746 related articles for article (PubMed ID: 18641031)
1. 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]
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. [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]
4. [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]
5. 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]
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. [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]
8. 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]
9. 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]
10. [Silent forms of hereditary spherocytosis].
Brabec V; Cermák J; Jarolím P
Vnitr Lek; 1999 Oct; 45(10):594-7. PubMed ID: 10951867
[TBL] [Abstract][Full Text] [Related]
11. [Hereditary spherocytosis: clinical characteristics and treatment with splenectomy].
Jonte F; Ramírez A; Medina J; García Gala J; Rosón C; Corte JR; Vargas M; Pérez Lozana L
Sangre (Barc); 1995 Feb; 40(1):45-8. PubMed ID: 7716671
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Diagnostic power of laboratory tests for hereditary spherocytosis: a comparison study in 150 patients grouped according to molecular and clinical characteristics.
Bianchi P; Fermo E; Vercellati C; Marcello AP; Porretti L; Cortelezzi A; Barcellini W; Zanella A
Haematologica; 2012 Apr; 97(4):516-23. PubMed ID: 22058213
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Using the eosin-5-maleimide binding test in the differential diagnosis of hereditary spherocytosis and hereditary pyropoikilocytosis.
King MJ; Telfer P; MacKinnon H; Langabeer L; McMahon C; Darbyshire P; Dhermy D
Cytometry B Clin Cytom; 2008 Jul; 74(4):244-50. PubMed ID: 18454487
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. [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]
18. Uniquely higher incidence of isolated or combined deficiency of band 3 and/or band 4.2 as the pathogenesis of autosomal dominantly inherited hereditary spherocytosis in the Japanese population.
Inoue T; Kanzaki A; Yawata A; Wada H; Okamoto N; Takahashi M; Sugihara T; Yamada O; Yawata Y
Int J Hematol; 1994 Dec; 60(4):227-38. PubMed ID: 7894027
[TBL] [Abstract][Full Text] [Related]
19. Variable clinical severity of hereditary spherocytosis: relation to erythrocytic spectrin concentration, osmotic fragility, and autohemolysis.
Eber SW; Armbrust R; Schröter W
J Pediatr; 1990 Sep; 117(3):409-16. PubMed ID: 2391596
[TBL] [Abstract][Full Text] [Related]
20. [Effectiveness of partial splenectomy in the treatment of hereditary spherocytosis].
Pavón Morán V; Estrada del Cueto M; Fernández Delgado N; Sánchez Damas M; Vergara Rivero R; González Otero A; Vilorio Barreras P; Svarch E
Rev Invest Clin; 2000; 52(3):229-33. PubMed ID: 10953604
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]