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You searched for: Author/Creator Dejkhamron, Prapai

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1. A Longitudinal Study of Growth and Relation With Anemia and Iron Overload in Pediatric Patients With Transfusion-dependent Thalassemia. Issue 6 (August 2016)

2. Cutis laxa with pulmonary emphysema, conjunctivochalasis, nasolacrimal duct obstruction, abnormal hair, and a novel FBLN5 mutation. Issue 9 (24th June 2014)

4. Juberg-Hayward syndrome and Roberts syndrome are allelic, caused by mutations in ESCO2. (November 2020)

5. Juberg-Hayward syndrome is a cohesinopathy, caused by mutation in ESCO2. (7th April 2020)

6. Type 1 diabetes management and outcomes: A multicenter study in Thailand. Issue 4 (4th October 2020)

7. Vitamin D deficiency and its relationship with cardiac iron and function in patients with transfusion-dependent thalassemia at Chiang Mai University Hospital. (2nd January 2018)

8. Young‐onset diabetes patients in Thailand: Data from Thai Type 1 Diabetes and Diabetes diagnosed Age before 30 years Registry, Care and Network (T1DDAR CN). Issue 5 (6th January 2022)