Zobrazeno 1 - 10
of 160
pro vyhledávání: '"Komvilaisak P"'
Autor:
Pimpitcha Youthong, Samart Pakakasama, Patcharee Komvilaisak, Piya Rujkijyanont, Chane Choed-Amphai, Kamon Phuakpet, Chatphatai Moonla, Chantana Polprasert, Darintr Sosothikul
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-8 (2024)
Abstract Background Subcutaneous panniculitis-like T-cell lymphoma (SPTCL) is a rare subtype of non-Hodgkin lymphoma associated with hemophagocytic lymphohistiocytosis (HLH)/HLH-like systemic illnesses and germline HAVCR2 mutations. Although previous
Externí odkaz:
https://doaj.org/article/890cdac32e8c42a499c86081d2da6cc7
Autor:
Chanaporn Pinsuwan, Chalongpon Santong, Su-on Chainansamit, Patcharee Komvilaisak, Prapassara Sirikarn, Surachai Phimha, Kunanya Suwannaying
Publikováno v:
BMC Public Health, Vol 24, Iss 1, Pp 1-9 (2024)
Abstract Background In Thailand, the national health care system and nationwide standard treatment protocols have evolved over time, potentially influencing the trends in the incidence and survival rates of childhood cancers. However, further investi
Externí odkaz:
https://doaj.org/article/ab49895818ea4ea0b0eaae376c436554
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:
Patcharee Komvilaisak, Najwa Yudhasompop, Kittima Kanchanakamhaeng, Suradej Hongeng, Samart Pakakasama, Usanarat Anurathapan, Pongpak Pongphitcha, Duantida Songdej, Werasak Sasanakul, Nongnuch Sirachainan
Publikováno v:
BMC Pediatrics, Vol 23, Iss 1, Pp 1-7 (2023)
Abstract Background Congenital neutropenia is a rare disease. Recurrent infections since young age are the presentation. The most common mutation causing severe congenital neutropenia (SCN) and cyclic neutropenia (CyN) is the ELANE gene. The objectiv
Externí odkaz:
https://doaj.org/article/55db97815d6840198156412f03f6e48d
Akademický článek
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Akademický článek
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Autor:
Ampaiwan Chuansumrit, Surapan Parapakpenjune, Rungrote Natesirinilkul, Patcharee Komvilaisak, Werasak Sasanakul, Nongnuch Sirachainan, Anchalee Aramthienthamrong, Chorthip Wattanasutthipong, Kittima Kanchanakumhan, Kunrada Inthawong, Montana Chantaraniyom, Naonpan Pongpaothai, Nattaporntira Phalakornkul, Nisakorn Khumchan, Pacharapan Surapolchai, Panjarat Sowittayasakul, Somporn Wangruangsathit
Publikováno v:
Pediatric Hematology Oncology Journal, Vol 7, Iss 4, Pp 130-135 (2022)
Objective: The phenotypic and genotypic analysis of patients with congenital factor VII deficiency were retrospectively conducted. Methods: The study included 26 patients defined as severe (n = 25) and moderate (n = 1) degree by FVII 3% did not exhib
Externí odkaz:
https://doaj.org/article/cdadc6bb0b204cb8982be3f95df55ccb
Akademický článek
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Autor:
Chantana Polprasert, Chatphatai Moonla, Patcharee Komvilaisak, Thanawat Rattanathammethee, Sunisa Kongkiatkamon, Kitsada Wudhikarn, Sirorat Kobbuaklee, Pitchayut Boonyabaramee, Samart Pakakasama, Piya Rujkijyanont, Chane Choed-Amphai, Kamon Phuakpet, Saranya Pongudom, Udomsak Bunworasate, Darintr Sosothikul, Ponlapat Rojnuckarin
Publikováno v:
HemaSphere, Vol 7, p e18386d6 (2023)
Externí odkaz:
https://doaj.org/article/7b0070768955468caf0dff3eaf66a95d
Autor:
Kunanya Suwannaying, Piti Techavichit, Patcharee Komvilaisak, Napat Laoaroon, Nattee Narkbunnam, Kleebsabai Sanpakit, Kanhatai Chiengthong, Thirachit Chotsampancharoen, Lalita Sathitsamitphong, Chalongpon Santong, Panya Seksarn, Suradej Hongeng, Surapon Wiangnon
Publikováno v:
Clinical and Experimental Pediatrics, Vol 65, Iss 9, Pp 453-458 (2022)
Background In 2013, the Thai Pediatric Oncology Group (ThaiPOG) introduced a national protocol in which high-dose chemotherapy plus stem cell rescue is performed without immunotherapy. Methods This study aimed to elucidate the outcomes of high-risk n
Externí odkaz:
https://doaj.org/article/8374e7f7343a47a5b4f0cf8b997c9172