Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Sorawit Viravan"'
Publikováno v:
Journal of Health Science and Medical Research (JHSMR), Vol 40, Iss 3, Pp 301-308 (2022)
Objective: To identify the common causal gene mutations in Thai children with the Dravet (DS) phenotype, using single gene analysis. Material and Methods: The study was carried out on 20 DS patients at Siriraj Hospital, Bangkok, Thailand. Sanger sequ
Externí odkaz:
https://doaj.org/article/f801afb29cd746a5a283456938fd1f6b
Publikováno v:
Pediatric Reports, Vol 10, Iss 2 (2018)
Patients with Takayasu arteritis (TA) generally present with non-specific symptoms that, if unrecognized and untreated, may develop vessel stenosis and/or aneurysm. There is limited data regarding chronic monoarthritis as the initial presentation in
Externí odkaz:
https://doaj.org/article/0805068459d9467f8f730da52fa66cca
Autor:
Piradee Suwanpakdee, Burachat Saksritavee, Napakjira Likasitthananon, Thitiwan Simasathien, Tayard Deesudchit, Chaiyos Khongkhatithum, Sorawit Viravan, Charcrin Nabangchang
Publikováno v:
Seizure. 100:103-108
To evaluate the effectiveness and tolerability of perampanel (PER) in real-world settings in patients between 1 month and 18 years of age with drug resistant epilepsy (DRE) waiting for epilepsy surgery.In this multicenter study, patients between 1 mo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2aed3d9abd41710a1041ba3849b2e83
https://doi.org/10.1016/j.seizure.2022.06.015
https://doi.org/10.1016/j.seizure.2022.06.015
Publikováno v:
Journal of Health Science and Medical Research.
Objective: To identify the common causal gene mutations in Thai children with the Dravet (DS) phenotype, using single gene analysis.Material and Methods: The study was carried out on 20 DS patients at Siriraj Hospital, Bangkok, Thailand. Sanger seque
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cec781e460e3b05150299d21684372d4
https://doi.org/10.31584/jhsmr.2021838
https://doi.org/10.31584/jhsmr.2021838
Publikováno v:
Brain Pathol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::21ac3aec8d5c80559e0e7722850d06f0
https://pubmed.ncbi.nlm.nih.gov/26276028
https://pubmed.ncbi.nlm.nih.gov/26276028
Publikováno v:
Brain Pathology. 25:651-652
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::008a3bd13d3c4cd91c53bd89c6445d47
https://doi.org/10.1111/bpa.12284
https://doi.org/10.1111/bpa.12284
Autor:
Sorawit, Viravan, Cristina, Go, Ayako, Ochi, Tomoyuki, Akiyama, O, Carter Snead, Hiroshi, Otsubo
Publikováno v:
Epilepsia. 52(7)
Jeavons syndrome (JS) is one of the underreported epileptic syndromes characterized by eyelid myoclonia (EM), eye closure-induced seizures/electroencephalography (EEG) paroxysms, and photosensitivity. JS has been proposed as idiopathic generalized ep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4ba8fee1987f26f9b6ecf0ec28dec3c7
https://pubmed.ncbi.nlm.nih.gov/21729035
https://pubmed.ncbi.nlm.nih.gov/21729035