182 related articles for article (PubMed ID: 9844481)
21. [Contribution of the spleen to the lipid metabolism in plasma and red cells. On hereditary spherocytosis and hereditary high red cell membrane phosphatidylcholine hemolytic anemia].
Sugihara T; Otsuka A; Yawata Y
Rinsho Ketsueki; 1989 Aug; 30(8):1248-55. PubMed ID: 2601042
[TBL] [Abstract][Full Text] [Related]
22. [Alteration of erythrocyte membrane proteins in a family with hereditary spherocytosis].
Inoue F; Matsuyama R; Yoneyama S
Nihon Ketsueki Gakkai Zasshi; 1989 Nov; 52(7):1122-7. PubMed ID: 2618557
[TBL] [Abstract][Full Text] [Related]
23. Changes in proteolytic susceptibility of erythrocyte membrane proteins in hereditary spherocytosis.
Gaczyńska M; Bartosz G; Judkiewicz L
Clin Chim Acta; 1991 May; 198(3):267-70. PubMed ID: 1889126
[No Abstract] [Full Text] [Related]
24. [Study of erythrocyte ion permeability in hereditary spherocytosis: contribution to its diagnosis].
Merino A; Vives Corrons L; Aguilar i Bascompte JL; Berga L; Reverter JC
Sangre (Barc); 1987; 32(3):323-32. PubMed ID: 2443989
[No Abstract] [Full Text] [Related]
25. [Studies on the protein composition of red-cell membrane in hereditary spherocytosis (author's transl)].
Mazo E; Fernández J; Zubizarreta A; Rocha E
Sangre (Barc); 1979; 24(4):376-88. PubMed ID: 483115
[No Abstract] [Full Text] [Related]
26. Abnormal degradation of erythrocyte membrane proteins in hereditary spherocytosis.
Gaczyńska M; Bartosz G; Judkiewicz L; Rosin J
Clin Chim Acta; 1987 Sep; 168(1):7-11. PubMed ID: 3665105
[TBL] [Abstract][Full Text] [Related]
27. Homozygosity for dominant form of hereditary spherocytosis.
Duru F; Gürgey A; Oztürk G; Yörükan S; Altay C
Br J Haematol; 1992 Nov; 82(3):596-600. PubMed ID: 1486040
[TBL] [Abstract][Full Text] [Related]
28. 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]
29. 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]
30. [Current theories on the etiopathogenesis of congenital spherocytosis].
Zelenay E; Ochocka M
Pediatr Pol; 1985 Jan; 60(1):91-4. PubMed ID: 3898003
[No Abstract] [Full Text] [Related]
31. [Hereditary spherocytosis. Cases from the Pediatric Clinic].
Cottafava F; Di Maio A; Tosca P; Fedi M; Cosso D; Brida di Priò S
Minerva Pediatr; 1985 Jun; 37(11-12):429-34. PubMed ID: 4069090
[No Abstract] [Full Text] [Related]
32. Occurrence and characteristics of hereditary spherocytosis in Algeria.
Zerhouni F; Guetarni D; Henni T; Colonna P
Eur J Haematol; 1991 Jul; 47(1):42-7. PubMed ID: 1868913
[TBL] [Abstract][Full Text] [Related]
33. 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]
34. Hereditary Spherocytosis: Can Next-Generation Sequencing of the Five Most Frequently Affected Genes Replace Time-Consuming Functional Investigations?
Häuser F; Rossmann H; Adenaeuer A; Shrestha A; Marandiuc D; Paret C; Faber J; Lackner KJ; Lämmle B; Beck O
Int J Mol Sci; 2023 Nov; 24(23):. PubMed ID: 38069343
[TBL] [Abstract][Full Text] [Related]
35. Flow cytometric measurement (H-1 Technicon) of microcytic and hyperchromic red cell populations in pediatric patients affected by hereditary spherocytosis (HS).
Ialongo P; Vignetti M; Cigliano G; Amadori S; Mandelli F
Haematologica; 1989; 74(6):547-53. PubMed ID: 2628236
[TBL] [Abstract][Full Text] [Related]
36. Decreased membrane mechanical stability and in vivo loss of surface area reflect spectrin deficiencies in hereditary spherocytosis.
Chasis JA; Agre P; Mohandas N
J Clin Invest; 1988 Aug; 82(2):617-23. PubMed ID: 3403720
[TBL] [Abstract][Full Text] [Related]
37. Growth of Plasmodium falciparum in human erythrocytes containing abnormal membrane proteins.
Schulman S; Roth EF; Cheng B; Rybicki AC; Sussman II; Wong M; Wang W; Ranney HM; Nagel RL; Schwartz RS
Proc Natl Acad Sci U S A; 1990 Sep; 87(18):7339-43. PubMed ID: 2205856
[TBL] [Abstract][Full Text] [Related]
38. Abnormal oxidant sensitivity and beta-chain structure of spectrin in hereditary spherocytosis associated with defective spectrin-protein 4.1 binding.
Becker PS; Morrow JS; Lux SE
J Clin Invest; 1987 Aug; 80(2):557-65. PubMed ID: 3611357
[TBL] [Abstract][Full Text] [Related]
39. Effects of
Herrera-Tirado IM; Espinoza-Mata LL; Rizo-delaTorre LDC; Becerra-Solano LE; Ibarra-Cortés B; Perea-Díaz FJ
Genet Test Mol Biomarkers; 2022 May; 26(5):270-276. PubMed ID: 35638908
[No Abstract] [Full Text] [Related]
40. Hereditary spherocytosis.
Boyd AS
Am Fam Physician; 1989 Feb; 39(2):167-72. PubMed ID: 2644787
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
