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g(HbF): a genetic model of fetal hemoglobin in sickle cell disease.
Gardner K, Fulford T, Silver N, Rooks H, Angelis N, Allman M, Nkya S, Makani J, Howard J, Kesse-Adu R, Rees DC, Stuart-Smith S, Yeghen T, Awogbade M, Sangeda RZ, Mgaya J, Patel H, Newhouse S, Menzel S, Thein SL. Gardner K, et al. Among authors: menzel s. Blood Adv. 2018 Feb 13;2(3):235-239. doi: 10.1182/bloodadvances.2017009811. Blood Adv. 2018. PMID: 29437638 Free PMC article.
Genome wide association study of fetal hemoglobin in sickle cell anemia in Tanzania.
Mtatiro SN, Singh T, Rooks H, Mgaya J, Mariki H, Soka D, Mmbando B, Msaki E, Kolder I, Thein SL, Menzel S, Cox SE, Makani J, Barrett JC. Mtatiro SN, et al. Among authors: menzel s. PLoS One. 2014 Nov 5;9(11):e111464. doi: 10.1371/journal.pone.0111464. eCollection 2014. PLoS One. 2014. PMID: 25372704 Free PMC article.
F cell numbers are associated with an X-linked genetic polymorphism and correlate with haematological parameters in patients with sickle cell disease.
Urio F, Nkya S, Rooks H, Mgaya JA, Masamu U, Zozimus Sangeda R, Mmbando BP, Brumat M, Mselle T, Menzel S, Luzzatto L, Makani J. Urio F, et al. Among authors: menzel s. Br J Haematol. 2020 Dec;191(5):888-896. doi: 10.1111/bjh.17102. Epub 2020 Oct 19. Br J Haematol. 2020. PMID: 33073380 Free article. Clinical Trial.
Genetic variants of PKLR are associated with acute pain in sickle cell disease.
Wang X, Gardner K, Tegegn MB, Dalgard CL, Alba C, Menzel S, Patel H, Pirooznia M, Fu YP, Seifuddin FT, Thein SL. Wang X, et al. Among authors: menzel s. Blood Adv. 2022 Jun 14;6(11):3535-3540. doi: 10.1182/bloodadvances.2021006668. Blood Adv. 2022. PMID: 35271708 Free PMC article.
274 results