Zobrazeno 1 - 10
of 78
pro vyhledávání: '"Preamrudee Poomthavorn"'
Autor:
Somboon Wankanit, Pat Mahachoklertwattana, Thipwimol Tim-Aroon, Kinnaree Sorapipatcharoen,, Preamrudee Poomthavorn
Publikováno v:
JCRPE, Vol 14, Iss 4, Pp 485-489 (2022)
Pseudohypoparathyroidism (PHP) type 1A (PHP1A) is a disorder of multiple hormone resistance, mainly parathyroid hormone. It is associated with Albright hereditary osteodystrophy phenotypes. Patients with PHP1A may initially present with hypothyroidis
Externí odkaz:
https://doaj.org/article/146d45e5ce5643909def03d62e4bc5ed
Autor:
Papatsorn Suppasit, Soamarat Vilaiyuk, Preamrudee Poomthavorn, Sarunyu Pongratanakul, Patcharin Khlairit, Pat Mahachoklertwattana
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 20, Iss 1, Pp 1-8 (2022)
Abstract Background Systemic juvenile idiopathic arthritis (SJIA) is a chronic systemic inflammatory disease in children. Overproduction of inflammatory cytokines in SJIA resembles that in adult onset Still disease. Chronic inflammation causes insuli
Externí odkaz:
https://doaj.org/article/85fc9e11d33f48ddb06adadfa43ae1ff
Autor:
Lalita Ponin, Preamrudee Poomthavorn, Kwanchai Pirojsakul, Butsabong Lerkvaleekul, Sirisucha Soponkanaporn, Niyata Chitrapazt, Soamarat Vilaiyuk
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 20, Iss 1, Pp 1-11 (2022)
Abstract Background Growth impairment is the most common complication in patients with childhood-onset systemic lupus erythematosus (cSLE). There are limited data on risk factors affecting growth development in Asian patients with cSLE. This study ai
Externí odkaz:
https://doaj.org/article/cfdace3c869e4516abb94c90041e1b90
Autor:
Weenita Pipitprapat, Oraluck Pattanaprateep, Nareenart Iemwimangsa, Insee Sensorn, Bhakbhoom Panthan, Poramate Jiaranai, Wasun Chantratita, Kinnaree Sorapipatcharoen, Preamrudee Poomthavorn, Pat Mahachoklertwattana, Thanyachai Sura, Atchara Tunteeratum, Kanoknan Srichan, Chutintorn Sriphrapradang
Publikováno v:
Annals of Medicine, Vol 53, Iss 1, Pp 1244-1256 (2021)
AbstractIntroduction Pheochromocytomas and paragangliomas (PPGLs) are highly heritable tumours, with up to 40% of cases carrying germline variants. Current guidelines recommend genetic testing for all patients with PPGLs. Next-generation sequencing (
Externí odkaz:
https://doaj.org/article/c86466637b7a4d32898cf10bf9c6359f
Autor:
Kinnaree Sorapipatcharoen, Thipwimol Tim-Aroon, Pat Mahachoklertwattana, Wasun Chantratita, Nareenart Iemwimangsa, Insee Sensorn, Bhakbhoom Panthan, Poramate Jiaranai, Saisuda Noojarern, Patcharin Khlairit, Sarunyu Pongratanakul, Chittiwat Suprasongsin, Manassawee Korwutthikulrangsri, Chutintorn Sriphrapradang, Preamrudee Poomthavorn
Publikováno v:
Endocrine Connections, Vol 9, Iss 11, Pp 1121-1134 (2020)
Objective: To identify the genetic etiologies of congenital primary hypothyroidism (CH) in Thai patients. Design and methods: CH patients were enrolled. Clinical characteristics including age, signs and symptoms of CH, pedigree, family history, scree
Externí odkaz:
https://doaj.org/article/a1a308f866004555bf0676538b2eff7a
Autor:
Sira Korpaisarn, Dararat Chiewchalermsri, Jiraporn Arunakul, Orawee Chinthakanan, Preamrudee Poomthavorn, Chutintorn Sriphrapradang
Publikováno v:
SAGE Open Medicine, Vol 9 (2021)
Objectives: Data regarding gender-affirming hormone therapy in the Asian population are sparse. We aimed to evaluate the efficacy and safety of testosterone therapy in transgender men. Methods: A retrospective study chart review was conducted in a si
Externí odkaz:
https://doaj.org/article/3e50419d05f540f3a2d64008ba233d77
Autor:
Kochakorn Sithinamsuwan, Pat Mahachoklertwattana, Somboon Wankanit, Suwannee Chanprasertyothin, Sarunyu Pongratanakul, Patcharin Khlairit, Preamrudee Poomthavorn
Publikováno v:
International Journal of Endocrinology, Vol 2020 (2020)
Objective. Kisspeptin, a puberty control neuropeptide, has been discovered to have an additional role in metabolism and glucose homeostasis regulation. This study aimed to determine the association of serum kisspeptin with metabolic parameters and gl
Externí odkaz:
https://doaj.org/article/58f14b164c7d43c6bbecf687b0a1ef4c
Publikováno v:
Journal of Paediatrics and Child Health. 59:526-532
Autor:
Preamrudee Poomthavorn, Thipwimol Tim-Aroon, Kinnaree Sorapipatcharoen, Somboon Wankanit, Pat Mahachoklertwattana
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology. 14:485-489
Pseudohypoparathyroidism type 1A (PHP1A) is a disorder of multiple hormone resistance, mainly parathyroid hormone. It is associated with Albright hereditary osteodystrophy phenotypes. Patients with PHP1A may initially present with hypothyroidism duri
Autor:
Suparat Ekawaravong, Suporn Treepongkaruna, Preamrudee Poomthavorn, Sarunyu Pongratanakul, Patcharin Khlairit, Suwanee Chanprasertyothin, Pat Mahachoklertwattana
Publikováno v:
Clinical Pediatric Endocrinology.