Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Supavadee Jantasuwan"'
Autor:
Suphalak Chokvithaya, Natarin Caengprasath, Aayalida Buasong, Supavadee Jantasuwan, Kanokwan Santawong, Netchanok Leela-adisorn, Siraprapa Tongkobpetch, Chupong Ittiwut, Vitchayaporn Emarach Saengow, Wuttichart Kamolvisit, Ponghatai Boonsimma, Saknan Bongsebandhu-phubhakdi, Vorasuk Shotelersuk
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-11 (2023)
Abstract Mutations in KCNQ2 encoding for voltage-gated K channel subunits underlying the neuronal M-current have been associated with infantile-onset epileptic disorders. The clinical spectrum ranges from self-limited neonatal seizures to epileptic e
Externí odkaz:
https://doaj.org/article/34faeeb0f7da4b4c958907783b71d468
Autor:
Suphalak Chokvithaya, Natarin Caengprasath, Aayalida Buasong, Supavadee Jantasuwan, Kanokwan Santawong, Netchanok Leela-adisorn, Siraprapa Tongkobpetch, Chupong Ittiwut, Vitchayaporn Saengow, Wuttichart Kamolvisit, Ponghatai Boonsimma, Saknan Bongsebandhu-Phubhakdi, Vorasuk Shotelersuk
Mutations in KCNQ2 encoding for voltage-gated K channel subunits underlying the neuronal M-current, have been associated with infantile-onset epileptic disorders. The clinical spectrum ranges from self-limited neonatal seizures to epileptic encephalo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::68f7b61e5694874ad03eb603ccc80588
https://doi.org/10.21203/rs.3.rs-1966853/v1
https://doi.org/10.21203/rs.3.rs-1966853/v1
Autor:
Karn Wejaphikul, Khomsak Srilanchakon, Wuttichart Kamolvisit, Supavadee Jantasuwan, Kanokwan Santawong, Siraprapa Tongkobpetch, Thanakorn Theerapanon, Alisara Damrongmanee, Nattaphorn Hongsawong, Nuthapong Ukarapol, Prapai Dejkhamron, Vichit Supornsilchai, Thantrira Porntaveetus, Vorasuk Shotelersuk
Publikováno v:
The Journal of clinical endocrinology and metabolism.
Context Biallelic pathogenic variants in the NEUROG3 gene cause malabsorptive diarrhea, insulin-dependent diabetes mellitus (IDDM), and rarely hypogonadotropic hypogonadism. With only 17 reported cases, the clinical and mutational spectra of this dis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a573a0bfe82b65910df3960b693bbc3c
https://pubmed.ncbi.nlm.nih.gov/36149814
https://pubmed.ncbi.nlm.nih.gov/36149814