201 related articles for article (PubMed ID: 3069829)
1. Clinical disorders of the erythrocyte membrane skeleton.
McGuire M; Agre P
Hematol Pathol; 1988; 2(1):1-14. PubMed ID: 3069829
[TBL] [Abstract][Full Text] [Related]
2. [Hereditary diseases of the human erythrocyte membrane skeleton (author's transl)].
Boivin P
Nouv Presse Med; 1982 Jul; 11(31):2347-51. PubMed ID: 7111000
[TBL] [Abstract][Full Text] [Related]
3. [Molecular pathology of the erythrocyte membrane].
Delaunay J
Rev Prat; 1993 Jun; 43(11):1392-6. PubMed ID: 8235389
[TBL] [Abstract][Full Text] [Related]
4. [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]
5. 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]
6. [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]
7. Red cell membrane skeleton: structure-function relationships.
Palek J; Liu SC
Prog Clin Biol Res; 1980; 43():21-44. PubMed ID: 6999502
[TBL] [Abstract][Full Text] [Related]
8. Molecular pathology of inherited erythrocyte membrane disorders: hereditary spherocytosis and elliptocytosis.
Iolascon A; Miraglia del Giudice E; Camaschella C
Haematologica; 1992; 77(1):60-72. PubMed ID: 1356891
[TBL] [Abstract][Full Text] [Related]
9. Disorders of red cell membrane.
An X; Mohandas N
Br J Haematol; 2008 May; 141(3):367-75. PubMed ID: 18341630
[TBL] [Abstract][Full Text] [Related]
10. [Hereditary diseases of erythrocyte membrane: from clinical aspects to underlying genetical and molecular mechanisms].
Bichis M; Huber AR
Ann Biol Clin (Paris); 2000; 58(3):277-89. PubMed ID: 10846232
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. The molecular basis for membrane - cytoskeleton association in human erythrocytes.
Bennett V
J Cell Biochem; 1982; 18(1):49-65. PubMed ID: 6461664
[TBL] [Abstract][Full Text] [Related]
13. Membrane proteins in hereditary spherocytosis, elliptocytosis and stomatocytosis.
Sakal M; Chorváth B; Duraj J; Sakalová A
Folia Haematol Int Mag Klin Morphol Blutforsch; 1982; 109(5):787-91. PubMed ID: 6188665
[TBL] [Abstract][Full Text] [Related]
14. [Congenital hemolytic anemia with erythrocyte thermal instability and defect of spectrin tetrameric polymerization. Study of erythrocyte deformability in a new case of hereditary pyropoikilocytosis using diffraction viscosimetry].
Dhermy D; Féo C; Garbarz M; Bournier O; Dommergues JP; Garcia J; Boivin P; Tchernia G
Nouv Rev Fr Hematol (1978); 1983; 25(1):7-16. PubMed ID: 6835836
[TBL] [Abstract][Full Text] [Related]
15. Spectrin oligomerization is cooperatively coupled to membrane assembly: a linkage targeted by many hereditary hemolytic anemias?
Giorgi M; Cianci CD; Gallagher PG; Morrow JS
Exp Mol Pathol; 2001 Jun; 70(3):215-30. PubMed ID: 11418000
[TBL] [Abstract][Full Text] [Related]
16. Red blood cell membrane defects.
Iolascon A; Perrotta S; Stewart GW
Rev Clin Exp Hematol; 2003 Mar; 7(1):22-56. PubMed ID: 14692233
[TBL] [Abstract][Full Text] [Related]
17. Recent advances in the understanding of the erythrocyte membrane.
Lam SK; Quah TC
J Singapore Paediatr Soc; 1991; 33(3-4):140-8. PubMed ID: 1812330
[TBL] [Abstract][Full Text] [Related]
18. [Hemolytic anemia caused by congenital anomalies of the erythrocyte membrane].
Boivin P
J Genet Hum; 1986 Nov; 34(5):393-412. PubMed ID: 3540209
[No Abstract] [Full Text] [Related]
19. 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]
20. Molecular defect in the sickle erythrocyte skeleton. Abnormal spectrin binding to sickle inside-our vesicles.
Platt OS; Falcone JF; Lux SE
J Clin Invest; 1985 Jan; 75(1):266-71. PubMed ID: 2578138
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
