Cargando…

Sickle cell disease and albuminuria: recent advances in our understanding of sickle cell nephropathy

Albuminuria is considered to be a relevant biomarker for the detection of early glomerular damage in patients with sickle cell disease (SCD). Improvements in our understanding of the pathophysiological processes and molecular mechanisms underlying albuminuria are required, because increasing numbers...

Descripción completa

Detalles Bibliográficos
Autores principales:	Audard, Vincent, Bartolucci, Pablo, Stehlé, Thomas
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Oxford University Press 2017
Materias:	Genetic Kidney Disease
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5570022/ https://www.ncbi.nlm.nih.gov/pubmed/28852484 http://dx.doi.org/10.1093/ckj/sfx027

Ejemplares similares

Prevalence and determinants of microalbuminuria in children suffering from sickle cell anemia in steady state
por: Aloni, Michel N., et al.
Publicado: (2017)

UMOD genetic variations and myeloma cast nephropathy
por: Belliere, Julie, et al.
Publicado: (2019)

Diacylglycerol kinase epsilon nephropathy: late diagnosis and therapeutic implications
por: de Holanda, Maria Izabel, et al.
Publicado: (2019)

G1 is the major APOL1 risk allele for hypertension-attributed nephropathy in Central Africa
por: Sumaili, Ernest K, et al.
Publicado: (2018)

Balkan Nephropathy: Evolution of Our Knowledge
por: Bamias, Giorgos, et al.
Publicado: (2008)

First evidence of subclinical renal tubular injury during sickle-cell crisis
por: Audard, Vincent, et al.
Publicado: (2014)

Development of multi-level standards of care recommendations for sickle cell disease: Experience from SickleInAfrica
por: Paintsil, Vivian, et al.
Publicado: (2023)

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

Biomarkers of sickle cell nephropathy in Senegal
por: Ndour, El Hadji Malick, et al.
Publicado: (2022)

Sickle Cell Nephropathy and Associated Factors among Asymptomatic Children with Sickle Cell Anaemia
por: Nnaji, Uchenna Modestus, et al.
Publicado: (2020)

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

Natural history and variability in albuminuria in pediatric and murine sickle cell anemia
por: Kasztan, Malgorzata, et al.
Publicado: (2023)

Renal Function, Albuminuria, and the Risk of Cardiovascular Events After Kidney Transplantation
por: Lam, Ngan N., et al.
Publicado: (2018)

Iron Status in Sickle Cell Anemia: Deficiency or Overload?
por: Patel, Varsha P, et al.
Publicado: (2023)

SICKLE CELL DISEASE AND COVID-19
por: HANNA, SANDRINE, et al.
Publicado: (2021)

Establishing a Sickle Cell Disease Registry in Africa: Experience From the Sickle Pan-African Research Consortium, Kumasi-Ghana
por: Paintsil, Vivian, et al.
Publicado: (2022)

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

Establishing a database for sickle cell disease patient mapping and survival tracking: The sickle pan-african research consortium Nigeria example
por: Nnodu, Obiageli, et al.
Publicado: (2022)

Nephrotic syndrome and adrenal insufficiency caused by a variant in SGPL1
por: Linhares, Natália Duarte, et al.
Publicado: (2018)

Two brothers with identical variants of the CLCN5 gene—one developing Dent’s disease
por: Fischer, Anne Sophie, et al.
Publicado: (2018)

Exocrine pancreatic dysfunction is common in hepatocyte nuclear factor 1β-associated renal disease and can be symptomatic
por: Clissold, Rhian L, et al.
Publicado: (2018)

Late-onset Bartter syndrome type II
por: Gollasch, Benjamin, et al.
Publicado: (2017)

Potential and pitfalls in the genetic diagnosis of kidney diseases
por: Kesselheim, Anne, et al.
Publicado: (2017)

Rare diseases, rare presentations: recognizing atypical inherited kidney disease phenotypes in the age of genomics
por: Ars, Elisabet, et al.
Publicado: (2017)

Rare genetic variants in Shiga toxin-associated haemolytic uraemic syndrome: genetic analysis prior to transplantation is essential
por: Dowen, Frances, et al.
Publicado: (2017)

Diabetes, deafness and renal disease
por: Godinho, Iolanda, et al.
Publicado: (2017)

Long-term outcome in inherited nephrogenic diabetes insipidus
por: Sharma, Sonia, et al.
Publicado: (2018)

Uromodulin-related autosomal-dominant tubulointerstitial kidney disease—pathogenetic insights based on a case
por: Reindl, Johanna, et al.
Publicado: (2018)

Persistent pruritus as a rare and potentially serious manifestation of liver involvement in autosomal dominant polycystic kidney disease
por: García-Prieto, Ana, et al.
Publicado: (2018)

Variable phenotype in HNF1B mutations: extrarenal manifestations distinguish affected individuals from the population with congenital anomalies of the kidney and urinary tract
por: Madariaga, Leire, et al.
Publicado: (2018)

Genomic architecture of sickle cell disease in West African children
por: Quinlan, Jacklyn, et al.
Publicado: (2014)

Whole Blood Transcriptome Analysis in Children with Sickle Cell Anemia
por: Gee, Beatrice E., et al.
Publicado: (2022)

Editorial: Building capacity for sickle cell disease research and healthcare
por: Nembaware, Victoria, et al.
Publicado: (2023)

Classification of Kidney Transplant Recipients Using a Combination of Estimated GFR and Albuminuria Reflects Risk
por: White, Christine A., et al.
Publicado: (2016)

Advancements in Sickle Cell Disease (SCD) Treatment: A Review of Novel Pharmacotherapies and Their Impact on Patient Outcomes
por: Khan, Salman J, et al.
Publicado: (2023)

Diabetic nephropathy as the cause of end-stage kidney disease reported on the medical evidence form CMS2728 at a single center
por: Yuan, Christina M., et al.
Publicado: (2017)

Biomarkers and recent advances in the management and therapy of sickle cell disease
por: Telen, Marilyn J.
Publicado: (2015)

Albuminuria Is Associated with Endothelial Dysfunction and Elevated Plasma Endothelin-1 in Sickle Cell Anemia
por: Ataga, Kenneth I., et al.
Publicado: (2016)

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)

Donor-derived Cell-free DNA and the Prediction of BK Virus-associated Nephropathy
por: Kant, Sam, et al.
Publicado: (2020)

Cannot write session to /tmp/vufind_sessions/sess_entbd7ol4a23qbjc919j6i9vji