Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Duangkamol Tangviriyapaiboon"'
Publikováno v:
IBRO Neuroscience Reports, Vol 15, Iss , Pp S126- (2023)
Externí odkaz:
https://doaj.org/article/f6a44165ad6b4fee90a9839582a0055a
Publikováno v:
Songklanakarin Journal of Science and Technology (SJST), Vol 43, Iss 3, Pp 816-823 (2021)
Fragile X (FRAXA) syndrome and fragile XE (FRAXE) syndrome are caused by the expansion of a trinucleotide repeat in the FMR1 and FMR2 genes, respectively. Currently, there are several methods available for fragile X syndrome screening in a large po
Externí odkaz:
https://doaj.org/article/6ff69f215829476e841a9ed1066d2b1c
Autor:
Chuphong Thongnak, Areerat Hnoonual, Duangkamol Tangviriyapaiboon, Suchaya Silvilairat, Apichaya Puangpetch, Ekawat Pasomsub, Wasun Chantratita, Pornprot Limprasert, Chonlaphat Sukasem
Publikováno v:
International Journal of Genomics, Vol 2018 (2018)
Autism spectrum disorder (ASD) has a strong genetic basis, although the genetics of autism is complex and it is unclear. Genetic testing such as microarray or sequencing was widely used to identify autism markers, but they are unsuccessful in several
Externí odkaz:
https://doaj.org/article/7c82c0961eea489080bc0dc09371a0fd
Autor:
Duangkamol Tangviriyapaiboon, Patrinee Traisathit, Vorasith Siripornpanich, Chidawan Suyakong, Hataichanok Apikomonkon, Nontiya Homkham, Salinee Thumronglaohapun, Pimwarat Srikummoon
Publikováno v:
Healthcare; Volume 10; Issue 10; Pages: 1969
Epilepsy often causes more severe behavioral problems in children with autism spectrum disorder (ASD) and is strongly associated with poor cognitive functioning. Interestingly, individuals with ASD without a history of epilepsy can have abnormal elec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::954be2cab774c7cad4dadc395b6d6e3f
https://pubmed.ncbi.nlm.nih.gov/36292416
https://pubmed.ncbi.nlm.nih.gov/36292416
Autor:
Duangkamol Tangviriyapaiboon, Suttipong Kawilapat, Samai Sirithongthaworn, Hataichanok Apikomonkon, Chidawan Suyakong, Pimwarat Srikummoon, Salinee Thumronglaohapun, Patrinee Traisathit
Publikováno v:
Healthcare; Volume 10; Issue 10; Pages: 1868
The Thai Diagnostic Autism Scale (TDAS) was developed to diagnose autism spectrum disorder (ASD) under the context and characteristics of the Thai population. Although the tool has an excellent agreement, the interpretation of diagnostic results need
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f530a92ef276162178dfb1e6f55c996f
https://pubmed.ncbi.nlm.nih.gov/36292315
https://pubmed.ncbi.nlm.nih.gov/36292315
Autor:
Pimwarat Srikummoon, Suttipong Kawilapat, Samai Sirithongthaworn, Hataichanok Apikomonkon, Patrinee Traisathit, Chidawan Suyakong, Duangkamol Tangviriyapaiboon
Publikováno v:
Autism research : official journal of the International Society for Autism Research. 15(2)
The Thai Diagnostic Autism Scale (TDAS) was developed for use as a diagnostic tool for the early diagnosis of Autism Spectrum Disorder (ASD) in Thai children aged 12-48 months old. TDAS consists of 23 items (13 and 17 items in the observational and i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0215b23eefdd46d4a607f5031d0db297
https://pubmed.ncbi.nlm.nih.gov/34697914
https://pubmed.ncbi.nlm.nih.gov/34697914
Autor:
Suchaya Silvilairat, Areerat Hnoonual, Duangkamol Tangviriyapaiboon, Chonlaphat Sukasem, Wasun Chantratita, Apichaya Puangpetch, Pornprot Limprasert, Ekawat Pasomsub, Chuphong Thongnak
Publikováno v:
International Journal of Genomics, Vol 2018 (2018)
Autism spectrum disorder (ASD) has a strong genetic basis, although the genetics of autism is complex and it is unclear. Genetic testing such as microarray or sequencing was widely used to identify autism markers, but they are unsuccessful in several
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19156e29015d7ab939f89834bea0c9a7
https://doaj.org/article/7c82c0961eea489080bc0dc09371a0fd
https://doaj.org/article/7c82c0961eea489080bc0dc09371a0fd
Autor:
Chuphong, Thongnak, Areerat, Hnoonual, Duangkamol, Tangviriyapaiboon, Suchaya, Silvilairat, Apichaya, Puangpetch, Ekawat, Pasomsub, Wasun, Chantratita, Pornprot, Limprasert, Chonlaphat, Sukasem
Publikováno v:
International Journal of Genomics
Autism spectrum disorder (ASD) has a strong genetic basis, although the genetics of autism is complex and it is unclear. Genetic testing such as microarray or sequencing was widely used to identify autism markers, but they are unsuccessful in several
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a6b7e34d74fd04166dc410d10e6398c5
https://pubmed.ncbi.nlm.nih.gov/29888248
https://pubmed.ncbi.nlm.nih.gov/29888248
Autor:
Ekawat Pasomsub, Pornprot Limprasert, Chonlaphat Sukasem, Apichaya Puangpetch, Wasun Chantratita, Chuphong Thongnak, Duangkamol Tangviriyapaiboon, Suchaya Silvilairat
Publikováno v:
Disease Markers
Disease Markers, Vol 2016 (2016)
Disease Markers, Vol 2016 (2016)
Background. Congenital heart block is characterized by blockage of electrical impulses from the atrioventricular node (AV node) to the ventricles. This blockage can be caused by ion channel impairment that is the result of genetic variation. This stu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1b8341ff087fc8f622b22c5a772b5ad
http://europepmc.org/articles/PMC5149683
http://europepmc.org/articles/PMC5149683
Journal of Mental Health of Thailand, 24, 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d13266a89e8d0a764e766db36d6b56eb
