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Items: 1 to 20 of 203

2.

A new abnormal variant of spectrin in black patients with hereditary elliptocytosis.

Lecomte MC, Dhermy D, Solis C, Ester A, Féo C, Gautero H, Bournier O, Boivin P.

Blood. 1985 May;65(5):1208-17.

3.

Molecular basis of clinical and morphological heterogeneity in hereditary elliptocytosis (HE) with spectrin alpha I variants.

Lecomte MC, Garbarz M, Gautero H, Bournier O, Galand C, Boivin P, Dhermy D.

Br J Haematol. 1993 Nov;85(3):584-95.

PMID:
8136282
6.

Hereditary elliptocytosis: clinical, morphological and biochemical studies of 38 cases.

Dhermy D, Garbarz M, Lecomte MC, Féo C, Bournier O, Chaveroche I, Gautero H, Galand C, Boivin P.

Nouv Rev Fr Hematol. 1986;28(3):129-40.

PMID:
3748797
7.

Spectrin-alpha I/61: a new structural variant of alpha-spectrin in a double-heterozygous form of hereditary pyropoikilocytosis.

Lawler J, Coetzer TL, Mankad VN, Moore RB, Prchal JT, Palek J.

Blood. 1988 Oct;72(4):1412-5.

8.

Molecular determinants of clinical expression of hereditary elliptocytosis and pyropoikilocytosis.

Coetzer T, Lawler J, Prchal JT, Palek J.

Blood. 1987 Sep;70(3):766-72.

9.

Mutant forms of spectrin alpha-subunits in hereditary elliptocytosis.

Marchesi SL, Letsinger JT, Speicher DW, Marchesi VT, Agre P, Hyun B, Gulati G.

J Clin Invest. 1987 Jul;80(1):191-8.

11.

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.

Blood. 1989 Aug 15;74(3):1126-33.

12.

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.

Blood. 1990 Apr 15;75(8):1691-8.

13.
14.

Sp alpha I/65 hereditary elliptocytosis in North Africa.

Alloisio N, Guetarni D, Morlé L, Pothier B, Ducluzeau MT, Soun A, Colonna P, Clerc M, Philippe N, Delaunay J.

Am J Hematol. 1986 Oct;23(2):113-22.

PMID:
3752066
15.
16.

Pathologic and nonpathologic variants of the spectrin molecule in two black families with hereditary elliptocytosis.

Lecomte MC, Dhermy D, Garbarz M, Feo C, Gautero H, Bournier O, Picat C, Chaveroche I, Ester A, Galand C, et al.

Hum Genet. 1985;71(4):351-7.

PMID:
4077050
17.

Viscoelastic properties of red cell membrane in hereditary elliptocytosis.

Chabanel A, Sung KL, Rapiejko J, Prchal JT, Palek J, Liu SC, Chien S.

Blood. 1989 Feb;73(2):592-5.

18.

Abnormal spectrin in hereditary elliptocytosis.

Marchesi SL, Knowles WJ, Morrow JS, Bologna M, Marchesi VT.

Blood. 1986 Jan;67(1):141-51.

19.

Sp alpha I/65: a new variant of the alpha subunit of spectrin in hereditary elliptocytosis.

Lawler J, Coetzer TL, Palek J, Jacob HS, Luban N.

Blood. 1985 Sep;66(3):706-9.

20.

Clinical expression of alpha spectrin mutants in hereditary elliptocytosis.

Palek J, Coetzer T.

Blood Cells. 1987;13(1-2):237-50. Review.

PMID:
3311220

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