Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Oradawan Plong-On"'
Autor:
Kanoot Jaruthamsophon, Pornsiri Sangmanee, Oradawan Plong‐on, Chariyawan Charalsawadi, Chonlaphat Sukasem, Areerat Hnoonual
Publikováno v:
Clinical and Translational Science, Vol 17, Iss 6, Pp n/a-n/a (2024)
Abstract Genetic screening for HLA‐B*15:02 before prescribing carbamazepine is standard practice to prevent severe cutaneous adverse reactions in Asian populations. These reactions are associated not only with this allele but also with closely rela
Externí odkaz:
https://doaj.org/article/550eaba2accc423587a46a44dae04519
Publikováno v:
Medicine
Supplemental Digital Content is available in the text
Autism spectrum disorder (ASD) is a form of pervasive developmental disorder manifested by impairment in social interactions and repetitive behaviors. Although genetic contribution is strongl
Autism spectrum disorder (ASD) is a form of pervasive developmental disorder manifested by impairment in social interactions and repetitive behaviors. Although genetic contribution is strongl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b396029a8386048a17602b3a6cba215d
https://doi.org/10.1097/md.0000000000021946
https://doi.org/10.1097/md.0000000000021946
Autor:
Anannit Visudtibhan, Fadell Hayeeduereh, Utcharee Intusoma, Sasipa Thammongkol, Apasri Lusawat, Punnee Vasiknanonte, Supachai Janjindamai, Pornprot Limprasert, Oradawan Plong-On, Thanya Sripo
Publikováno v:
European Journal of Paediatric Neurology. 15:432-438
Purposes To perform CDKL5 mutation screening in Thai children with cryptogenic infantile intractable epilepsy and to determine the clinical sensitivity of CDKL5 screening when different inclusion criteria were applied. Methods Children with cryptogen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::790519dd0165c32f6454b962b5269b8b
https://doi.org/10.1016/j.ejpn.2011.01.005
https://doi.org/10.1016/j.ejpn.2011.01.005
Autor:
Supaporn Yangngam, Juthamas Wirojanan, Tippawan Hansakunachai, Rawiwan Roongpraiwan, Thanya Sripo, Tasnawat Sombuntham, Pornprot Limprasert, Nichara Ruangdaraganon, Oradawan Plong-On
Aim: Neurexin 1 has two major protein isoforms using alternative promoters, coding for the alpha-neurexin 1 (α-NRXN1) and beta-neurexin 1 (β-NRXN1) genes. This study is to explore the possibility that variants of the NRXN1 gene predispose to intell
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c46930d818c71139b8fc5d793b72769
https://europepmc.org/articles/PMC4094023/
https://europepmc.org/articles/PMC4094023/
Autor:
Rawiwan Roongpraiwan, Tasnawat Sombuntham, Thanya Sripo, John B. Vincent, Nichara Ruangdaraganon, Anna Mikhailov, Oradawan Plong-On, Pornprot Limprasert, Alanna Fennell, Tippawan Hansakunachai
Publikováno v:
Psychiatric genetics. 24(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::372cd2e6f1aa978a1b63f875aca47d24
https://pubmed.ncbi.nlm.nih.gov/24362370
https://pubmed.ncbi.nlm.nih.gov/24362370