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Journal of Pediatric Hematology/Oncology|April 25, 2000
Low-molecular-weight heparin in thrombotic disease in children and adolescentsR C Punzalan, C A Hillery, R R Montgomery, et al.
Molecular Pain|September 12, 2012
Sickle cell mice exhibit mechanical allodynia and enhanced responsiveness in light touch cutaneous mechanoreceptorsSheldon R Garrison, Audra A Kramer, Nashaat Z Gerges, et al.
Blood|March 29, 2003
Single-chain antibody fragments derived from a human synthetic phage-display library bind thrombospondin and inhibit sickle cell adhesionNicholas A Watkins, Lily M Du, J Paul Scott, et al.
American Journal of Hematology|November 2, 2012
Patients with sickle cell disease have increased sensitivity to cold and heatAmanda M Brandow, Cheryl L Stucky, Cheryl A Hillery, et al.
Pediatric Emergency Care|January 13, 2004
Patient-controlled analgesia for sickle cell pain crisis in a pediatric emergency departmentMarlene D Melzer-Lange, Christine M Walsh-Kelly, Gwen Lea, et al.
British Journal of Haematology|October 14, 2017
Characterization of a mouse model of sickle cell trait: parallels to human trait and a novel finding of cutaneous sensitizationKatherine J Zappia, Yihe Guo, Dawn Retherford, et al.
Pediatrics|June 5, 2003
Delayed hemolytic transfusion reaction/hyperhemolysis syndrome in children with sickle cell diseaseJulie-An M Talano, Cheryl A Hillery, Jerome L Gottschall, et al.
JCI Insight|March 8, 2024
High-mobility group box 1 increases platelet surface P2Y12 and platelet activation in sickle cell diseaseDeirdre Nolfi-Donegan, Gowtham K Annarapu, Claudette St Croix, et al.
British Journal of Haematology|November 10, 2007
Phase I study of magnesium pidolate in combination with hydroxycarbamide for children with sickle cell anaemiaJane S Hankins, Lynn W Wynn, Carlo Brugnara, et al.
Annals of Surgery|February 1, 2003
Clinical and hematologic benefits of partial splenectomy for congenital hemolytic anemias in childrenHenry E Rice, Keith T Oldham, Cheryl A Hillery, et al.
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