: feo c. J Clin Invest. 1982 Oct;70(4):707-15. doi: 10.1172/jci110666. J Clin Invest. 1982. PMID: 7119110 Free PMC article.

3

A nonsense mutation in the erythrocyte band 3 gene associated with decreased mRNA accumulation in a kindred with dominant hereditary spherocytosis.

Jenkins PB, Abou-Alfa GK, Dhermy D, Bursaux E, Féo C, Scarpa AL, Lux SE, Garbarz M, Forget BG, Gallagher PG. Jenkins PB, et al. Among authors: feo c. J Clin Invest. 1996 Jan 15;97(2):373-80. doi: 10.1172/JCI118425. J Clin Invest. 1996. PMID: 8567957 Free PMC article.

4

Spectrin Jendouba: an alpha II/31 spectrin variant that is associated with elliptocytosis and carries a mutation distant from the dimer self-association site.

Alloisio N, Wilmotte R, Morlé L, Baklouti F, Maréchal J, Ducluzeau MT, Denoroy L, Féo C, Forget BG, Kastally R, et al. Alloisio N, et al. Among authors: feo c. Blood. 1992 Aug 1;80(3):809-15. Blood. 1992. PMID: 1638030 Free article.

5

Hereditary pyropoikilocytosis and elliptocytosis in a white French family with the spectrin alpha I/74 variant related to a CGT to CAT codon change (Arg to His) at position 22 of the spectrin alpha I domain.

Garbarz M, Lecomte MC, Féo C, Devaux I, Picat C, Lefebvre C, Galibert F, Gautero H, Bournier O, Galand C, et al. Garbarz M, et al. Among authors: feo c. Blood. 1990 Apr 15;75(8):1691-8. Blood. 1990. PMID: 2328319 Free article.

6

Severe recessive poikilocytic anaemia with a new spectrin alpha chain variant.

Lecomte MC, Feo C, Gautero H, Bournier O, Galand C, Garbarz M, Boivin P, Dhermy D. Lecomte MC, et al. Among authors: feo c. Br J Haematol. 1990 Apr;74(4):497-507. doi: 10.1111/j.1365-2141.1990.tb06341.x. Br J Haematol. 1990. PMID: 2346729

7

Sp alpha I/78: a mutation of the alpha I spectrin domain in a white kindred with HE and HPP phenotypes.

Lecomte MC, Garbarz M, Grandchamp B, Féo C, Gautero H, Devaux I, Bournier O, Galand C, d'Auriol L, Galibert F, et al. Lecomte MC, et al. Among authors: feo c. Blood. 1989 Aug 15;74(3):1126-33. Blood. 1989. PMID: 2568862 Free article.

8

Confirming or ruling out hereditary elliptocytosis.

Feo C, Dhermy D. Feo C, et al. Acta Haematol. 1988;79(2):116. doi: 10.1159/000205736. Acta Haematol. 1988. PMID: 3124471 Free article. No abstract available.

9

Spectrin Nice (beta 220/216): a shortened beta-chain variant associated with an increase of the alpha I/74 fragment in a case of elliptocytosis.

Pothier B, Morlé L, Alloisio N, Ducluzeau MT, Caldani C, Féo C, Garbarz M, Chaveroche I, Dhermy D, Lecomte MC, et al. Pothier B, et al. Among authors: feo c. Blood. 1987 Jun;69(6):1759-65. Blood. 1987. PMID: 3580577 Free article.

10

Prenatal diagnosis of hereditary elliptocytosis with molecular defect of spectrin.

Dhermy D, Feo C, Garbarz M, Lecomte MC, Bournier O, Chaveroche I, Gautero H, Boivin P, Daffos F, Forestier F. Dhermy D, et al. Among authors: feo c. Prenat Diagn. 1987 Sep;7(7):471-83. doi: 10.1002/pd.1970070703. Prenat Diagn. 1987. PMID: 3671334

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