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Life cycle assessment (LCA) of digested sewage sludge incineration for heat and power production

Journal of cleaner production, 2017-01, Vol.142, p.1684-1692

2017

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Crizanlizumab for the Prevention of Pain Crises in Sickle Cell Disease

The New England journal of medicine, 2017-02, Vol.376 (5), p.429-439

2017

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The clinical spectrum of HbSC sickle cell disease‐not a benign condition

British journal of haematology, 2024-08, Vol.205 (2), p.653-663

2024

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A comparative thermodynamic and economic analysis and assessment of a conventional HVAC and a VRF system in a social and cultural center building

Energy and buildings, 2017-04, Vol.140, p.196-209

2017

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(281) Genetic variability of UGT2B7, CYP3A4, CYP3A5 and CYP2B6 DMETs in a sickle cell disease patient cohort

The journal of pain, 2016-04, Vol.17 (4), p.S46-S46

2016

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A Navier-Stokes Solver for Compressible Turbulent Flows on Quadtree and Octree Based Cartesian Grids

Journal of applied fluid mechanics, 2019-01, Vol.12 (2), p.539-549

2019

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140EMF Pulmonary Hypertension as a Sickle Cell Disease Emergency: Is There a Role for Preemptive Pharmacogenetic Testing?

Annals of emergency medicine, 2016-10, Vol.68 (4), p.S56-S56

2016

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5613436 EXPERT CONSENSUS ON THE MANAGEMENT OF INFUSION‐RELATED REACTIONS (IRRS) PRESENTING WITH PAIN IN PATIENTS RECEIVING CRIZANLIZUMAB

HemaSphere, 2023-04, Vol.7 (S1), p.10-10

2023

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181 Admission Rates for an Observation Unit Clinical Pathway for the Treatment of Uncomplicated Sickle Cell Disease Vasoocclusive Crisis

Annals of emergency medicine, 2014-10, Vol.64 (4), p.S65-S66

2014

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Evaluating the implementation of a multi-level mHealth study to improve hydroxyurea utilization in sickle cell disease

Frontiers in health services, 2023-01, Vol.2, p.1024541-1024541

2023

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Fetal hemoglobin in sickle cell anemia: genetic determinants of response to hydroxyurea

The pharmacogenomics journal, 2007-12, Vol.7 (6), p.386-394

2007

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(258) CYP2C8 and CYP2C9 metabolic profiles and frequency of emergency department visits for sickle cell disease pain management

The journal of pain, 2015-04, Vol.16 (4), p.S40-S40

2015

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(275) CYP2C8 allele and genotype frequencies in adult Sickle Cell Disease Patients: implications for NSAIDs metabolism

The journal of pain, 2014-04, Vol.15 (4), p.S44-S44

2014

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NSAIDs pharmacotherapy and CYP2C9 allele frequency in pediatric sickle cell disease patients

The journal of pain, 2012-04, Vol.13 (4), p.S42-S42

2012

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CFD analysis of the Ahmed Glaucoma Valve and design of an alternative device

Computer methods in biomechanics and biomedical engineering, 2010-12, Vol.13 (6), p.655-662

2010

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Purified poloxamer 188 for treatment of acute vaso-occlusive crisis of sickle cell disease: A randomized controlled trial

JAMA : the journal of the American Medical Association, 2001-11, Vol.286 (17), p.2099

2001

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Transcranial Doppler ultrasonography in adults with sickle cell disease

Neurology, 2006-08, Vol.67 (4), p.572-574

2006

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The risks and benefits of long‐term use of hydroxyurea in sickle cell anemia: A 17.5 year follow‐up

American journal of hematology, 2010-06, Vol.85 (6), p.403-408

2010

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101: The Utility of Routine Reticulocyte Count in Uncomplicated Vaso-Occlusive Crisis Due to Sickle Cell Disease

Annals of emergency medicine, 2009, Vol.54 (3), p.S33-S33

2009

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P-Selectin Blockade in the Treatment of Painful Vaso-Occlusive Crises in Sickle Cell Disease: A Spotlight on Crizanlizumab

Journal of pain research, 2021-01, Vol.14, p.849-856

2021

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A randomized clinical trial of the efficacy and safety of rivipansel for sickle cell vaso-occlusive crisis

Blood, 2023-01, Vol.141 (2), p.168-179

2023

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Hb M Dothan [β 25/26 (B7/B8)/(GGT/GAG→GAG//Gly/Glu→Glu]; a new mechanism of unstable methemoglobin variant and molecular characteristics

Blood cells, molecules, & diseases, 2009-11, Vol.43 (3), p.235-238

2009

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Neuropsychological dysfunction and neuroimaging abnormalities in neurologically intact adults with sickle cell anemia

JAMA : the journal of the American Medical Association, 2010-05, Vol.303 (18), p.1823

2010

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Exergy analyses of green hydrogen production methods from biogas-based electricity and sewage sludge

International journal of hydrogen energy, 2017-04, Vol.42 (16), p.10986-10996

2017

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A New Sickling Variant ‘Hb S-Wake β[(Glu6Val-Asn139 Ser)]’ Found in a Compound Heterozygote with Hb S β(Glu6Val) Coinherited with Homozygous α-Thalassemia-2: Phenotype and Molecular Characteristics

Acta haematologica, 2010-01, Vol.124 (2), p.120-124

2010

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Life cycle assessment (LCA) of digested sewage sludge incineration for heat and power production

Crizanlizumab for the Prevention of Pain Crises in Sickle Cell Disease

The clinical spectrum of HbSC sickle cell disease‐not a benign condition

A comparative thermodynamic and economic analysis and assessment of a conventional HVAC and a VRF system in a social and cultural center building

(281) Genetic variability of UGT2B7, CYP3A4, CYP3A5 and CYP2B6 DMETs in a sickle cell disease patient cohort

A Navier-Stokes Solver for Compressible Turbulent Flows on Quadtree and Octree Based Cartesian Grids

140EMF Pulmonary Hypertension as a Sickle Cell Disease Emergency: Is There a Role for Preemptive Pharmacogenetic Testing?

5613436 EXPERT CONSENSUS ON THE MANAGEMENT OF INFUSION‐RELATED REACTIONS (IRRS) PRESENTING WITH PAIN IN PATIENTS RECEIVING CRIZANLIZUMAB

181 Admission Rates for an Observation Unit Clinical Pathway for the Treatment of Uncomplicated Sickle Cell Disease Vasoocclusive Crisis

Evaluating the implementation of a multi-level mHealth study to improve hydroxyurea utilization in sickle cell disease

Fetal hemoglobin in sickle cell anemia: genetic determinants of response to hydroxyurea

(258) CYP2C8 and CYP2C9 metabolic profiles and frequency of emergency department visits for sickle cell disease pain management

(275) CYP2C8 allele and genotype frequencies in adult Sickle Cell Disease Patients: implications for NSAIDs metabolism

NSAIDs pharmacotherapy and CYP2C9 allele frequency in pediatric sickle cell disease patients

CFD analysis of the Ahmed Glaucoma Valve and design of an alternative device

Purified poloxamer 188 for treatment of acute vaso-occlusive crisis of sickle cell disease: A randomized controlled trial

Transcranial Doppler ultrasonography in adults with sickle cell disease

The risks and benefits of long‐term use of hydroxyurea in sickle cell anemia: A 17.5 year follow‐up

101: The Utility of Routine Reticulocyte Count in Uncomplicated Vaso-Occlusive Crisis Due to Sickle Cell Disease

P-Selectin Blockade in the Treatment of Painful Vaso-Occlusive Crises in Sickle Cell Disease: A Spotlight on Crizanlizumab

A randomized clinical trial of the efficacy and safety of rivipansel for sickle cell vaso-occlusive crisis

Hb M Dothan [β 25/26 (B7/B8)/(GGT/GAG→GAG//Gly/Glu→Glu]; a new mechanism of unstable methemoglobin variant and molecular characteristics

Neuropsychological dysfunction and neuroimaging abnormalities in neurologically intact adults with sickle cell anemia

Exergy analyses of green hydrogen production methods from biogas-based electricity and sewage sludge

A New Sickling Variant ‘Hb S-Wake β[(Glu6Val-Asn139 Ser)]’ Found in a Compound Heterozygote with Hb S β(Glu6Val) Coinherited with Homozygous α-Thalassemia-2: Phenotype and Molecular Characteristics

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