Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Kinnaree Sorapipatcharoen,"'
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:
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::316b24174a236dc5218e9e81e195db88
https://doi.org/10.4274/jcrpe.galenos.2021.2021.0141
https://doi.org/10.4274/jcrpe.galenos.2021.2021.0141
Autor:
Chutintorn Sriphrapradang, Poramate Jiaranai, Saisuda Noojarern, Preamrudee Poomthavorn, Kinnaree Sorapipatcharoen, Thipwimol Tim-Aroon, Nareenart Iemwimangsa, Wasun Chantratita, Manassawee Korwutthikulrangsri, Pat Mahachoklertwattana, Insee Sensorn, Patcharin Khlairit, Chittiwat Suprasongsin, Sarunyu Pongratanakul, Bhakbhoom Panthan
Publikováno v:
Endocrine Connections
Endocrine Connections, Vol 9, Iss 11, Pp 1121-1134 (2020)
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, screene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f1d2d2911049dd8c33b7b204201ddd2
http://europepmc.org/articles/PMC7774760
http://europepmc.org/articles/PMC7774760
Autor:
Somboon, Wankanit, Pat, Mahachoklertwattana, Thipwimol, Tim-Aroon, Kinnaree, Sorapipatcharoen, Preamrudee, Poomthavorn
Publikováno v:
Journal of clinical research in pediatric endocrinology. 14(4)
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://explore.openaire.eu/search/publication?articleId=pmid________::dda10d7a9e6bdab93f56d79697464705
https://pubmed.ncbi.nlm.nih.gov/34327978
https://pubmed.ncbi.nlm.nih.gov/34327978
Autor:
Atchara Tunteeratum, Kinnaree Sorapipatcharoen, Weenita Pipitprapat, Kanoknan Srichan, Insee Sensorn, Nareenart Iemwimangsa, Wasun Chantratita, Thanyachai Sura, Pat Mahachoklertwattana, Preamrudee Poomthavorn, Chutintorn Sriphrapradang, Bhakbhoom Panthan, Oraluck Pattanaprateep, Poramate Jiaranai
Publikováno v:
Annals of Medicine
article-version (VoR) Version of Record
article-version (VoR) Version of Record
Introduction 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 (NGS) ena
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::306f4f6eba693956b715bb176efafd3a
https://pubmed.ncbi.nlm.nih.gov/34309460
https://pubmed.ncbi.nlm.nih.gov/34309460
Autor:
Pat Mahachoklertwattana, Thipwimol Tim-Aroon, Sathit Karanes, Kinnaree Sorapipatcharoen, Preamrudee Poomthavorn, Duangrurdee Wattanasirichaigoon, Sani Molagool
Publikováno v:
Journal of Paediatrics and Child Health. 56:1144-1146
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4f9bb112af6295144aa42dbe342bc29f
https://doi.org/10.1111/jpc.14757
https://doi.org/10.1111/jpc.14757
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