Yu-wen Cheng

Jun 4, 2024 | mdpi.com | William Winardi |Sin-Hua Moi |Yu-wen Cheng |Thomas Winardi

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Apr 29, 2024 | mdpi.com | Yu-wen Cheng |Jia-Hau Lee |Chih-Hui Chang |Tzu-Ting Tseng

All articles published by MDPI are made immediately available worldwide under an open access license. No specialpermission is required to reuse all or part of the article published by MDPI, including figures and tables. Forarticles published under an open access Creative Common CC BY license, any part of the article may be reused withoutpermission provided that the original article is clearly cited. For more information, please refer tohttps://www.mdpi.com/openaccess.

Apr 4, 2024 | preprints.org | Yu-wen Cheng |Chih-Hui Chang |Tzu-Ting Tseng |Jia-Hau Lee

Preprint Article Version 1 This version is not peer-reviewed Version 1 : Received: 2 April 2024 / Approved: 3 April 2024 / Online: 4 April 2024 (17:26:13 CEST) Cheng, Y.; Lee, J.; Chang, C.; Tseng, T.; Chai, C.; Lieu, A.; Kwan, A. High PGC-1α Expression as a Poor Prognostic Indicator in Intracranial Glioma. Preprints 2024, 2024040347. https://doi.org/10.20944/preprints202404.0347.v1 Cheng, Y.; Lee, J.; Chang, C.; Tseng, T.; Chai, C.; Lieu, A.; Kwan, A.

Feb 28, 2024 | onlinelibrary.wiley.com | Wei-Ting Tu |Chun-Lin Su |Yu-wen Cheng |Yi-Chia Tsai

CONFLICT OF INTEREST STATEMENT There is no conflict of interest to report. REFERENCES 1, , , . Cloning of human type VII collagen. Complete primary sequence of the alpha 1(VII) chain and identification of intragenic polymorphisms. J Biol Chem. 1994; 269(32): 20256-20262. 2, , , , , . Rare compound heterozygous frameshift mutations in ALMS1 gene identified through exome sequencing in a Taiwanese patient with Alström syndrome. Front Genet. 2018; 9: 110. 3, , , et al.

Aug 31, 2023 | n.neurology.org | Ruiting Zhang |Chih-Hao Chen |Yu-wen Cheng |Jessica Lebenberg

AbstractBackground and objectives: Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and leukoencephalopathy (CADASIL) is the most frequent genetic cerebrovascular disease. The clinical aspects of the disease in relation to the various types of lesions on MRI vary widely within families but also between different cohorts reported worldwide. Many limitations prevent comparison of imaging data obtained with different scanners and sequences in different patients cohorts.