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Acta Haematologica|November 25, 2010
Plasma glial fibrillary acidic protein levels in a child with sickle cell disease and strokeWilliam J Savage, Allen D Everett, James F CasellaJournal of Pediatric Hematology/Oncology|November 1, 1996
Skull infarction and epidural hematomas in a patient with sickle cell anemiaL M Resar, M M Oliva, J F CasellaThe New England Journal of Medicine|December 18, 1986
Inheritance pattern and clinical response to splenectomy as a reflection of erythrocyte spectrin deficiency in hereditary spherocytosisP Agre, A Asimos, J F Casella, et al.Cell Motility and the Cytoskeleton|January 1, 1995
Quantitation of Cap Z in conventional actin preparations and methods for further purification of actinJ F Casella, E A Barron-Casella, M A TorresJournal of Orthopaedics and Traumatology : Official Journal of the Italian Society of Orthopaedics and Traumatology|April 23, 2009
Perspectives on metaphyseal conservative stemsF Falez, F Casella, G Panegrossi, et al.Journal of Pediatric Hematology/Oncology|July 27, 2013
Partial manual exchange reduces iron accumulation during chronic red cell transfusions for sickle cell diseaseWilliam J Savage, Shirley Reddoch, Jaime Wolfe, et al.American Journal of Preventive Medicine|June 21, 2016
Newborn Screening Programs and Sickle Cell Disease: A Public Health Services and Systems ApproachCynthia S Minkovitz, Holly Grason, Marjory Ruderman, et al.Medical Decision Making : an International Journal of the Society for Medical Decision Making|March 16, 2011
Decision modeling of disagreements: pediatric hematologists' management of idiopathic thrombocytopenic purpuraHarold P Lehmann, Nkossi Dambita, George R Buchanan, et al.American Journal of Hematology|July 23, 2009
The excess burden of stroke in hospitalized adults with sickle cell diseaseJohn J Strouse, Lori C Jordan, Sophie Lanzkron, et al.FEBS Letters|January 15, 1996
Cap Z, a calcium insensitive capping protein in resting and activated plateletsV T Nachmias, R Golla, J F Casella, et al.Pageof 18