Candidate sequence variants and fetal hemoglobin in children with sickle cell disease treated with hydroxyurea
Green, Nancy S, Ender, Katherine L, Pashankar, Farzana, Driscoll, Catherine, Giardina, Patricia J, Mullen, Craig A, Clark, Lorraine N, Manwani, Deepa, Crotty, Jennifer, Kisselev, Sergey, Neville, Kathleen A, Hoppe, Carolyn, Barral, Sandra
Published in PloS one (07.02.2013)
Published in PloS one (07.02.2013)
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Use of a clinical pathway to improve the acute management of vaso-occlusive crisis pain in pediatric sickle cell disease
Ender, Katherine L., Krajewski, Jennifer A., Babineau, John, Tresgallo, Mary, Schechter, William, Saroyan, John M., Kharbanda, Anupam
Published in Pediatric blood & cancer (01.04.2014)
Published in Pediatric blood & cancer (01.04.2014)
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Exploring social media for patient perspectives of sickle cell disease
Liao, Benita T., Busse, Jennifer, Ender, Katherine L., Schechter, William S.
Published in Pediatric hematology and oncology (17.02.2016)
Published in Pediatric hematology and oncology (17.02.2016)
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Fetal hemoglobin levels in African American and Hispanic children with sickle cell disease at baseline and in response to hydroxyurea
Ender, Katherine L, Lee, Margaret T, Sheth, Sujit, Licursi, Maureen, Crotty, Jennifer, Barral, Sandra, Green, Nancy S
Published in Journal of pediatric hematology/oncology (01.10.2011)
Published in Journal of pediatric hematology/oncology (01.10.2011)
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