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Lisa M Shook

Showing results (11-20 of 21) with videos related to

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Complementary Therapies in Medicine|March 10, 2020
Vitamin D supplementation and pain-related emergency department visits in children with sickle cell diseaseAnna M Hood, Charles T Quinn, Christopher D King, et al.
Ethnicity & Health|September 8, 2020
The influence of perceived racial bias and health-related stigma on quality of life among children with sickle cell diseaseAnna M Hood, Lori E Crosby, Eva Hanson, et al.
AJPM Focus|January 27, 2025
Challenges of Engaging Primary Care Providers in Specialized Telementoring Education About Sickle Cell Disease for Sickle Cell Specialists: Results from the Sickle Cell Disease Training and Mentoring Program for Primary Care Providers (STAMP) Project ECHOLisa M Shook, Bailey House, Christina Bennett Farrell, et al.
Journal of Pediatric Hematology/Oncology|July 26, 2018
Development of a Hydroxyurea Decision Aid for Parents of Children With Sickle Cell AnemiaLori E Crosby, Ashley Walton, Lisa M Shook, et al.
Journal of Pediatric Hematology/Oncology|May 22, 2024
Attitudes, Beliefs, and Intention to Receive a COVID-19 Vaccine for Pediatric Patients With Sickle Cell DiseaseLisa M Shook, Brittany L Rosen, Constance A Mara, et al.
Medical Education Online|November 27, 2016
Translating sickle cell guidelines into practice for primary care providers with Project ECHOLisa M Shook, Christina B Farrell, Karen A Kalinyak, et al.
Blood Advances|August 14, 2020
Building access to care in adult sickle cell disease: defining models of care, essential components, and economic aspectsJulie Kanter, Wally R Smith, Payal C Desai, et al.
Trials|November 28, 2020
Hydroxyurea Optimization through Precision Study (HOPS): study protocol for a randomized, multicenter trial in children with sickle cell anemiaEmily R Meier, Susan E Creary, Matthew M Heeney, et al.
British Journal of Haematology|July 31, 2025
Grandchildren of GRNDaD: Shifts in disease-modifying therapy at the adolescent transition in sickle cell diseaseMatthew Chang, Daniel Semakula, Jane A Little, et al.
Pediatric Blood & Cancer|March 7, 2025
Engaging Parents of Children With Sickle Cell Disease in Shared Decision-Making for Hydroxyurea: The ENGAGE-HU StudyAimee K Hildenbrand, Constance A Mara, Bridget Murphy, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
Complementary Therapies in Medicine|March 10, 2020
Vitamin D supplementation and pain-related emergency department visits in children with sickle cell diseaseAnna M Hood, Charles T Quinn, Christopher D King, et al.
Ethnicity & Health|September 8, 2020
The influence of perceived racial bias and health-related stigma on quality of life among children with sickle cell diseaseAnna M Hood, Lori E Crosby, Eva Hanson, et al.
AJPM Focus|January 27, 2025
Challenges of Engaging Primary Care Providers in Specialized Telementoring Education About Sickle Cell Disease for Sickle Cell Specialists: Results from the Sickle Cell Disease Training and Mentoring Program for Primary Care Providers (STAMP) Project ECHOLisa M Shook, Bailey House, Christina Bennett Farrell, et al.
Journal of Pediatric Hematology/Oncology|July 26, 2018
Development of a Hydroxyurea Decision Aid for Parents of Children With Sickle Cell AnemiaLori E Crosby, Ashley Walton, Lisa M Shook, et al.
Journal of Pediatric Hematology/Oncology|May 22, 2024
Attitudes, Beliefs, and Intention to Receive a COVID-19 Vaccine for Pediatric Patients With Sickle Cell DiseaseLisa M Shook, Brittany L Rosen, Constance A Mara, et al.
Medical Education Online|November 27, 2016
Translating sickle cell guidelines into practice for primary care providers with Project ECHOLisa M Shook, Christina B Farrell, Karen A Kalinyak, et al.
Blood Advances|August 14, 2020
Building access to care in adult sickle cell disease: defining models of care, essential components, and economic aspectsJulie Kanter, Wally R Smith, Payal C Desai, et al.
Trials|November 28, 2020
Hydroxyurea Optimization through Precision Study (HOPS): study protocol for a randomized, multicenter trial in children with sickle cell anemiaEmily R Meier, Susan E Creary, Matthew M Heeney, et al.
British Journal of Haematology|July 31, 2025
Grandchildren of GRNDaD: Shifts in disease-modifying therapy at the adolescent transition in sickle cell diseaseMatthew Chang, Daniel Semakula, Jane A Little, et al.
Pediatric Blood & Cancer|March 7, 2025
Engaging Parents of Children With Sickle Cell Disease in Shared Decision-Making for Hydroxyurea: The ENGAGE-HU StudyAimee K Hildenbrand, Constance A Mara, Bridget Murphy, et al.
Pageof 3