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Physiology and pathophysiology of iron in hemoglobin-associated diseases

Free radical biology & medicine, 2014-07, Vol.72, p.23-40

Coates, Thomas D.

2014

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Higher hemoglobin is better in thalassemia

Blood, 2024-03, Vol.143 (10), p.842

Coates, Thomas D

2024

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American Society of Hematology 2019 guidelines for sickle cell disease: cardiopulmonary and kidney disease

Blood advances, 2019-12, Vol.3 (23), p.3867-3897

2019

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Contrasting resting-state fMRI abnormalities from sickle and non-sickle anemia

PloS one, 2017-10, Vol.12 (10), p.e0184860-e0184860

2017

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Biophysical markers of the peripheral vasoconstriction response to pain in sickle cell disease

PloS one, 2017-05, Vol.12 (5), p.e0178353-e0178353

2017

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Iron overload in transfusion-dependent patients

Hematology, 2019-12, Vol.2019 (1), p.337-344

Coates, Thomas D

2019

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Vasoconstriction Response to Mental Stress in Sickle Cell Disease: The Role of the Cardiac and Vascular Baroreflexes

Frontiers in physiology, 2021-11, Vol.12, p.698209-698209

2021

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McDAPS: A multi-channel physiological signals display and analysis system for clinical researchers

SoftwareX, 2023-07, Vol.23, p.101482, Article 101482

2023

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Sickle Cell Disease Subjects Have a Distinct Abnormal Autonomic Phenotype Characterized by Peripheral Vasoconstriction With Blunted Cardiac Response to Head-Up Tilt

Frontiers in physiology, 2019-04, Vol.10, p.381-381

2019

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Vaso-Occlusion in Sickle Cell Disease: Is Autonomic Dysregulation of the Microvasculature the Trigger?

Journal of clinical medicine, 2019-10, Vol.8 (10), p.1690

2019

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How we manage iron overload in sickle cell patients

British journal of haematology, 2017-06, Vol.177 (5), p.703-716

2017

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Iron and oxidative stress in cardiomyopathy in thalassemia

Free radical biology & medicine, 2015-11, Vol.88 (Pt A), p.3-9

2015

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Introduction to a How I Treat series on sickle cell disease and thalassemia

Blood, 2018-10, Vol.132 (17), p.1729-1730

2018

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Hemoglobin and mean platelet volume predicts diffuse T1-MRI white matter volume decrease in sickle cell disease patients

NeuroImage clinical, 2017-01, Vol.15, p.239-246

2017

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Diminished cerebral oxygen extraction and metabolic rate in sickle cell disease using T2 relaxation under spin tagging MRI

Magnetic resonance in medicine, 2018-07, Vol.80 (1), p.294-303

2018

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Introduction to a review series on human neutrophils

Blood, 2019-05, Vol.133 (20), p.2111-2112

2019

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You don't always get what you want: Does hypoxia cause sickle cell crisis?

American journal of hematology, 2018-04, Vol.93 (4), p.475-477

Coates, Thomas D.

2018

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Splenic iron decreases without change in volume or liver parameters during luspatercept therapy

Blood, 2023-11, Vol.142 (22), p.1932

2023

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Transplantation in thalassemia: Revisiting the Pesaro risk factors 25 years later

American journal of hematology, 2017-05, Vol.92 (5), p.411-413

2017

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Introduction to a review series on iron metabolism and its disorders

Blood, 2019-01, Vol.133 (1), p.1-2

2019

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Identifying Elevated Risk for Future Pain Crises in Sickle-Cell Disease Using Photoplethysmogram Patterns Measured During Sleep: A Machine Learning Approach

Frontiers in digital health, 2021-07, Vol.3

2021

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Management of luspatercept therapy in patients with transfusion‐dependent β‐thalassaemia

British journal of haematology, 2023-06, Vol.201 (5), p.824-831

2023

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Unchanneling cardiac iron in humans

Blood, 2016-09, Vol.128 (12), p.1538-1540

Coates, Thomas D.

2016

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Relationship between labile plasma iron, liver iron concentration and cardiac response in a deferasirox monotherapy trial

Haematologica (Roma), 2011-07, Vol.96 (7), p.1055

2011

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Shared Care for Adults with Sickle Cell Disease: An Analysis of Care from Eight Health Systems

Journal of clinical medicine, 2019-08, Vol.8 (8), p.1154

2019

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Physiology and pathophysiology of iron in hemoglobin-associated diseases

Higher hemoglobin is better in thalassemia

American Society of Hematology 2019 guidelines for sickle cell disease: cardiopulmonary and kidney disease

Contrasting resting-state fMRI abnormalities from sickle and non-sickle anemia

Biophysical markers of the peripheral vasoconstriction response to pain in sickle cell disease

Iron overload in transfusion-dependent patients

Vasoconstriction Response to Mental Stress in Sickle Cell Disease: The Role of the Cardiac and Vascular Baroreflexes

McDAPS: A multi-channel physiological signals display and analysis system for clinical researchers

Sickle Cell Disease Subjects Have a Distinct Abnormal Autonomic Phenotype Characterized by Peripheral Vasoconstriction With Blunted Cardiac Response to Head-Up Tilt

Vaso-Occlusion in Sickle Cell Disease: Is Autonomic Dysregulation of the Microvasculature the Trigger?

How we manage iron overload in sickle cell patients

Iron and oxidative stress in cardiomyopathy in thalassemia

Introduction to a How I Treat series on sickle cell disease and thalassemia

Hemoglobin and mean platelet volume predicts diffuse T1-MRI white matter volume decrease in sickle cell disease patients

Diminished cerebral oxygen extraction and metabolic rate in sickle cell disease using T2 relaxation under spin tagging MRI

Introduction to a review series on human neutrophils

You don't always get what you want: Does hypoxia cause sickle cell crisis?

Splenic iron decreases without change in volume or liver parameters during luspatercept therapy

Transplantation in thalassemia: Revisiting the Pesaro risk factors 25 years later

Introduction to a review series on iron metabolism and its disorders

Identifying Elevated Risk for Future Pain Crises in Sickle-Cell Disease Using Photoplethysmogram Patterns Measured During Sleep: A Machine Learning Approach

Management of luspatercept therapy in patients with transfusion‐dependent β‐thalassaemia

Unchanneling cardiac iron in humans

Relationship between labile plasma iron, liver iron concentration and cardiac response in a deferasirox monotherapy trial

Shared Care for Adults with Sickle Cell Disease: An Analysis of Care from Eight Health Systems

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