1. Srinakharinwirot University Institutional Repository

Search


Current filters:



Start a new search
Add filters:

Use filters to refine the search results.

 | 
Results 51-58 of 58 (Search time: 0.002 seconds).
Item hits:
Issue DateTitleAuthor(s)
2009Renal thrombotic microangiopathy after hematopoietic cell transplant: Role of GVHD in pathogenesisChangsirikulchai S.; Myerson D.; Guthrie K.A.; McDonald G.B.; Alpers C.E.; Hingorani S.R.
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.
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.
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.
2004Meniscal lesions in the anterior cruciate insufficient knee: The accuracy of clinical evaluationPookarnjanamorakot C.; Korsantirat T.; Woratanarat P.
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