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Journal Articles

Raising hemoglobin level with erythropoietin improves cerebral but not muscle tissue oxygenation in patients with sickle cell disease

Nelly Kiriza, Lara Abdelmohsen, Elizabeth Meinert-Spyker, John Tukakira, Feyisayo Oluwole, Adeniyi Adiat, Joel Dzidzorvi Kwame Disu, Nahom Mossazghi, Jude Jonassaint, D. Akinsanya Olesugun-Joseph, Vincent Osunkalu, Olubusola Oluwole, Laura DeCastro, Enrico Novelli, Titilope Adeyemo, Sossena Wood, Julia Xu

Blood (2025) 146 (Supplement 1): 2964.

https://doi.org/10.1182/blood-2025-2964

Published: 2025

Journal Articles

Feasibility of wearable technology for remote monitoring in high-risk adults with sickle cell disease: Baseline data from the SCD-carre trial

Charles Jonassaint, Alicia Colvin, Colleen Ballantyne, Marnie Bertolet, Jude Jonassaint, Carissa Low, Nirmish Shah, Ella Zadorozny, Fuad El Rassi, Santosh Saraf, Wally Smith, Maria Brooks, Darrell Triulzi, Mark Gladwin

Blood (2025) 146 (Supplement 1): 2600.

https://doi.org/10.1182/blood-2025-2600

Published: 2025

Journal Articles

EPO treatment in combination with hydroxyurea improves pain and other quality of life measures in sickle cell disease

Kseniya Anishchenko, Nelly Kiriza, Feyisayo Oluwole, Adeniyi Adiat, John Tukakira, Jude Jonassaint, D. Akinsanya Olesugun-Joseph, Vincent Osunkalu, Olubusola Oluwole, Laura DeCastro, Enrico Novelli, Titilope Adeyemo, Julia Xu

Blood (2025) 146 (Supplement 1): 614.

https://doi.org/10.1182/blood-2025-614

Published: 2025

Journal Articles

A Phase 1b/2 Study of the Efficacy and Safety of Combination Hydroxyurea and Dose-Escalated Erythropoietin for Treatment of Anemia in Sickle Cell Disease (ACHiEvE-SCD)

Titilope A Adeyemo, Nelly Kiriza, Feyisayo T. Oluwole, Mark Jelinek, Jude Jonassaint, Olubusola Oluwole, Christine Saber, Brian J Philips, Olusegun-Joseph D Akinsanya, Vincent O Osunkalu, Laura M. DeCastro, Enrico M Novelli, Julia Z Xu

Blood (2024) 144 (Supplement 1): 178.

https://doi.org/10.1182/blood-2024-205261

Published: 2024

Journal Articles

Novel Multidimensional Pain Assessment Tool Is a Feasible, Valid, and Enjoyable Approach to Communication of Pain Symptoms in Pediatric Sickle Cell Disease

Erica Mamauag, Charles R. Jonassaint, Jude Jonassaint, Li Wang, Nathan Matten, Cheryl Hillery

Blood (2023) 142 (Supplement 1): 251.

https://doi.org/10.1182/blood-2023-173878

Published: 2023

Journal Articles

Liver-to-lung microembolic NETs promote gasdermin D–dependent inflammatory lung injury in sickle cell disease

Ravi Vats, Tomasz W. Kaminski, Tomasz Brzoska, John A. Leech, Egemen Tutuncuoglu, Omika Katoch, Jude Jonassaint, Jesus Tejero, Enrico M. Novelli, Tirthadipa Pradhan-Sundd, Mark T. Gladwin, Prithu Sundd

Blood (2022) 140 (9): 1020–1037.

https://doi.org/10.1182/blood.2021014552

Published: 2022

Includes: Multimedia, Supplemental data

Journal Articles

Assessing Dynamic Cerebral Autoregulation in Patients with Sickle Cell Disease Using Near-Infrared Spectroscopy and Paced Breathing

Sossena Wood, PhD, Abeselom Fanta, M.S., Atinuke Dosunmu-Ogunbi, B.S., Alexander Ruesch, PhD, Jude Jonassaint, R.N., Theodore Huppert, PhD, Enrico M Novelli, MD, M.S., Jana Kainerstorfer, PhD

Blood (2020) 136 (Supplement 1): 57–58.

https://doi.org/10.1182/blood-2020-137624

Published: 2020

Journal Articles

Integrating Mobile Health Technology for Symptom Management in Acute Pediatric Blood and Marrow Transplant Patients

Jacqueline Vaughn, BSN, Sid Gollarahalli, BA, Erika Summers-Goeckerman, RN, MSN, CPNP-AC, Jude Jonassaint, RN, Nirmish Shah, MD

Blood (2018) 132 (Supplement 1): 4726.

https://doi.org/10.1182/blood-2018-99-118815

Published: 2018

Journal Articles

Use of Mobile Health (mHealth) Apps and Wearable Technology to Assess Changes in Pain during Treatment of Acute Pain in Sickle Cell Disease

Amanda Johnson, MD, Siddharth Gollarahalli, Daniel Abrams, Jude Jonassaint, Nirmish Shah, MD

Blood (2017) 130 (Supplement 1): 2230.

https://doi.org/10.1182/blood.V130.Suppl_1.2230.2230

Published: 2017

Journal Articles

Understanding Sleep in Pediatric Patients with Sickle Cell Disease Admitted for Vaso-Occlusive Pain Crisis through Objective Data

Kalindi Narine, MD, Fan Yang, Tanvi Banerjee, Jude Jonassaint, Nirmish Shah, MD

Blood (2017) 130 (Supplement 1): 4791.

https://doi.org/10.1182/blood.V130.Suppl_1.4791.4791

Published: 2017

Journal Articles

Use of Mobile Technology to Monitor Pain and Reduce Outpatient, Emergency Department (ED), and Hospital Visits for Sickle Cell Pain Crisis

Kalindi Yajnik Narine, MD, Jennifer Minjia Chang, Jude Jonassaint, RN, Marilyn J. Telen, MD, Nirmish Shah, MD

Blood (2016) 128 (22): 2390.

https://doi.org/10.1182/blood.V128.22.2390.2390

Published: 2016

Journal Articles

The Impact of Cognitive Function on Adherence to Hydroxyurea Therapy in Patients with Sickle Cell Disease

Cristina Merkhofer, MD, Susan Sylvester, MS, BSN, RN, CCM, Michelle Zmuda, Jude Jonassaint, RN, Laura M. De Castro, MD, Gregory J Kato, MD, Meryl A. Butters, PhD, Enrico M. Novelli, MD MS

Blood (2016) 128 (22): 2493.

https://doi.org/10.1182/blood.V128.22.2493.2493

Published: 2016

Journal Articles

Effects of Sulforaphane Obtained from Broccoli Sprout Homogenate in Patients with Sickle Cell Disease (SCD)

Jennifer Doss, BS, Jude Jonassaint, RN, Nirmish Shah, MD, Marilyn J. Telen, MD, Jen-Tsan A. Chi, MD, PhD

Blood (2014) 124 (21): 4931.

https://doi.org/10.1182/blood.V124.21.4931.4931

Published: 2014

Journal Articles

The Use of Mobile Technology for Intensive Training in Medication Management in the Pediatric Population

Sarah Leonard, MD MPH, Jude Jonassaint, RN, Lindsay Anderson, MA, Nirmish Shah, MD

Blood (2014) 124 (21): 4842.

https://doi.org/10.1182/blood.V124.21.4842.4842

Published: 2014

Journal Articles

Genetic and Epigenetic Regulation of the Gamma Globin Locus Is Associated with Fetal Hemoglobin Levels and Frequency of Pain in Sickle Cell Disease

Blair Anderson, Ebenezer Enchia, Karen Soldano, B.S., Melanie Garrett, MS, Jude Jonassaint, RN, Laura M. De Castro, MD, Marilyn J. Telen, MD, Allison E Ashley-Koch, PhD

Blood (2012) 120 (21): 3230.

https://doi.org/10.1182/blood.V120.21.3230.3230

Published: 2012

Journal Articles

Information Technology Use by Patients with Hemoglobinopathies

Jude Jonassaint, RN, Laura M. De Castro, MD

Blood (2012) 120 (21): 4698.

https://doi.org/10.1182/blood.V120.21.4698.4698

Published: 2012

Journal Articles

Genetic Variation In MYH9 Is Associated with Sickle Cell Disease Nephropathy

Emmanuel Okocha, MBBS, Melanie Garrett, MS, Karen Soldano, BS, Laura M. De Castro, MD, Jude Jonassaint, RN, Eugene P. Orringer, MD, James R. Eckman, MD, Marilyn J. Telen, MD, Allison E Ashley-Koch, PhD

Blood (2010) 116 (21): 1648.

https://doi.org/10.1182/blood.V116.21.1648.1648

Published: 2010

Journal Articles

Retrospective Review of the Natural History of Pulmonary Hypertension in Sickle Cell Disease Demonstrates That Progressive Enlargement of the Left Atrium Is a Strong Predictor of Death.

Damian Silbermins, MD, Agustin Calatroni, MS, Jude Jonassaint, RN, Marilyn J. Telen, MD, Laura M. De Castro, MD

Blood (2009) 114 (22): 1529.

https://doi.org/10.1182/blood.V114.22.1529.1529

Published: 2009

Journal Articles

Identification of genetic polymorphisms associated with risk for pulmonary hypertension in sickle cell disease

Allison E. Ashley-Koch, Laine Elliott, Melanie E. Kail, Laura M. De Castro, Jude Jonassaint, Terry L. Jackson, Jennifer Price, Kenneth I. Ataga, Marc C. Levesque, J. Brice Weinberg, Eugene P. Orringer, Ann Collins, Jeffery M. Vance, Marilyn J. Telen

Blood (2008) 111 (12): 5721–5726.

https://doi.org/10.1182/blood-2007-02-074849

Published: 2008

Includes: Supplemental data

Journal Articles

Further Investigation of the Role of Factor XIII in Priapism Associated with SCD.

Aya El Khatib, Allison Ashley-Koch, PhD, Melanie Kail, MS, Ann Collins, PhD, Jude Jonassaint, RN, Soheir S. Adam, MD, Kenneth I. Ataga, MD, James R. Eckman, MD, Eugene P. Orringer, MD, Charles S. Greenberg, MD, Marilyn J. Telen, MD

Blood (2007) 110 (11): 3407.

https://doi.org/10.1182/blood.V110.11.3407.3407

Published: 2007

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Raising hemoglobin level with erythropoietin improves cerebral but not muscle tissue oxygenation in patients with sickle cell disease

Feasibility of wearable technology for remote monitoring in high-risk adults with sickle cell disease: Baseline data from the SCD-carre trial

EPO treatment in combination with hydroxyurea improves pain and other quality of life measures in sickle cell disease

A Phase 1b/2 Study of the Efficacy and Safety of Combination Hydroxyurea and Dose-Escalated Erythropoietin for Treatment of Anemia in Sickle Cell Disease (ACHiEvE-SCD)

Novel Multidimensional Pain Assessment Tool Is a Feasible, Valid, and Enjoyable Approach to Communication of Pain Symptoms in Pediatric Sickle Cell Disease

Liver-to-lung microembolic NETs promote gasdermin D–dependent inflammatory lung injury in sickle cell disease

Assessing Dynamic Cerebral Autoregulation in Patients with Sickle Cell Disease Using Near-Infrared Spectroscopy and Paced Breathing

Integrating Mobile Health Technology for Symptom Management in Acute Pediatric Blood and Marrow Transplant Patients

Use of Mobile Health (mHealth) Apps and Wearable Technology to Assess Changes in Pain during Treatment of Acute Pain in Sickle Cell Disease

Understanding Sleep in Pediatric Patients with Sickle Cell Disease Admitted for Vaso-Occlusive Pain Crisis through Objective Data

Use of Mobile Technology to Monitor Pain and Reduce Outpatient, Emergency Department (ED), and Hospital Visits for Sickle Cell Pain Crisis

The Impact of Cognitive Function on Adherence to Hydroxyurea Therapy in Patients with Sickle Cell Disease

Effects of Sulforaphane Obtained from Broccoli Sprout Homogenate in Patients with Sickle Cell Disease (SCD)

The Use of Mobile Technology for Intensive Training in Medication Management in the Pediatric Population

Genetic and Epigenetic Regulation of the Gamma Globin Locus Is Associated with Fetal Hemoglobin Levels and Frequency of Pain in Sickle Cell Disease

Information Technology Use by Patients with Hemoglobinopathies

Genetic Variation In MYH9 Is Associated with Sickle Cell Disease Nephropathy

Retrospective Review of the Natural History of Pulmonary Hypertension in Sickle Cell Disease Demonstrates That Progressive Enlargement of the Left Atrium Is a Strong Predictor of Death.

Identification of genetic polymorphisms associated with risk for pulmonary hypertension in sickle cell disease

Further Investigation of the Role of Factor XIII in Priapism Associated with SCD.

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American Society of Hematology

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