about
Pulmonary hypertension in well-transfused thalassemia major patientsChronic transfusion therapy improves but does not normalize systemic and pulmonary vasculopathy in sickle cell disease.The heart in sickle cell disease, a model for heart failure with preserved ejection fractionIn Vivo T1 of Blood Measurements in Children with Sickle Cell Disease Improve Cerebral Blood Flow Quantification from Arterial Spin-Labeling MRI.Pseudo continuous arterial spin labeling quantification in anemic subjects with hyperemic cerebral blood flow.Liver MRI is more precise than liver biopsy for assessing total body iron balance: a comparison of MRI relaxometry with simulated liver biopsy results.Unwinding the path from anemia to stroke.Patients with sickle-cell disease exhibit greater functional connectivity and centrality in the locus coeruleus compared to anemic controlsFixing the MRI R2-iron calibration in liverLower white matter volume in beta-thalassemia associated with anemia and cognitive performanceIncreased brain iron deposition in patients with sickle cell disease: an MRI quantitative susceptibility mapping studyWhite matter has impaired resting oxygen delivery in sickle cell patientsPostoperative Serum Troponin Trends in Infants Undergoing Cardiac SurgeryBrain O2 reserve in sickle cell diseaseIn vivo validation of T2- and susceptibility-based Sv O2 measurements with jugular vein catheterization under hypoxia and hypercapniaProgressive Vasoconstriction with Sequential Thermal Stimulation Indicates Vascular Dysautonomia in Sickle Cell Disease
P50
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P50
description
researcher ORCID ID = 0000-0003-0996-3439
@en
name
John Wood
@ast
John Wood
@en
John Wood
@es
John Wood
@nl
type
label
John Wood
@ast
John Wood
@en
John Wood
@es
John Wood
@nl
prefLabel
John Wood
@ast
John Wood
@en
John Wood
@es
John Wood
@nl
P31
P496
0000-0003-0996-3439