These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

142 related articles for article (PubMed ID: 24862439)

  • 1. Different haematological picture of congenital sideroblastic anaemia in a hemizygote and a heterozygote.
    Aguiar E; Freitas MI; Barbot J
    Br J Haematol; 2014 Aug; 166(4):469. PubMed ID: 24862439
    [No Abstract]   [Full Text] [Related]  

  • 2. A novel hemizygous I418S mutation in the ALAS2 gene in a young Korean man with X-linked sideroblastic anemia.
    Moon SY; Jun IJ; Kim JE; Lee SJ; Kim HK; Yoon SS
    Ann Lab Med; 2014 Mar; 34(2):159-62. PubMed ID: 24624355
    [No Abstract]   [Full Text] [Related]  

  • 3. A novel mutation, Ile289Thr, in the ALAS2 gene in a family with pyridoxine responsive sideroblastic anaemia.
    Percy MJ; Cuthbert RJ; May A; McMullin MF
    J Clin Pathol; 2006 Sep; 59(9):1002. PubMed ID: 16935983
    [No Abstract]   [Full Text] [Related]  

  • 4. 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]  

  • 5. X-linked sideroblastic anaemia due to ALAS₂ mutations in the Netherlands: a disease in disguise.
    Donker AE; Raymakers RA; Nieuwenhuis HK; Coenen MJ; Janssen MC; MacKenzie MA; Brons PP; Swinkels DW
    Neth J Med; 2014 May; 72(4):210-7. PubMed ID: 24829177
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Disparate phenotypic expression of ALAS2 R452H (nt 1407 G --> A) in two brothers, one with severe sideroblastic anemia and iron overload, hepatic cirrhosis, and hepatocellular carcinoma.
    Barton JC; Lee PL
    Blood Cells Mol Dis; 2006; 36(3):342-6. PubMed ID: 16540354
    [TBL] [Abstract][Full Text] [Related]  

  • 7. X-linked sideroblastic anemia due to ALAS2 intron 1 enhancer element GATA-binding site mutations.
    Campagna DR; de Bie CI; Schmitz-Abe K; Sweeney M; Sendamarai AK; Schmidt PJ; Heeney MM; Yntema HG; Kannengiesser C; Grandchamp B; Niemeyer CM; Knoers NV; Swart S; Marron G; van Wijk R; Raymakers RA; May A; Markianos K; Bottomley SS; Swinkels DW; Fleming MD
    Am J Hematol; 2014 Mar; 89(3):315-9. PubMed ID: 24166784
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mutation Analysis of X-linked Sideroblastic Anemia in a 12-Month-Old Boy by Massively Parallel Sequencing.
    Yu HJ; Lee YJ; Shim JW; Kim DS; Shim JY; Park MS; Woo HY; Park H; Jung HL; Kwon MJ
    Ann Lab Med; 2018 Jul; 38(4):389-392. PubMed ID: 29611395
    [No Abstract]   [Full Text] [Related]  

  • 9. A hemizygous p.R204Q mutation in the ALAS2 gene underlies X-linked sideroblastic anemia in an adult Chinese Han man.
    Huang J; Ge M; Shao Y; Wang M; Jin P; Huo J; Li X; Zhang J; Nie N; Zheng Y
    BMC Med Genomics; 2021 Apr; 14(1):107. PubMed ID: 33858445
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A Novel
    Lee JS; Gu J; Yoo HJ; Koh Y; Kim HK
    Ann Clin Lab Sci; 2017 May; 47(3):319-322. PubMed ID: 28667034
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. A double red cells population in a woman with a microcytic anemia.
    Garçon L; Kannengiesser C
    Blood; 2014 Feb; 123(6):808. PubMed ID: 24660232
    [No Abstract]   [Full Text] [Related]  

  • 13. Gene symbol: ALAS2. Disease: sideroblastic anaemia.
    Gonçalves P; Pereira JC; Ribeiro ML
    Hum Genet; 2004 Nov; 115(6):532. PubMed ID: 15678585
    [No Abstract]   [Full Text] [Related]  

  • 14. 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]  

  • 15. A novel mutation of the erythroid-specific delta-aminolaevulinate synthase gene in a patient with X-linked sideroblastic anaemia.
    Harigae H; Furuyama K; Kimura A; Neriishi K; Tahara N; Kondo M; Hayashi N; Yamamoto M; Sassa S; Sasaki T
    Br J Haematol; 1999 Jul; 106(1):175-7. PubMed ID: 10444183
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Congenital sideroblastic anaemia with a novel frameshift mutation in SLC25A38.
    Wong WS; Wong HF; Cheng CK; Chang KO; Chan NP; Ng MH; Wong KF
    J Clin Pathol; 2015 Mar; 68(3):249-51. PubMed ID: 25512395
    [No Abstract]   [Full Text] [Related]  

  • 18. Novel human pathological mutations. Gene symbol: ALAS2. Disease: sideroblastic anaemia.
    Pereira JC; Barbot J; Ribeiro ML
    Hum Genet; 2009 Aug; 126(2):333. PubMed ID: 19693999
    [No Abstract]   [Full Text] [Related]  

  • 19. [Congenital sideroblastic anemia-a new family with identification of K156E mutation of ALAS2 gene and literature review].
    Cui R; Xu Z; Qin T; Zhang Y; Xiao Z
    Zhonghua Xue Ye Xue Za Zhi; 2014 Feb; 35(2):142-6. PubMed ID: 24606657
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Progress of study on sideroblastic anemia and its possible gene therapy--review].
    Wang YQ; Zhu P
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2005 Jun; 13(3):524-8. PubMed ID: 15972158
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.