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White matter has impaired resting oxygen delivery in sickle cell patients

American journal of hematology, 2019-04, Vol.94 (4), p.467-474

2019

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Tissue iron evaluation in chronically transfused children shows significant levels of iron loading at a very young age

American journal of hematology, 2013-11, Vol.88 (11), p.E283-E285

2013

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Pancreatic iron and glucose dysregulation in thalassemia major

American journal of hematology, 2012-02, Vol.87 (2), p.155-160

2012

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Pituitary iron and volume predict hypogonadism in transfusional iron overload

American journal of hematology, 2012-02, Vol.87 (2), p.167-171

2012

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Fixing the MRI R2‐iron calibration in liver

American journal of hematology, 2020-05, Vol.95 (5), p.E120-E122

2020

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Cardiac iron overload in sickle‐cell disease

American journal of hematology, 2014-07, Vol.89 (7), p.678-683

2014

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Determinants of resting cerebral blood flow in sickle cell disease

American journal of hematology, 2016-09, Vol.91 (9), p.912-917

2016

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Reduced global cerebral oxygen metabolic rate in sickle cell disease and chronic anemias

American journal of hematology, 2021-08, Vol.96 (8), p.901-913

2021

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Ferritin trends do not predict changes in total body iron in patients with transfusional iron overload

American journal of hematology, 2014-04, Vol.89 (4), p.391-394

2014

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The role of carbon monoxide and heme oxygenase in the prevention of sickle cell disease vaso‐occlusive crises

American journal of hematology, 2017-06, Vol.92 (6), p.569-582

2017

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Anemia predicts lower white matter volume and cognitive performance in sickle and non‐sickle cell anemia syndrome

American journal of hematology, 2019-10, Vol.94 (10), p.1055-1065

2019

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Loss of alpha‐globin genes in human subjects is associated with improved nitric oxide‐mediated vascular perfusion

American journal of hematology, 2021-03, Vol.96 (3), p.277-281

2021

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Tricuspid regurgitant jet velocity and myocardial tissue Doppler parameters predict mortality in a cohort of patients with sickle cell disease spanning from pediatric to adult age groups ‐ revisiting this controversial concept after 16 years of additional evidence

American journal of hematology, 2021-01, Vol.96 (1), p.31-39

2021

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Individuals with sickle cell disease have a significantly greater vasoconstriction response to thermal pain than controls and have significant vasoconstriction in response to anticipation of pain

American journal of hematology, 2017-11, Vol.92 (11), p.1137-1145

2017

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Sickle cell microvascular paradox—oxygen supply‐demand mismatch

American journal of hematology, 2019-06, Vol.94 (6), p.678-688

2019

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Nutritional deficiencies in iron overloaded patients with hemoglobinopathies

American journal of hematology, 2009-06, Vol.84 (6), p.344-348

2009

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Comparison of biventricular dimensions and function between pediatric sickle‐cell disease and thalassemia major patients without cardiac iron

American journal of hematology, 2013-03, Vol.88 (3), p.213-218

2013

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Electrocardiographic consequences of cardiac iron overload in thalassemia major

American journal of hematology, 2012-02, Vol.87 (2), p.139-144

2012

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Tricuspid regurgitant jet velocity and myocardial tissue Doppler parameters predict mortality in a cohort of patients with sickle cell disease spanning from pediatric to adult age groups ‐ revisiting this controversial concept after 16years of additional evidence

American journal of hematology, 2021-01, Vol.96 (1), p.31-39

2021

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Tricuspid regurgitant jet velocity and myocardial tissue doppler parameters predict mortality in a cohort of patients with sickle cell disease spanning from pediatric to adult age groups – revisiting this controversial concept after sixteen years of additional evidence

American journal of hematology, 2020-10, Vol.96 (1), p.31-39

2020

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Iron chelation adherence to deferoxamine and deferasirox in thalassemia

American journal of hematology, 2011-05, Vol.86 (5), p.433-436

2011

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Patterns of hepatic iron distribution in patients with chronically transfused thalassemia and sickle cell disease

American journal of hematology, 2009-08, Vol.84 (8), p.480-483

2009

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Follow‐up report on the 2‐year cardiac data from a deferasirox monotherapy trial

American journal of hematology, 2010-10, Vol.85 (10), p.818-819

2010

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Exercise performance in thalassemia major: Correlation with cardiac iron burden

American journal of hematology, 2013-03, Vol.88 (3), p.193-197

2013

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Quality of life in thalassemia: A comparison of SF‐36 results from the thalassemia longitudinal cohort to reported literature and the US norms

American journal of hematology, 2011-01, Vol.86 (1), p.92-95

2011

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White matter has impaired resting oxygen delivery in sickle cell patients

Tissue iron evaluation in chronically transfused children shows significant levels of iron loading at a very young age

Pancreatic iron and glucose dysregulation in thalassemia major

Pituitary iron and volume predict hypogonadism in transfusional iron overload

Fixing the MRI R2‐iron calibration in liver

Cardiac iron overload in sickle‐cell disease

Determinants of resting cerebral blood flow in sickle cell disease

Reduced global cerebral oxygen metabolic rate in sickle cell disease and chronic anemias

Ferritin trends do not predict changes in total body iron in patients with transfusional iron overload

The role of carbon monoxide and heme oxygenase in the prevention of sickle cell disease vaso‐occlusive crises

Anemia predicts lower white matter volume and cognitive performance in sickle and non‐sickle cell anemia syndrome

Loss of alpha‐globin genes in human subjects is associated with improved nitric oxide‐mediated vascular perfusion

Tricuspid regurgitant jet velocity and myocardial tissue Doppler parameters predict mortality in a cohort of patients with sickle cell disease spanning from pediatric to adult age groups ‐ revisiting this controversial concept after 16 years of additional evidence

Individuals with sickle cell disease have a significantly greater vasoconstriction response to thermal pain than controls and have significant vasoconstriction in response to anticipation of pain

Sickle cell microvascular paradox—oxygen supply‐demand mismatch

Nutritional deficiencies in iron overloaded patients with hemoglobinopathies

Comparison of biventricular dimensions and function between pediatric sickle‐cell disease and thalassemia major patients without cardiac iron

Electrocardiographic consequences of cardiac iron overload in thalassemia major

Tricuspid regurgitant jet velocity and myocardial tissue Doppler parameters predict mortality in a cohort of patients with sickle cell disease spanning from pediatric to adult age groups ‐ revisiting this controversial concept after 16years of additional evidence

Tricuspid regurgitant jet velocity and myocardial tissue doppler parameters predict mortality in a cohort of patients with sickle cell disease spanning from pediatric to adult age groups – revisiting this controversial concept after sixteen years of additional evidence

Iron chelation adherence to deferoxamine and deferasirox in thalassemia

Patterns of hepatic iron distribution in patients with chronically transfused thalassemia and sickle cell disease

Follow‐up report on the 2‐year cardiac data from a deferasirox monotherapy trial

Exercise performance in thalassemia major: Correlation with cardiac iron burden

Quality of life in thalassemia: A comparison of SF‐36 results from the thalassemia longitudinal cohort to reported literature and the US norms

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