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Journal of Clinical Nursing
|
March 18, 2011
Family caregiver distress with children having rare genetic disorders: a qualitative study involving Russell-Silver Syndrome in Taiwan
Hsin-Ju Weng, Dau-Ming Niu, Sue Turale, et al.
Orphanet Journal of Rare Diseases
|
June 15, 2019
Cardiac characteristics and natural progression in Taiwanese patients with mucopolysaccharidosis III
Hsiang-Yu Lin, Ming-Ren Chen, Shan-Miao Lin, et al.
American Journal of Medical Genetics. Part A
|
September 6, 2025
Marked Improvements in Airway Abnormalities and Multifaceted Outcomes After 2 Years Switching to Avalglucosidase Alfa: Evaluation of A 19-Year-Old Male Diagnosed With Late-Onset Pompe Disease
Chih-Hsuan Lu, Dau-Ming Niu, Yuh-Jing Yeou, et al.
Journal of the Chinese Medical Association : JCMA
|
September 19, 2009
Growth hormone therapy in neonatal patients with methylmalonic acidemia
Chuan-Hong Kao, Mei-Ying Liu, Tze-Tze Liu, et al.
Eye (London, England)
|
November 27, 2022
Ophthalmic characteristics and retinal vasculature changes in Williams syndrome, and its association with systemic diseases
Tsai-Chu Yeh, Hui-Chen Cheng, Hsing-Yuan Li, et al.
Prenatal Diagnosis
|
September 8, 2006
Paternal gonadal mosaicism of NIPBL mutation in a father of siblings with Cornelia de Lange syndrome
Dau-Ming Niu, Jing-Ying Huang, Hsin-Yang Li, et al.
Science Advances
|
April 9, 2025
Invention of an oral medication for cardiac Fabry disease caused by RNA mis-splicing
Tomonari Awaya, Masahiko Ajiro, Hiroko Kobayashi, et al.
The Prostate
|
April 28, 2012
Activation of silenced tumor suppressor genes in prostate cancer cells by a novel energy restriction-mimetic agent
Hsiang-Yu Lin, Yi-Chiu Kuo, Yu-I Weng, et al.
Clinical Nutrition (Edinburgh, Scotland)
|
December 18, 2014
Heterozygous carriers of classical homocystinuria tend to have higher fasting serum homocysteine concentrations than non-carriers in the presence of folate deficiency
Yung-Hsiu Lu, Li-Mei Cheng, Yu-Hsiu Huang, et al.
Journal of Medical Genetics
|
May 19, 2006
A common SCN5A polymorphism attenuates a severe cardiac phenotype caused by a nonsense SCN5A mutation in a Chinese family with an inherited cardiac conduction defect
Dau-Ming Niu, Betau Hwang, Han-Wei Hwang, et al.
Page
of 19
Search research articles
Search
Showing results (81-90 of 184) with videos related to
Sort By:
Page
of 19
Journal of Clinical Nursing
|
March 18, 2011
Family caregiver distress with children having rare genetic disorders: a qualitative study involving Russell-Silver Syndrome in Taiwan
Hsin-Ju Weng, Dau-Ming Niu, Sue Turale, et al.
Orphanet Journal of Rare Diseases
|
June 15, 2019
Cardiac characteristics and natural progression in Taiwanese patients with mucopolysaccharidosis III
Hsiang-Yu Lin, Ming-Ren Chen, Shan-Miao Lin, et al.
American Journal of Medical Genetics. Part A
|
September 6, 2025
Marked Improvements in Airway Abnormalities and Multifaceted Outcomes After 2 Years Switching to Avalglucosidase Alfa: Evaluation of A 19-Year-Old Male Diagnosed With Late-Onset Pompe Disease
Chih-Hsuan Lu, Dau-Ming Niu, Yuh-Jing Yeou, et al.
Journal of the Chinese Medical Association : JCMA
|
September 19, 2009
Growth hormone therapy in neonatal patients with methylmalonic acidemia
Chuan-Hong Kao, Mei-Ying Liu, Tze-Tze Liu, et al.
Eye (London, England)
|
November 27, 2022
Ophthalmic characteristics and retinal vasculature changes in Williams syndrome, and its association with systemic diseases
Tsai-Chu Yeh, Hui-Chen Cheng, Hsing-Yuan Li, et al.
Prenatal Diagnosis
|
September 8, 2006
Paternal gonadal mosaicism of NIPBL mutation in a father of siblings with Cornelia de Lange syndrome
Dau-Ming Niu, Jing-Ying Huang, Hsin-Yang Li, et al.
Science Advances
|
April 9, 2025
Invention of an oral medication for cardiac Fabry disease caused by RNA mis-splicing
Tomonari Awaya, Masahiko Ajiro, Hiroko Kobayashi, et al.
The Prostate
|
April 28, 2012
Activation of silenced tumor suppressor genes in prostate cancer cells by a novel energy restriction-mimetic agent
Hsiang-Yu Lin, Yi-Chiu Kuo, Yu-I Weng, et al.
Clinical Nutrition (Edinburgh, Scotland)
|
December 18, 2014
Heterozygous carriers of classical homocystinuria tend to have higher fasting serum homocysteine concentrations than non-carriers in the presence of folate deficiency
Yung-Hsiu Lu, Li-Mei Cheng, Yu-Hsiu Huang, et al.
Journal of Medical Genetics
|
May 19, 2006
A common SCN5A polymorphism attenuates a severe cardiac phenotype caused by a nonsense SCN5A mutation in a Chinese family with an inherited cardiac conduction defect
Dau-Ming Niu, Betau Hwang, Han-Wei Hwang, et al.
Page
of 19