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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 children
Shang-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 syndrome
Tzong-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 syndrome
Tze-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 Workshop
Ming-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 deficiency
Shu-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 deficiency
Hsien-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 syndrome
Li-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 case
Jui-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 reversal
Hui-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 hyperplasia
Li-Ping Tsai, Ching-Feng Cheng, Jo-Ping Hsieh, et al.
Page
of 5
Search research articles
Search
Showing results (11-20 of 50) with videos related to
Sort By:
Page
of 5
Pediatric Nephrology (Berlin, Germany)
|
February 13, 2015
Elevated postvoid residual urine volume predicting recurrence of urinary tract infections in toilet-trained children
Shang-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 syndrome
Tzong-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 syndrome
Tze-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 Workshop
Ming-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 deficiency
Shu-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 deficiency
Hsien-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 syndrome
Li-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 case
Jui-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 reversal
Hui-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 hyperplasia
Li-Ping Tsai, Ching-Feng Cheng, Jo-Ping Hsieh, et al.
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of 5