Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Nattiya, Teawtrakul"'
Autor:
Siriyakorn Chansai, Supawadee Yamsri, Supan Fucharoen, Goonnapa Fucharoen, Nattiya Teawtrakul
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 14, Iss 1 (2022)
Introduction: Extramedullary hematopoiesis (EMH) is one of the main complications in patients with thalassemia in compensation for the underlying ineffective erythropoiesis. This study aimed to evaluate the association between ineffective erythropoie
Externí odkaz:
https://doaj.org/article/fea35046cb5146d4862ca39c25fe4b90
Autor:
Chinadol Wanitpongpun, Nattiya Teawtrakul, Theerin Lanamtieng, Kanchana Chansung, Chittima Sirijeerachai, Worakamol Amampai, Kittisak Sawanyawisuth
Publikováno v:
Leukemia Research Reports, Vol 17, Iss , Pp 100296- (2022)
Febrile neutropenia (FN) is considered an oncologic emergency in acute leukemia. There were 250 FN events in 124 hospitalized patients with hematologic malignancy. These data imply that two FN events may occur per patient, yet data on the prevalence,
Externí odkaz:
https://doaj.org/article/19097aa3f7b443309beef57f98534420
Autor:
Nang Noon Shean Aye, Pornsuda Maraming, Ratree Tavichakorntrakool, Attawut Chaibunruang, Patcharee Boonsiri, Sakda Daduang, Nattiya Teawtrakul, Prinya Prasongdee, Vittaya Amornkitbamrung, Jureerut Daduang
Publikováno v:
Applied Sciences, Vol 11, Iss 21, p 10315 (2021)
Glycated albumin (GA) has been previously introduced as a promising biomarker for glycemic monitoring in diabetes patients with thalassemia. In this study, a label-free graphene oxide (GO)-modified aptasensor was developed for the rapid detection of
Externí odkaz:
https://doaj.org/article/bfddcb40f8ed40b297ca5b211cea125e
Autor:
Nattiya Teawtrakul, Sukanya Chukanhom, Suranut Charoensri, Charoonsak Somboonporn, Chatlert Pongchaiyakul
Publikováno v:
Anemia, Vol 2020 (2020)
Introduction. Thalassemia bone disease is one of the disease-related complications in patients with thalassemia. Prevalence of fractures and the role of a trabecular bone score (TBS) as a predictive factor for fractures were evaluated in patients wit
Externí odkaz:
https://doaj.org/article/1a23cbfcffc94c5a99b44e42a84c3d9b
Autor:
Itthiphat Arunsurat, Wipa Reechaipichitkul, Apichart So-Ngern, Piti Ungareevittaya, Nipon Chaisuriya, Nattiya Teawtrakul, Pailin Ratanawatkul, Worawat Chumpangern
Publikováno v:
Respiratory Medicine Case Reports, Vol 29, Iss , Pp - (2020)
Multiple myeloma (MM) is a hematologic malignancy of plasma cell origin. Incidence of pleural effusion in multiple myeloma patients is approximately 6%. Myelomatous pleural effusions (MPE) are rare and occur in less than 1% of all MM cases. MPE is as
Externí odkaz:
https://doaj.org/article/91b95ef2f9dd473cb9ef21112d3ba1db
Autor:
Maxwell Chappell, Laura Breda, Danuta Jadwiga Jarocha, Michael Triebwasser, Tyler E Papp, Valentina Ghiaccio, Megan T Fedorky, Amaliris Guerra, Kandace Gollomp, Osheiza Y. Abdulmalik, Nattiya Teawtrakul, Stavros Glentis, Antonis Kattamis, Hamideh Parhiz, Stefano Rivella
Publikováno v:
Blood. 140:300-302
Autor:
Chingching, Foocharoen, Ajanee, Mahakkanukrauh, Pewpan, Maleewong, Wanchai, Maleewong, Amonrat, Jumnainsong, Patnarin, Pongkulkiat, Nattiya, Teawtrakul, Siraphop, Suwannaroj, Ratanavadee, Nanagara
Publikováno v:
The American Journal of the Medical Sciences. 363:519-525
Peripheral eosinophilia (eosinophilia) is observed among systemic sclerosis (SSc) patients. The association between eosinophilia and SSc in terms of pathogenesis remains uncertain. We aimed to determine the prevalence of the clinical, serological, an
Autor:
Phaosin Thongsaen, Pantipa Tonsawan, Chinadol Wanitpongpun, Theerin Lanamtieng, Pisa Phiphitaporn, Nattiya Teawtrakul
Publikováno v:
International Urology and Nephrology.
Autor:
Paramee Phanrahan, Supawadee Yamsri, Nattiya Teawtrakul, Goonnapa Fucharoen, Kanokwan Sanchaisuriya, Supan Fucharoen
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 11, Iss 1 (2019)
Background: The finding of many Thai Hb E-β0-thalassemia patients with non-transfusion dependent thalassemia (NTDT) phenotype without co-inheritance of α-thalassemia has prompted us to investigate the existence of other genetic modifying factors.
Externí odkaz:
https://doaj.org/article/cb81ad789b944d488bac3cc31326e738
Publikováno v:
PLoS ONE, Vol 14, Iss 3, p e0214148 (2019)
Disease-related complications and management are different among patients with thalassemia. This study was aimed to review the prevalence, clinical risk factors for the complications and the management in patients with thalassemia in Thailand. A mult
Externí odkaz:
https://doaj.org/article/ad711e793e8046cf9ea2bca3981433c0