295 related articles for article (PubMed ID: 16540354)
41. H63D homozygotes with hyperferritinaemia: Is this genotype, the primary cause of iron overload?
de Diego C; Opazo S; Murga MJ; Martínez-Castro P
Eur J Haematol; 2007 Jan; 78(1):66-71. PubMed ID: 17042772
[TBL] [Abstract][Full Text] [Related]
42. X-linked sideroblastic anaemia due to a mutation in the erythroid 5-aminolaevulinate synthase gene leading to an arginine170 to leucine substitution.
Edgar AJ; Vidyatilake HM; Wickramasinghe SN
Eur J Haematol; 1998 Jul; 61(1):55-8. PubMed ID: 9688293
[TBL] [Abstract][Full Text] [Related]
43. Association of HLA-linked hemochromatosis with idiopathic refractory sideroblastic anemia.
Cartwright GE; Edwards CQ; Skolnick MH; Amos DB
J Clin Invest; 1980 May; 65(5):989-92. PubMed ID: 7364949
[TBL] [Abstract][Full Text] [Related]
44. Molecular pathophysiology and genetic mutations in congenital sideroblastic anemia.
Fujiwara T; Harigae H
Free Radic Biol Med; 2019 Mar; 133():179-185. PubMed ID: 30098397
[TBL] [Abstract][Full Text] [Related]
45. X-linked macrocytic dyserythropoietic anemia in females with an ALAS2 mutation.
Sankaran VG; Ulirsch JC; Tchaikovskii V; Ludwig LS; Wakabayashi A; Kadirvel S; Lindsley RC; Bejar R; Shi J; Lovitch SB; Bishop DF; Steensma DP
J Clin Invest; 2015 Apr; 125(4):1665-9. PubMed ID: 25705881
[TBL] [Abstract][Full Text] [Related]
46. Does rapidly progressive iron overload in a young girl with sideroblastic anemia also signify the presence of hereditary hemochromatosis?
Scimeca PG; Weinblatt ME; Kahn E; Kochen JA
Pediatr Hematol Oncol; 1994; 11(1):99-104. PubMed ID: 8155505
[TBL] [Abstract][Full Text] [Related]
47. X-linked Sideroblastic Anemia in a Malay Boy With ALAS2 S568G Mutation.
Susanto TAK; Bhattacharyya R
J Pediatr Hematol Oncol; 2017 Jul; 39(5):408-409. PubMed ID: 28644307
[TBL] [Abstract][Full Text] [Related]
48. Non syndromic childhood onset congenital sideroblastic anemia: A report of 13 patients identified with an ALAS2 or SLC25A38 mutation.
Le Rouzic MA; Fouquet C; Leblanc T; Touati M; Fouyssac F; Vermylen C; Jäkel N; Guichard JF; Maloum K; Toutain F; Lutz P; Perel Y; Manceau H; Kannengiesser C; Vannier JP
Blood Cells Mol Dis; 2017 Jul; 66():11-18. PubMed ID: 28772256
[TBL] [Abstract][Full Text] [Related]
49. Gene symbol: ALAS2. Disease: sideroblastic anaemia.
Pereira JC; Gutiérrez EO; Ribeiro ML
Hum Genet; 2004 Nov; 115(6):533. PubMed ID: 15678587
[No Abstract] [Full Text] [Related]
50. Phenotypic expression of ferroportin disease in a family with the N144H mutation.
Rosmorduc O; Wendum D; Arrivé L; Elnaggar A; Ennibi K; Hannoun L; Charlotte F; Grangé JD; Poupon R
Gastroenterol Clin Biol; 2008 Mar; 32(3):321-7. PubMed ID: 18403150
[TBL] [Abstract][Full Text] [Related]
51. Hereditary sideroblastic anaemia due to a mutation in exon 10 of the erythroid 5-aminolaevulinate synthase gene.
Edgar AJ; Wickramasinghe SN
Br J Haematol; 1998 Feb; 100(2):389-92. PubMed ID: 9488633
[TBL] [Abstract][Full Text] [Related]
52. Hepatocellular carcinoma associated with hereditary hemochromatosis occurring in non-cirrhotic liver.
von Delius S; Lersch C; Schulte-Frohlinde E; Fend F; Dobritz M; Schmid RM; Eckel F
Z Gastroenterol; 2006 Jan; 44(1):39-42. PubMed ID: 16397838
[TBL] [Abstract][Full Text] [Related]
53. Hereditary spherocytosis and hemochromatosis.
Brandenberg JB; Demarmels Biasiutti F; Lutz HU; Wuillemin WA
Ann Hematol; 2002 Apr; 81(4):202-9. PubMed ID: 11976822
[TBL] [Abstract][Full Text] [Related]
54. Gene symbol: ALAS2. Disease: sideroblastic anaemia.
Pereira JC; Gonçalves P; Cuhna E; Ribeiro ML
Hum Genet; 2004 Nov; 115(6):533. PubMed ID: 15678586
[No Abstract] [Full Text] [Related]
55. Gene symbol: ALAS2. Disease: sideroblastic anaemia.
Gonçalves P; Pereira JC; Rebelo U; Ribeiro ML
Hum Genet; 2004 Nov; 115(6):531. PubMed ID: 15565468
[No Abstract] [Full Text] [Related]
56. Homozygous p.M172K mutation of the TFR2 gene in an Italian family with type 3 hereditary hemochromatosis and early onset iron overload.
Majore S; Milano F; Binni F; Stuppia L; Cerrone A; Tafuri A; De Bernardo C; Palka G; Grammatico P
Haematologica; 2006 Aug; 91(8 Suppl):ECR33. PubMed ID: 16923517
[TBL] [Abstract][Full Text] [Related]
57. Two novel mutations, L490R and V561X, of the transferrin receptor 2 gene in Japanese patients with hemochromatosis.
Koyama C; Wakusawa S; Hayashi H; Suzuki R; Yano M; Yoshioka K; Kozuru M; Takayamam Y; Okada T; Mabuchi H
Haematologica; 2005 Mar; 90(3):302-7. PubMed ID: 15749661
[TBL] [Abstract][Full Text] [Related]
58. Hereditary sideroblastic anemias: pathophysiology, diagnosis, and treatment.
Camaschella C
Semin Hematol; 2009 Oct; 46(4):371-7. PubMed ID: 19786205
[TBL] [Abstract][Full Text] [Related]
59. [X-linked sideroblastic anemia].
Muramatsu M; Usuki K; Izutsu K; Yamaguchi Y; Iki S; Furuyama K; Kondo M; Urabe A
Rinsho Ketsueki; 1999 Jul; 40(7):593-8. PubMed ID: 10483144
[TBL] [Abstract][Full Text] [Related]
60. [Vitamin B6-sensitive hereditary sideroblastic anemia].
Heller T; Höchstetter V; Basler M; Borck V
Dtsch Med Wochenschr; 2004 Jan; 129(4):141-4. PubMed ID: 14724775
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]