Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Wanwisa Maneechay"'
Autor:
Nattapon Khongcharoen, Wison Laochareonsuk, Pongsakorn Choochuen, Wanwisa Maneechay, Surasak Sangkhathat
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 79, Iss , Pp 102216- (2022)
Introduction: Juvenile polyposis syndrome (JPS), a rare polyposis syndrome in childhood, is characterized by multiple diffuse hamartomatous polyps in the gastrointestinal tract (GI) with an estimated incidence of one in 50,000 to 100,000 live births.
Externí odkaz:
https://doaj.org/article/94f2daf9bfd94d3aa8084c2111b1c700
Publikováno v:
Songklanakarin Journal of Science and Technology (SJST), Vol 42, Iss 3, Pp 596-601 (2020)
Hirschsprung disease (HSCR) is complex genetic disorder of the enteric nervous system (ENS) characterized by an absence of ganglion cells in various parts of the intestine. The disease has a strong genetic association with RET-protooncogene (RET) a
Externí odkaz:
https://doaj.org/article/0cd83a8dda1c49cfb5164cfa7f7c0a85
Autor:
Wison Laochareonsuk, Seksit Osatakul, Utcharee Intusoma, Wanwisa Maneechay, Surasak Sangkhathat
Publikováno v:
Journal of Pediatric Genetics.
Hyperornithinemia–hyperammonemia–homocitrullinuria (HHH) syndrome, an inborn error of metabolism, is an inherited syndrome caused by loss-of-function mutations in the SLC25A15, resulting in ornithine translocase1 (ORNT1) deficiency. Disrupted orn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6c2a45c46d8f62b7dab1a0547371b4c7
https://doi.org/10.1055/s-0041-1742247
https://doi.org/10.1055/s-0041-1742247
Publikováno v:
Urological Science. 32:40
17-Hydroxylase/17,20-lyase deficiency is a rare congenital disorder accounting for 1% of congenital adrenal hyperplasia. This disease is recessively expressed as autosomal inheritance through mutations in the CYP17A1 gene, leading to defective levels
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::150c794ad8a8efec54af8c5fa76bdd1a
https://doi.org/10.4103/uros.uros_43_20
https://doi.org/10.4103/uros.uros_43_20
Autor:
Wanwisa Maneechay, Anuwat Palanusont, Teeranut Boonpipattanapong, Jirakrit Saetang, Surasak Sangkhathat
Publikováno v:
Asian Pacific Journal of Cancer Prevention. 17:2119-2123
Background: There is an established link between obesity related metabolic derangement and colorectal cancer development. Recently, we developed a metabolic-colorectal cancer risk score. In this follow-up study, we studied its association with colore
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13cf7e028b74498200bf5c488690a3a1
https://doi.org/10.7314/apjcp.2016.17.4.2119
https://doi.org/10.7314/apjcp.2016.17.4.2119
Autor:
Surasak Sangkhathat, Kanita Kayasut, Wison Laochareonsuk, Piyawan Chiengkriwate, Wanwisa Maneechay
Biliary atresia (BA) is the most severe form of obstructive cholangiopathy occurring in infants. Definitive diagnosis of BA usually relies on operative findings together with supporting pathological patterns found in the extrahepatic bile duct. In in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d955ce02809a179f019c0f1aa2937c50
https://europepmc.org/articles/PMC5916803/
https://europepmc.org/articles/PMC5916803/
Autor:
Surasak Sangkhathat, Wanwisa Maneechay, Teeranut Boonpipattanapong, Samornmas Kanngern, Welawee Chaiyapan
Publikováno v:
Molecular and Clinical Oncology. 3:1401-1405
Colorectal cancer (CRC) is one of the leading causes of cancer-related mortality worldwide. Our recent study demonstrated that the expression of Wilms' tumor 1 gene (WT1) is associated with surgical outcome in CRC patients. The present study aimed to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0299d5b1dc4c4333cf76110c774f5826
https://doi.org/10.3892/mco.2015.647
https://doi.org/10.3892/mco.2015.647
Autor:
Puttisak Puttawibul, Surasak Sangkhathat, Sarayut Lucien Geater, Teeranut Boonpipattanapong, Samornmas Kanngurn, Wanwisa Maneechay
Publikováno v:
Asian Pacific journal of cancer prevention : APJCP. 16(8)
Background: This case-control study aimed to determine if there were any associations between the two single nucleotide polymorphisms (SNPs) in Gc, rs7041 (Asp416Glu) and rs4588 (Thr420Lys) and 3 common cancers (breast, lung and colorectal) in Thai p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31b752dfa5b1d1e2600bad44016efa46
https://pubmed.ncbi.nlm.nih.gov/25921141
https://pubmed.ncbi.nlm.nih.gov/25921141
Autor:
Welawee Chaiyapan, Podchanaporn Gridist, Wanwisa Maneechay, Surasak Sangkhathat, Samornmas Kanngurn
Wilms’ tumor 1 gene (WT1) is known to be a tumor suppressor gene in the subset of nephroblastomas that harbors WT1 mutations. However, its role in nephroblastomas without mutations remains unclear. This study aimed to evaluate the expression of WT1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76074827d814aff0f8d19e42c8986b85
https://europepmc.org/articles/PMC3436438/
https://europepmc.org/articles/PMC3436438/
Autor:
Walawee Chaiyapan, Kittima Pornsuksiri, Wanwisa Maneechay, Siripong Chewatanakornkul, Samornmas Kanngurn, Surasak Sangkhathat
Publikováno v:
World Journal of Gastrointestinal Oncology. 4:216
AIM: To review a single institutional experience in clinical management of gastrointestinal stromal tumors (GIST) and analyze for factors determining treatment outcome. METHODS: Clinicopathological data of patients with a diagnosis of GIST who were t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0178892db6abee19438332f7be4300d
https://doi.org/10.4251/wjgo.v4.i11.216
https://doi.org/10.4251/wjgo.v4.i11.216