Page 1 | Search Results | Blood | American Society of Hematology

1-12 of 12

Sort by

Sort Order Select

Journal Articles

RACGAP1 variants in a sporadic case of CDA III implicate the dysfunction of centralspindlin as the basis of the disease

Sandeep N. Wontakal, Mishan Britto, Huan Zhang, Yongshuai Han, Chengjie Gao, Sarah Tannenbaum, Benjamin H. Durham, Margaret T. Lee, Xiuli An, Masanori Mishima

Blood (2022) 139 (9): 1413–1418.

https://doi.org/10.1182/blood.2021012334

Published: 2022

Includes: Supplemental data

Journal Articles

Food Insecurity Is a Common Problem Affecting Dietary Quality in a Clinic-Based Pediatric Sickle Cell Disease Sample

Cristina R. Fernández, MDMPH, Maureen Licursi, PNP, Randi Wolf, PhD MPH, Margaret T. Lee, MD, Nancy S. Green, MD

Blood (2020) 136 (Supplement 1): 8–9.

https://doi.org/10.1182/blood-2020-143096

Published: 2020

Journal Articles

Vitamin D and Inflammatory Markers in Children with Sickle Cell Disease

Margaret T. Lee, MD, Adiba Ashrafi, MS, Mady Hornig, MA, MD, Amelia Boehme, PhD MSPH, Nancy S. Green, MD, Gary M. Brittenham, MD

Blood (2019) 134 (Supplement_1): 2312.

https://doi.org/10.1182/blood-2019-129771

Published: 2019

Journal Articles

Association between Inflammatory Markers and Abnormal Neurological, Neurocognitive and Magnetic Resonance Imaging (MRI) Findings in Children with Sickle Cell Anemia in Uganda

Amelia Boehme, PhD MSPH, Adiba Ashrafi, MS, Richard Idro, MMED, PhD, Paul Bangirana, MS, PhD, Deogratias Munube, MD, Robert Opoka, MMED, Philip Kasirye, MMED, Margaret T. Lee, MD, Nancy S. Green, MD, Mady Hornig, MA, MD

Blood (2019) 134 (Supplement_1): 2300.

https://doi.org/10.1182/blood-2019-131560

Published: 2019

Journal Articles

Variation in Serial TCD Velocity Measurements in the TCD with Transfusions Changing to Hydroxyurea (TWiTCH) Trial

Russell E. Ware, MD PhD, Adam Lane, PhD, William H Schultz, MHS PA, Hamayun Imran, MD, Margaret T. Lee, MD, Matthew M Heeney, MD, Clark Brown, MD PhD, Lori Luchtman-Jones, MD, Jennifer Webb, MD, Sherron Jackson, MD, Banu Aygun, MD, Scott T. Miller, MD, Jennifer A Rothman, MD, Alexis A. Thompson, MD MPH, Judy Luden, CCRP, Barry R Davis, MD PhD, Robert J. Adams, MD

Blood (2016) 128 (22): 1019.

https://doi.org/10.1182/blood.V128.22.1019.1019

Published: 2016

Journal Articles

Case Series of Pediatric Sickle Retinopathy By Sensitive Clinical Imaging Technologies Suggests Frequent Early Pathology

Pahl A. Daniel, BS, Nancy S. Green, MD, Monica Bhatia, MD, Maureen Licursi, Courtney Briamonte, NP, Elana Smilow, NP, Jonathan S. Chang, MD, Margaret T. Lee, MD MS, Royce W.S. Chen, MD

Blood (2016) 128 (22): 3672.

https://doi.org/10.1182/blood.V128.22.3672.3672

Published: 2016

Journal Articles

Enhanced MRI Evaluation of Children with Sickle Cell Following Hematopoietic Stem Cell Transplantation

Nancy S. Green, MD, Monica Bhatia, MD, Erica Griffin, BS, Mahvish Qureshi, MD MBA, Courtney Briamonte, NP, Mirko Savone, BA, Stephen Sands, PsyD, Margaret T. Lee, MD MS, Angela Lignelli, MD, Adam M. Brickman, PhD

Blood (2015) 126 (23): 981.

https://doi.org/10.1182/blood.V126.23.981.981

Published: 2015

Journal Articles

TCD with Transfusions Changing to Hydroxyurea (TWiTCH): Hydroxyurea Therapy As an Alternative to Transfusions for Primary Stroke Prevention in Children with Sickle Cell Anemia

Russell E. Ware, MD PhD, Barry R Davis, MD PhD, William H Schultz, MHS PA, Clark Brown, MD PhD, Banu Aygun, MD, Sharada A. Sarnaik, MD, Isaac Odame, MD, Beng Fuh, MD, Alex George, MD, PhD, William Owen, MD, Lori Luchtman-Jones, MD, Zora R. Rogers, MD, Lee Hilliard, MD, Cynthia Gauger, MD, Connie M. Piccone, MD, Margaret T. Lee, MD, Janet Kwiatkowski, MD, Sherron Jackson, MD, Scott T. Miller, MD, Carla W Roberts, MD, Matthew M. Heeney, MD FRCP(C), Theodosia A. Kalfa, MD PhD, Stephen C Nelson, MD, Hamayun Imran, MD, Kerri A Nottage, MD MPH, Ofelia A. Alvarez, MD, Melissa Rhodes, MD, Alexis A. Thompson, MD, Jennifer Rothman, MD, Kathleen J. Helton, MD, Donna Roberts, MD, Jamie Coleman, MD, Melanie J Bonner, PhD, Abdullah Kutlar, MD, Niren Patel, MD, John C Wood, MD PhD, Linda Piller, MD, Peng Wei, PhD, Judy Luden, CCRP, Nicole A. Mortier, MHS, PA-C, Susan Stuber, MA, Naomi L.C. Luban, MD, Alan R. Cohen, MD, Sara L Pressel, MS, Robert J. Adams, MD MS

Blood (2015) 126 (23): 3.

https://doi.org/10.1182/blood.V126.23.3.3

Published: 2015

Journal Articles

Altered Regulation of Immune Responses in Alloimmunized Chronically Transfused Patients with Sickle Cell Disease.

Weili Bao, MS, Susanne Heck, PhD, Wu He, PhD, Maureen Licursi, MSN,CPNP, Genia Billote, RN, MPH, MFA, Hannah Stephens, RN, Joan Uehlinger, MD, Margaret T. Lee, MD, Sujit Sheth, MD, Karina Yazdanbakhsh, PhD

Blood (2009) 114 (22): 637.

https://doi.org/10.1182/blood.V114.22.637.637

Published: 2009

Journal Articles

Serum ferritin level changes in children with sickle cell disease on chronic blood transfusion are nonlinear and are associated with iron load and liver injury

Blood (2009) 114 (21): 4632–4638.

https://doi.org/10.1182/blood-2009-02-203323

Published: 2009

Journal Articles

Pulmonary Hypertension Is Not Associated with An Increased Risk of Death in Children with Sickle-Cell Disease Followed for a Mean of 3 Years.

Margaret T. Lee, MD, Tania Small, MD, Muhammad Amar Khan, MD, Erika Berman Rosenzweig, MD, Robyn J. Barst, MD, Gary M. Brittenham, MD

Blood (2008) 112 (11): 1443.

https://doi.org/10.1182/blood.V112.11.1443.1443

Published: 2008

Journal Articles

Stroke Prevention Trial in Sickle Cell Anemia (STOP): extended follow-up and final results

Margaret T. Lee, Sergio Piomelli, Suzanne Granger, Scott T. Miller, Shannon Harkness, Donald J. Brambilla, Robert J. Adams, for the STOP Study Investigators

Blood (2006) 108 (3): 847–852.

https://doi.org/10.1182/blood-2005-10-009506

Published: 2006

NARROW

RACGAP1 variants in a sporadic case of CDA III implicate the dysfunction of centralspindlin as the basis of the disease

Food Insecurity Is a Common Problem Affecting Dietary Quality in a Clinic-Based Pediatric Sickle Cell Disease Sample

Vitamin D and Inflammatory Markers in Children with Sickle Cell Disease

Association between Inflammatory Markers and Abnormal Neurological, Neurocognitive and Magnetic Resonance Imaging (MRI) Findings in Children with Sickle Cell Anemia in Uganda

Variation in Serial TCD Velocity Measurements in the TCD with Transfusions Changing to Hydroxyurea (TWiTCH) Trial

Case Series of Pediatric Sickle Retinopathy By Sensitive Clinical Imaging Technologies Suggests Frequent Early Pathology

Enhanced MRI Evaluation of Children with Sickle Cell Following Hematopoietic Stem Cell Transplantation

TCD with Transfusions Changing to Hydroxyurea (TWiTCH): Hydroxyurea Therapy As an Alternative to Transfusions for Primary Stroke Prevention in Children with Sickle Cell Anemia

Altered Regulation of Immune Responses in Alloimmunized Chronically Transfused Patients with Sickle Cell Disease.

Serum ferritin level changes in children with sickle cell disease on chronic blood transfusion are nonlinear and are associated with iron load and liver injury

Pulmonary Hypertension Is Not Associated with An Increased Risk of Death in Children with Sickle-Cell Disease Followed for a Mean of 3 Years.

Stroke Prevention Trial in Sickle Cell Anemia (STOP): extended follow-up and final results

Email alerts

ASH Publications

American Society of Hematology

Email alerts

ASH Publications

American Society of Hematology

This Feature Is Available To Subscribers Only