Zobrazeno 1 - 10
of 39
pro vyhledávání: '"Lertwilaiwittaya P"'
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:
Min Gao, Yunjia Chen, Pongtawat Lertwilaiwittaya, Anna Hurst, Ali Al-Beshri, Andrew Carroll, Fady Mikhail
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101640- (2024)
Externí odkaz:
https://doaj.org/article/2520512b6e094ae4978e0ffaa31cad73
Autor:
Pongtawat Lertwilaiwittaya, Narisa Tantai, Satanun Maneeon, Sophittha Kongbunrak, Nongyao Nonpanya, Anna C. E. Hurst, Varalak Srinonprasert, Manop Pithukpakorn
Publikováno v:
Frontiers in Public Health, Vol 11 (2023)
BackgroundScreening for germline pathogenic BRCA1 or BRCA2 variants (gBRCA) in high-risk breast cancer patients is known to be cost-effective in high-income countries. Nationwide adoption of genetics testing in high-risk breast cancer population rema
Externí odkaz:
https://doaj.org/article/9c42fe475ab340979c9f9ea2b5f9d63c
Autor:
Pongtawat Lertwilaiwittaya, Manop Pithukpakorn, Varalak Srinonprasert, Narisa Tantai, Satanun Maneeon, Ryan Kraemer, Anna Hurst
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100405- (2023)
Externí odkaz:
https://doaj.org/article/8e02b434cee3404db2ec2881ed835fca
Autor:
Pornpatr A. Dharmasaroja, Jintana Assanasen, Sunsanee Pongpakdee, Kankamol Jaisin, Praween Lolekha, Muthita Phanasathit, Laksanun Cheewakriengkrai, Chanisa Chotipanich, Pirada Witoonpanich, Sutisa Pitiyarn, Pongtawat Lertwilaiwittaya, Charungthai Dejthevaporn, Chanin Limwongse, Kammant Phanthumchinda
Publikováno v:
Dementia and Geriatric Cognitive Disorders Extra, Vol 11, Iss 1, Pp 64-70 (2021)
Introduction: Molecular imaging has been developed and validated in Thai patients, comprising a portion of patients in the dementia registry. This should provide a more accurate diagnosis of the etiology of dementia, which was the focus of this study
Externí odkaz:
https://doaj.org/article/c4754b96d88e4afa8d86b6e95df01fc6
Akademický článek
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Autor:
Pongtawat Lertwilaiwittaya, Bhoom Suktitipat, Phongphak Khongthon, Warut Pongsapich, Chanin Limwongse, Manop Pithukpakorn
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 7, Pp n/a-n/a (2021)
Abstract Background Osteopetrosis is a rare form of skeletal dysplasia characterized by increased bone density that leads to bone marrow failure, compressive neuropathy, and skeletal dysmorphism. Molecular diagnosis is essential as it guides treatmen
Externí odkaz:
https://doaj.org/article/fac9f534a4f34dcfa11d82ceb8724321
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Carlos Alva-Diaz, Christoper A. Alarcon-Ruiz, Kevin Pacheco-Barrios, Nicanor Mori, Josmel Pacheco-Mendoza, Bryan J. Traynor, Andrea Rivera-Valdivia, Pongtawat Lertwilaiwittaya, Thomas D. Bird, Mario Cornejo-Olivas
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
Introduction: Patients with Huntington-Like disorders (HLD) comprise a variety of allelic disorders sharing a Huntington phenotype. The hexanucleotide repeat expansion of the C9orf72 gene could explain part of the HLD etiology. We aimed to conduct a
Externí odkaz:
https://doaj.org/article/ab9ce89add9f4206b2a0a4c6e8dce082