Search research articles
Contact Us
Filters
Showing results (41-50 of 184) with videos related to
Page
of 19
Sort By:
Molecular Genetics and Metabolism
|
February 10, 2009
The gene founder effect of two spontaneous mutations in ethnic Chinese (Taiwanese) CAH patients with 21-hydroxylase deficiency
Yann-Jinn Lee, Li-Ping Tsai, Dau-Ming Niu, et al.
Journal of the Chinese Medical Association : JCMA
|
August 10, 2014
Anesthetic management of comprehensive dental restoration in a child with glutaric aciduria type 1 using volatile sevoflurane
Wei-Nung Teng, Su-Man Lin, Dau-Ming Niu, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi
|
December 3, 2014
Electroencephalography and transcranial Doppler ultrasonography in neonatal citrullinemia
Pen-Hua Su, Jia-Yuh Chen, Yung-Jung Chen, et al.
Current Genomics
|
November 14, 2025
Neurological Insights into 16p11.2- And 22q11.2-Related Disorders: A Mini-Review
Yung-Hsiu Lu, Yann-Jang Chen, Shan-Ju Lin, et al.
Genes
|
July 29, 2025
Comparative Evaluation of AAV8 and AAV9 Gene Therapy in Fabry Knockout (<i>Gla</i><sup>-/y</sup>) and Symptomatic (G3S<sup>Tg/+</sup><i>Gla</i><sup>-/y</sup>) Murine Models
Fu-Pang Chang, Ya-Ting Lee, Pao-Hsung Liu, et al.
Cornea
|
July 28, 2023
Novel Manifestation of Corneal Dystrophy After Keratorefractive Surgery
Tsai-Chu Yeh, Chih-Chien Hsu, Yung-Hsiu Lu, et al.
Journal of Child Neurology
|
September 23, 2016
Cognitive Development in Infantile-Onset Pompe Disease Under Very Early Enzyme Replacement Therapy
Chih-Jou Lai, Ting-Rong Hsu, Chia-Feng Yang, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi
|
November 29, 2011
Assessment of body composition using bioelectrical impedance analysis in Prader-Willi syndrome
Hsiang-Yu Lin, Ming-Ren Chen, Chih-Kuang Chuang, et al.
Medicine
|
November 3, 2017
Muscle ultrasound: A useful tool in newborn screening for infantile onset pompe disease
Hsuen-En Hwang, Ting-Rong Hsu, Yueh-Hui Lee, et al.
Journal of Human Genetics
|
October 1, 2010
Identification of a microdeletion at Xp22.13 in a Taiwanese family presenting with Nance-Horan syndrome
Hsiao-Mei Liao, Dau-Ming Niu, Yan-Jang Chen, et al.
Page
of 19
Search research articles
Search
Showing results (41-50 of 184) with videos related to
Sort By:
Page
of 19
Molecular Genetics and Metabolism
|
February 10, 2009
The gene founder effect of two spontaneous mutations in ethnic Chinese (Taiwanese) CAH patients with 21-hydroxylase deficiency
Yann-Jinn Lee, Li-Ping Tsai, Dau-Ming Niu, et al.
Journal of the Chinese Medical Association : JCMA
|
August 10, 2014
Anesthetic management of comprehensive dental restoration in a child with glutaric aciduria type 1 using volatile sevoflurane
Wei-Nung Teng, Su-Man Lin, Dau-Ming Niu, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi
|
December 3, 2014
Electroencephalography and transcranial Doppler ultrasonography in neonatal citrullinemia
Pen-Hua Su, Jia-Yuh Chen, Yung-Jung Chen, et al.
Current Genomics
|
November 14, 2025
Neurological Insights into 16p11.2- And 22q11.2-Related Disorders: A Mini-Review
Yung-Hsiu Lu, Yann-Jang Chen, Shan-Ju Lin, et al.
Genes
|
July 29, 2025
Comparative Evaluation of AAV8 and AAV9 Gene Therapy in Fabry Knockout (<i>Gla</i><sup>-/y</sup>) and Symptomatic (G3S<sup>Tg/+</sup><i>Gla</i><sup>-/y</sup>) Murine Models
Fu-Pang Chang, Ya-Ting Lee, Pao-Hsung Liu, et al.
Cornea
|
July 28, 2023
Novel Manifestation of Corneal Dystrophy After Keratorefractive Surgery
Tsai-Chu Yeh, Chih-Chien Hsu, Yung-Hsiu Lu, et al.
Journal of Child Neurology
|
September 23, 2016
Cognitive Development in Infantile-Onset Pompe Disease Under Very Early Enzyme Replacement Therapy
Chih-Jou Lai, Ting-Rong Hsu, Chia-Feng Yang, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi
|
November 29, 2011
Assessment of body composition using bioelectrical impedance analysis in Prader-Willi syndrome
Hsiang-Yu Lin, Ming-Ren Chen, Chih-Kuang Chuang, et al.
Medicine
|
November 3, 2017
Muscle ultrasound: A useful tool in newborn screening for infantile onset pompe disease
Hsuen-En Hwang, Ting-Rong Hsu, Yueh-Hui Lee, et al.
Journal of Human Genetics
|
October 1, 2010
Identification of a microdeletion at Xp22.13 in a Taiwanese family presenting with Nance-Horan syndrome
Hsiao-Mei Liao, Dau-Ming Niu, Yan-Jang Chen, et al.
Page
of 19