166 related articles for article (PubMed ID: 8136278)
1. Coexistence of hereditary spherocytosis (HS) due to band 3 deficiency and beta-thalassaemia trait: partial correction of HS phenotype.
Miraglia del Giudice E; Perrotta S; Nobili B; Pinto L; Cutillo L; Iolascon A
Br J Haematol; 1993 Nov; 85(3):553-7. PubMed ID: 8136278
[TBL] [Abstract][Full Text] [Related]
2. Hereditary spherocytosis (HS) due to loss of anion exchange transporter.
Iolascon A; Miraglia del Giudice E; Perrotta S; Pinto L; Fiorelli G; Cappellini DM; Vasseur C; Bursaux E; Cutillo S
Haematologica; 1992; 77(6):450-6. PubMed ID: 1289181
[TBL] [Abstract][Full Text] [Related]
3. Red cell membrane protein abnormalities in hereditary spherocytosis in Brazil.
Saad ST; Costa FF; Vicentim DL; Salles TS; Pranke PH
Br J Haematol; 1994 Oct; 88(2):295-9. PubMed ID: 7803273
[TBL] [Abstract][Full Text] [Related]
4. [Hereditary spherocytosis: one year study of erythrocyte membrane proteins].
Tshilolo L; Kagambega F; Sztern B; Vertongen F; Gulbis B
Rev Med Brux; 1998 Oct; 19(5 Pt 1):417-23. PubMed ID: 9844481
[TBL] [Abstract][Full Text] [Related]
5. Identification of quantitative trait loci that modify the severity of hereditary spherocytosis in wan, a new mouse model of band-3 deficiency.
Peters LL; Swearingen RA; Andersen SG; Gwynn B; Lambert AJ; Li R; Lux SE; Churchill GA
Blood; 2004 Apr; 103(8):3233-40. PubMed ID: 15070709
[TBL] [Abstract][Full Text] [Related]
6. Hereditary spherocytosis associated with protein band 3 defect in a Swiss kindred.
Reinhart WH; Wyss EJ; Arnold D; Ott P
Br J Haematol; 1994 Jan; 86(1):147-55. PubMed ID: 8011524
[TBL] [Abstract][Full Text] [Related]
7. Red blood cell indexes in patients in patients with hereditary spherocytosis and beta-thalassemia combination.
Akar N; Gökçe H
Pediatr Hematol Oncol; 2002 Dec; 19(8):569-73. PubMed ID: 12487832
[TBL] [Abstract][Full Text] [Related]
8. Partial pyruvate kinase deficiency aggravates the phenotypic expression of band 3 deficiency in a family with hereditary spherocytosis.
van Zwieten R; van Oirschot BA; Veldthuis M; Dobbe JG; Streekstra GJ; van Solinge WW; Schutgens RE; van Wijk R
Am J Hematol; 2015 Mar; 90(3):E35-9. PubMed ID: 25388786
[TBL] [Abstract][Full Text] [Related]
9. Study of a kindred with hereditary spherocytosis and glyceraldehyde-3-phosphate dehydrogenase deficiency.
McCann SR; Finkel B; Cadman S; Allen DW
Blood; 1976 Feb; 47(2):171-81. PubMed ID: 1244916
[TBL] [Abstract][Full Text] [Related]
10. Enhanced haemolysis with beta-thalassaemia trait due to the unstable beta chain variant, Hb Gunma, accompanied by hereditary elliptocytosis due to protein 4.1 deficiency in a Japanese family.
Maehara T; Tsukamoto N; Nojima Y; Karasawa M; Murakami H; Hattori Y; Ideguchi H
Br J Haematol; 2002 Apr; 117(1):193-7. PubMed ID: 11918554
[TBL] [Abstract][Full Text] [Related]
11. Heterogenous band 3 deficiency in hereditary spherocytosis related to different band 3 gene defects.
Dhermy D; Galand C; Bournier O; Boulanger L; Cynober T; Schismanoff PO; Bursaux E; Tchernia G; Boivin P; Garbarz M
Br J Haematol; 1997 Jul; 98(1):32-40. PubMed ID: 9233560
[TBL] [Abstract][Full Text] [Related]
12. Uniquely higher incidence of isolated or combined deficiency of band 3 and/or band 4.2 as the pathogenesis of autosomal dominantly inherited hereditary spherocytosis in the Japanese population.
Inoue T; Kanzaki A; Yawata A; Wada H; Okamoto N; Takahashi M; Sugihara T; Yamada O; Yawata Y
Int J Hematol; 1994 Dec; 60(4):227-38. PubMed ID: 7894027
[TBL] [Abstract][Full Text] [Related]
13. Search for the candidate genes in dominant hereditary spherocytosis using linkage analysis.
Garbarz M; Bibas D; Cynober T; Galand C; Bournier O; Devaux I; Tchernia G; Dhermy D
C R Acad Sci III; 1996 Oct; 319(10):913-9. PubMed ID: 8977772
[TBL] [Abstract][Full Text] [Related]
14. Band 3Tambaú: a de novo mutation in the AE1 gene associated with hereditary spherocytosis. Implications for anion exchange and insertion into the red blood cell membrane.
Lima PR; Baratti MO; Chiattone ML; Costa FF; Saad ST
Eur J Haematol; 2005 May; 74(5):396-401. PubMed ID: 15813913
[TBL] [Abstract][Full Text] [Related]
15. Abnormalities of erythrocyte membrane proteins in Korean patients with hereditary spherocytosis.
Lee YK; Cho HI; Park SS; Lee YJ; Ra E; Chang YH; Hur M; Shin HY; Ahn HS
J Korean Med Sci; 2000 Jun; 15(3):284-8. PubMed ID: 10895969
[TBL] [Abstract][Full Text] [Related]
16. Characterization of 13 novel band 3 gene defects in hereditary spherocytosis with band 3 deficiency.
Jarolim P; Murray JL; Rubin HL; Taylor WM; Prchal JT; Ballas SK; Snyder LM; Chrobak L; Melrose WD; Brabec V; Palek J
Blood; 1996 Dec; 88(11):4366-74. PubMed ID: 8943874
[TBL] [Abstract][Full Text] [Related]
17. 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
J Clin Invest; 1996 Jan; 97(2):373-80. PubMed ID: 8567957
[TBL] [Abstract][Full Text] [Related]
18. Interaction of hereditary spherocytosis and alpha thalassaemia: a family study.
Li CK; Ng MH; Cheung KL; Lam TK; Shing MM
Acta Haematol; 1994; 91(4):201-5. PubMed ID: 7976119
[TBL] [Abstract][Full Text] [Related]
19. Hereditary spherocytosis: identification of several HS families with ankyrin and band 3 deficiency in a population of southwestern Poland.
Bogusławska DM; Heger E; Chorzalska A; Nierzwicka M; Hołojda J; Swiderska A; Straburzyńska A; Paździor G; Langner M; Sikorski AF
Ann Hematol; 2004 Jan; 83(1):28-33. PubMed ID: 14517693
[TBL] [Abstract][Full Text] [Related]
20. Characteristic features of the genotype and phenotype of hereditary spherocytosis in the Japanese population.
Yawata Y; Kanzaki A; Yawata A; Doerfler W; Ozcan R; Eber SW
Int J Hematol; 2000 Feb; 71(2):118-35. PubMed ID: 10745622
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
