Cargando…

P115: REAL-WORLD DATA ON THE EFFICACY OF PHARMACEUTICAL-GRADE L-GLUTAMINE IN PREVENTING SICKLE CELL DISEASE-RELATED ACUTE COMPLICATIONS AND HEMOLYSIS IN PEDIATRIC AND ADULT PATIENTS.

Detalles Bibliográficos
Autores principales:	Elenga, N, Loko, G, Etienne-Julan, M, AlOkka, R, Adel, A, Yassin, M
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Lippincott Williams & Wilkins 2022
Materias:	Poster Presentations
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8811860/ http://dx.doi.org/10.1097/01.HS9.0000821552.41573.26

Ejemplares similares

P1503: REAL WORLD DATA ON EFFICACY OF PHARMACEUTICAL-GRADE L-GLUTAMINE IN PREVENTING SICKLE CELL DISEASE-RELATED ACUTE COMPLICATIONS AND HEMOLYSIS IN PEDIATRIC AND ADULT PATIENTS.
por: Elenga, N., et al.
Publicado: (2022)

Real-World data on efficacy of L-glutamine in preventing sickle cell disease-related complications in pediatric and adult patients
por: Elenga, Narcisse, et al.
Publicado: (2022)

PB2529: RENAL FUNCTIONS EVOLUTION OF 6 SCD PATIENTS TREATED BY L-GLUTAMINE PHARMACEUTICAL GRADE FOR 30 MONTHS: A REAL-WORLD STUDY.
por: Yassin, Mohamed, et al.
Publicado: (2023)

Fetal hemoglobin and hemolysis markers in sickle cell anemia()
por: Colella, Marina Pereira, et al.
Publicado: (2015)

Selenium Status and Hemolysis in Sickle Cell Disease Patients
por: Delesderrier, Emília, et al.
Publicado: (2019)

Newborn Screening for Sickle Cell Disease in the Caribbean: An Update of the Present Situation and of the Disease Prevalence
por: Knight-Madden, Jennifer, et al.
Publicado: (2019)

Uncommon Posterior Reversible Encephalopathy Syndrome in a Sickle-Cell Patient
por: Landais, Anne, et al.
Publicado: (2015)

Long-Term L-Glutamine Treatment Reduces Hemolysis without Ameliorating Hepatic Vaso-Occlusion and Liver Fibrosis in a Mouse Model of Sickle Cell Disease
por: Katoch, Omika, et al.
Publicado: (2023)

Chronic Hyper-Hemolysis in Sickle Cell Anemia: Association of Vascular Complications and Mortality with Less Frequent Vasoocclusive Pain
por: Taylor, James G., et al.
Publicado: (2008)

Higher Rates of Hemolysis Are Not Associated with Albuminuria in Jamaicans with Sickle Cell Disease
por: Asnani, Monika R., et al.
Publicado: (2011)

Sickle Retinopathy in a Person with Hemoglobin S/New York Disease
por: Calder, Donovan, et al.
Publicado: (2012)

Alloimmunization in Patients with Sickle Cell Disease in French Guiana
por: Elenga, Narcisse, et al.
Publicado: (2015)

Thrombotic Complications in Patients with Immune-Mediated Hemolysis
por: Capecchi, Marco, et al.
Publicado: (2021)

Severe hemolysis and vaso‐occlusive crisis due to COVID‐19 infection in a sickle cell disease patient improved after red blood cell exchange
por: Okar, Lina, et al.
Publicado: (2021)

Low bone mass density is associated with hemolysis in brazilian patients with sickle cell disease
por: Baldanzi, Gabriel, et al.
Publicado: (2011)

Doppler velocimetry of the orbital arteries in patients with sickle cell anemia: relationship with biomarkers of hemolysis
por: Ferrão, Thiago de Oliveira, et al.
Publicado: (2017)

Lactate dehydrogenase and hemolysis index to predict vaso-occlusive crisis in sickle cell disease
por: Feugray, Guillaume, et al.
Publicado: (2023)

Increased retention of functional mitochondria in mature sickle red blood cells is associated with increased sickling tendency, hemolysis and oxidative stress
por: Esperti, Sofia, et al.
Publicado: (2023)

115 The Beef Industry in a Post-Pandemic World
por: Peel, Derrell S
Publicado: (2021)

S115: LONG-TERM EFFICACY AND SAFETY OF DEFERIPRONE FOR PATIENTS WITH SICKLE CELL DISEASE OR OTHER ANEMIAS
por: Inusa, B, et al.
Publicado: (2022)

Pattern of hemolysis parameters and association with fetal hemoglobin in sickle cell anemia patients in steady state
por: Moreira, Juliane Almeida, et al.
Publicado: (2015)

Elevated Pulse Pressure is Associated with Hemolysis, Proteinuria and Chronic Kidney Disease in Sickle Cell Disease
por: Novelli, Enrico M., et al.
Publicado: (2014)

Primary Hyperparathyroidism in Homozygous Sickle Cell Patients: A Hemolysis-Mediated Hypocalciuric Hypercalcemia Phenotype?
por: Khan, Edmat Akhtar, et al.
Publicado: (2021)

More Unnecessary Imaginary Worlds – Part 4: The ICER Evidence Report for Crizanlizumab, Voxelotor and L-Glutamine for Sickle Cell Disease
por: Langley, Paul C
Publicado: (2020)

Sickle Cell Trait Increases Red Blood Cell Storage Hemolysis and Post-Transfusion Clearance in Mice
por: Osei-Hwedieh, David O., et al.
Publicado: (2016)

Hemolysis dictates monocyte differentiation via two distinct pathways in sickle cell disease vaso-occlusion
por: Liu, Yunfeng, et al.
Publicado: (2023)

Production of l-alanyl-l-glutamine by immobilized Pichia pastoris GS115 expressing α-amino acid ester acyltransferase
por: Li, Yi-Min, et al.
Publicado: (2019)

Prognostic value of the hemolysis index in patients with significant hemolysis
por: Cortés, Diego O, et al.
Publicado: (2015)

Evaluation of Outcomes and Quality of Care in Children with Sickle Cell Disease Diagnosed by Newborn Screening: A Real-World Nation-Wide Study in France
por: Brousse, Valentine, et al.
Publicado: (2019)

Can Hydroxychloroquine Cause G6PD-Related Hemolysis? A Case Study
por: Obeidat, Khaldun, et al.
Publicado: (2020)

Albuminuria, serum antioxidant enzyme levels and markers of hemolysis and inflammation in steady state children with sickle cell anemia
por: Itokua, Karen E., et al.
Publicado: (2016)

Inflammation, Hemolysis, and Erythropoiesis Lead to Competitive Regulation of Hepcidin and Possibly Systemic Iron Status in Sickle Cell Disease
por: Ginzburg, Yelena Z., et al.
Publicado: (2018)

Study of PMT FEU-115M and FEU-115M-10
por: Brekhovskikh, V, et al.
Publicado: (2000)

Low grade intravascular hemolysis associates with peripheral nerve injury in type 2 diabetes
por: Le Jeune, Sylvain, et al.
Publicado: (2022)

MECHANISM OF HEMOLYSIS BY COMPLEMENT : I. COMPLEMENT FIXATION AS AN ESSENTIAL PRELIMINARY TO HEMOLYSIS.
por: Eagle, Harry, et al.
Publicado: (1929)

Associations between TGF-β1 Levels and Markers of Hemolysis, Inflammation, and Tissue Remodeling in Pediatric Sickle Cell Patients
por: Santiago, Rayra P., et al.
Publicado: (2021)

P1431: ACCURATE CELL-FREE HEME DOSAGE IN PLASMA CORRELATES WITH ANEMIA, HEMOLYSIS AND SICKLE CELL NEPHROPATHY SEVERITY
por: Bencheikh, Laura, et al.
Publicado: (2023)

Blood Thixotropy in Patients with Sickle Cell Anaemia: Role of Haematocrit and Red Blood Cell Rheological Properties
por: Vent-Schmidt, Jens, et al.
Publicado: (2014)

p115 untethered
por: Wells, William A.
Publicado: (2001)

On knots (AM-115)
por: Kauffman, Louis H
Publicado: (1988)

Cannot write session to /tmp/vufind_sessions/sess_b7c0dpos4q2uipe5nn9aqp3ug1