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Mechanisms of vasculopathy in sickle cell disease and thalassemia

Hematology, 2008, Vol.2008 (1), p.177-185

Morris, Claudia R

2008

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Reply to Letter to the Editor regarding hospital-based triage travel screens during the COVID-19 pandemic

International journal of infectious diseases, 2021-06, Vol.107, p.165-165

2021

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Acquired Amino Acid Deficiencies: A Focus on Arginine and Glutamine

Nutrition in Clinical Practice, 2017-04, Vol.32 (1_suppl), p.30S-47S

2017

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An Official American Thoracic Society Clinical Practice Guideline: Diagnosis, Risk Stratification, and Management of Pulmonary Hypertension of Sickle Cell Disease

American journal of respiratory and critical care medicine, 2014-03, Vol.189 (6), p.727-740

2014

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Special issue: Pediatric pain and sickle cell disease

Complementary therapies in medicine, 2022-12, Vol.71, p.102880, Article 102880

2022

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Asthma management: Reinventing the wheel in sickle cell disease

American journal of hematology, 2009-04, Vol.84 (4), p.234-241

Morris, Claudia R.

2009

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Dysregulated arginine metabolism, hemolysis-associated pulmonary hypertension, and mortality in sickle cell disease

JAMA : the journal of the American Medical Association, 2005-07, Vol.294 (1), p.81

2005

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Arginine Dysregulation and Myocardial Dysfunction in a Mouse Model and Children with Chronic Kidney Disease

Nutrients, 2023-04, Vol.15 (9), p.2162

2023

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A randomized, placebo-controlled trial of arginine therapy for the treatment of children with sickle cell disease hospitalized with vaso-occlusive pain episodes

Haematologica (Roma), 2013-09, Vol.98 (9), p.1375

2013

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Decreased Arginine Bioavailability and Increased Serum Arginase Activity in Asthma

American journal of respiratory and critical care medicine, 2004-07, Vol.170 (2), p.148-153

2004

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The effects of glutamine supplementation on markers of apoptosis and autophagy in sickle cell disease peripheral blood mononuclear cells

Complementary therapies in medicine, 2022-11, Vol.70, p.102856-102856, Article 102856

2022

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Implications for the metabolic fate of oral glutamine supplementation within plasma and erythrocytes of patients with sickle cell disease: A pharmacokinetics study

Complementary therapies in medicine, 2022-03, Vol.64, p.102803-102803, Article 102803

2022

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Pediatric emergency department-based asthma education tools and parent/child asthma knowledge

Allergy, asthma, and clinical immunology, 2024-03, Vol.20 (1), p.24-24

2024

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The capacity of red blood cells to reduce nitrite determines nitric oxide generation under hypoxic conditions

PloS one, 2014-07, Vol.9 (7), p.e101626

2014

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Erythrocyte glutamine depletion, altered redox environment, and pulmonary hypertension in sickle cell disease

Blood, 2008-01, Vol.111 (1), p.402-410

2008

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Prevalence of SARS-CoV-2 antibodies in pediatric healthcare workers

International journal of infectious diseases, 2021-04, Vol.105, p.474-481

2021

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Sex and frequency of pain episodes are associated with acute pain trajectories in adolescents with sickle cell disease

Pain reports, 2023-09, Vol.8 (5), p.e1084-e1084

2023

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Arginine Therapy and Cardiopulmonary Hemodynamics in Hospitalized Children with Sickle Cell Anemia: A Prospective, Double-blinded, Randomized Placebo-controlled Clinical Trial

American journal of respiratory and critical care medicine, 2022-07, Vol.206 (1), p.70-80

2022

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A multicenter evaluation of viral bloodstream detections in children presenting to the Emergency Department with suspected systemic infection

BMC pediatrics, 2021-05, Vol.21 (1), p.238-238, Article 238

2021

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Alterations of the arginine metabolome in sickle cell disease: a growing rationale for arginine therapy

Hematology/oncology clinics of North America, 2014-04, Vol.28 (2), p.301

Morris, Claudia R

2014

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Predictive value of clinician impression for readmission and postdischarge mortality among neonates and young children in Dar es Salaam, Tanzania and Monrovia, Liberia

BMJ paediatrics open, 2023-06, Vol.7 (1), p.e001972

2023

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Arginine Therapy Shows Promise for Treatment of Sickle Cell Disease Clinical Subphenotypes of Hemolysis and Arginine Deficiency

Anesthesia and analgesia, 2017-04, Vol.124 (4), p.1369-1370

Morris, Claudia R

2017

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Variability in firearm injury among major pediatric trauma centers across the USA

Trauma surgery & acute care open, 2023-05, Vol.8 (1), p.e001014-e001014

2023

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Mechanisms of vasculopathy in sickle cell disease and thalassemia

Reply to Letter to the Editor regarding hospital-based triage travel screens during the COVID-19 pandemic

Acquired Amino Acid Deficiencies: A Focus on Arginine and Glutamine

An Official American Thoracic Society Clinical Practice Guideline: Diagnosis, Risk Stratification, and Management of Pulmonary Hypertension of Sickle Cell Disease

Special issue: Pediatric pain and sickle cell disease

Asthma management: Reinventing the wheel in sickle cell disease

Dysregulated arginine metabolism, hemolysis-associated pulmonary hypertension, and mortality in sickle cell disease

Arginine Dysregulation and Myocardial Dysfunction in a Mouse Model and Children with Chronic Kidney Disease

A randomized, placebo-controlled trial of arginine therapy for the treatment of children with sickle cell disease hospitalized with vaso-occlusive pain episodes

Severe COVID-19 Is Characterized by an Impaired Type I Interferon Response and Elevated Levels of Arginase Producing Granulocytic Myeloid Derived Suppressor Cells

Decreased Arginine Bioavailability and Increased Serum Arginase Activity in Asthma

The effects of glutamine supplementation on markers of apoptosis and autophagy in sickle cell disease peripheral blood mononuclear cells

Implications for the metabolic fate of oral glutamine supplementation within plasma and erythrocytes of patients with sickle cell disease: A pharmacokinetics study

Pediatric emergency department-based asthma education tools and parent/child asthma knowledge

The capacity of red blood cells to reduce nitrite determines nitric oxide generation under hypoxic conditions

Identifying neonates at risk for post-discharge mortality in Dar es Salaam, Tanzania, and Monrovia, Liberia: Derivation and internal validation of a novel risk assessment tool

Erythrocyte glutamine depletion, altered redox environment, and pulmonary hypertension in sickle cell disease

Prevalence of SARS-CoV-2 antibodies in pediatric healthcare workers

Sex and frequency of pain episodes are associated with acute pain trajectories in adolescents with sickle cell disease

Arginine Therapy and Cardiopulmonary Hemodynamics in Hospitalized Children with Sickle Cell Anemia: A Prospective, Double-blinded, Randomized Placebo-controlled Clinical Trial

A multicenter evaluation of viral bloodstream detections in children presenting to the Emergency Department with suspected systemic infection

Alterations of the arginine metabolome in sickle cell disease: a growing rationale for arginine therapy

Predictive value of clinician impression for readmission and postdischarge mortality among neonates and young children in Dar es Salaam, Tanzania and Monrovia, Liberia

Arginine Therapy Shows Promise for Treatment of Sickle Cell Disease Clinical Subphenotypes of Hemolysis and Arginine Deficiency

Variability in firearm injury among major pediatric trauma centers across the USA

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