Chang Yy
Chang Gung University
8 Papers
43 Citations
Chang Yy is an academic researcher from Chang Gung University. The author has contributed to research in topics: Hereditary spastic paraplegia & Multiplex ligation-dependent probe amplification. The author has an hindex of 5, co-authored 8 publications.
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Papers
•Journal Article
A case of Graves' diseases associated with intracranial moyamoya vessels and tubular stenosis of extracranial internal carotid arteries.
TL;DR: A 28-year-old woman presented with a clinical picture of hyperthyroidism, goiter, ophthalmopathy, and an ensuing ischemic stroke and Cerebral angiography demonstrated moyamoya vessels around the Willis's circle and tubular stenosis of the bilateral extracranial internal carotid arteries.
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Large SGCE deletion contributes to Taiwanese myoclonus–dystonia syndrome
Chia Ling Huang,Min-Yu Lan,Chang Yy,Chia-Yu Hsu,Szu-Chia Lai,Rou-Shayn Chen,Hsiu Chen Chang,Chin-Song Lu,Yah-Huei Wu-Chou +8 more
TL;DR: Three novel deletions of the SGCE gene are reported in three families with myoclonus-dystonia (M-D) syndrome in Taiwan which might implicate an important contribution to Taiwanese M-D syndrome.
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•Journal Article
Amphotericin B-induced leukoencephalopathy in a patient with cryptococcal meningitis
TL;DR: A 43-year-old male was diagnosed as having cryptococcal meningitis based on his clinical condition, cerebrospinal fluid (CSF) profile and high titer CSF cryptococ Cal antigen, and the patient's clinical condition was partially reversed after low-dose steroid therapy.
10
Clinical and genetic characterization of hereditary spastic paraplegia type 3A in Taiwan.
Shao-Lun Hsu,Hsueh-Wen Hsueh,Shih-Ying Chen,Chang Yy,Shennie Tan,Chien-Tai Hong,Yu-Shuen Tsai,Kai-Wei Yu,Hsiu-Mei Wu,Yi-Chu Liao,Bing-Wen Soong,Chaur-Jong Hu,Min-Yu Lan,Yi-Chung Lee +13 more
TL;DR: In this article, the authors investigated the clinical and genetic features of hereditary spastic paraplegia (HSP) type 3A (SPG3A) in Taiwan and provided useful information for the diagnosis and management, especially in patients of Han Chinese descent.
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Clinical and genetic analysis of four Taiwanese families with autosomal dominant hereditary spastic paraplegia
TL;DR: Mutation patterns and phenotypic expressivity are heterogeneous in Taiwanese patients with SPG4-related HSP, and genetic rearrangements could be a significant cause of SPG 4- related HSP in the Taiwanese population.
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