1. Srinakharinwirot University Institutional Repository

Search


Current filters:




Start a new search
Add filters:

Use filters to refine the search results.

 | 
Results 51-60 of 60 (Search time: 0.003 seconds).
Item hits:
Issue DateTitleAuthor(s)
2015Apolipoprotein E receptor 2 gene polymorphisms associated with dyslipidemia among thai populationThongket P.; Rattanathanawan K.; Seesom W.; Sukhumsirichart W.
2016Children’s eating behavior questionnaire: Factorial validation and differences in sex and educational level in Thai school-age childrenSirirassamee T.; Hunchangsith P.
2012Association of CTXN3-SLC12A2 polymorphisms and schizophrenia in a Thai populationPanichareon B.; Nakayama K.; Iwamoto S.; Thurakitwannakarn W.; Sukhumsirichart W.
2018Assessment of preeclampsia risk by use of serum ionized magnesium-based equationKreepala C.; Kitporntheranunt M.; Sangwipasnapaporn W.; Rungsrithananon W.; Wattanavaekin K.
2019Comparison of Endothelial Keratoplasty Techniques in Patients With Prior Glaucoma Surgery: A Case-Matched StudyLin S.R.; Prapaipanich P.; Yu F.; Law S.K.; Caprioli J.; Aldave A.J.; Deng S.X.
2017Comparison of Breastfeeding Outcomes between Using the Laid-Back and Side-Lying Breastfeeding Positions in Mothers Delivering by Cesarean Section: A Randomized Controlled TrialPuapornpong P.; Raungrongmorakot K.; Laosooksathit W.; Hanprasertpong T.; Ketsuwan S.
2016The effect of ginger on breast milk volume in the early postpartum period: A randomized, double-blind controlled trialParitakul P.; Ruangrongmorakot K.; Laosooksathit W.; Suksamarnwong M.; Puapornpong P.
2013Polymorphisms in nitric oxide synthase and endothelin genes among children with obstructive sleep apneaChatsuriyawong S.; Gozal D.; Kheirandish-Gozal L.; Bhattacharjee R.; Khalyfa A.A.; Wang Y.; Sukhumsirichart W.; Khalyfa A.
2011Genome-wide association study identifies variations in 6p21.3 associated with nevirapine-induced rashChantarangsu S.; Mushiroda T.; Mahasirimongkol S.; Kiertiburanakul S.; Sungkanuparph S.; Manosuthi W.; Tantisiriwat W.; Charoenyingwattana A.; Sura T.; Takahashi A.; Kubo M.; Kamatani N.; Chantratita W.; Nakamura Y.
2019Strong Linkage of the Single Nucleotide Polymorphism rs77308790 with an α0-Thalassemia (– –SEA deletion) Allele and Application for Double-Check Diagnosis of Hb Bart’s Hydrops Fetalis Syndrome in ThailandJomoui W.; Tepakhan W.; Karnpean R.

Discover