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9. Hereditary sideroblastic anaemia and ataxia: an X linked recessive disorder. Pagon RA; Bird TD; Detter JC; Pierce I J Med Genet; 1985 Aug; 22(4):267-73. PubMed ID: 4045952 [TBL] [Abstract][Full Text] [Related]
10. Pyridoxine-refractory congenital sideroblastic anaemia with evidence for autosomal inheritance: exclusion of linkage to ALAS2 at Xp11.21 by polymorphism analysis. Jardine PE; Cotter PD; Johnson SA; Fitzsimons EJ; Tyfield L; Lunt PW; Bishop DF J Med Genet; 1994 Mar; 31(3):213-8. PubMed ID: 7912287 [TBL] [Abstract][Full Text] [Related]
11. A family study of congenital X linked sideroblastic anaemia. Holmes J; May A; Geddes D; Jacobs A J Med Genet; 1990 Jan; 27(1):26-8. PubMed ID: 2308152 [TBL] [Abstract][Full Text] [Related]
13. Acquired hypochromic and microcytic sideroblastic anaemia responsive to pyridoxine with low value of free erythrocyte protoporphyrin: a possible subgroup of idiopathic acquired sideroblastic anaemia (IASA). Takeda Y; Sawada H; Sawai H; Toi-Matsuda T; Tashima M; Okuma M; Watanabe S; Ohmori S; Kondo M Br J Haematol; 1995 May; 90(1):207-9. PubMed ID: 7786786 [TBL] [Abstract][Full Text] [Related]
14. [Refractory sideroblastic anaemia of primary and acquired appearance (author's transl)]. Albahary C; Boiron M; Najean Y Nouv Presse Med; 1979 Feb; 8(6):425-6. PubMed ID: 162300 [TBL] [Abstract][Full Text] [Related]
16. Iron overload in mild sideroblastic anaemias. Peto TE; Pippard MJ; Weatherall DJ Lancet; 1983 Feb; 1(8321):375-8. PubMed ID: 6130377 [TBL] [Abstract][Full Text] [Related]
17. Lethal ALAS2 mutation in males X-linked sideroblastic anaemia. Rose C; Callebaut I; Pascal L; Oudin C; Fournier M; Gouya L; Lambilliotte A; Kannengiesser C Br J Haematol; 2017 Aug; 178(4):648-651. PubMed ID: 27292130 [No Abstract] [Full Text] [Related]
18. Linkage analysis of a large pedigree with hereditary sideroblastic anaemia. Noble JS; Taylor GR; Losowsky MS; Hall R; Turner G; Mueller RF; Stewart AD J Med Genet; 1995 May; 32(5):389-92. PubMed ID: 7616548 [TBL] [Abstract][Full Text] [Related]
19. Haema synthesis during pyridoxine therapy in two families with different types of hereditary sideroblastic anaemia. Pasanen AV; Salmi M; Tenhunen R; Vuopio P Ann Clin Res; 1982 Apr; 14(2):61-5. PubMed ID: 7149613 [TBL] [Abstract][Full Text] [Related]
20. RDW: a helpful diagnostic parameter in the malabsorption syndrome? Gambella O; Vignetti G Haematologica; 1992; 77(4):368. PubMed ID: 1427451 [No Abstract] [Full Text] [Related] [Next] [New Search]