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Li-Ping Tsai

Showing results (11-20 of 50) with videos related to

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Pediatric Nephrology (Berlin, Germany)|February 13, 2015
Elevated postvoid residual urine volume predicting recurrence of urinary tract infections in toilet-trained childrenShang-Jen Chang, Li-Ping Tsai, Chun-Kai Hsu, et al.
Tzu Chi Medical Journal|April 10, 2020
Clinical characteristics and epilepsy in genomic imprinting disorders: Angelman syndrome and Prader-Willi syndromeTzong-Shi Wang, Wen-Hsin Tsai, Li-Ping Tsai, et al.
Neurourology and Urodynamics|April 3, 2021
High prevalence of lower urinary tract dysfunction in patients with Prader-Willi syndromeTze-Chen Chao, Stephen S-D Yang, Shang-Jen Chang, et al.
International Journal of Environmental Research and Public Health|July 28, 2022
Accelerometer-Measured Physical Activity and Sedentary Behavior of Adults with Prader-Willi Syndrome Attending and Not Attending a Small-Scale Community WorkshopMing-Ju Wu, Li-Ping Tsai, Ting-Fu Lai, et al.
Pediatrics and Neonatology|July 26, 2019
A 2-year-old twin boy with pancytopenia caused due to nutritional cobalamin deficiencyShu-Huey Chen, Yung-Ting Kuo, Li-Ping Tsai, et al.
The Journal of Clinical Endocrinology and Metabolism|June 6, 2003
Mutation of IVS2 -12A/C>G in combination with 707-714delGAGACTAC in the CYP21 gene is caused by deletion of the C4-CYP21 repeat module with steroid 21-hydroxylase deficiencyHsien-Hsiung Lee, Shwu-Fen Chang, Fuu-Jen Tsai, et al.
Journal of Pediatric Orthopedics. Part B|November 29, 2022
Scoliosis and BMI in patients with Prader-Willi syndromeLi-Ping Tsai, Shiau-Tzu Tzeng, Tsung-Han Hsieh, et al.
Acta Paediatrica Taiwanica = Taiwan Er Ke Yi Xue Hui Za Zhi|November 24, 2005
Partial androgen insensitivity syndrome with R840H mutation in androgen receptor: report of one caseJui-Lung Yen, Kuang-Huey Chang, Jin-Cherng Sheu, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi|December 23, 2006
Novel SOX9 gene mutation in campomelic dysplasia with autosomal sex reversalHui-Pin Hsiao, Li-Ping Tsai, Mei-Chyn Chao, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 26, 2009
Application of the DHPLC method for mutational detection of the CYP21A2 gene in congenital adrenal hyperplasiaLi-Ping Tsai, Ching-Feng Cheng, Jo-Ping Hsieh, et al.
Pageof 5

Showing results (11-20 of 50) with videos related to

Sort By:
Pageof 5
Pediatric Nephrology (Berlin, Germany)|February 13, 2015
Elevated postvoid residual urine volume predicting recurrence of urinary tract infections in toilet-trained childrenShang-Jen Chang, Li-Ping Tsai, Chun-Kai Hsu, et al.
Tzu Chi Medical Journal|April 10, 2020
Clinical characteristics and epilepsy in genomic imprinting disorders: Angelman syndrome and Prader-Willi syndromeTzong-Shi Wang, Wen-Hsin Tsai, Li-Ping Tsai, et al.
Neurourology and Urodynamics|April 3, 2021
High prevalence of lower urinary tract dysfunction in patients with Prader-Willi syndromeTze-Chen Chao, Stephen S-D Yang, Shang-Jen Chang, et al.
International Journal of Environmental Research and Public Health|July 28, 2022
Accelerometer-Measured Physical Activity and Sedentary Behavior of Adults with Prader-Willi Syndrome Attending and Not Attending a Small-Scale Community WorkshopMing-Ju Wu, Li-Ping Tsai, Ting-Fu Lai, et al.
Pediatrics and Neonatology|July 26, 2019
A 2-year-old twin boy with pancytopenia caused due to nutritional cobalamin deficiencyShu-Huey Chen, Yung-Ting Kuo, Li-Ping Tsai, et al.
The Journal of Clinical Endocrinology and Metabolism|June 6, 2003
Mutation of IVS2 -12A/C>G in combination with 707-714delGAGACTAC in the CYP21 gene is caused by deletion of the C4-CYP21 repeat module with steroid 21-hydroxylase deficiencyHsien-Hsiung Lee, Shwu-Fen Chang, Fuu-Jen Tsai, et al.
Journal of Pediatric Orthopedics. Part B|November 29, 2022
Scoliosis and BMI in patients with Prader-Willi syndromeLi-Ping Tsai, Shiau-Tzu Tzeng, Tsung-Han Hsieh, et al.
Acta Paediatrica Taiwanica = Taiwan Er Ke Yi Xue Hui Za Zhi|November 24, 2005
Partial androgen insensitivity syndrome with R840H mutation in androgen receptor: report of one caseJui-Lung Yen, Kuang-Huey Chang, Jin-Cherng Sheu, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi|December 23, 2006
Novel SOX9 gene mutation in campomelic dysplasia with autosomal sex reversalHui-Pin Hsiao, Li-Ping Tsai, Mei-Chyn Chao, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 26, 2009
Application of the DHPLC method for mutational detection of the CYP21A2 gene in congenital adrenal hyperplasiaLi-Ping Tsai, Ching-Feng Cheng, Jo-Ping Hsieh, et al.
Pageof 5