Zobrazeno 1 - 10
of 52
pro vyhledávání: '"Tunteeratum, A."'
Autor:
T. Sukarayothin, M. Phattaravittakon, N. Poprom, R. Suvikapakornkul, P. Chirappapha, Y. Wasuthit, M. Leesombatpaiboon, A. Tunteeratum, S. Charoenratana, P. Lertsithichai
Publikováno v:
Breast, Vol 68, Iss , Pp S75-S76 (2023)
Externí odkaz:
https://doaj.org/article/6501c3379a3d4b9a9adbcc7b37393371
Autor:
Songporn Oranratnachai, Watchalawalee Yamkaew, Atchara Tunteeratum, Thongchai Sukarayothin, Nareenart Iemwimangsa, Ravat Panvichien
Publikováno v:
Cancer Reports, Vol 6, Iss 1, Pp n/a-n/a (2023)
Abstract Introduction Germline mutations in BRCA1/2 are the most common cause of hereditary breast and ovarian cancer (HBOC) syndrome. Few studies published during the past decade reported the prevalence of germline BRCA mutations in Asian patients w
Externí odkaz:
https://doaj.org/article/fb78aec7f7824ab1ad4f901bb1403c78
Autor:
Weenita Pipitprapat, Oraluck Pattanaprateep, Nareenart Iemwimangsa, Insee Sensorn, Bhakbhoom Panthan, Poramate Jiaranai, Wasun Chantratita, Kinnaree Sorapipatcharoen, Preamrudee Poomthavorn, Pat Mahachoklertwattana, Thanyachai Sura, Atchara Tunteeratum, Kanoknan Srichan, Chutintorn Sriphrapradang
Publikováno v:
Annals of Medicine, Vol 53, Iss 1, Pp 1244-1256 (2021)
AbstractIntroduction Pheochromocytomas and paragangliomas (PPGLs) are highly heritable tumours, with up to 40% of cases carrying germline variants. Current guidelines recommend genetic testing for all patients with PPGLs. Next-generation sequencing (
Externí odkaz:
https://doaj.org/article/c86466637b7a4d32898cf10bf9c6359f
Publikováno v:
Clinical Medicine Insights: Endocrinology and Diabetes, Vol 10 (2017)
Mutations in the VHL, RET, SDHB , and SDHD genes are responsible for von Hippel-Lindau (VHL) disease, multiple endocrine neoplasia type 2 (MEN2), and familial paraganglioma, respectively. However, genotype-phenotype correlation data are lacking in So
Externí odkaz:
https://doaj.org/article/fae773d96b25482396b66df8ba615af7
Autor:
Oranratnachai, Songporn, Yamkaew, Watchalawalee, Tunteeratum, Atchara, Sukarayothin, Thongchai, Iemwimangsa, Nareenart, Panvichien, Ravat
Publikováno v:
Cancer Reports; Jan2023, Vol. 6 Issue 1, p1-11, 11p
Autor:
Atchara Tunteeratum, Kinnaree Sorapipatcharoen, Weenita Pipitprapat, Kanoknan Srichan, Insee Sensorn, Nareenart Iemwimangsa, Wasun Chantratita, Thanyachai Sura, Pat Mahachoklertwattana, Preamrudee Poomthavorn, Chutintorn Sriphrapradang, Bhakbhoom Panthan, Oraluck Pattanaprateep, Poramate Jiaranai
Publikováno v:
Annals of Medicine
article-version (VoR) Version of Record
article-version (VoR) Version of Record
Introduction Pheochromocytomas and paragangliomas (PPGLs) are highly heritable tumours, with up to 40% of cases carrying germline variants. Current guidelines recommend genetic testing for all patients with PPGLs. Next-generation sequencing (NGS) ena
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::306f4f6eba693956b715bb176efafd3a
https://pubmed.ncbi.nlm.nih.gov/34309460
https://pubmed.ncbi.nlm.nih.gov/34309460
Autor:
Donniphat Dejsuphong, Piyamitr Sritara, Atchara Tunteeratum, Pollawat Khemthong, Aruchalean Taweewongsounton, Thanyachai Sura, Sermsiri Chitphuk, Wasana Stitchantrakul
Publikováno v:
Neurological Sciences. 40:1729-1732
Spinal muscular atrophy (SMA) is one of the leading causes of death in infants and young children from heritable diseases. Patients diagnosed with SMA develop symmetrical progressive muscle weakness and atrophy from degeneration of alpha motor neuron
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::880486edd0dfc36955577f291cde75d2
https://doi.org/10.1007/s10072-019-03885-5
https://doi.org/10.1007/s10072-019-03885-5
Autor:
Watchalawalee Yamkaew, Songporn Oranratnachai, Nareenart Iemwimangsa, Ravat Panvichian, Atchara Tunteeratum, Thongchai Sukarayothin
Germline mutations in BRCA1/2 are the most common cause of hereditary breast and ovarian cancer (HBOC) syndrome. A few studies have reported the prevalence of germline BRCA mutations in Asian patients with breast cancer. Here, we aimed to explore the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6799988f83fe30cd803bc42e3fa649ad
https://doi.org/10.21203/rs.3.rs-591403/v1
https://doi.org/10.21203/rs.3.rs-591403/v1
Akademický článek
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Autor:
Sukarayothin, T., Phattaravittakon, M., Poprom, N., Suvikapakornkul, R., Chirappapha, P., Wasuthit, Y., Leesombatpaiboon, M., Tunteeratum, A., Charoenratana, S., Lertsithichai, P.
Publikováno v:
In The Breast April 2023 68 Supplement:S75-S76