Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Chien-Hong Lee"'
Autor:
Hsiu-Huei Peng, Chien-Hong Lee, Sheng-Yuan Su, Kuan-Ju Chen, Yen-Chang Lee, Shu-Han You, Wen-Fang Lee, Po-Jen Cheng
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 58, Iss 5, Pp 662-666 (2019)
Objective: Prenatal diagnosis of de novo segmental amplification or deletion by microarray-based comparative genomic hybridization (array CGH) is uncommon. The study aimed to know about the incidence, abnormal ultrasound findings, and pregnancy outco
Externí odkaz:
https://doaj.org/article/c64c55ac45414b69938eb600ed2db5c9
Autor:
Chin-Chieh Hsu, Chien-Hong Lee, Shuenn-Dyh Chang, Tsang-Ming Ko, Shir-Hwa Ueng, Yu-Hsiu Chen, Mei-Chia Wang, Yao-Lung Chang
Publikováno v:
Genes. 13:245
Placental mesenchymal dysplasia is an uncommon vascular anomaly of the placenta with characteristics of placentomegaly and multicystic appearance and with or without association with fetal chromosomal anomaly. We present a unique placental mesenchyma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8b199a09aa5a1ad83623863297ca6a72
https://doi.org/10.3390/genes13020245
https://doi.org/10.3390/genes13020245
Publikováno v:
Genes
Volume 12
Issue 10
Genes, Vol 12, Iss 1480, p 1480 (2021)
Volume 12
Issue 10
Genes, Vol 12, Iss 1480, p 1480 (2021)
The copy number variation (CNV) of 15q11.2, an emerging and common condition observed during prenatal counseling, is encompassed by four highly conserved and non-imprinted genes—TUBGCP5, CYFIP1, NIPA1, and NIPA2—which are reportedly related to de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8e78dd81dc020509933a6e658a22fb2
https://doi.org/10.3390/genes12101480
https://doi.org/10.3390/genes12101480
Autor:
Tsu-Lan Wu, Chien-Hong Lee, Daniel T. Y. Chiu, Shue-Wei Cheng, Mei-Hui Lin, Kuo-Chien Tsao, Jui-Der Liou, Chien-Feng Sun, D.C. Chu
Publikováno v:
Clinical Genetics. 60:305-309
Since homozygosity of the α-thalassemia-1 of Southeast Asian (SEA) type deletion results in hydrops fetalis, a novel protocol based on the real-time quantitating polymerase chain reaction (PCR) technique has been developed to quantify the intact and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ade517b164a0b5389cc973c5e2df6ec7
https://doi.org/10.1034/j.1399-0004.2001.600409.x
https://doi.org/10.1034/j.1399-0004.2001.600409.x
Autor:
Ding-Ping Chen, Daniel T. Y. Chiu, Kuo-Chien Tsao, D.C. Chu, Ming-De Lo, Shu-Wei Cheng, Tsu-Lan Wu, Chien-Hong Lee, Chien-Feng Sun
Publikováno v:
American Journal of Medical Genetics. 95:332-335
α-Thalassemia has been estimated to account for over 60% of hydrops fetalis cases in Taiwan. The most common genotypic lesion found in α-thalassemia-1 cases in Taiwan is deletion of a large segment of the α-globin gene cluster, termed the Southeas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0b1513f941089a8ba8d69a02fe4a6dd5
https://doi.org/10.1002/1096-8628(20001211)95:4<332::aid-ajmg7>3.0.co
https://doi.org/10.1002/1096-8628(20001211)95:4<332::aid-ajmg7>3.0.co
Intrathoracic extramedullary haematopoiesis complicated by massive haemothorax in alpha-thalassaemia
Publikováno v:
Thorax. 54:466-468
Intrathoracic extramedullary haematopoiesis (EMH) is a rare entity that is usually asymptomatic. A 44 year old man with alpha-thalassaemia is described who developed dyspnoea and massive left sided haemothorax. The haemoglobin disorder was establishe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::63fc74e1a5b51c24fa66d1df3953ce93
https://doi.org/10.1136/thx.54.5.466
https://doi.org/10.1136/thx.54.5.466
Autor:
Hsiu-chuan Tseng, Chien-Hong Lee, Daniel Tsun-Yee Chiu, Hung-Yao Ho, Mei-Ling Cheng, Lee-Yung Shih
Publikováno v:
British journal of haematology. 128(1)
alpha-Thalassaemia is a common red cell disorder in Taiwan, affecting 6-8% of Taiwanese. Previous studies have shown that reactive oxygen species are generated in increased amounts in thalassaemic red cells. This implies the possible alteration of re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1bdf2476df125c88e8696b826b4958ab
https://pubmed.ncbi.nlm.nih.gov/15606558
https://pubmed.ncbi.nlm.nih.gov/15606558
Autor:
Po-Jen, Cheng, Da-Chang, Chu, Chien-Hong, Lee, Ho-Yen, Chiueh, Yu-Ting, Lin, Yung-Kwei, Soong
Publikováno v:
Chang Gung medical journal. 26(1)
Alpha-thalassemia is a common hereditary disease in Taiwan. Affected patients always carry a heavy burden of morbidity and early death. Prenatal diagnosis has reduced the disease burden on families and the health care system. This study evaluated a n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::357b6ec0a3a87f7bd330a688bb355a34
https://pubmed.ncbi.nlm.nih.gov/12656305
https://pubmed.ncbi.nlm.nih.gov/12656305
Autor:
Cheng, Mei-ling, Hung-yao Ho, Hsiu-chuan Tseng, Chien-Hong Lee, Lee-yung Shih, Daniel Tsun-yee Chiu
Publikováno v:
British Journal of Haematology; Jan2005, Vol. 128 Issue 1, p119-127, 9p
Publikováno v:
Thorax; May1999, p466-468, 3p