Clinical and genetic predictors of renal dysfunctions in sickle cell anaemia in Cameroon-Reference-Cited by-同舟云学术

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Clinical and genetic predictors of renal dysfunctions in sickle cell anaemia in Cameroon

Published:2017-05-03 Issue:4 Volume:178 Page:629-639
ISSN:0007-1048
Container-title:British Journal of Haematology
language:en
Short-container-title:Br J Haematol

Author:

Geard Amy¹,Pule Gift D.¹,Chetcha Chemegni Bernard²,Ngo Bitoungui Valentina J.²,Kengne Andre P.³,Chimusa Emile R.¹,Wonkam Ambroise¹^ORCID

Affiliation:

1. Division of Human Genetics; Department of Pathology; Faculty of Health Sciences; University of Cape Town; Cape Town South Africa

2. Faculty of Medicine and Biomedical Sciences; University of Yaoundé; Yaoundé Cameroon

3. Non-Communicable Diseases Research Unit; South African Medical Research Council; Cape Town South Africa

Funder

National Health Laboratory Services (NHLS), South Africa

National Institutes of Health

Wellcome Trust

Publisher

Wiley

Subject

Hematology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/bjh.14724/fullpdf

Reference68 articles.

1. Cardiorenal risk prevalence in sickle cell hemoglobinopathy;Abo-Zenah;Nephron Clinical Practice,2009

2. Renal function in children suffering from sickle cell disease: challenge of early detection in highly resource-scarce settings;Aloni;PLoS ONE,2014

3. Congolese children with sickle cell trait may exhibit glomerular hyperfiltration: a case control study;Aloni;Journal of Clinical Laboratory Analysis,2017

4. Early blood transfusions protect against microalbuminuria in children with sickle cell disease;Alvarez;Pediatric Blood & Cancer,2006

5. Determination of the best method to estimate glomerular filtration rate from serum creatinine in adult patients with sickle cell disease: a prospective observational cohort study;Arlet;BMC Nephrology,2012

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1. Priorities for sickle cell disease global research and implementation;The Lancet;2024-07

2. Relevance of repeated analyses of albuminuria and glomerular filtration rate in African children with sickle cell anaemia;British Journal of Haematology;2024-06-27

3. Systematic Review of Genetic Modifiers Associated with the Development and/or Progression of Nephropathy in Patients with Sickle Cell Disease;International Journal of Molecular Sciences;2024-05-16

4. Interplay between α‐thalassemia and β‐hemoglobinopathies: Translating genotype–phenotype relationships into therapies;HemaSphere;2024-05

5. Comparison between serum nephrin and microalbuminuria as biomarkers for sickle cell nephropathy;Pediatric Hematology/Oncology and Immunopathology;2023-12-20

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