Zobrazeno 1 - 10
of 93
pro vyhledávání: '"Somchit Jaruratanasirikul"'
Publikováno v:
Journal of Health Science and Medical Research (JHSMR), Vol 42, Iss 5, Pp e20241055-e20241055 (2024)
We describe a 13-year-old girl who presented at her local hospital with a diffuse goiter and had discrepant thyroid function test (TFT) of elevated free T4 (FT4), free T3 (FT3) levels with mildly elevated thyroid-stimulating hormone (TSH) and a pitui
Externí odkaz:
https://doaj.org/article/93d4899416b147cb88d61e3f1c76e8fa
Autor:
Maneerat Puwanant, Somchit Jaruratanasirikul, Praenapa Chaithaweesup, Sasivara Boonrusmee, Kanjana Chimrung, Hutcha Sriplung
Publikováno v:
Journal of Health Science and Medical Research (JHSMR), Vol 42, Iss 4, Pp e20231016-e20231016 (2024)
Objective: To determine complementary food intake, food group diversity and nutritional adequacy of 6-12-month-old infants in southern Thailand. Material and Methods: A total of 120 healthy infants, aged 6-12 months, were enrolled: from December 2020
Externí odkaz:
https://doaj.org/article/1a47eb63a34d4e4ba9178b6bda7fb3c2
Publikováno v:
Journal of Health Science and Medical Research (JHSMR), Vol 42, Iss 4, Pp e20241033-e20241033 (2024)
We describe a 14-year-old girl who was referred for management of a prolactin-secreting pituitary adenoma as she had persistent milky discharge from her nipples, an elevated prolactin level and pituitary enlargement. Upon reviewing the medical histor
Externí odkaz:
https://doaj.org/article/76c28e939a5549629d13d70208c4a67f
Autor:
Somchit Jaruratanasirikul, Sasivara Boonrusmee, Staporn Kasemsripitak, Tansit Saengkaew, Kanjana Chimrung, Hutcha Sriplung
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-9 (2023)
Abstract Vitamin D inadequacy is a global problem in all age groups. Although there are various studies of vitamin D status in pregnant women in Southeast Asia, to date there are few studies from Southeast Asia examining vitamin D status in non-pregn
Externí odkaz:
https://doaj.org/article/d8a318cffb2e478992c4b1669e84b0e8
Autor:
Staporn Kasemsripitak, Somchit Jaruratanasirikul, Sasivara Boonrusmee, Tansit Saengkaew, Hutcha Sriplung
Publikováno v:
BMC Pediatrics, Vol 22, Iss 1, Pp 1-9 (2022)
Abstract Background Vitamin D is an essential micronutrient for bone mineralization and bone growth in children. There have been few studies to date of vitamin D status in infants aged 6–12 months in Southeast Asian countries. Aim To examine the pr
Externí odkaz:
https://doaj.org/article/2ffdca55ee974058b64d6e2bbf724aec
Autor:
Maneerat Puwanant, Sasivara Boonrusmee, Somchit Jaruratanasirikul, Kanjana Chimrung, Hutcha Sriplung
Publikováno v:
BMC Nutrition, Vol 8, Iss 1, Pp 1-11 (2022)
Abstract Introduction Adequate nutritional intake of both macronutrients and micronutrients is essential for maintaining good health throughout life, particularly for women of reproductive age (WRA). The Minimum Dietary Diversity for WRA (MDD-W), or
Externí odkaz:
https://doaj.org/article/e0d3c967f7d04013be45ec942cc3349c
Autor:
Wannapong Chonnapasatid, Nita Viwattanatipa, Somchai Manopatanakul, Somchit Jaruratanasirikul
Publikováno v:
BMC Health Services Research, Vol 22, Iss 1, Pp 1-10 (2022)
Abstract Background This study assessed the cleft lip/palate (CL/P) healthcare provision using data from the Thailand National Health Security Office from fiscal years 2012–2016. Methods Four national databases of Thailand comprising 1) admitted pa
Externí odkaz:
https://doaj.org/article/664517812eb04c7ba27e2b193f290d82
Publikováno v:
Journal of Health Science and Medical Research (JHSMR), Vol 39, Iss 6, Pp 517-522 (2021)
Wolman disease is a very rare autosomal recessive genetic disorder. The patients have the typical clinical finding of hepatosplenomegaly but with an abnormal lipid profile of high levels of total cholesterol (TC), triglycerides, and low-density lipop
Externí odkaz:
https://doaj.org/article/9c712b813e3242dc967bdc1e9e84d3fd
Autor:
Chariyawan Charalsawadi, Somchit Jaruratanasirikul, Areerat Hnoonual, Aussanai Chantarapong, Pornsiri Sangmanee, Sasipong Trongnit, Natini Jinawath, Pornprot Limprasert
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Chimerism is a very rare genetic finding in human. Most reported cases have a chi 46,XX/46,XY karyotype. Only three non-twin cases carrying both trisomy 21 and a normal karyotype have been reported, including two cases with a chi 47,XY,+21/46,XX kary
Externí odkaz:
https://doaj.org/article/7f3cb4dac637481ab4278b544c6bc714
Autor:
Chariyawan Charalsawadi, Sasipong Trongnit, Kanoot Jaruthamsophon, Juthamas Wirojanan, Somchit Jaruratanasirikul, Anupong Nitiruangjaras, Pornprot Limprasert
Publikováno v:
International Journal of Pediatrics, Vol 2021 (2021)
Background. Little is currently known about the genetics of pilomatricoma. A number of studies have reported some evidence that this disease may have a genetic association with mutations of CTNNB1 gene or expression of the beta-catenin protein. In th
Externí odkaz:
https://doaj.org/article/ccb0545f17274e4cb6d3ed34a4ef6946