279 related articles for article (PubMed ID: 3982506)
1. Partial deficiency of erythrocyte spectrin in hereditary spherocytosis.
Agre P; Casella JF; Zinkham WH; McMillan C; Bennett V
Nature; 1985 Mar 28-Apr 3; 314(6009):380-3. PubMed ID: 3982506
[TBL] [Abstract][Full Text] [Related]
2. Inheritance pattern and clinical response to splenectomy as a reflection of erythrocyte spectrin deficiency in hereditary spherocytosis.
Agre P; Asimos A; Casella JF; McMillan C
N Engl J Med; 1986 Dec; 315(25):1579-83. PubMed ID: 3785322
[TBL] [Abstract][Full Text] [Related]
3. [Disorders of the membrane skeleton of erythrocytes in hereditary spherocytosis and elliptocytosis: significance of the molecular defect for pathogenesis and clinical severity].
Eber SW
Klin Padiatr; 1991; 203(4):284-95. PubMed ID: 1942935
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Deficient red-cell spectrin in severe, recessively inherited spherocytosis.
Agre P; Orringer EP; Bennett V
N Engl J Med; 1982 May; 306(19):1155-61. PubMed ID: 7070419
[No Abstract] [Full Text] [Related]
6. [Erythrocyte membrane and hereditary spherocytosis].
Ideguchi H
Rinsho Byori; 1990 Apr; 38(4):360-4. PubMed ID: 2195190
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Beta spectrin PRAGUE: a truncated beta spectrin producing spectrin deficiency, defective spectrin heterodimer self-association and a phenotype of spherocytic elliptocytosis.
Jarolim P; Wichterle H; Hanspal M; Murray J; Rubin HL; Palek J
Br J Haematol; 1995 Oct; 91(2):502-10. PubMed ID: 8547102
[TBL] [Abstract][Full Text] [Related]
9. [Determination of spectrin in erythrocytes: an important aid in the diagnosis of hereditary spherocytosis].
van Zwieten R; Bolscher BG; Schouten-van Meeteren AY; Hoffmann JJ; Roos D
Ned Tijdschr Geneeskd; 1995 Nov; 139(44):2256-61. PubMed ID: 7501052
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Hereditary spherocytosis with spectrin deficiency due to an unstable truncated beta spectrin.
Hassoun H; Vassiliadis JN; Murray J; Yi SJ; Hanspal M; Johnson CA; Palek J
Blood; 1996 Mar; 87(6):2538-45. PubMed ID: 8630421
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. Reductions of erythrocyte membrane viscoelastic coefficients reflect spectrin deficiencies in hereditary spherocytosis.
Waugh RE; Agre P
J Clin Invest; 1988 Jan; 81(1):133-41. PubMed ID: 3335631
[TBL] [Abstract][Full Text] [Related]
15. [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]
16. 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]
17. 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]
18. Lipid loss in spectrin deficient mouse erythrocytes.
Shohet SB
Prog Clin Biol Res; 1979; 30():471-4. PubMed ID: 531038
[No Abstract] [Full Text] [Related]
19. Hereditary spherocytosis of man. Altered binding of cytoskeletal components to the erythrocyte membrane.
Hill JS; Sawyer WH; Howlett GJ; Wiley JS
Biochem J; 1982 Feb; 201(2):259-66. PubMed ID: 7082289
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
