Chelation Therapy and Bone Metabolism Markers in Thalassemia Major-Reference-Cited by-同舟云学术

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Chelation Therapy and Bone Metabolism Markers in Thalassemia Major

Published:2006-01 Issue:11 Volume:19 Page:
ISSN:2191-0251
Container-title:Journal of Pediatric Endocrinology and Metabolism
language:
Short-container-title:

Author:

Pratelli L.,Verri E.,Fortini M.,Marconi S.,Zolezzi C.,Fornasari P.M.,Gamberini M R.,De Sanctis V.

Publisher

Walter de Gruyter GmbH

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology and Child Health

Link

https://www.degruyter.com/document/doi/10.1515/JPEM.2006.19.11.1335/pdf

Reference15 articles.

1. Osteochondrodystrophic Lesions in Chelated Thalassemic Patients: An Histological Analysis

2. Biochemical markers of bone turnover and bone mineral density in patients with β-thalassaemia major

3. Bone mineral density in prepubertal children with β-thalassemia: Correlation with growth and hormonal data

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1. Active hematopoiesis triggers exosomal release of PRDX2 that promotes osteoclast formation;Physiological Reports;2021-02

2. Impact of iron overload on bone remodeling in thalassemia;Archives of Osteoporosis;2020-09-14

3. Consumption of a green tea extract–curcumin drink decreases blood urea nitrogen and redox iron in β-thalassemia patients;Food & Function;2020

4. Intestinal calcium transport and its regulation in thalassemia: interaction between calcium and iron metabolism;The Journal of Physiological Sciences;2018-02-26

5. Bone turnover and mineral density in adult thalassemic patients: relationships with growth hormone secretory status and circulating somatomedins;Endocrine;2016-01-29

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