295 related articles for article (PubMed ID: 11030038)
1. The diagnosis and management of hereditary spherocytosis.
Bolton-Maggs PH
Baillieres Best Pract Res Clin Haematol; 2000 Sep; 13(3):327-42. PubMed ID: 11030038
[TBL] [Abstract][Full Text] [Related]
2. Guidelines for the diagnosis and management of hereditary spherocytosis.
Bolton-Maggs PH; Stevens RF; Dodd NJ; Lamont G; Tittensor P; King MJ;
Br J Haematol; 2004 Aug; 126(4):455-74. PubMed ID: 15287938
[TBL] [Abstract][Full Text] [Related]
3. [Hereditary spherocytosis: guidelines for the diagnosis and management in children].
Guitton C; Garçon L; Cynober T; Gauthier F; Tchernia G; Delaunay J; Leblanc T; Thuret I; Bader-Meunier B
Arch Pediatr; 2008 Sep; 15(9):1464-73. PubMed ID: 18556182
[TBL] [Abstract][Full Text] [Related]
4. [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]
5. Protein deficiency balance as a predictor of clinical outcome in hereditary spherocytosis.
Rocha S; Rebelo I; Costa E; Catarino C; Belo L; Castro EM; Cabeda JM; Barbot J; Quintanilha A; Santos-Silva A
Eur J Haematol; 2005 May; 74(5):374-80. PubMed ID: 15813910
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Guidelines for the diagnosis and management of hereditary spherocytosis--2011 update.
Bolton-Maggs PH; Langer JC; Iolascon A; Tittensor P; King MJ;
Br J Haematol; 2012 Jan; 156(1):37-49. PubMed ID: 22055020
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. [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]
10. Hereditary spherocytosis.
Bellingham AJ; Prankerd TA
Clin Haematol; 1975 Feb; 4(1):139-44. PubMed ID: 1102180
[No Abstract] [Full Text] [Related]
11. Erythropoietin levels in the different clinical forms of hereditary spherocytosis.
Rocha S; Costa E; Catarino C; Belo L; Castro EM; Barbot J; Quintanilha A; Santos-Silva A
Br J Haematol; 2005 Nov; 131(4):534-42. PubMed ID: 16281946
[TBL] [Abstract][Full Text] [Related]
12. Red cell membrane disorders.
Gallagher PG
Hematology Am Soc Hematol Educ Program; 2005; ():13-8. PubMed ID: 16304353
[TBL] [Abstract][Full Text] [Related]
13. [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]
14. [Hereditary stomatocytoses--diagnostic problems and their molecular basis].
Bogusławska DM; Machnicka B; Sikorski AF
Pol Merkur Lekarski; 2010 Aug; 29(170):119-24. PubMed ID: 20842826
[TBL] [Abstract][Full Text] [Related]
15. [3 generations of a family affected by hereditary microspherocytic anemia treated by splenectomy].
Judkiewicz L; Pawlowska-Krykowska D; Polkowska-Kulesza E; Pluzańska A
Pol Tyg Lek; 1973 Nov; 28(45):1768-70. PubMed ID: 4765944
[No Abstract] [Full Text] [Related]
16. Clinical and molecular aspects of disorders of the erythrocyte membrane skeleton.
Gallagher PG; Tse WT; Forget BG
Semin Perinatol; 1990 Oct; 14(5):351-67. PubMed ID: 2287951
[No Abstract] [Full Text] [Related]
17. The effect of splenectomy in hereditary spherocytosis by dual angle laser light cytometry.
Ricard MP; Gilsanz F
Clin Lab Haematol; 1996 Dec; 18(4):249-51. PubMed ID: 9054697
[TBL] [Abstract][Full Text] [Related]
18. Spectrin oligomers of the red cell membrane extracts in hereditary spherocytosis.
Marík T; Kodícek M; Brabec V
Biomed Biochim Acta; 1983; 42(11-12):S32-7. PubMed ID: 6675711
[TBL] [Abstract][Full Text] [Related]
19. ICSH guidelines for the laboratory diagnosis of nonimmune hereditary red cell membrane disorders.
King MJ; Garçon L; Hoyer JD; Iolascon A; Picard V; Stewart G; Bianchi P; Lee SH; Zanella A;
Int J Lab Hematol; 2015 Jun; 37(3):304-25. PubMed ID: 25790109
[TBL] [Abstract][Full Text] [Related]
20. Laboratory markers of thrombosis risk in children with hereditary spherocytosis.
Troendle SB; Adix L; Crary SE; Buchanan GR
Pediatr Blood Cancer; 2007 Nov; 49(6):781-5. PubMed ID: 17854065
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]