Peroxisome Proliferator-Activated Receptor-γ Pro12Ala Polymorphism and Risk of Osteopenia in β-Thalassemia Major Patients-Reference-Cited by-同舟云学术

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Peroxisome Proliferator-Activated Receptor-γ Pro12Ala Polymorphism and Risk of Osteopenia in β-Thalassemia Major Patients

Published:2013-08-05 Issue:6 Volume:37 Page:564-573
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Sahmani Mehdi,Gholami Abdollah,Azarkeivan Azita,Darabi Masoud,Ahmadi Mohammad Hossein,Sabet Majid Sirati,Najafipour Reza

Publisher

Informa UK Limited

Subject

Biochemistry, medical,Clinical Biochemistry,Genetics(clinical),Hematology

Link

http://www.tandfonline.com/doi/pdf/10.3109/03630269.2013.814035

Reference29 articles.

1. New insights into the pathophysiology and management of osteoporosis in patients with beta thalassaemia

2. The genetics of osteoporosis: ‘complexities and difficulties’

3. Low Bone Mass in Prepubertal Children with Thalassemia Major: Insights into the Pathogenesis of Low Bone Mass in Thalassemia

4. The association of Pro12Ala polymorphism of peroxisome proliferator-activated receptor-γ gene with serum osteoprotegerin levels in healthy Korean women

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Association of Bone Disorder and Gene Polymorphism of PPAR-γ Pro12 Ala in Egyptian Children with β-Thalassemia;Thalassemia Reports;2023-09-30

2. Bone health in pediatric transfusion‐dependent beta‐thalassemia: Circulating osteoprotegerin and RANKL system;Pediatric Blood & Cancer;2021-10-26

3. PPARγ Pro12Ala and C161T polymorphisms, but not PPARα L162V, are associated with osteoporosis risk in Turkish postmenopausal women;Istanbul Journal of Pharmacy;2019-05-17

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