203 related articles for article (PubMed ID: 3886234)
1. 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]
2. [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]
3. Clinical and hematologic features of 300 patients affected by hereditary spherocytosis grouped according to the type of the membrane protein defect.
Mariani M; Barcellini W; Vercellati C; Marcello AP; Fermo E; Pedotti P; Boschetti C; Zanella A
Haematologica; 2008 Sep; 93(9):1310-7. PubMed ID: 18641031
[TBL] [Abstract][Full Text] [Related]
4. Physiologically important secondary modifications of red cell membrane in hereditary spherocytosis-evidence for in vivo oxidation and lipid rafts protein variations.
Margetis P; Antonelou M; Karababa F; Loutradi A; Margaritis L; Papassideri I
Blood Cells Mol Dis; 2007; 38(3):210-20. PubMed ID: 17208471
[TBL] [Abstract][Full Text] [Related]
5. [Erythrocyte membrane and hereditary spherocytosis].
Ideguchi H
Rinsho Byori; 1990 Apr; 38(4):360-4. PubMed ID: 2195190
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Ankyrin-1 mutations are a major cause of dominant and recessive hereditary spherocytosis.
Eber SW; Gonzalez JM; Lux ML; Scarpa AL; Tse WT; Dornwell M; Herbers J; Kugler W; Ozcan R; Pekrun A; Gallagher PG; Schröter W; Forget BG; Lux SE
Nat Genet; 1996 Jun; 13(2):214-8. PubMed ID: 8640229
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. [Molecular mechanism of hereditary spherocytosis].
Bogusławska DM; Heger E; Sikorski AF
Pol Merkur Lekarski; 2006 Jan; 20(115):112-6. PubMed ID: 16617750
[TBL] [Abstract][Full Text] [Related]
11. [Relation between types of erythrocyte membrane defects and the clinical picture in hereditary spherocytosis].
Brabec V; Palek J; Petrtýlová K; Cermák J; Jarolím P
Vnitr Lek; 1997 Feb; 43(2):91-4. PubMed ID: 9245075
[TBL] [Abstract][Full Text] [Related]
12. [Abnormal changes in erythrocyte membrane proteins in hereditary spherocytosis and their relation to clinical and biological aspects of the disease].
Ayala S; Besson I; Aymerich M; Berga L; Vives Corrons JL
Med Clin (Barc); 1995 Jun; 105(2):45-9. PubMed ID: 7603093
[TBL] [Abstract][Full Text] [Related]
13. Erythrocyte membrane protein defects in hereditary spherocytosis patients in Turkish population.
Ayhan AC; Yildiz I; Yüzbaşıoğlu S; Celkan T; Apak H; Ozkan A; Karaman S
Hematology; 2012 Jul; 17(4):232-6. PubMed ID: 22889517
[TBL] [Abstract][Full Text] [Related]
14. A genetic defect in the binding of protein 4.1 to spectrin in a kindred with hereditary spherocytosis.
Wolfe LC; John KM; Falcone JC; Byrne AM; Lux SE
N Engl J Med; 1982 Nov; 307(22):1367-74. PubMed ID: 6215583
[TBL] [Abstract][Full Text] [Related]
15. Hereditary spherocytosis--defects in proteins that connect the membrane skeleton to the lipid bilayer.
Eber S; Lux SE
Semin Hematol; 2004 Apr; 41(2):118-41. PubMed ID: 15071790
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. Role of the interaction between Lu/BCAM and the spectrin-based membrane skeleton in the increased adhesion of hereditary spherocytosis red cells to laminin.
Gauthier E; El Nemer W; Wautier MP; Renaud O; Tchernia G; Delaunay J; Le Van Kim C; Colin Y
Br J Haematol; 2010 Feb; 148(3):456-65. PubMed ID: 20092464
[TBL] [Abstract][Full Text] [Related]
19. Unchanged binding of 99molybdenum to red cell membrane proteins in hereditary spherocytosis.
Marík T; Kselíková M; Bíbr B; Brabec V; Lener J
Folia Haematol Int Mag Klin Morphol Blutforsch; 1983; 110(1):81-5. PubMed ID: 6192057
[TBL] [Abstract][Full Text] [Related]
20. [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]
[Next] [New Search]