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5. Combined spectrin and ankyrin deficiency is common in autosomal dominant hereditary spherocytosis. Savvides P; Shalev O; John KM; Lux SE Blood; 1993 Nov; 82(10):2953-60. PubMed ID: 8219186 [TBL] [Abstract][Full Text] [Related]
6. Molecular basis of spectrin and ankyrin deficiencies in severe hereditary spherocytosis: evidence implicating a primary defect of ankyrin. Hanspal M; Yoon SH; Yu H; Hanspal JS; Lambert S; Palek J; Prchal JT Blood; 1991 Jan; 77(1):165-73. PubMed ID: 1702027 [TBL] [Abstract][Full Text] [Related]
7. Combined ankyrin and spectrin deficiency in hereditary spherocytosis. Pekrun A; Eber SW; Kuhlmey A; Schröter W Ann Hematol; 1993 Aug; 67(2):89-93. PubMed ID: 8347735 [TBL] [Abstract][Full Text] [Related]
8. 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]
9. Erythrocyte membrane protein alterations underlying clinical heterogeneity in hereditary spherocytosis. Miraglia del Giudice E; Iolascon A; Pinto L; Nobili B; Perrotta S Br J Haematol; 1994 Sep; 88(1):52-5. PubMed ID: 7803256 [TBL] [Abstract][Full Text] [Related]
10. A genetic defect of erythrocyte band 4.2 protein associated with hereditary spherocytosis. Ideguchi H; Nishimura J; Nawata H; Hamasaki N Br J Haematol; 1990 Mar; 74(3):347-53. PubMed ID: 2139792 [TBL] [Abstract][Full Text] [Related]
11. Hereditary spherocytosis associated with deletion of human erythrocyte ankyrin gene on chromosome 8. Lux SE; Tse WT; Menninger JC; John KM; Harris P; Shalev O; Chilcote RR; Marchesi SL; Watkins PC; Bennett V Nature; 1990 Jun; 345(6277):736-9. PubMed ID: 2141669 [TBL] [Abstract][Full Text] [Related]
12. Clinical and molecular evaluation of non-dominant hereditary spherocytosis. Miraglia del Giudice E; Nobili B; Francese M; D'Urso L; Iolascon A; Eber S; Perrotta S Br J Haematol; 2001 Jan; 112(1):42-7. PubMed ID: 11167781 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. Ankyrin-1 mutations are a major cause of dominant and recessive hereditary spherocytosis. Eber SW; Gonzalez JM; Lux ML; Scarpa AL; Tse WT; Dornwell M; Herbers J; Kugler W; Ozcan R; Pekrun A; Gallagher PG; Schröter W; Forget BG; Lux SE Nat Genet; 1996 Jun; 13(2):214-8. PubMed ID: 8640229 [TBL] [Abstract][Full Text] [Related]
15. Membrane cation and anion transport activities in erythrocytes of hereditary spherocytosis: effects of different membrane protein defects. De Franceschi L; Olivieri O; Miraglia del Giudice E; Perrotta S; Sabato V; Corrocher R; Iolascon A Am J Hematol; 1997 Jul; 55(3):121-8. PubMed ID: 9256290 [TBL] [Abstract][Full Text] [Related]
16. [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]
17. Identification of the molecular defect in the erythrocyte membrane skeleton of some kindreds with hereditary spherocytosis. Goodman SR; Shiffer KA; Casoria LA; Eyster ME Blood; 1982 Sep; 60(3):772-84. PubMed ID: 7104494 [TBL] [Abstract][Full Text] [Related]
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