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Page 1
Inherited hemolytic anemia: a possessive beginner's guide.
Mohandas N. Mohandas N. Hematology Am Soc Hematol Educ Program. 2018 Nov 30;2018(1):377-381. doi: 10.1182/asheducation-2018.1.377. Hematology Am Soc Hematol Educ Program. 2018. PMID: 30504335 Free PMC article. Review.
Disorders of red cell membrane.
An X, Mohandas N. An X, et al. Among authors: mohandas n. Br J Haematol. 2008 May;141(3):367-75. doi: 10.1111/j.1365-2141.2008.07091.x. Epub 2008 Mar 12. Br J Haematol. 2008. PMID: 18341630 Review.
Membrane assembly during erythropoiesis.
Liu J, Mohandas N, An X. Liu J, et al. Among authors: mohandas n. Curr Opin Hematol. 2011 May;18(3):133-8. doi: 10.1097/MOH.0b013e32834521f3. Curr Opin Hematol. 2011. PMID: 21372707 Review.
Diagnostic tool for red blood cell membrane disorders: Assessment of a new generation ektacytometer.
Da Costa L, Suner L, Galimand J, Bonnel A, Pascreau T, Couque N, Fenneteau O, Mohandas N; Society of Hematology and Pediatric Immunology (SHIP) group; French Society of Hematology (SFH). Da Costa L, et al. Among authors: mohandas n. Blood Cells Mol Dis. 2016 Jan;56(1):9-22. doi: 10.1016/j.bcmd.2015.09.001. Epub 2015 Sep 16. Blood Cells Mol Dis. 2016. PMID: 26603718 Free PMC article.
Red cell membrane disorders.
Narla J, Mohandas N. Narla J, et al. Among authors: mohandas n. Int J Lab Hematol. 2017 May;39 Suppl 1:47-52. doi: 10.1111/ijlh.12657. Int J Lab Hematol. 2017. PMID: 28447420 Review.
Prognostic factors of disease severity in infants with sickle cell anemia: A comprehensive longitudinal cohort study.
Brousse V, El Hoss S, Bouazza N, Arnaud C, Bernaudin F, Pellegrino B, Guitton C, Odièvre-Montanié MH, Mames D, Brouzes C, Picard V, Nguyen-Khoa T, Pereira C, Lapouméroulie C, Pissard S, Gardner K, Menzel S, Le Van Kim C, Colin-Aronovicz Y, Buffet P, Mohandas N, Elie C, Maier-Redelsperger M, El Nemer W, de Montalembert M. Brousse V, et al. Among authors: mohandas n. Am J Hematol. 2018 Nov;93(11):1411-1419. doi: 10.1002/ajh.25260. Epub 2018 Sep 21. Am J Hematol. 2018. PMID: 30132969 Free article. Clinical Trial.
Heterogeneous phenotype of Hereditary Xerocytosis in association with PIEZO1 variants.
de Meira Oliveira P, Balan A, Muto NH, Cervato MC, Fonseca GHH, Suganuma LM, Gualandro S, Pinho JRR, Mohandas N, Silveira PAA, Sitnik R. de Meira Oliveira P, et al. Among authors: mohandas n. Blood Cells Mol Dis. 2020 May;82:102413. doi: 10.1016/j.bcmd.2020.102413. Epub 2020 Feb 8. Blood Cells Mol Dis. 2020. PMID: 32109669 Free article.
571 results