A KCNQ2 E515D mutation associated with benign familial neonatal seizures and continuous spike and waves during slow-wave sleep syndrome in Taiwan

by Inn-Chi Lee, Jiann-Jou Yang, Shuan-Yow Li
Published 2017-09-01

Seizure Recurrence in Children after Stopping Antiepileptic Medication: 5-Year Follow-Up

by Inn-Chi Lee, Shuan-Yow Li, Yung-Jung Chen
Published 2017-08-01

A Wide Spectrum of Genetic Disorders Causing Severe Childhood Epilepsy in Taiwan: A Case Series of Ultrarare Genetic Cause and Novel Mutation Analysis in a Pilot Study

by Syuan-Yu Hong, Jiann-Jou Yang, Shuan-Yow Li, Inn-Chi Lee
Published 2020-12-01

KCNQ2 mutations in childhood nonlesional epilepsy: Variable phenotypes and a novel mutation in a case series

by Inn‐Chi Lee, Tung‐Ming Chang, Jao‐Shwann Liang, Shuan‐Yow Li
Published 2019-07-01

Lenticulostriate Vasculopathy in Brain Ultrasonography is Associated with Cytomegalovirus Infection in Newborns

by Syuan-Yu Hong, Jiann-Jou Yang, Shuan-Yow Li, Inn-Chi Lee
Published 2015-12-01

Novel Mutations in the TMPRSS3 Gene May Contribute to Taiwanese Patients with Nonsyndromic Hearing Loss

by Swee-Hee Wong, Yung-Chang Yen, Shuan-Yow Li, Jiann-Jou Yang
Published 2020-03-01

Ferulic acid-mediated protection against neomycin-induced hair cell loss in transgenic zebrafish

by Ju Chang-Chien, Yung-Chang Yen, Shuan-Yow Li, Tsai-Ching Hsu, Jiann-Jou Yang
Published 2017-01-01

The Functional Role of CONNEXIN 26 Mutation in Nonsyndromic Hearing Loss, Demonstrated by Zebrafish Connexin 30.3 Homologue Model

by Hsuan-An Su, Ting-Wei Lai, Shuan-Yow Li, Tzu-Rong Su, Jiann-Jou Yang, Ching-Chyuan Su
Published 2020-05-01

A novel missense mutation in the connexin30 causes nonsyndromic hearing loss.

by Wen-Hung Wang, Yu-Fan Liu, Ching-Chyuan Su, Mao-Chang Su, Shuan-Yow Li, Jiann-Jou Yang
Published 2011-01-01

Polymorphisms of the RET Gene in Hirschsprung Disease, Anorectal Malformation and Intestinal Pseudo-obstruction in Taiwan

by Trang-Tiau Wu, Tsui-Wei Tsai, Han Chang, Ching-Chyuan Su, Shuan-Yow Li, Hong-Shiee Lai, Chuan Li
Published 2010-01-01

Study of functional-structural relationship of FMRP

by Yang, Jiann-Jou, 楊建洲

Molecular Study of Fragile X Syndrome

by Lin, Mei-Ling, 林玫伶

Functional study of CX30.2/CX31.3 using cell model

by Pin-Hua, 陳品樺
Published 2012

Functional study of GJB2 gene mutation in nonsyndromic deafness using cell model

by I-Ting, 鄭宜婷
Published 2012

Mutation in PDS causes non-syndromic deafness

by Chin-Chu Tsai, 蔡錦珠
Published 2003

Identification and function analysis of zebrafish tmprss gene

by Yi-Wen Wang, 王怡文
Published 2012

Functional analysis of the CX30.2/CX31.3 gene

by Jhih-Hao, 粘志豪
Published 2010

Functional study of mutant Cx29, Cx43 and pseudo-Cx43 in prelingual non-syndromic sensorineural deafness

by Huei Mei, 洪惠媚
Published 2010

Mutations in Cx43 gene cause non-syndromic deafness

by Wen-Chou Chang, 張文州
Published 2003

Study of the TMPRSS3 gene of patients with non-syndromic deafness

by Shu-Ting, 楊舒婷
Published 2007