Zobrazeno 1 - 10
of 73
pro vyhledávání: '"Wanna Thongnoppakhun"'
Autor:
Chalermkiat Kansuttiviwat, Pongtawat Lertwilaiwittaya, Ekkapong Roothumnong, Panee Nakthong, Peerawat Dungort, Chutima Meesamarnpong, Warisara Tansa-Nga, Khontawan Pongsuktavorn, Supakit Wiboonthanasarn, Warunya Tititumjariya, Nannipa Phuphuripan, Chittapat Lertbussarakam, Jantanee Wattanarangsan, Jiraporn Sritun, Kittiporn Punuch, Jirayu Kammarabutr, Pornthira Mutirangura, Wanna Thongnoppakhun, Chanin Limwongse, Manop Pithukpakorn
Publikováno v:
npj Genomic Medicine, Vol 9, Iss 1, Pp 1-13 (2024)
Abstract Multi-gene panel testing has led to the detection of pathogenic/likely pathogenic (P/LP) variants in many cancer susceptibility genes in patients with breast-ovarian cancer spectrum. However, the clinical and genomic data of Asian population
Externí odkaz:
https://doaj.org/article/8a7eaab7c4b041d89ecec331f8a811b5
Autor:
Chalermkiat Kansuttiviwat, Pongtawat Lertwilaiwittaya, Ekkapong Roothumnong, Panee Nakthong, Peerawat Dungort, Chutima Meesamarnpong, Warisara Tansa-Nga, Khontawan Pongsuktavorn, Supakit Wiboonthanasarn, Warunya Tititumjariya, Nannipa Phuphuripan, Chittapat Lertbussarakam, Jantanee Wattanarangsan, Jiraporn Sritun, Kittiporn Punuch, Jirayu Kammarabutr, Wanna Thongnoppakhun, Chanin Limwongse, Manop Pithukpakorn
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 100951- (2024)
Externí odkaz:
https://doaj.org/article/937a03ddca544aa29cfdb1ab886ac0b0
Autor:
Bundarika Suwanawiboon, Wannaphorn Rotchanapanya, Komkrit Mahaprom, Wanna Thongnoppakhun, Yupaporn Lalerd, Chanin Limwongse, Nuttawut Sermsathanasawadi, Weerapat Owattanapanich
Publikováno v:
Hematology, Vol 27, Iss 1, Pp 95-104 (2022)
Objectives The fact that a lower warfarin maintenance dose is required by Asian populations is well-known. Currently, the American College of Chest Physicians recommends commencing warfarin at a dose between 5 and 10 mg for venous thromboembolism (VT
Externí odkaz:
https://doaj.org/article/fb1c69c2867f4951adf11ededf7c3531
Autor:
Pantaree Laosuebsakulthai, Surachai Likasitwattanakul, Theerapong Pho-iam, Wanna Thongnoppakhun, Mongkol Chanvanichtrakool
Publikováno v:
Journal of Health Science and Medical Research (JHSMR), Vol 40, Iss 4, Pp 419-424 (2022)
Objective: To examine the frequency of the proline-rich transmembrane protein-2 (PRRT2) gene mutation in Thai patients with paroxysmal kinesigenic dyskinesia (PKD). Material and Methods: A retrospective study of children aged 0-18 years with a diagno
Externí odkaz:
https://doaj.org/article/4a0b6f75c3a44e8ea222586e250d71ed
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:
Egyptian Journal of Forensic Sciences, Vol 9, Iss 1, Pp 1-9 (2019)
Abstract Background Sudden unexplained nocturnal death syndrome (SUNDS) is a genetic disorder that can cause sudden death in young and healthy adults during sleep at night. Cardiac arrhythmia has been proposed as the factor responsible for such death
Externí odkaz:
https://doaj.org/article/4211e608c8d24b8d8d1a3a872198b694
Autor:
Suvimol Niyomnaitham, Napa Parinyanitikul, Ekkapong Roothumnong, Worapoj Jinda, Norasate Samarnthai, Taywin Atikankul, Bhoom Suktitipat, Wanna Thongnoppakhun, Chanin Limwongse, Manop Pithukpakorn
Publikováno v:
PeerJ, Vol 7, p e6501 (2019)
Background Triple negative breast cancer (TNBC) is a breast cancer subtype characterized by absence of both hormonal receptors and human epithelial growth factor receptor 2 (HER2). TNBC accounts for 15–20% of breast cancer. TNBC is associated with
Externí odkaz:
https://doaj.org/article/31a4b574358745fba8ee20ccc033470b
Autor:
Benjaporn Panichareon, Thanawat Seedapan, Wanna Thongnoppakhun, Chanin Limwongse, Manop Pithukpakorn, Thawornchai Limjindaporn
Publikováno v:
Case Reports in Dermatology, Vol 7, Iss 2, Pp 212-219 (2015)
Dyskeratosis congenita (DKC) is a rare inherited disease that is characterized by abnormal skin pigmentation, nail dystrophy and mucosal leukoplakia. DKC is caused by an abnormality in a component of the telomerase and shelterin complexes. TINF2 enco
Externí odkaz:
https://doaj.org/article/33a79c121c9a4e238fa689e3819f89d2
Autor:
Bhoom Suktitipat, Sakda Sathirareuangchai, Ekkapong Roothumnong, Wanna Thongnoppakhun, Purin Wangkiratikant, Nutchavadee Vorasan, Rungroj Krittayaphong, Manop Pithukpakorn, Warangkna Boonyapisit
Publikováno v:
PLoS ONE, Vol 12, Iss 7, p e0180056 (2017)
Sudden unexpected death syndrome (SUDS) is an important cause of death in young healthy adults with a high incident rate in Southeast Asia; however, there are no molecular autopsy reports about these victims. We performed a combination of both a deta
Externí odkaz:
https://doaj.org/article/aacf9dd2c48248c59050975c2625fb54
Autor:
Manop Pithukpakorn, Ekkapong Roothumnong, Nasikarn Angkasekwinai, Bhoom Suktitipat, Anunchai Assawamakin, Voravich Luangwedchakarn, Pinklow Umrod, Wanna Thongnoppakhun, Suporn Foongladda, Yupin Suputtamongkol
Publikováno v:
PLoS ONE, Vol 10, Iss 5, p e0128481 (2015)
Recently a newly identified clinical syndrome of disseminated non-tuberculous mycobacterial diseases (with or without other opportunistic infections in adult patients who were previously healthy, has been recognized in association with an acquired au
Externí odkaz:
https://doaj.org/article/6d95410365e34f199b8f8e36a431dc61