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Journal Articles

Impact of hematopoietic cell transplantation on myocardial fibrosis in young patients with sickle cell disease

Akshay Sharma, Subodh Selukar, Yu Bi, Anthony Merlocco, Cara E. Morin, Chris Goode, Parul Rai, Jeffrey A. Towbin, Jane S. Hankins, Stephen Gottschalk, Brandon Triplett, Jason N. Johnson

Blood (2024) 144 (6): 672–675.

https://doi.org/10.1182/blood.2023023028

Published: 2024

Includes: Supplemental data

Journal Articles

Executive Difficulties and Depressive Symptoms Predict Future Acute Pain Emergency Visits and Hospitalizations in Children with Sickle Cell Disease

Andrew M Heitzer, Shuyan Chen, Jennifer N Longoria, Jerlym S. Porter, Guolian Kang, Jane S Hankins, Clifford M Takemoto

Blood (2023) 142 (Supplement 1): 2378.

https://doi.org/10.1182/blood-2023-183016

Published: 2023

Journal Articles

Myocardial Fibrosis Improves in Young Patients with Sickle Cell Disease after Hematopoietic Cell Transplantation

Akshay Sharma, Anthony Merlocco, Cara Morin, Subodh Selukar, Yu Bi, Chris Goode, Parul Rai, Brandon M Triplett, Jeffrey Towbin, Jane S Hankins, Jason N Johnson

Blood (2023) 142 (Supplement 1): 2518.

https://doi.org/10.1182/blood-2023-178267

Published: 2023

Journal Articles

Cerebral Oxygen Metabolism Improves Following Hematopoietic Cell Transplantation in Children with Sickle Cell Disease

Chih-Chiang Chang, Matthew A. Scoggins, Ping Zou, Sydney Somogyi, Soniya Pinto, Kathleen Helton, Jane S Hankins, Brandon M Triplett, Akshay Sharma, Ranganatha Sitaram

Blood (2023) 142 (Supplement 1): 2519.

https://doi.org/10.1182/blood-2023-179363

Published: 2023

Journal Articles

Prevalence and Time Trends of Oral Anticoagulant Utilization in Adults with Sickle Cell Disease

Ming Chen, Jane S Hankins, Min Zhang, Justin Gatwood, James E Bailey, Kenneth I. Ataga

Blood (2023) 142 (Supplement 1): 5294.

https://doi.org/10.1182/blood-2023-188030

Published: 2023

Journal Articles

Sleep Fragmentation and Obstructive Sleep Apnea Are Associated with High Primary Stroke Risk in Children with Sickle Cell Disease

Zachary Abramson, La'Ron Browne, Ayobami Olanrewaju, Guolian Kang, Yunus Olufadi, Andrew M Heitzer, Ahsan Bashir, Kevin R. Krull, Jane S Hankins

Blood (2023) 142 (Supplement 1): 795.

https://doi.org/10.1182/blood-2023-185094

Published: 2023

Journal Articles

Impact of Acute Exercise Challenge on Airway Dynamics in Children and Young Adults with Sickle Cell Anemia

Robyn T. Cohen, Jane S Hankins, Kirsten K Ness, Lewis Hsu, Tracy Baynard, Amy Tang, Shlomit Radom-Aizik, Kevin Guerrero, Mark Rodeghier, Robert I. Liem

Blood (2023) 142 (Supplement 1): 794.

https://doi.org/10.1182/blood-2023-182904

Published: 2023

Journal Articles

Birth-Related Risk Factors Impact Cognitive and Academic Outcomes in Children with Sickle Cell Disease

Jennifer N Longoria, Andrew M Heitzer, Joshua Semko, Halle T McCracken, Erin MacArthur, Guolian Kang, Catherine R Hoyt, Jane S Hankins, Clifford M Takemoto

Blood (2023) 142 (Supplement 1): 5128.

https://doi.org/10.1182/blood-2023-186586

Published: 2023

Journal Articles

Optimization of RH Genotyping from Whole Exon Sequencing Data By Machine Learning

Ti-Cheng Chang, Jing Yu, Zhaoming Wang, Jane S Hankins, Mitchell Weiss, Gang Wu, Connie M. Westhoff, Sunitha Vege, Stella Chou, Yan Zheng

Blood (2023) 142 (Supplement 1): 4034.

https://doi.org/10.1182/blood-2023-182089

Published: 2023

Journal Articles

Evaluation of Capacity for Implementation of Pediatric-to-Adult Care Transition for Sickle Cell Disease in Brazil

Kelly Pimenta, Tarun Aurora, Perla Vicari, Thais Oliveira, Heloisa Helena Miranda, Maria Stella Figueiredo, Patricia Moura, Josefina Braga, Clarisse Lobo, Andrea Angel, Thiago Vilela, Patricia Blum, Maria Jose de Farias Ramos Reis, Ana Baumann, Jane S Hankins

Blood (2023) 142 (Supplement 1): 2296.

https://doi.org/10.1182/blood-2023-178672

Published: 2023

Journal Articles

Impact of an Individualized Pain Plan (IPP) for Adults with Sickle Cell Disease Experiencing a Vaso-Occlusive Episode (VOE) on Patient Satisfaction and ED Provider Confidence in Treating Pain

Rita V Masese, Lauren Siewny, Siera Gollan, Jeffrey A. Glassberg, Victor R. Gordeuk, Jane S Hankins, Cathy Melvin, Liliana Preiss, Paula Jean Tanabe, Marsha Treadwell, Allison A. King

Blood (2023) 142 (Supplement 1): 3671.

https://doi.org/10.1182/blood-2023-186906

Published: 2023

Journal Articles

Engagement with Incharge App - a Mobile Health Intervention to Improve Adherence to Hydroxyurea Among Individuals with Sickle Cell Disease

Christina M Abrams, Natalia Davila, Cathy Melvin, Sherif M. Badawy, Michael B Potter, Robert Gibson, Allison A King, Victor R. Gordeuk, Chinonyelum Nwosu, Jerlym S. Porter, Sophie Li, Jeffrey A. Glassberg, Richard Lottenberg, Lisa Klesges, Nirmish Shah, Jane S Hankins

Blood (2023) 142 (Supplement 1): 1144.

https://doi.org/10.1182/blood-2023-179272

Published: 2023

Journal Articles

Outpatient Costs of Patients with Sickle Cell Disease with or without Hydroxyurea at an Institution in Rio De Janeiro, Brazil

Tarun Aurora, Patricia Moura, Delaine Fidlarczyk, Jane Duran, Roberto Barbosa, Thais Oliveira, Emilia Nascimento, Jane S Hankins, Clarisse Lobo

Blood (2023) 142 (Supplement 1): 7325.

https://doi.org/10.1182/blood-2023-179610

Published: 2023

Journal Articles

Diffuse myocardial fibrosis occurs in young patients with sickle cell anemia despite early disease-modifying therapy

Cara E. Morin, Akshay Sharma, Subodh Selukar, Gary Beasley, Anthony Merlocco, Chris Goode, Parul Rai, Jeffrey A. Towbin, Jane S. Hankins, Jason N. Johnson

Blood (2023) 141 (11): 1358–1362.

https://doi.org/10.1182/blood.2022018209

Published: 2023

Includes: Supplemental data

Journal Articles

Optimizing the Frequency of Transcranial Doppler (TCD) Exams in Children with Sickle Cell Anemia

Ayobami Olanrewaju, Zachary Abramson, Jane S Hankins, Clifford Takemoto, M. Beth McCarville, Andrew M Heitzer, Guolian Kang, Victoria Okhomina, Winfred C. Wang

Blood (2022) 140 (Supplement 1): 2142–2144.

https://doi.org/10.1182/blood-2022-159500

Published: 2022

Journal Articles

High Rate of Recurrent Venous Thromboembolism Is Children with Sickle Cell Disease and History of VTE: Analysis of the Trinetx Research Network Database

Marisol Betensky, Ernest Amankwah, Jane S Hankins, Neil Goldenberg

Blood (2021) 138 (Supplement 1): 778.

https://doi.org/10.1182/blood-2021-154003

Published: 2021

Journal Articles

Successful HPV Vaccination in Adolescents with Sickle Cell Disease Following a Quality Improvement Bundle Intervention

Tarun Aurora, Audrey Cole, Parul Rai, Paul T Lavoie, Carrie McIvor, Lisa Klesges, Guolian Kang, Juan Ding, Heather Brandt, Jane S Hankins

Blood (2021) 138 (Supplement 1): 914.

https://doi.org/10.1182/blood-2021-151461

Published: 2021

Journal Articles

Optimization of Autologous Hematopoietic Progenitor Stem Cell Apheresis Collection from Plerixafor-Mobilized Patients with Sickle Cell Disease

Blood (2021) 138 (Supplement 1): 1770.

https://doi.org/10.1182/blood-2021-146669

Published: 2021

Journal Articles

Vitamin D Levels: Associations with Acute Pain Events and Self-Reported Pain in Children with Sickle Cell Disease

Latika Puri, Nicole M Alberts, Guolian Kang, Juan Ding, Jane S Hankins, Amanda M. Brandow, Doralina Anghelescu

Blood (2021) 138 (Supplement 1): 3089.

https://doi.org/10.1182/blood-2021-145914

Published: 2021

Journal Articles

Cost Analysis of ACUTE Care Resource Utilization Among Individuals with Sickle Cell Disease in a Middle-Income Country

Clarisse Lobo, Jane S Hankins, Nickhill Bhakta, Emilia Nascimento, Patricia Gomes Moura, Delaine Fidlarczyk, Thais Oliveira Figueiredo, Roberto Barbosa, Jane Duran

Blood (2021) 138 (Supplement 1): 2987.

https://doi.org/10.1182/blood-2021-149639

Published: 2021

NARROW

Impact of hematopoietic cell transplantation on myocardial fibrosis in young patients with sickle cell disease

Executive Difficulties and Depressive Symptoms Predict Future Acute Pain Emergency Visits and Hospitalizations in Children with Sickle Cell Disease

Myocardial Fibrosis Improves in Young Patients with Sickle Cell Disease after Hematopoietic Cell Transplantation

Cerebral Oxygen Metabolism Improves Following Hematopoietic Cell Transplantation in Children with Sickle Cell Disease

Prevalence and Time Trends of Oral Anticoagulant Utilization in Adults with Sickle Cell Disease

Sleep Fragmentation and Obstructive Sleep Apnea Are Associated with High Primary Stroke Risk in Children with Sickle Cell Disease

Impact of Acute Exercise Challenge on Airway Dynamics in Children and Young Adults with Sickle Cell Anemia

Birth-Related Risk Factors Impact Cognitive and Academic Outcomes in Children with Sickle Cell Disease

Optimization of RH Genotyping from Whole Exon Sequencing Data By Machine Learning

Evaluation of Capacity for Implementation of Pediatric-to-Adult Care Transition for Sickle Cell Disease in Brazil

Impact of an Individualized Pain Plan (IPP) for Adults with Sickle Cell Disease Experiencing a Vaso-Occlusive Episode (VOE) on Patient Satisfaction and ED Provider Confidence in Treating Pain

Engagement with Incharge App - a Mobile Health Intervention to Improve Adherence to Hydroxyurea Among Individuals with Sickle Cell Disease

Outpatient Costs of Patients with Sickle Cell Disease with or without Hydroxyurea at an Institution in Rio De Janeiro, Brazil

Diffuse myocardial fibrosis occurs in young patients with sickle cell anemia despite early disease-modifying therapy

Optimizing the Frequency of Transcranial Doppler (TCD) Exams in Children with Sickle Cell Anemia

High Rate of Recurrent Venous Thromboembolism Is Children with Sickle Cell Disease and History of VTE: Analysis of the Trinetx Research Network Database

Successful HPV Vaccination in Adolescents with Sickle Cell Disease Following a Quality Improvement Bundle Intervention

Optimization of Autologous Hematopoietic Progenitor Stem Cell Apheresis Collection from Plerixafor-Mobilized Patients with Sickle Cell Disease

Vitamin D Levels: Associations with Acute Pain Events and Self-Reported Pain in Children with Sickle Cell Disease

Cost Analysis of ACUTE Care Resource Utilization Among Individuals with Sickle Cell Disease in a Middle-Income Country

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American Society of Hematology

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American Society of Hematology

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