Zobrazeno 1 - 10
of 94
pro vyhledávání: '"Pat Mahachoklertwattana"'
Autor:
Sirada Chongthavornvasana, Chatmanee Lertudomphonwanit, Pat Mahachoklertwattana, Manassawee Korwutthikulrangsri
Publikováno v:
BMC Pediatrics, Vol 23, Iss 1, Pp 1-8 (2023)
Abstract Background Vitamin D deficiency in patients with cholestasis is due to impaired intestinal vitamin D absorption, which results from decreased intestinal bile acid concentration. Patients with cholestasis usually do not achieve optimal vitami
Externí odkaz:
https://doaj.org/article/b4c8b4cb66d146469f147af7620a91ba
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:
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:
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
Autor:
Pat Mahachoklertwattana
Publikováno v:
Siriraj Medical Journal, Vol 58, Iss 4 (2006)
Externí odkaz:
https://doaj.org/article/e0a374342cf947aa8e549a8ee3b41616
Autor:
Wittayathorn Pornsiripratharn, Suporn Treepongkaruna, Phatthawit Tangkittithaworn, Niyata Chitrapaz, Chatmanee Lertudomphonwanit, Songpon Getsuwan, Pornthep Tanpowpong, Pat Mahachoklertwattana
Publikováno v:
Pediatric Gastroenterology, Hepatology & Nutrition; May2024, Vol. 27 Issue 3, p158-167, 10p
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