241 related articles for article (PubMed ID: 3604989)
1. Clinical and laboratory study of two Caucasian families with hereditary pyropoikilocytosis and hereditary elliptocytosis.
Peterson LC; Dampier C; Coetzer T; Lawler J; White J; Palek J
Am J Clin Pathol; 1987 Jul; 88(1):58-65. PubMed ID: 3604989
[TBL] [Abstract][Full Text] [Related]
2. 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. PubMed ID: 3167214
[TBL] [Abstract][Full Text] [Related]
3. Hereditary pyropoikilocytosis and elliptocytosis in a Caucasian family. Transmission of the same molecular defect in spectrin through three generations with different clinical expression.
Lecomte MC; Dhermy D; Garbarz M; Feo C; Gautero H; Bournier O; Picat C; Chaveroche I; Galand C; Boivin P
Hum Genet; 1987 Dec; 77(4):329-34. PubMed ID: 3692477
[TBL] [Abstract][Full Text] [Related]
4. 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
Blood; 1990 Apr; 75(8):1691-8. PubMed ID: 2328319
[TBL] [Abstract][Full Text] [Related]
5. Structural and functional heterogeneity of alpha spectrin mutations involving the spectrin heterodimer self-association site: relationships to hematologic expression of homozygous hereditary elliptocytosis and hereditary pyropoikilocytosis.
Coetzer T; Palek J; Lawler J; Liu SC; Jarolim P; Lahav M; Prchal JT; Wang W; Alter BP; Schewitz G
Blood; 1990 Jun; 75(11):2235-44. PubMed ID: 2346784
[TBL] [Abstract][Full Text] [Related]
6. Heterogeneity of the molecular basis of hereditary pyropoikilocytosis and hereditary elliptocytosis associated with increased levels of the spectrin alpha I/74-kilodalton tryptic peptide.
Floyd PB; Gallagher PG; Valentino LA; Davis M; Marchesi SL; Forget BG
Blood; 1991 Sep; 78(5):1364-72. PubMed ID: 1878597
[TBL] [Abstract][Full Text] [Related]
7. Abnormal tryptic peptide from the spectrin alpha-chain resulting from alpha- or beta-chain mutations: two genetically distinct forms of the Sp alpha I/74 variant.
Lecomte MC; Gautero H; Garbarz M; Boivin P; Dhermy D
Br J Haematol; 1990 Nov; 76(3):406-13. PubMed ID: 2261350
[TBL] [Abstract][Full Text] [Related]
8. Alteration of the erythrocyte membrane skeletal ultrastructure in hereditary spherocytosis, hereditary elliptocytosis, and pyropoikilocytosis.
Liu SC; Derick LH; Agre P; Palek J
Blood; 1990 Jul; 76(1):198-205. PubMed ID: 2364170
[TBL] [Abstract][Full Text] [Related]
9. Molecular heterogeneity of hereditary pyropoikilocytosis: identification of a second variant of the spectrin alpha-subunit.
Lawler J; Palek J; Liu SC; Prchal J; Butler WM
Blood; 1983 Dec; 62(6):1182-9. PubMed ID: 6640107
[TBL] [Abstract][Full Text] [Related]
10. Molecular defect of spectrin in the family of a child with congenital hemolytic poikilocytic anemia.
Dhermy D; Lecomte MC; Garbarz M; Feo C; Gautero H; Bournier O; Galand C; Herrera A; Gretillat F; Boivin P
Pediatr Res; 1984 Oct; 18(10):1005-12. PubMed ID: 6493844
[TBL] [Abstract][Full Text] [Related]
11. A common type of the spectrin alpha I 46-50a-kD peptide abnormality in hereditary elliptocytosis and pyropoikilocytosis is associated with a mutation distant from the proteolytic cleavage site. Evidence for the functional importance of the triple helical model of spectrin.
Gallagher PG; Tse WT; Coetzer T; Lecomte MC; Garbarz M; Zarkowsky HS; Baruchel A; Ballas SK; Dhermy D; Palek J
J Clin Invest; 1992 Mar; 89(3):892-8. PubMed ID: 1541680
[TBL] [Abstract][Full Text] [Related]
12. Abnormal spectrin in hereditary elliptocytosis.
Marchesi SL; Knowles WJ; Morrow JS; Bologna M; Marchesi VT
Blood; 1986 Jan; 67(1):141-51. PubMed ID: 3940543
[TBL] [Abstract][Full Text] [Related]
13. Hereditary poikilocytic anemia associated with the co-inheritance of two alpha spectrin abnormalities.
Iarocci TA; Wagner GM; Mohandas N; Lane PA; Mentzer WC
Blood; 1988 May; 71(5):1390-6. PubMed ID: 3359047
[TBL] [Abstract][Full Text] [Related]
14. Molecular basis and haplotyping of the alphaII domain polymorphisms of spectrin: application to the study of hereditary elliptocytosis and pyropoikilocytosis.
Gallagher PG; Kotula L; Wang Y; Marchesi SL; Curtis PJ; Speicher DW; Forget BG
Am J Hum Genet; 1996 Aug; 59(2):351-9. PubMed ID: 8755921
[TBL] [Abstract][Full Text] [Related]
15. Red cell ektacytometry in two patients with chronic hemolytic anemia and three new α-spectrin variants.
Vives-Corrons JL; Krishnevskaya E; Hernández-Rodriguez I; Payán-Pernia S; Sevilla ÁFR; Badell I
Ann Hematol; 2022 Mar; 101(3):549-555. PubMed ID: 34845540
[TBL] [Abstract][Full Text] [Related]
16. Partial spectrin deficiency in hereditary pyropoikilocytosis.
Coetzer TL; Palek J
Blood; 1986 Apr; 67(4):919-24. PubMed ID: 3955236
[TBL] [Abstract][Full Text] [Related]
17. 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
Blood; 1989 Aug; 74(3):1126-33. PubMed ID: 2568862
[TBL] [Abstract][Full Text] [Related]
18. 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. PubMed ID: 8136282
[TBL] [Abstract][Full Text] [Related]
19. Hematologically important mutations: spectrin variants in hereditary elliptocytosis and hereditary pyropoikilocytosis.
Gallagher PG; Forget BG
Blood Cells Mol Dis; 1996; 22(3):254-8. PubMed ID: 9075575
[No Abstract] [Full Text] [Related]
20. Clinical expression of alpha spectrin mutants in hereditary elliptocytosis.
Palek J; Coetzer T
Blood Cells; 1987; 13(1-2):237-50. PubMed ID: 3311220
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
