Zobrazeno 1 - 10
of 51
pro vyhledávání: '"Meng Ju Li"'
Autor:
Wen-Li Lu, Yin-Hsiu Chien, Fuu-Jen Tsai, Wuh-Liang Hwu, Yen-Yin Chou, Shao-Yin Chu, Meng-Ju Li, An-Ju Lee, Chao-Chuan Liao, Chung-Hsing Wang, Ni-Chung Lee
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-11 (2023)
Abstract Background Gaucher disease (GD) is a lysosomal storage disorder characterized by deficient glucocerebrosidase activity that results from biallelic mutations in the GBA1 gene. Its phenotypic variability allows GD to be classified into 3 subty
Externí odkaz:
https://doaj.org/article/5f203ea9af2e4503addb3c547dbeafed
Publikováno v:
Journal of the Formosan Medical Association, Vol 119, Iss 1, Pp 69-74 (2020)
Background: Nationwide newborn screening for glucose-6-phosphate dehydrogenase (G6PD) deficiency has been implemented in Taiwan since 1987 and the G6PD enzyme activity levels were applied for diagnosis confirmation. As the reference value of G6PD enz
Externí odkaz:
https://doaj.org/article/3e16e23c051849819c37fac6da0a936b
Autor:
Chih-Hsiang Yu, Gang Wu, Chia-Ching Chang, Shiann-Tarng Jou, Meng-Yao Lu, Kai-Hsin Lin, Shu-Huey Chen, Kang-Hsi Wu, Fang-Liang Huang, Chao-Neng Cheng, Hsiu-Hao Chang, Dale Hedges, Jinn-Li Wang, Hsiu-Ju Yen, Meng-Ju Li, Shu-Wei Chou, Chen-Ting Hung, Ze-Shiang Lin, Chien-Yu Lin, Hsuan-Yu Chen, Yu-Ling Ni, Yin-Chen Hsu, Dong-Tsamn Lin, Shu-Wha Lin, Jun J. Yang, Ching-Hon Pui, Sung-Liang Yu, Yung-Li Yang
Publikováno v:
The Journal of Molecular Diagnostics. 24:1195-1206
Identification of specific leukemia subtypes is a key to successful risk-directed therapy in childhood acute lymphoblastic leukemia (ALL). Although RNA sequencing (RNA-seq) is the best approach to identify virtually all specific leukemia subtypes, th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da3d1991b23f2bf80357287571b6c65b
https://doi.org/10.1016/j.jmoldx.2022.08.001
https://doi.org/10.1016/j.jmoldx.2022.08.001
Publikováno v:
Journal of the Formosan Medical Association, Vol 119, Iss 2, Pp 660-661 (2020)
Externí odkaz:
https://doaj.org/article/e45c1599a3de4c679215796285166520
Autor:
Meng-Ju Li, Yung-Li Yang, Ni-Chung Lee, Shiann-Tarng Jou, Meng-Yao Lu, Hsiu-Hao Chang, Kai-Hsin Lin, Ching-Tien Peng, Dong-Tsamn Lin
Publikováno v:
Journal of the Formosan Medical Association, Vol 115, Iss 9, Pp 801-806 (2016)
Mutations in the tet oncogene family member 2 gene (TET2) are frequently found in adult patients with acute myeloid leukemia (AML). Reports of TET2 mutations in children are limited. We assessed the prevalence of TET2 mutations in Taiwanese children
Externí odkaz:
https://doaj.org/article/43ad8c99feba49468da7bd5b10508831
Autor:
Meng-Ju Li, Ni-Chung Lee, Yung-Li Yang, Hsiu-Ju Yen, Hsiu-Hao Chang, Yin-Hsiu Chien, Meng-Yao Lu, Shiann-Tarng Jou, Kai-Hsin Lin, Wuh-Liang Hwu, Dong-Tsamn Lin
Publikováno v:
Journal of the Formosan Medical Association, Vol 115, Iss 2, Pp 94-99 (2016)
Although Down syndrome (DS) patients have a higher risk of developing transient myeloproliferative disorder (TMD) and acute leukemia, very little data is available on long-term outcome in Taiwanese patients. The current study was designed to determin
Externí odkaz:
https://doaj.org/article/4a700b093f7648f8b86591004d9c9343
Autor:
Boon Fatt Tan, Chun-Min Fu, Chi-Nien Chen, Po-Jung Kung, Ling-Chun Liao, Meng-Ju Li, Po-Yu Su, An-Kuo Chou
Publikováno v:
Journal of Infection and Chemotherapy. 28:103-107
Imatinib is a crucial therapeutic strategy against chronic myeloid leukemia. Though superficial edema is a common adverse effect of imatinib, massive fluid retention is rarely reported. Here, we report the case of an adolescent who had tolerated imat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae76fcdcb06654f1d9789b32ee7ac99c
https://doi.org/10.1016/j.jiac.2021.10.002
https://doi.org/10.1016/j.jiac.2021.10.002
Autor:
Meng-Ju Li, Chih-Hsiang Yu, Shu-Wei Chou, Ying-Hui Su, Kuang-Wen Liao, Hsiu-Hao Chang, Yung-Li Yang
Publikováno v:
JCO Precision Oncology.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c33039b9fb72125c79a3274c40345fa3
https://doi.org/10.1200/po.22.00236
https://doi.org/10.1200/po.22.00236
Autor:
Wen-Li Lu, Yin-Hsiu Chien, Fuu-Jen Tsai, Wuh-Liang Hwu, Yen-Yin Chou, Shao-Yin Chu, Meng-Ju Li, An-Ju Lee, Chao-Chuan Liao, Chung-Hsing Wang, Ni-Chung Lee
Background Gaucher disease (GD) is a lysosomal storage disorder characterized by deficient glucocerebrosidase activity that results from biallelic mutations in the GBA gene. Its phenotypic variability allows GD to be classified into 3 subtypes based
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7c12d0c2f1ba405095d50d21b03fa264
https://doi.org/10.21203/rs.3.rs-1799385/v1
https://doi.org/10.21203/rs.3.rs-1799385/v1
Autor:
Meng-Ju Li, Po-Ren Hsueh, Chun-Yi Lu, Hung-Chieh Chou, Ping-Ing Lee, Luan-Yin Chang, Li-Min Huang
Publikováno v:
Journal of the Formosan Medical Association, Vol 111, Iss 1, Pp 46-50 (2012)
Systemic fungal infections have high morbidity and mortality rates in neonates, especially neonates with an extremely low birth weight (ELBW). Here, we describe a 21-day-old ELBW female infant with an amphotericin B-unresponsive congenital Candida al
Externí odkaz:
https://doaj.org/article/0a4315111ede4f55b3179e8b93dc06ff