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Annals of Human Genetics
|
January 5, 2011
Genetic studies of Prader-Willi patients provide evidence for conservation of genomic architecture in proximal chromosome 15q
Aihua Hou, Shuan-Pei Lin, Shi Yun Ho, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
May 4, 2020
HLA-DQ genotype and biochemical characterization of anti-transglutaminase 2 antibodies in patients with type 1 diabetes mellitus in Taiwan
Yann-Jinn Lee, Wei-Hsin Ting, Yi-Wen Yang, et al.
Acta Paediatrica (Oslo, Norway : 1992)
|
June 1, 2007
Genotype and phenotype in patients with Prader-Willi syndrome in Taiwan
Hsiang-Yu Lin, Shuan-Pei Lin, Chih-Kuang Chuang, et al.
Pediatrics and Neonatology
|
February 11, 2026
Declining trends in diabetic ketoacidosis after type 1 diabetes Diagnosis: A 22-year experience at a pediatric medical center in Northern Taiwan
Kai-Hsiang Chang, Wei-Hsin Ting, Yann-Jinn Lee, et al.
Plos One
|
October 7, 2020
Acute kidney injury is a common complication in children and adolescents hospitalized for diabetic ketoacidosis
Shih-Kang Huang, Chi-Yu Huang, Chao-Hsu Lin, et al.
Oncotarget
|
April 18, 2018
Autoantibodies against islet cell antigens in children with type 1 diabetes mellitus
Bi-Wen Cheng, Fu-Sung Lo, An-Mei Wang, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi
|
October 27, 2017
Factors associated with diabetic nephropathy in children, adolescents, and adults with type 1 diabetes
Chi-Yu Huang, Wei-Hsin Ting, Fu-Sung Lo, et al.
Pediatrics and Neonatology
|
January 26, 2020
Long-term outcomes of graves disease in children treated with anti-thyroid drugs
Ya-Ting Chiang, Wei-Hsin Ting, Chi-Yu Huang, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease
|
November 23, 2018
Mutations in glucokinase and other genes detected in neonatal and type 1B diabetes patient using whole exome sequencing may lead to disease-causing changes in protein activity
Dao-Chen Lin, Chi-Yu Huang, Wei-Hsin Ting, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
September 11, 2008
Association of CT60 polymorphism of the CTLA4 gene with Graves' disease in Taiwanese children
Suei-Tsau Tsai, Chi-Yu Huang, Fu-Sung Lo, et al.
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of 6
Search research articles
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Showing results (41-50 of 55) with videos related to
Sort By:
Page
of 6
Annals of Human Genetics
|
January 5, 2011
Genetic studies of Prader-Willi patients provide evidence for conservation of genomic architecture in proximal chromosome 15q
Aihua Hou, Shuan-Pei Lin, Shi Yun Ho, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
May 4, 2020
HLA-DQ genotype and biochemical characterization of anti-transglutaminase 2 antibodies in patients with type 1 diabetes mellitus in Taiwan
Yann-Jinn Lee, Wei-Hsin Ting, Yi-Wen Yang, et al.
Acta Paediatrica (Oslo, Norway : 1992)
|
June 1, 2007
Genotype and phenotype in patients with Prader-Willi syndrome in Taiwan
Hsiang-Yu Lin, Shuan-Pei Lin, Chih-Kuang Chuang, et al.
Pediatrics and Neonatology
|
February 11, 2026
Declining trends in diabetic ketoacidosis after type 1 diabetes Diagnosis: A 22-year experience at a pediatric medical center in Northern Taiwan
Kai-Hsiang Chang, Wei-Hsin Ting, Yann-Jinn Lee, et al.
Plos One
|
October 7, 2020
Acute kidney injury is a common complication in children and adolescents hospitalized for diabetic ketoacidosis
Shih-Kang Huang, Chi-Yu Huang, Chao-Hsu Lin, et al.
Oncotarget
|
April 18, 2018
Autoantibodies against islet cell antigens in children with type 1 diabetes mellitus
Bi-Wen Cheng, Fu-Sung Lo, An-Mei Wang, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi
|
October 27, 2017
Factors associated with diabetic nephropathy in children, adolescents, and adults with type 1 diabetes
Chi-Yu Huang, Wei-Hsin Ting, Fu-Sung Lo, et al.
Pediatrics and Neonatology
|
January 26, 2020
Long-term outcomes of graves disease in children treated with anti-thyroid drugs
Ya-Ting Chiang, Wei-Hsin Ting, Chi-Yu Huang, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease
|
November 23, 2018
Mutations in glucokinase and other genes detected in neonatal and type 1B diabetes patient using whole exome sequencing may lead to disease-causing changes in protein activity
Dao-Chen Lin, Chi-Yu Huang, Wei-Hsin Ting, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
September 11, 2008
Association of CT60 polymorphism of the CTLA4 gene with Graves' disease in Taiwanese children
Suei-Tsau Tsai, Chi-Yu Huang, Fu-Sung Lo, et al.
Page
of 6