Zobrazeno 1 - 10
of 803
pro vyhledávání: '"P, Charoenkwan"'
Autor:
Natnipa Parapob, Suree Lekawanvijit, Theera Tongsong, Kittipat Charoenkwan, Charuwan Tantipalakorn
Publikováno v:
Obstetrics & Gynecology Science, Vol 67, Iss 6, Pp 557-564 (2024)
Objective The primary objective of this study was to compare the detection rate of high-risk human papillomavirus (HPV) infection between self-sampling to collect vaginal specimens and clinician sampling to collect cervical specimens, as well as the
Externí odkaz:
https://doaj.org/article/65ae6b4d0b854986ab1d4313772cf809
Autor:
Nalini Schaduangrat, Phisit Khemawoot, Apisada Jiso, Phasit Charoenkwan, Watshara Shoombuatong
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-19 (2024)
Abstract Migraine is considered one of the debilitating primary headache conditions with an estimated worldwide occurrence of approximately 14–15%, contributing highly to factors responsible for global disability. Calcitonin gene-related peptide (C
Externí odkaz:
https://doaj.org/article/d47c0c84d1c54b899fafea42fbcfb6eb
Autor:
Piyatida Natsrita, Phasit Charoenkwan, Watshara Shoombuatong, Panupong Mahalapbutr, Kiatichai Faksri, Sorujsiri Chareonsudjai, Thanyada Rungrotmongkol, Chonlatip Pipattanaboon
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-14 (2024)
Abstract Several computational methods have been developed to identify neutralizing antibodies (NAbs) covering four dengue virus serotypes (DENV-1 to DENV-4); however, limitations of the dataset and the resulting performance remain. Here, we develope
Externí odkaz:
https://doaj.org/article/ec1523c3a247476889938b9865ef254a
Autor:
Pannarai Somboonchai, Pimlak Charoenkwan, Sirivipa Piyamongkol, Worashorn Lattiwongsakorn, Tawiwan Pantasri, Wirawit Piyamongkol
Publikováno v:
BMC Genomics, Vol 25, Iss 1, Pp 1-10 (2024)
Abstract Hb H disease is the most severe form of α-thalassemia compatible with post-natal life. Compound heterozygous α0-thalassemia− SEA deletion/α+-thalassemia− 3.7kb deletion is the commonest cause of Hb H disease in Thailand. Preimplantati
Externí odkaz:
https://doaj.org/article/7c62aea24d224adba5f2a8c596231028
Publikováno v:
Heliyon, Vol 10, Iss 20, Pp e39103- (2024)
Background: The study aims to establish prediction model derived from red blood cell indices to improve the accuracy of α0-thalassemia trait screening in non-anemic pregnant women. Method: A diagnostic study as secondary analysis on the prospective
Externí odkaz:
https://doaj.org/article/ffe87b2aae5d4110aae3e6bb58e0778b
Autor:
Varit Jan-ngam, Siriraj Boontha, Alisa Tubsuwan, Somsakul Pop Wongpalee, Kanda Fanhchaksai, Adisak Tantiworawit, Pimlak Charoenkwan, Pinyaphat Khamphikham
Publikováno v:
Heliyon, Vol 10, Iss 18, Pp e38020- (2024)
Reactivation of fetal hemoglobin (HbF, α2γ2) potentially alleviates clinical presentation in β-thalassemia. Prolyl hydroxylase domain enzymes (PHDs) play roles in the canonical oxygen-sensing pathway and maintain the stability of cellular hypoxia-
Externí odkaz:
https://doaj.org/article/e639dce5a1d3423e9be7472e82a74b31
Autor:
Pimlak Charoenkwan, Patcharee Komvilaisak, Kaewjai Thepsuthummarat, Panya Seksarn, Kitti Torcharus
Publikováno v:
Thalassemia Reports, Vol 14, Iss 1, Pp 10-17 (2024)
Thalassemia is a hereditary hemolytic anemia that is prevalent in Southeast Asia. The primary treatment for severe thalassemia involves red cell transfusion, iron chelation, and the treatment of long-term complications, leading to frequent hospital v
Externí odkaz:
https://doaj.org/article/685d06c1161b4fa2a17a816cd170bf25
Autor:
Adisak Tantiworawit, Thansita Kamolsripat, Pokpong Piriyakhuntorn, Thanawat Rattanathammethee, Sasinee Hantrakool, Chatree Chai-Adisaksopha, Ekarat Rattarittamrong, Lalita Norasetthada, Kanda Fanhchaksai, Pimlak Charoenkwan
Publikováno v:
Annals of Medicine, Vol 56, Iss 1 (2024)
AbstractBackground Thalassemia is the most prevalent hereditary anaemia worldwide. Severe forms of thalassemia can lead to reduced life expectancy due to disease-related complications.Objectives To investigate the survival of thalassemia patients acr
Externí odkaz:
https://doaj.org/article/166113d9379f45c0bb5171dc6e65f711
Autor:
Natnicha Ananvutisombat, Adisak Tantiworawit, Teerachat Punnachet, Nonthakorn Hantrakun, Pokpong Piriyakhuntorn, Thanawat Rattanathammethee, Sasinee Hantrakool, Chatree Chai-Adisaksopha, Ekarat Rattarittamrong, Lalita Norasetthada, Kanda Fanhchaksai, Pimlak Charoenkwan
Publikováno v:
Frontiers in Endocrinology, Vol 15 (2024)
BackgroundA common complication of thalassemia is secondary osteoporosis. This study aimed to assess the prevalence and factors associated with low BMD in thalassemic patients.MethodThis is a cross-sectional study. Eligible patients were males aged w
Externí odkaz:
https://doaj.org/article/56f9d143c4c8451db702d02d152d1ee9
Autor:
Kittipat Charoenkwan, Nattayaporn Apaijai, Sirawit Sriwichaiin, Nipon Chattipakorn, Siriporn C. Chattipakorn
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-9 (2024)
Abstract Metabolic alterations play an essential role in ovarian carcinogenesis. The flexibility of mitochondrial functions facilitates cellular adaptation to the tough environment associated with carcinogenesis. An understanding of the differences i
Externí odkaz:
https://doaj.org/article/65ad9de24a7d44ea8ecd5d8bf552125b