Assessment of cystatin C in pediatric sickle cell disease and β-thalassemia as a marker of subclinical cardiovascular dysfunction: a case-control study-Reference-Cited by-同舟云学术

Assessment of cystatin C in pediatric sickle cell disease and β-thalassemia as a marker of subclinical cardiovascular dysfunction: a case-control study

Published:2021-03-16 Issue:7 Volume:38 Page:620-632
ISSN:0888-0018
Container-title:Pediatric Hematology and Oncology
language:en
Short-container-title:Pediatric Hematology and Oncology

Author:

Hanna Diana¹,Beshir Mohamed¹,Khalifa Naglaa²,Baz Eman¹,Elhewala Ahmed¹

Affiliation:

1. Pediatric Department, Faculty of Medicine, Zagazig University, Sharkia, Egypt

2. Clinical pathology Department, Faculty of Medicine, Zagazig University, Sharkia, Egypt

Publisher

Informa UK Limited

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Link

https://www.tandfonline.com/doi/pdf/10.1080/08880018.2021.1894280

Reference46 articles.

1. Takeuchi R, Groudine MT, Stoddard BL, Bender MA. Compositions and methods for the treatment of hemoglobinopathies. US patent 10,619,140. 2020.

2. Comparative study of sickle cell anemia and hemoglobin SC disease: clinical characterization, laboratory biomarkers and genetic profiles

3. Genetic diminution of circulating prothrombin ameliorates multiorgan pathologies in sickle cell disease mice

4. Cardiovascular Abnormalities in Sickle Cell Disease

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1. Correlation Analysis and Diagnostic Value of Serum Homocysteine, Cystatin C and Uric Acid Levels with the Severity of Coronary Artery Stenosis in Patients with Coronary Heart Disease;International Journal of General Medicine;2023-06

2. Hemolysis scavenger proteins and renal function marker in children with sickle cell disease at steady state: A cross‐sectional study;Health Science Reports;2023-03-30