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Year Number of Results
2010 1
2012 3
2013 3
2014 5
2015 3
2016 6
2017 1
2018 3
2019 2
2020 1
2021 1
2024 0

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24 results

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Page 1
The molecular genetics of sideroblastic anemia.
Ducamp S, Fleming MD. Ducamp S, et al. Blood. 2019 Jan 3;133(1):59-69. doi: 10.1182/blood-2018-08-815951. Epub 2018 Nov 6. Blood. 2019. PMID: 30401706 Free PMC article. Review.
Sideroblastic anemia: diagnosis and management.
Bottomley SS, Fleming MD. Bottomley SS, et al. Hematol Oncol Clin North Am. 2014 Aug;28(4):653-70, v. doi: 10.1016/j.hoc.2014.04.008. Epub 2014 Jun 2. Hematol Oncol Clin North Am. 2014. PMID: 25064706 Review.
Ringed sideroblasts in β-thalassemia.
Cattivelli K, Campagna DR, Schmitz-Abe K, Heeney MM, Yaish HM, Caruso Brown AE, Kearney S, Walkovich K, Markianos K, Fleming MD, Neufeld EJ. Cattivelli K, et al. Pediatr Blood Cancer. 2017 May;64(5):10.1002/pbc.26324. doi: 10.1002/pbc.26324. Epub 2016 Nov 3. Pediatr Blood Cancer. 2017. PMID: 27808451 Free PMC article.
SLC25A38 congenital sideroblastic anemia: Phenotypes and genotypes of 31 individuals from 24 families, including 11 novel mutations, and a review of the literature.
Heeney MM, Berhe S, Campagna DR, Oved JH, Kurre P, Shaw PJ, Teo J, Shanap MA, Hassab HM, Glader BE, Shah S, Yoshimi A, Ameri A, Antin JH, Boudreaux J, Briones M, Dickerson KE, Fernandez CV, Farah R, Hasle H, Keel SB, Olson TS, Powers JM, Rose MJ, Shimamura A, Bottomley SS, Fleming MD. Heeney MM, et al. Hum Mutat. 2021 Nov;42(11):1367-1383. doi: 10.1002/humu.24267. Epub 2021 Aug 5. Hum Mutat. 2021. PMID: 34298585 Free PMC article. Review.
Mitochondrial heme: an exit strategy at last.
Fleming MD, Hamza I. Fleming MD, et al. J Clin Invest. 2012 Dec;122(12):4328-30. doi: 10.1172/JCI66607. Epub 2012 Nov 26. J Clin Invest. 2012. PMID: 23187133 Free PMC article.
Characterization of mitochondrial ferritin-deficient mice.
Bartnikas TB, Campagna DR, Antiochos B, Mulhern H, Pondarré C, Fleming MD. Bartnikas TB, et al. Am J Hematol. 2010 Dec;85(12):958-60. doi: 10.1002/ajh.21872. Am J Hematol. 2010. PMID: 20960432 Free PMC article. No abstract available.
Mutations in TRNT1 cause congenital sideroblastic anemia with immunodeficiency, fevers, and developmental delay (SIFD).
Chakraborty PK, Schmitz-Abe K, Kennedy EK, Mamady H, Naas T, Durie D, Campagna DR, Lau A, Sendamarai AK, Wiseman DH, May A, Jolles S, Connor P, Powell C, Heeney MM, Giardina PJ, Klaassen RJ, Kannengiesser C, Thuret I, Thompson AA, Marques L, Hughes S, Bonney DK, Bottomley SS, Wynn RF, Laxer RM, Minniti CP, Moppett J, Bordon V, Geraghty M, Joyce PB, Markianos K, Rudner AD, Holcik M, Fleming MD. Chakraborty PK, et al. Blood. 2014 Oct 30;124(18):2867-71. doi: 10.1182/blood-2014-08-591370. Epub 2014 Sep 5. Blood. 2014. PMID: 25193871 Free PMC article.
24 results