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Unraveling the mystery of the spleen

American journal of hematology, 2024-02, Vol.99 (2), p.150-151

Tubman, Venée N.

2024

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Indications for transfusion in the management of sickle cell disease

Hematology, 2021-12, Vol.2021 (1), p.696-703

2021

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New ASH initiatives to improve patient care in the long-overlooked sickle cell disease

Blood, 2023-07, Vol.142 (3), p.230-234

2023

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Mother knows best: The caregiver's perspective on clinical trials for sickle cell disease highlights the challenges of providing care in Africa

Pediatric blood & cancer, 2020-02, Vol.67 (2), p.e28054-n/a

Tubman, Venée N.

2020

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Turf wars: exploring splenomegaly in sickle cell disease in malaria‐endemic regions

British journal of haematology, 2017-06, Vol.177 (6), p.938-946

2017

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Fever Management in Sickle Cell Disease in Low- and Middle-Income Countries: A Survey of SCD Management Programs

The American journal of tropical medicine and hygiene, 2020-04, Vol.102 (4), p.902-904

2020

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X-linked gray platelet syndrome due to a GATA1 Arg216Gln mutation

Blood, 2007-04, Vol.109 (8), p.3297-3299

2007

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Sickle solubility test to screen for sickle cell trait: what's the harm?

Hematology, 2015-12, Vol.2015 (1), p.433-435

2015

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Determinants of retention in care of newborns diagnosed with sickle cell disease in Liberia: Results from a mixed-methods study of caregivers

PLOS global public health, 2023, Vol.3 (4), p.e0001705-e0001705

2023

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Clinical and laboratory outcomes following total or partial splenectomy in patients with hereditary spherocytosis

Pediatric hematology and oncology, 2019-08, Vol.36 (6), p.382-389

2019

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Building partnerships to target sickle cell anemia in Africa

American journal of hematology, 2013-12, Vol.88 (12), p.983-983

2013

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Progressive Thrombocytopenia, Splenomegaly, and Abnormal Tone in an Infant With Growth Faltering

Pediatrics (Evanston), 2024-07, Vol.154 (1), p.1

2024

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Allele-Specific Recombinase Polymerase Amplification to Detect Sickle Cell Disease in Low-Resource Settings

Analytical chemistry (Washington), 2021-03, Vol.93 (11), p.4832-4840

2021

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Multi-center retrospective study of children with sickle cell disease admitted to pediatric intensive care units in the United States

Scientific reports, 2023-04, Vol.13 (1), p.6758-10, Article 6758

2023

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A multiplexed, allele-specific recombinase polymerase amplification assay with lateral flow readout for sickle cell disease detection

Lab on a chip, 2024-08, Vol.24 (17), p.4115-4127

2024

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Global perspectives on cellular therapy for children with sickle cell disease

Current opinion in hematology, 2022-11, Vol.29 (6), p.275-280

2022

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Ketamine for Pain in Sickle Cell Disease Reduces Opioid Usage

Journal of pain and symptom management, 2024-03, Vol.67 (3), p.e169-e175

2024

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Concomitant sickle cell disease and systemic lupus erythematosus: A single‐center case series

Pediatric blood & cancer, 2024-10, Vol.71 (10), p.e31194-n/a

2024

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Unswitched memory B cell deficiency in children with sickle cell disease and response to pneumococcal polysaccharide vaccine

American journal of hematology, 2024-06, Vol.99 (6), p.1084-1094

2024

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Newborn Screening for Sickle Cell Disease in Liberia: A Pilot Study

Pediatric blood & cancer, 2016-04, Vol.63 (4), p.671-676

2016

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Acute lymphoblastic leukemia in a patient with MonoMAC syndrome/GATA2 haploinsufficiency

Pediatric blood & cancer, 2016-10, Vol.63 (10), p.1844-1847

2016

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Unique Hemoglobinopathy Pattern Following Treatment with Voxelotor

Annals of clinical and laboratory science, 2023-07, Vol.53 (4), p.647

2023

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Expert consensus on the management of infusion-related reactions (IRRs) in patients with sickle cell disease (SCD) receiving crizanlizumab: a RAND/UCLA modified Delphi panel

Annals of hematology, 2024-06, Vol.103 (6), p.1909-1917

2024

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Regional anesthesia for sickle cell disease vaso‐occlusive crisis: A single‐center case series

Pediatric blood & cancer, 2022-06, Vol.69 (6), p.e29695-n/a

2022

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Guidelines for the Standard Monitoring of Patients With Thalassemia: Report of the Thalassemia Longitudinal Cohort

Journal of pediatric hematology/oncology, 2015-04, Vol.37 (3), p.e162-e169

2015

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Unraveling the mystery of the spleen

Indications for transfusion in the management of sickle cell disease

New ASH initiatives to improve patient care in the long-overlooked sickle cell disease

Mother knows best: The caregiver's perspective on clinical trials for sickle cell disease highlights the challenges of providing care in Africa

Turf wars: exploring splenomegaly in sickle cell disease in malaria‐endemic regions

Fever Management in Sickle Cell Disease in Low- and Middle-Income Countries: A Survey of SCD Management Programs

X-linked gray platelet syndrome due to a GATA1 Arg216Gln mutation

Sickle solubility test to screen for sickle cell trait: what's the harm?

Determinants of retention in care of newborns diagnosed with sickle cell disease in Liberia: Results from a mixed-methods study of caregivers

Clinical and laboratory outcomes following total or partial splenectomy in patients with hereditary spherocytosis

Building partnerships to target sickle cell anemia in Africa

Progressive Thrombocytopenia, Splenomegaly, and Abnormal Tone in an Infant With Growth Faltering

Allele-Specific Recombinase Polymerase Amplification to Detect Sickle Cell Disease in Low-Resource Settings

Multi-center retrospective study of children with sickle cell disease admitted to pediatric intensive care units in the United States

A multiplexed, allele-specific recombinase polymerase amplification assay with lateral flow readout for sickle cell disease detection

Global perspectives on cellular therapy for children with sickle cell disease

Ketamine for Pain in Sickle Cell Disease Reduces Opioid Usage

Concomitant sickle cell disease and systemic lupus erythematosus: A single‐center case series

Unswitched memory B cell deficiency in children with sickle cell disease and response to pneumococcal polysaccharide vaccine

Newborn Screening for Sickle Cell Disease in Liberia: A Pilot Study

Acute lymphoblastic leukemia in a patient with MonoMAC syndrome/GATA2 haploinsufficiency

Unique Hemoglobinopathy Pattern Following Treatment with Voxelotor

Expert consensus on the management of infusion-related reactions (IRRs) in patients with sickle cell disease (SCD) receiving crizanlizumab: a RAND/UCLA modified Delphi panel

Regional anesthesia for sickle cell disease vaso‐occlusive crisis: A single‐center case series

Guidelines for the Standard Monitoring of Patients With Thalassemia: Report of the Thalassemia Longitudinal Cohort

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