Výsledky vyhledávání - "A. Tunteeratum"

Akademický článek

Genotype-Phenotype Correlation in Patients With Germline Mutations of VHL, RET, SDHB, and SDHD Genes: Thai Experience

Autor: Chutintorn Sriphrapradang, Kitjapong Choopun, Atchara Tunteeratum, Thanyachai Sura

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

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Akademický článek

Characteristics of breast cancer patients tested for germline BRCA1/2 mutations by next‐generation sequencing in Ramathibodi Hospital, Mahidol University.

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

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Cost-minimization analysis of sequential genetic testing versus targeted next-generation sequencing gene panels in patients with pheochromocytoma and paraganglioma

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

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

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Carrier frequency of spinal muscular atrophy in Thailand

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

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Characteristics of breast cancer patients tested for germline BRCA1/2 mutations by next-generation sequencing in Ramathibodi Hospital, Mahidol University

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