Assessing Patient Preferences for Treatment Options for Pediatric Sickle Cell Disease: A Critical Review of Quantitative and Qualitative Studies by Katoch D, Krishnamurti L

Get full text

Presence of pain on three or more days of the week is associated with worse patient reported outcomes in adults with sickle cell disease by Bakshi N, Ross D, Krishnamurti L

Get full text

Quantitative sensory testing is feasible and is well-tolerated in patients with sickle cell disease following a vaso-occlusive episode by Bakshi N, Lukombo I, Belfer I, Krishnamurti L

Get full text

Pain catastrophizing is associated with poorer health-related quality of life in pediatric patients with sickle cell disease by Bakshi N, Lukombo I, Belfer I, Krishnamurti L

Get full text

Association of genetic variation in COMT gene with pain related to sickle cell disease in patients from the walk-PHaSST study by Zhang Y, Belfer I, Nouraie M, Zeng Q, Goel R, Chu Y, Krasiy I, Krishnamurti L

Get full text

Effects of Music Therapy on Quality of Life in Adults with Sickle Cell Disease (MUSIQOLS): A Mixed Methods Feasibility Study [Erratum] by Rodgers-Melnick SN, Lin L, Gam K, Souza de Santana Carvalho E, Jenerette C, Rowland DY, Little JA, Dusek JA, Bakshi N, Krishnamurti L

Get full text