181 related articles for article (PubMed ID: 9844481)
1. [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]
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. [Erythrocyte membrane and hereditary spherocytosis].
Ideguchi H
Rinsho Byori; 1990 Apr; 38(4):360-4. PubMed ID: 2195190
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Hereditary spherocytosis and related disorders.
Becker PS; Lux SE
Clin Haematol; 1985 Feb; 14(1):15-43. PubMed ID: 3886234
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. [Hereditary elliptocytosis caused by a spectrin deficiency (Sp alpha I/46). 1st patient described in Cuba].
Estrada del Cueto M; García Meneses M; Pérez Díez de los Ríos G; Lagarde Ampudia M
Sangre (Barc); 1992 Dec; 37(6):461-3. PubMed ID: 1293798
[TBL] [Abstract][Full Text] [Related]
8. [Erythrocyte membrane protein abnormalities in hereditary hemolytic anemias].
Boivin P; Galand C
Nouv Rev Fr Hematol Blood Cells; 1977; 18(1):95-116. PubMed ID: 197487
[TBL] [Abstract][Full Text] [Related]
9. [Measurement of phospholipids in erythrocytes, plasma and platelets in a patient with hereditary spherocytosis].
César JM; Fernández I; Navarro JL
Sangre (Barc); 1989 Aug; 34(4):300-2. PubMed ID: 2772783
[TBL] [Abstract][Full Text] [Related]
10. [Cytoskeleton anomalies in disorders of red cell membrane proteins].
Kanzaki A; Wada H; Yawata Y
Rinsho Ketsueki; 1991 Jun; 32(6):573-9. PubMed ID: 1832469
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. The genetic disorders of the red cell skeleton.
Delaunay J; Alloisio N; Morle L; Baklouti F
Nouv Rev Fr Hematol (1978); 1991; 33(2):63-70. PubMed ID: 1766857
[TBL] [Abstract][Full Text] [Related]
13. Ankyrin deficiency in dominant hereditary spherocytosis: report of three cases.
Iolascon A; Miraglia del Giudice E; Camaschella C; Pinto L; Nobili B; Perrotta S; Cutillo S
Br J Haematol; 1991 Aug; 78(4):551-4. PubMed ID: 1832935
[TBL] [Abstract][Full Text] [Related]
14. Partial ankyrin and spectrin deficiency in severe, atypical hereditary spherocytosis.
Coetzer TL; Lawler J; Liu SC; Prchal JT; Gualtieri RJ; Brain MC; Dacie JV; Palek J
N Engl J Med; 1988 Jan; 318(4):230-4. PubMed ID: 2961992
[No Abstract] [Full Text] [Related]
15. Spectrin/band 3 ratio as diagnostic tool in hereditary spherocytosis.
Cutillo S; Pinto L; Nobili B; Miraglia del Giudice E; Iolascon A
Eur J Pediatr; 1992 Jan; 151(1):35-7. PubMed ID: 1728542
[TBL] [Abstract][Full Text] [Related]
16. [Molecular pathology of the erythrocyte membrane. Erythrocyte membrane defects as a cause of congenital hemolytic anemia].
Schröter W; Eber SW
Monatsschr Kinderheilkd; 1989 Jul; 137(7):368-79. PubMed ID: 2677683
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. Oxidative erythrocyte membrane damage in hereditary spherocytosis.
Caprari P; Bozzi A; Ferroni L; Strom R; Salvati AM
Biochem Int; 1992 Feb; 26(2):265-74. PubMed ID: 1558539
[TBL] [Abstract][Full Text] [Related]
20. Marked reduction of spectrinin hereditary spherocytosis in the common house mouse.
Greenquist AC; Shohet SB; Bernstein SE
Blood; 1978 Jun; 51(6):1149-55. PubMed ID: 647119
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]