Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Nawaporn Numbenjapon"'
Autor:
Craig F Munns, Han‐Wook Yoo, Muhammad Yazid Jalaludin, Rashida Vasanwala, Manju Chandran, Yumie Rhee, Wai Man BUT, Alice Pik‐Shan Kong, Pen‐Hua Su, Nawaporn Numbenjapon, Noriyuki Namba, Yasuo Imanishi, Roderick J Clifton‐Bligh, Xiaoping Luo, Weibo Xia
Publikováno v:
JBMR Plus, Vol 7, Iss 6, Pp n/a-n/a (2023)
ABSTRACT X‐linked hypophosphatemia (XLH) is a rare, inherited, multisystem disorder characterized by hypophosphatemia that occurs secondary to renal phosphate wasting. Mutations in PHEX gene (located at Xp22.1) in XLH alter bone mineral metabolism,
Externí odkaz:
https://doaj.org/article/738ef1c63308428f943cc4cf638b2ada
Autor:
Prapai Dejkhamron, Jeerunda Santiprabhob, Supawadee Likitmaskul, Chaicharn Deerochanawong, Petch Rawdaree, Thipaporn Tharavanij, Sirimon Reutrakul, Chawkaew Kongkanka, Chittiwat Suprasongsin, Nawaporn Numbenjapon, Taninee Sahakitrungruang, Raweewan Lertwattanarak, Pontipa Engkakul, Apiradee Sriwijitkamol, Manassawee Korwutthikulrangsri, Rattana Leelawattana, Mattabhorn Phimphilai, Somkiat Potisat, Panthep Khananuraksa, Kemarasami Kunsuikmengrai, Wannee Nitiyanant, for the Thai Type 1 Diabetes and Diabetes diagnosed Age before 30 years Registry, Care and Network (T1DDAR CN)
Publikováno v:
Journal of Diabetes Investigation, Vol 13, Iss 5, Pp 796-809 (2022)
ABSTRACT Aims/Introduction There is a lack of current information regarding young‐onset diabetes in Thailand. Thus, the objectives of this study were to describe the types of diabetes, the clinical characteristics, the treatment regimens and achiev
Externí odkaz:
https://doaj.org/article/b5e4af8feb9d42d582a9ddf8dccf782d
Autor:
Prapai Dejkhamron, Jeerunda Santiprabhob, Supawadee Likitmaskul, Chaicharn Deerochanawong, Petch Rawdaree, Thipaporn Tharavanij, Sirimon Reutrakul, Chawkaew Kongkanka, Chittiwat Suprasongsin, Nawaporn Numbenjapon, Taninee Sahakitrungruang, Raweewan Lertwattanarak, Pontipa Engkakul, Apiradee Sriwijitkamol, Manassawee Korwutthikulrangsri, Rattana Leelawattana, Mattabhorn Phimphilai, Somkiat Potisat, Panthep Khananuraksa, Cherdchai Nopmaneejumruslers, Wannee Nitiyanant, the Thai Type 1 Diabetes and Diabetes Diagnosed Before Age 30 Years Registry, Care, and Network (T1DDAR CN)
Publikováno v:
Journal of Diabetes Investigation, Vol 12, Iss 4, Pp 516-526 (2021)
Abstract Aims/Introduction The Thai Type 1 Diabetes and Diabetes Diagnosed Before Age 30 Years Registry, Care and Network was established in 2014 and involved 31 hospitals. The objective of the registry was to evaluate glycemic control and complicati
Externí odkaz:
https://doaj.org/article/1011925228b949979f90c7fec54a2a9a
Autor:
Suchavadee Vichutavate, Piradee Suwanpakdee, Napakjira Likasitthananon, Nawaporn Numbenjapon, Charcrin Nabangchang, Voraluck Phatarakijnirund
Publikováno v:
Journal of pediatric endocrinologymetabolism : JPEMReferences. 35(11)
Objectives Children with epilepsy are at increased risk of vitamin D deficiency. We aimed to compare the effect of two ergocalciferol regimens given for 90 days. Methods Epileptic patients aged 5–18 years who received at least one antiepileptic dru
Autor:
Pacharin Mungklarat, Anothai Juttuporn, Wiphakorn Suphaphimon, Warissara Sanor, Chula Kooanantkul, Nawaporn Numbenjapon, Voraluck Phatarakijinirund
Publikováno v:
Journal of Southeast Asian Medical Research. 3:59-66
Background: The prevalence of childhood obesity is in creasingly worldwide. Abnormal glucose metabolism (ASM) including impaired fasting glucose (IFG), impaired glucose tolerance (IGT) and type 2 diabetes (T2DM) is a common endocrine complication amo
Autor:
Prapai, Dejkhamron, Jeerunda, Santiprabhob, Supawadee, Likitmaskul, Chaicharn, Deerochanawong, Petch, Rawdaree, Thipaporn, Tharavanij, Sirimon, Reutrakul, Chawkaew, Kongkanka, Chittiwat, Suprasongsin, Nawaporn, Numbenjapon, Taninee, Sahakitrungruang, Raweewan, Lertwattanarak, Pontipa, Engkakul, Apiradee, Sriwijitkamol, Manassawee, Korwutthikulrangsri, Rattana, Leelawattana, Mattabhorn, Phimphilai, Somkiat, Potisat, Panthep, Khananuraksa, Kemarasami, Kunsuikmengrai, Wannee, Nitiyanant, Palinee, Nantarakchaikul
Publikováno v:
Journal of diabetes investigation. 13(5)
There is a lack of current information regarding young-onset diabetes in Thailand. Thus, the objectives of this study were to describe the types of diabetes, the clinical characteristics, the treatment regimens and achievement of glycemic control in
Autor:
Sirimon Reutrakul, Somkiat Potisat, Cherdchai Nopmaneejumruslers, Raweewan Lertwattanarak, Wannee Nitiyanant, Thai Type Diabetes, Chittiwat Suprasongsin, Taninee Sahakitrungruang, Nawaporn Numbenjapon, Petch Rawdaree, Prapai Dejkhamron, Care Diabetes Diagnosed Before Age Years Registry, Mattabhorn Phimphilai, Rattana Leelawattana, Supawadee Likitmaskul, Manassawee Korwutthikulrangsri, Jeerunda Santiprabhob, Pontipa Engkakul, Chawkaew Kongkanka, Panthep Khananuraksa, Chaicharn Deerochanawong, Thipaporn Tharavanij, Apiradee Sriwijitkamol
Publikováno v:
Journal of Diabetes Investigation
Journal of Diabetes Investigation, Vol 12, Iss 4, Pp 516-526 (2021)
Journal of Diabetes Investigation, Vol 12, Iss 4, Pp 516-526 (2021)
Aims/Introduction The Thai Type 1 Diabetes and Diabetes Diagnosed Before Age 30 Years Registry, Care and Network was established in 2014 and involved 31 hospitals. The objective of the registry was to evaluate glycemic control and complications of pa
Autor:
Oranut Komkhum, Phairuch Chaiyakul, Voraluck Phatarakijnirund, Wasawee Sakdinun, Nawaporn Numbenjapon
Publikováno v:
Journal of the Endocrine Society
Background: GnRH stimulation test is the gold standard for the diagnosis of central precocious puberty (CPP). However, it is invasive and costly. Previous studies showed that increased urinary gonadotropins (Gn) level in first morning voided (FMV) ur
Autor:
Voraluck Phatarakijnirund, Nawaporn Numbenjapon, Piriya Chantrathammachart, Boonchai Boonyawat
Publikováno v:
Journal of Southeast Asian Medical Research. 1:81-84
Background:Adrenal hypoplasia congenita (AHC) is a rare inherited disorder of adrenal development resulting in hypoplasia of adrenal gland and inability to produce glucocorticoids, mineralocorticoids and sex steroids. X-linked AHC is the most common
Autor:
Nawaporn Numbenjapon, Voraluck Phatarakijnirund, Chanisa Chotipanich, Chawkaew Kongkarnka, Puwadon Veerapan
Publikováno v:
Bone Abstracts.