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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2009 | 1 |
2011 | 1 |
2012 | 1 |
2015 | 1 |
2016 | 1 |
2017 | 1 |
2024 | 0 |
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Page 1
Prevention of conversion to abnormal transcranial Doppler with hydroxyurea in sickle cell anemia: A Phase III international randomized clinical trial.
Am J Hematol. 2015 Dec;90(12):1099-105. doi: 10.1002/ajh.24198. Epub 2015 Nov 17.
Am J Hematol. 2015.
PMID: 26414435
Free PMC article.
Clinical Trial.
EXpanding Treatment for Existing Neurological Disease (EXTEND): An Open-Label Phase II Clinical Trial of Hydroxyurea Treatment in Sickle Cell Anemia.
Rankine-Mullings AE, Little CR, Reid ME, Soares DP, Taylor-Bryan C, Knight-Madden JM, Stuber SE, Badaloo AV, Aldred K, Wisdom-Phipps ME, Latham T, Ware RE.
Rankine-Mullings AE, et al.
JMIR Res Protoc. 2016 Sep 12;5(3):e185. doi: 10.2196/resprot.5872.
JMIR Res Protoc. 2016.
PMID: 27619954
Free PMC article.
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Decision analysis of treatment strategies in children with severe sickle cell disease.
O'Brien SH, Hankins JS.
O'Brien SH, et al.
J Pediatr Hematol Oncol. 2009 Nov;31(11):873-8. doi: 10.1097/MPH.0b013e3181b83cab.
J Pediatr Hematol Oncol. 2009.
PMID: 19829150
Free PMC article.
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Fetal haemoglobin levels and haematological characteristics of compound heterozygotes for haemoglobin S and deletional hereditary persistence of fetal haemoglobin.
Ngo DA, Aygun B, Akinsheye I, Hankins JS, Bhan I, Luo HY, Steinberg MH, Chui DH.
Ngo DA, et al.
Br J Haematol. 2012 Jan;156(2):259-64. doi: 10.1111/j.1365-2141.2011.08916.x. Epub 2011 Oct 24.
Br J Haematol. 2012.
PMID: 22017641
Free PMC article.
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The clinical severity of hemoglobin S/Black (A γδβ)0 -thalassemia.
Cancio MI, Aygun B, Chui DHK, Rothman JA, Scott JP, Estepp JH, Hankins JS.
Cancio MI, et al.
Pediatr Blood Cancer. 2017 Nov;64(11):10.1002/pbc.26596. doi: 10.1002/pbc.26596. Epub 2017 Apr 28.
Pediatr Blood Cancer. 2017.
PMID: 28453928
Free PMC article.
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