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Journal of Neurodevelopmental Disorders
|
July 31, 2020
Firing activity of locus coeruleus noradrenergic neurons decreases in necdin-deficient mice, an animal model of Prader-Willi syndrome
Rui-Ni Wu, Wei-Chen Hung, Ching-Tsuey Chen, et al.
Pediatric Pulmonology
|
August 28, 2007
Polysomnographic characteristics in patients with Prader-Willi syndrome
Hsiang-Yu Lin, Shuan-Pei Lin, Ching-Chi Lin, et al.
Journal of Biomedicine & Biotechnology
|
November 7, 2009
Methyl-CpG-binding PCR of bloodspots for confirmation of fragile X syndrome in males
Ching-Cherng Tzeng, Chiou-Ping Liou, Chien-Feng Li, et al.
Journal of Neurodevelopmental Disorders
|
December 31, 2025
GABAergic regulation of Locus coeruleus activity in necdin-deficient mice, an animal model of Prader-Willi syndrome
Li-Ping Tsai, Hao Chan, Wei-Chen Hung, et al.
Sleep & Breathing = Schlaf & Atmung
|
April 10, 2016
Drug-induced sleep endoscopy in children with Prader-Willi syndrome
Ming-Chin Lan, Yen-Bin Hsu, Ming-Ying Lan, et al.
Metabolism: Clinical and Experimental
|
August 31, 2004
Lack of relationship between beta3-adrenergic receptor gene polymorphism and gestational diabetes mellitus in a Taiwanese population
Po-Jung Tsai, Su-Chen Ho, Li-Ping Tsai, et al.
Pediatrics and Neonatology
|
June 18, 2026
Homozygous p.Arg227Gln mutation with isolated micropenis is the major presentation of 5α-reductase type 2 deficiency in Taiwan
Siew-Yin Chee, Cynthia Sze-Ya Ting, Shu-Hua Chuang, et al.
Life (Basel, Switzerland)
|
November 27, 2021
Whole Exome Sequencing Identifies a Novel Homozygous Missense Mutation in the CSB Protein-Encoding <i>ERCC6</i> Gene in a Taiwanese Boy with Cockayne Syndrome
Ching-Ming Lin, Jay-How Yang, Hwei-Jen Lee, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi
|
January 26, 2015
Incidence of severe combined immunodeficiency through newborn screening in a Chinese population
Yin-Hsiu Chien, Shu-Chuan Chiang, Kai-Ling Chang, et al.
American Journal of Medical Genetics. Part A
|
January 8, 2005
Prevalence of the FMR1 mutation in Taiwan assessed by large-scale screening of newborn boys and analysis of DXS548-FRAXAC1 haplotype
Ching-Cherng Tzeng, Li-Ping Tsai, Wuh-Liang Hwu, et al.
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Search research articles
Search
Showing results (31-40 of 50) with videos related to
Sort By:
Page
of 5
Journal of Neurodevelopmental Disorders
|
July 31, 2020
Firing activity of locus coeruleus noradrenergic neurons decreases in necdin-deficient mice, an animal model of Prader-Willi syndrome
Rui-Ni Wu, Wei-Chen Hung, Ching-Tsuey Chen, et al.
Pediatric Pulmonology
|
August 28, 2007
Polysomnographic characteristics in patients with Prader-Willi syndrome
Hsiang-Yu Lin, Shuan-Pei Lin, Ching-Chi Lin, et al.
Journal of Biomedicine & Biotechnology
|
November 7, 2009
Methyl-CpG-binding PCR of bloodspots for confirmation of fragile X syndrome in males
Ching-Cherng Tzeng, Chiou-Ping Liou, Chien-Feng Li, et al.
Journal of Neurodevelopmental Disorders
|
December 31, 2025
GABAergic regulation of Locus coeruleus activity in necdin-deficient mice, an animal model of Prader-Willi syndrome
Li-Ping Tsai, Hao Chan, Wei-Chen Hung, et al.
Sleep & Breathing = Schlaf & Atmung
|
April 10, 2016
Drug-induced sleep endoscopy in children with Prader-Willi syndrome
Ming-Chin Lan, Yen-Bin Hsu, Ming-Ying Lan, et al.
Metabolism: Clinical and Experimental
|
August 31, 2004
Lack of relationship between beta3-adrenergic receptor gene polymorphism and gestational diabetes mellitus in a Taiwanese population
Po-Jung Tsai, Su-Chen Ho, Li-Ping Tsai, et al.
Pediatrics and Neonatology
|
June 18, 2026
Homozygous p.Arg227Gln mutation with isolated micropenis is the major presentation of 5α-reductase type 2 deficiency in Taiwan
Siew-Yin Chee, Cynthia Sze-Ya Ting, Shu-Hua Chuang, et al.
Life (Basel, Switzerland)
|
November 27, 2021
Whole Exome Sequencing Identifies a Novel Homozygous Missense Mutation in the CSB Protein-Encoding <i>ERCC6</i> Gene in a Taiwanese Boy with Cockayne Syndrome
Ching-Ming Lin, Jay-How Yang, Hwei-Jen Lee, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi
|
January 26, 2015
Incidence of severe combined immunodeficiency through newborn screening in a Chinese population
Yin-Hsiu Chien, Shu-Chuan Chiang, Kai-Ling Chang, et al.
American Journal of Medical Genetics. Part A
|
January 8, 2005
Prevalence of the FMR1 mutation in Taiwan assessed by large-scale screening of newborn boys and analysis of DXS548-FRAXAC1 haplotype
Ching-Cherng Tzeng, Li-Ping Tsai, Wuh-Liang Hwu, et al.
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of 5