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Diverse phenotypic expression of sickle cell hemoglobin C disease in an Indian family.
Patel DK, Patel S, Mashon RS, Dash PM, Mukherjee MB. Patel DK, et al. Among authors: patel s. Ann Hematol. 2011 Mar;90(3):357-8. doi: 10.1007/s00277-010-1014-1. Epub 2010 Jun 17. Ann Hematol. 2011. PMID: 20556388 No abstract available.
Higher fetal hemoglobin concentration in patients with sickle cell disease in eastern India reduces frequency of painful crisis.
Mashon RS, Dash PM, Khalkho J, Dash L, Mohanty PK, Patel S, Mohanty RC, Das BS, Das UK, Das PK, Patel DK. Mashon RS, et al. Among authors: patel s, patel dk. Eur J Haematol. 2009 Oct;83(4):383-4. doi: 10.1111/j.1600-0609.2009.01290.x. Epub 2009 Jun 8. Eur J Haematol. 2009. PMID: 19508686 No abstract available.
Fetal hemoglobin and alpha thalassemia modulate the phenotypic expression of HbSD-Punjab.
Patel DK, Purohit P, Dehury S, Das P, Dutta A, Meher S, Patel S, Bag S, Mashon RS, Das K. Patel DK, et al. Among authors: patel s. Int J Lab Hematol. 2014 Aug;36(4):444-50. doi: 10.1111/ijlh.12165. Epub 2013 Nov 19. Int J Lab Hematol. 2014. PMID: 24245819
Association of plasma homocysteine level with vaso-occlusive crisis in sickle cell anemia patients of Odisha, India.
Meher S, Patel S, Das K, Dehury S, Jit BP, Maske MM, Das P, Dash BP, Mohanty PK. Meher S, et al. Among authors: patel s. Ann Hematol. 2019 Oct;98(10):2257-2265. doi: 10.1007/s00277-019-03776-x. Epub 2019 Aug 22. Ann Hematol. 2019. PMID: 31440871 Clinical Trial.
Association of fetal hemoglobin level with frequency of acute pain episodes in sickle cell disease (HbS-only phenotype) patients.
Jit BP, Mohanty PK, Purohit P, Das K, Patel S, Meher S, Mohanty JR, Sinha S, Behera RK, Das P. Jit BP, et al. Among authors: patel s. Blood Cells Mol Dis. 2019 Mar;75:30-34. doi: 10.1016/j.bcmd.2018.12.003. Epub 2018 Dec 20. Blood Cells Mol Dis. 2019. PMID: 30597429
Clinical and molecular characterization of Hb Hofu in eastern India.
Purohit P, Mashon RS, Patel S, Dehury S, Pattanayak C, Das K, Nair S, Italia K, Bag S, Colah R, Patel DK. Purohit P, et al. Among authors: patel s, patel dk. Int J Lab Hematol. 2014 Feb;36(1):71-6. doi: 10.1111/ijlh.12128. Epub 2013 Jul 25. Int J Lab Hematol. 2014. PMID: 23889802
Fetal Hemoglobin Modifies the Disease Manifestation of Severe Plasmodium Falciparum Malaria in Adult Patients with Sickle Cell Anemia.
Purohit P, Patel S, Mohanty PK, Das P, Panigrahi J. Purohit P, et al. Among authors: patel s. Mediterr J Hematol Infect Dis. 2016 Nov 1;8(1):e2016055. doi: 10.4084/MJHID.2016.055. eCollection 2016. Mediterr J Hematol Infect Dis. 2016. PMID: 27872735 Free PMC article. No abstract available.
Low dose hydroxyurea is effective in reducing the incidence of painful crisis and frequency of blood transfusion in sickle cell anemia patients from eastern India.
Patel DK, Mashon RS, Patel S, Das BS, Purohit P, Bishwal SC. Patel DK, et al. Among authors: patel s. Hemoglobin. 2012;36(5):409-20. doi: 10.3109/03630269.2012.709897. Hemoglobin. 2012. PMID: 22881992
Clinical and molecular characterization of β(S) and (G)γ((A)γδβ)⁰-thalassemia in eastern India.
Patel DK, Patel M, Mashon RS, Patel S, Dash PM, Das BS. Patel DK, et al. Among authors: patel m, patel s. Hemoglobin. 2010;34(6):604-9. doi: 10.3109/03630269.2010.526890. Hemoglobin. 2010. PMID: 21077771
Procalcitonin as a biomarker of bacterial infection in sickle cell vaso-occlusive crisis.
Patel DK, Mohapatra MK, Thomas AG, Patel S, Purohit P. Patel DK, et al. Among authors: patel s. Mediterr J Hematol Infect Dis. 2014 Feb 17;6(1):e2014018. doi: 10.4084/MJHID.2014.018. eCollection 2014. Mediterr J Hematol Infect Dis. 2014. PMID: 24678395 Free PMC article.
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