Lisa M. Shook

Building access to care in adult sickle cell disease: defining models of care, essential components, and economic aspects

Julie Kanter, Wally R. Smith, Payal Desai et al. · Blood Advances · 2020 · 113 citations · Full text

Disease Management, Healthcare Provision, Primary Care +22

The influence of perceived racial bias and health-related stigma on quality of life among children with sickle cell disease

Anna Hood, Lori E. Crosby, Eva Hanson et al. · Ethnicity and Health · 2020 · 56 citations · Full text

School Performance and Disease Interference in Adolescents with Sickle Cell Disease

Lori E. Crosby, Naomi E. Joffe, Mary Kay Irwin et al. · Physical Disabilities Education and Related Services · 2015 · 39 citations · Full text

Translating sickle cell guidelines into practice for primary care providers with Project ECHO

Lisa M. Shook, Christina Bennett Farrell, Karen Kalinyak et al. · Medical Education Online · 2016 · 38 citations · Full text

Patient Perspectives on Gene Transfer Therapy for Sickle Cell Disease

Heather Strong, Monica J. Mitchell, Alana Goldstein‐Leever et al. · Advances in Therapy · 2017 · 35 citations · Full text

Cell Therapy, Novel Therapy, Gene Transfer Therapy +9