148 related articles for article (PubMed ID: 1293798)
1. [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]
2. [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]
3. 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]
4. [Abnormalities of beta spectrin with hereditary elliptocytosis in mother and child].
Iyori H; Kobayashi N; Fujisawa K; Akatsuka J; Nakamura H; Mishima K; Kanzaki A; Wada H; Ata K; Yamada O
Rinsho Ketsueki; 1992 Feb; 33(2):167-72. PubMed ID: 1635163
[TBL] [Abstract][Full Text] [Related]
5. Molecular heterogeneity of hereditary elliptocytosis in Italy.
Miraglia del Giudice E; Perrotta S; Sannino E; De Angelis F; Nobili B; Iolascon A
Haematologica; 1994; 79(5):400-5. PubMed ID: 7843625
[TBL] [Abstract][Full Text] [Related]
6. [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]
7. 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]
8. [Application of 2 electrophoresis techniques to the analysis of erythrocyte membrane proteins in hereditary spherocytosis].
Ferrándiz F; Ródenas S; Villegas A
Sangre (Barc); 1993 Oct; 38(5):393-7. PubMed ID: 8140503
[TBL] [Abstract][Full Text] [Related]
9. [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]
10. Hemolytic anemias due to abnormalities in red cell spectrin: a brief review.
Lux SE; Wolfe LC; Pease B; Tomaselli MB; John KM; Bernstein SE
Prog Clin Biol Res; 1981; 45():159-68. PubMed ID: 7017750
[No Abstract] [Full Text] [Related]
11. Expression of spectrin alpha I/65 hereditary elliptocytosis in patients from Brazil.
Pranke PH; Basseres DS; Costa FF; Saad ST
Br J Haematol; 1996 Sep; 94(3):470-5. PubMed ID: 8790144
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. [Hereditary elliptocytosis in West Africa: frequency and repartition of spectrin variants].
Lecomte MC; Dhermy D; Gautero H; Bournier O; Galand C; Boivin P
C R Acad Sci III; 1988; 306(2):43-6. PubMed ID: 3126987
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. Hemolytic anemias associated with deficient or dysfunctional spectrin.
Lux SE; Pease B; Tomaselli MB; John KM; Bernstein SE
Prog Clin Biol Res; 1979; 30():463-9. PubMed ID: 531037
[TBL] [Abstract][Full Text] [Related]
17. Red cell membrane disorders in the Japanese population: clinical, biochemical, electron microscopic, and genetic studies.
Yawata Y; Kanzaki A; Inoue T; Ata K; Wada H; Okamoto N; Higo I; Yawata A; Sugihara T; Yamada O
Int J Hematol; 1994 Jul; 60(1):23-38. PubMed ID: 7919236
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. [Molecular aspects of erythrocyte membrane disorders].
Saad ST; Costa FF
Rev Assoc Med Bras (1992); 1994; 40(3):216-24. PubMed ID: 7787875
[No Abstract] [Full Text] [Related]
20. Update on the clinical spectrum and genetics of red blood cell membrane disorders.
Gallagher PG
Curr Hematol Rep; 2004 Mar; 3(2):85-91. PubMed ID: 14965483
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
