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

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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

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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

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Combining pain therapy with lifestyle: the role of personalized nutrition and nutritional supplements according to the SIMPAR Feed Your Destiny approach by De Gregori M, Muscoli C, Schatman ME, Stallone T, Intelligente F, Rondanelli M, Franceschi F, Arranz LI, Lorente Cebrián S, Salamone M, Ilari S, Belfer I, Allegri M

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Second edition of SIMPAR’s “Feed Your Destiny” workshop: the role of lifestyle in improving pain management by De Gregori M, Belfer I, De Giorgio R, Marchesini M, Muscoli C, Rondanelli M, Martini D, Mena P, Arranz LI, Lorente-Cebrián S, Perna S, Villarini A, Salamone M, Allegri M, Schatman ME

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A GCH1 haplotype confers sex-specific susceptibility to pain crises and altered endothelial function in adults with sickle cell anemia. by Belfer, I, Youngblood, V, Darbari, D, Wang, Z, Diaw, L, Freeman, L, Desai, K, Dizon, M, Allen, D, Cunnington, C, Channon, K, Milton, J, Hartley, S, Nolan, V, Kato, G, Steinberg, M, Goldman, D, Taylor, J