Cargando…

Proteomic analysis of plasma from children with sickle cell anemia and silent cerebral infarction

Silent cerebral infarction is the most common neurological abnormality in children with sickle cell anemia, affecting 30-40% of 14 year olds. There are no known biomarkers to identify children with silent cerebral infarcts, and the pathological basis is also unknown. We used an unbiased proteomic di...

Descripción completa

Detalles Bibliográficos
Autores principales:	Tewari, Sanjay, Renney, George, Brewin, John, Gardner, Kate, Kirkham, Fenella, Inusa, Baba, Barrett, James E, Menzel, Stephan, Thein, Swee Lay, Ward, Malcolm, Rees, David C.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Ferrata Storti Foundation 2018
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6029528/ https://www.ncbi.nlm.nih.gov/pubmed/29545349 http://dx.doi.org/10.3324/haematol.2018.187815

Ejemplares similares

Genome wide association study of silent cerebral infarction in sickle cell disease (HbSS and HbSC)
por: Brewin, John N., et al.
Publicado: (2020)

Quantification of Silent Cerebral Infarction on High-Resolution FLAIR and Cognition in Sickle Cell Anemia
por: Stotesbury, Hanne, et al.
Publicado: (2022)

Associations between environmental factors and hospital admissions for sickle cell disease
por: Piel, Frédéric B., et al.
Publicado: (2017)

Quantitative susceptibility mapping (QSM) and R2(*) of silent cerebral infarcts in sickle cell anemia
por: Murdoch, Russell, et al.
Publicado: (2022)

Early Markers of Sickle Nephropathy in Children With Sickle Cell Anemia Are Associated With Red Cell Cation Transport Activity
por: Brewin, John, et al.
Publicado: (2017)

Genetic variants at HbF‐modifier loci moderate anemia and leukocytosis in sickle cell disease in Tanzania
por: Mtatiro, Siana Nkya, et al.
Publicado: (2014)

Fetal Hemoglobin is Associated with Peripheral Oxygen Saturation in Sickle Cell Disease in Tanzania
por: Nkya, Siana, et al.
Publicado: (2017)

White matter integrity and processing speed in sickle cell anemia
por: Stotesbury, Hanne, et al.
Publicado: (2018)

Venous cerebral blood flow quantification and cognition in patients with sickle cell anemia
por: Stotesbury, Hanne, et al.
Publicado: (2022)

Individual Watershed Areas in Sickle Cell Anemia: An Arterial Spin Labeling Study
por: Stotesbury, Hanne, et al.
Publicado: (2022)

Genome Wide Association Study of Fetal Hemoglobin in Sickle Cell Anemia in Tanzania
por: Mtatiro, Siana Nkya, et al.
Publicado: (2014)

Experimental Generation of SNP Haplotype Signatures in Patients with Sickle Cell Anaemia
por: Menzel, Stephan, et al.
Publicado: (2010)

Precursors of Executive Function in Infants With Sickle Cell Anemia
por: Hogan, Alexandra M., et al.
Publicado: (2013)

Prevention of Morbidity in sickle cell disease - qualitative outcomes, pain and quality of life in a randomised cross-over pilot trial of overnight supplementary oxygen and auto-adjusting continuous positive airways pressure (POMS2a): study protocol for a randomised controlled trial
por: Howard, Jo, et al.
Publicado: (2015)

Executive Function and Processing Speed in Children Living with Sickle Cell Anemia
por: Kelleher, Stephanie C., et al.
Publicado: (2023)

Structural connectivity mediates the relationship between blood oxygenation and cognitive function in sickle cell anemia
por: Clayden, Jonathan D., et al.
Publicado: (2022)

COVID-19 and sickle cell disease
por: Menapace, Laurel A., et al.
Publicado: (2020)

Therapeutic advances in sickle cell disease in the last decade
por: Shet, Arun S., et al.
Publicado: (2017)

Silent cerebral infarct in sickle cell anemia patients of southern Turkey
por: NAFİLE SAYMAN, Ezgi, et al.
Publicado: (2020)

Genetic variants of PKLR are associated with acute pain in sickle cell disease
por: Wang, Xunde, et al.
Publicado: (2022)

The carrier state for sickle cell disease is not completely harmless
por: Xu, Julia Zhe, et al.
Publicado: (2019)

Research in Sickle Cell Disease: From Bedside to Bench to Bedside
por: Salinas Cisneros, Gabriel, et al.
Publicado: (2021)

A survey of genetic fetal-haemoglobin modifiers in Nigerian patients with sickle cell anaemia
por: Adeyemo, Titilope A., et al.
Publicado: (2018)

Hematological and Genetic Predictors of Daytime Hemoglobin Saturation in Tanzanian Children with and without Sickle Cell Anemia
por: Cox, Sharon E., et al.
Publicado: (2013)

The Effect of Antioxidants on the Properties of Red Blood Cells From Patients With Sickle Cell Anemia
por: Al Balushi, Halima, et al.
Publicado: (2019)

Biopsychosocial Predictors of Quality of Life in Paediatric Patients With Sickle Cell Disease
por: Hood, Anna M., et al.
Publicado: (2021)

The significance of spleen size in children with sickle cell anemia
por: Nardo‐Marino, Amina, et al.
Publicado: (2022)

Epidemiology of Stroke in Sickle Cell Disease
por: Kirkham, Fenella Jane, et al.
Publicado: (2021)

The effect of xanthine oxidase and hypoxanthine on the permeability of red cells from patients with sickle cell anemia
por: Al Balushi, Halima W. M., et al.
Publicado: (2018)

Effects of regional brain volumes on cognition in sickle cell anemia: A developmental perspective
por: Hamdule, Shifa, et al.
Publicado: (2023)

Neutrophils remain detrimentally active in hydroxyurea-treated patients with sickle cell disease
por: Barbu, Emilia Alina, et al.
Publicado: (2019)

World Sickle Cell Day 2016 : A time for appraisal
por: Thein, Mya S., et al.
Publicado: (2016)

Geographic Differences in Phenotype and Treatment of Children with Sickle Cell Anemia from the Multinational DOVE Study
por: Inusa, Baba Psalm Duniya, et al.
Publicado: (2019)

Genetic association of fetal-hemoglobin levels in individuals with sickle cell disease in Tanzania maps to conserved regulatory elements within the MYB core enhancer
por: Mtatiro, Siana N, et al.
Publicado: (2015)

Brain Volumes and Cognition in Patients with Sickle Cell Anaemia: A Systematic Review and Meta-Analysis
por: Hamdule, Shifa, et al.
Publicado: (2023)

Morbidity pattern of sickle cell disease in India: A single centre perspective
por: Tewari, Sanjay, et al.
Publicado: (2013)

Recent Advances in the Treatment of Sickle Cell Disease
por: Salinas Cisneros, Gabriel, et al.
Publicado: (2020)

Neuroimaging and Cognitive Function in Sickle Cell Disease: A Systematic Review
por: Abdi, Suad S., et al.
Publicado: (2023)

A ten year review of the sickle cell program in Muhimbili National Hospital, Tanzania
por: Makani, Julie, et al.
Publicado: (2018)

Overnight auto-adjusting continuous airway pressure + standard care compared with standard care alone in the prevention of morbidity in sickle cell disease phase II (POMS2b): study protocol for a randomised controlled trial
por: Howard, Jo, et al.
Publicado: (2018)

Cannot write session to /tmp/vufind_sessions/sess_25c0i8pif3mjc3rgl6ddfgvgor