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Critical Care (London, England)|August 24, 2014
Determining delayed admission to intensive care unit for mechanically ventilated patients in the emergency departmentShih-Chiang Hung, Chia-Te Kung, Chih-Wei Hung, et al.
General Hospital Psychiatry|June 16, 2016
Risk of bipolar disorder in patients with COPD: a population-based cohort studyPei-Jung Tsai, Yin-To Liao, Charles Tzu-Chi Lee, et al.
Prenatal Diagnosis|February 16, 2005
Perinatal findings and molecular cytogenetic analysis of de novo partial trisomy 16q (16q22.1-->qter) and partial monosomy 20q (20q13.3-->qter)Chih-Ping Chen, Shuan-Pei Lin, Chyi-Chyang Lin, et al.
The Journal of Heart and Lung Transplantation : the Official Publication of the International Society for Heart Transplantation|December 22, 2007
Lung transplantation in the management of patients with lymphangioleiomyomatosis: baseline data from the NHLBI LAM RegistryJanet R Maurer, Jay Ryu, Gerald Beck, et al.
Scientific Reports|August 11, 2019
Cucumber mosaic virus-induced gene silencing in bananaYuh Tzean, Ming-Chi Lee, Hsiao-Hsuan Jan, et al.
Science Immunology|April 26, 2020
IL-23 and IL-2 activation of STAT5 is required for optimal IL-22 production in ILC3s during colitisDavid Bauché, Barbara Joyce-Shaikh, Julie Fong, et al.
Taiwanese Journal of Obstetrics & Gynecology|July 28, 2011
Partial monosomy 13q (13q21.32--->qter) and partial trisomy 8p (8p1--->pter) presenting with anencephaly and increased nuchal translucency: array comparative genomic hybridization characterizationChih-Ping Chen, Yi-Ning Su, Fuu-Jen Tsai, et al.
Zhonghua Xin Xue Guan Bing Za Zhi|June 1, 2011
[Mechanism related to docosahexaenoic acid induced large conductance calcium-activated potassium channel currents increase in coronary smooth muscle cells]Ru-xing Wang, Ku-lin Li, Chang-ying Zhang, et al.
Taiwanese Journal of Obstetrics & Gynecology|October 28, 2011
Chromosome 1p32-p31 deletion syndrome: prenatal diagnosis by array comparative genomic hybridization using uncultured amniocytes and association with NFIA haploinsufficiency, ventriculomegaly, corpus callosum hypogenesis, abnormal external genitalia, and intrauterine growth restrictionChih-Ping Chen, Yi-Ning Su, Yi-Yung Chen, et al.
Gene|August 13, 2013
An interstitial deletion of 8q23.3-q24.22 associated with Langer-Giedion syndrome, Cornelia de Lange syndrome and epilepsyChih-Ping Chen, Shuan-Pei Lin, Yu-Peng Liu, et al.
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