Kinnaree Sorapipatcharoen

Cost-minimization analysis of sequential genetic testing versus targeted next-generation sequencing gene panels in patients with pheochromocytoma and paraganglioma

W. Chantratita, Weenita Pipitprapat, Chutintorn Sriphrapradang, 2021, Annals of medicine.

DUOX2 variants are a frequent cause of congenital primary hypothyroidism in Thai patients

W. Chantratita, Chutintorn Sriphrapradang, P. Mahachoklertwattana, 2020, Endocrine connections.

Successful parathyroidectomy with intra‐operative parathyroid hormone monitoring in a neonate with severe primary hyperparathyroidism caused by homozygous mutation in CASR gene

D. Wattanasirichaigoon, P. Mahachoklertwattana, P. Poomthavorn, 2019, Journal of paediatrics and child health.

Central Precocious Puberty in a Boy with Pseudohypoparathyroidism Type 1A due to a Novel GNAS Variant, with Congenital Hypothyroidism as the First Manifestation

P. Mahachoklertwattana, P. Poomthavorn, Thipwimol Tim-Aroon, 2021, Journal of clinical research in pediatric endocrinology.