Publications by authors named "Lisa Shook"

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Grandchildren of GRNDaD: Shifts in disease-modifying therapy at the adolescent transition in sickle cell disease.
Matthew Chang, Daniel Semakula, Jane A Little, Julie Kanter, Deepa G Manwani, Lisa M Shook

Br J Haematol· September 2025

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Engaging Parents of Children With Sickle Cell Disease in Shared Decision-Making for Hydroxyurea: The ENGAGE-HU Study.
Aimee K Hildenbrand, Constance A Mara, Bridget Murphy, Anna M Hood, Yolanda Johnson, Lisa M Shook

Pediatr Blood Cancer· May 2025

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Primary Stroke Screening and Hydroxyurea Treatment for Sickle Cell Anemia in Pediatric Healthcare Settings in East and Central Africa: A Narrative Review of Capacity Gaps and Opportunities.
Teresa Smith Latham, Katarzyna Czabanowska, Suzanne Babich, Faith Yego-Kosgei, Lisa M Shook

Public Health Rev· May 2025

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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 ECHO.
Lisa M Shook, Bailey House, Christina Bennett Farrell, Rosalyn Stewart, Sophie Lanzkron

AJPM Focus· February 2025

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Clinical Utility of the Addition of Molecular Genetic Testing to Newborn Screening for Hemoglobinopathies for Confirmation of Alpha-Thalassemia Trait.
Lisa M Shook, Deidra Haygood, Charles T Quinn

Int J Neonatal Screen· February 2025

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A health equity ECHO for clinicians of individuals with SCD.
Lisa M Shook, Lori E Crosby, Christina Bennett Farrell, Stephen C Nelson

J Sick Cell Dis· August 2024

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Attitudes, Beliefs, and Intention to Receive a COVID-19 Vaccine for Pediatric Patients With Sickle Cell Disease.
Lisa M Shook, Brittany L Rosen, Constance A Mara, Cami Mosley, Alexis A Thompson

J Pediatr Hematol Oncol· July 2024

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A Mixed-Methods Evaluation of a Project ECHO Program for the Evidence-Based Management of Sickle Cell Disease.
Cami Mosley, Christina Bennett Farrell, Charles T Quinn, Lisa Marie Shook

Int J Environ Res Public Health· April 2024

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Screening for haemoglobin disorders: One size may not fit all.
Lisa M Shook, Russell E Ware

Br J Haematol· January 2024

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The influence of perceived racial bias and health-related stigma on quality of life among children with sickle cell disease.
Anna M Hood, Lori E Crosby, Eva Hanson, Lisa M Shook, Jeffrey D Lebensburger

Ethn Health· May 2022

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Expanding a Regional Sickle Cell Disease Project ECHO to Rapidly Disseminate COVID-19 Education.
Lisa Marie Shook, Christina Bennett Farrell, Cami Mosley

Adv Med Educ Pract· May 2022

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Educational Needs of School Nurses Regarding the Evidence-Based Management of Sickle Cell Disease.
Lisa M Shook, Cami Mosley, Christina Bennett Farrell, Ann Connelly, Cheryl L Jones

Int J Environ Res Public Health· November 2021

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Clinical Utility of the Addition of Molecular Genetic Testing to Newborn Screening for Sickle Cell Anemia.
Lisa M Shook, Deidra Haygood, Charles T Quinn

Front Med (Lausanne)· November 2021

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Engaging Caregivers and Providers of Children With Sickle Cell Anemia in Shared Decision Making for Hydroxyurea: Protocol for a Multicenter Randomized Controlled Trial.
Anna M Hood, Heather Strong, Cara Nwankwo, Yolanda Johnson, James Peugh, Lisa M Shook

JMIR Res Protoc· May 2021

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Piloting a multidisciplinary virtual learning course about haemoglobinopathies.
Lisa M Shook, Christina B Farrell, Cami Mosley, Deidra Haygood

Med Educ· November 2020

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Hydroxyurea Optimization through Precision Study (HOPS): study protocol for a randomized, multicenter trial in children with sickle cell anemia.
Emily R Meier, Susan E Creary, Matthew M Heeney, Min Dong, Abena O Appiah-Kubi, Lisa M Shook

Trials· November 2020

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A National Measurement Framework to Assess and Improve Sickle Cell Care in 4 US Regions.
Elissa Z Faro, Lisa Shook, Marsha J Treadwell, Allison A King, Lauren N Whiteman

Public Health Rep· August 2020

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Building access to care in adult sickle cell disease: defining models of care, essential components, and economic aspects.
Julie Kanter, Wally R Smith, Payal C Desai, Marsha Treadwell, Biree Andemariam, Lisa M Shook

Blood Adv· August 2020

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Clinical Utility of Confirmatory Genetic Testing to Differentiate Sickle Cell Trait from Sickle-β-Thalassemia by Newborn Screening.
Lisa M Shook, Deidra Haygood, Charles T Quinn

Int J Neonatal Screen· March 2020

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Vitamin D supplementation and pain-related emergency department visits in children with sickle cell disease.
Anna M Hood, Charles T Quinn, Christopher D King, Lisa M Shook, James L Peugh

Complement Ther Med· March 2020

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Development of a Hydroxyurea Decision Aid for Parents of Children With Sickle Cell Anemia.
Lori E Crosby, Ashley Walton, Lisa M Shook, Russell E Ware, Marsha Treadwell

J Pediatr Hematol Oncol· January 2019

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Sickle cell screening in Europe: the time has come.
Lisa M Shook, Russell E Ware

Br J Haematol· November 2018

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Effective screening leads to better outcomes in sickle cell disease.
Lisa M Shook, Russell E Ware

Arch Dis Child· July 2018

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Erratum to: Patient Perspectives on Gene Transfer Therapy for Sickle Cell Disease.
Heather Strong, Monica J Mitchell, Alana Goldstein-Leever, Lisa Shook, Punam Malik

Adv Ther· September 2017

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Patient Perspectives on Gene Transfer Therapy for Sickle Cell Disease.
Heather Strong, Monica J Mitchell, Alana Goldstein-Leever, Lisa Shook, Punam Malik

Adv Ther· August 2017

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