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Search: authors:"Fu-Sung Lo"

7 papers found.
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A 26-week, randomized trial of insulin detemir versus NPH insulin in children and adolescents with type 2 diabetes (iDEAt2)

There are limited studies evaluating the safety and efficacy of treatments in young people with type 2 diabetes (T2D). This study compared the efficacy and safety of insulin detemir versus neutral protamine Hagedorn (NPH) insulin, both in combination with metformin and lifestyle intervention, in children and adolescents with T2D. This randomized, open-label, phase 3 trial...

Nomogram for prediction of non-proliferative diabetic retinopathy in juvenile-onset type 1 diabetes: a cohort study in an Asian population

, An-Ning Chao, Yih-Shiou Hwang, Yen-Po Chen & Yih-Hsin ChenChang Gung University, College of Medicine, Taoyuan, 333, TaiwanEugene Yu-Chuan Kang, Fu-Sung Lo, Lung-Kun Yeh, An-Lun Wu, Chun-Ting Yeh, Laura ... Search for Fu-Sung Lo in:Nature Research journals • PubMed • Google Scholar Search for Jung-Pan Wang in:Nature Research journals • PubMed • Google Scholar Search for Lung-Kun Yeh in:Nature Research

Short Form of the Chinese Version Diabetes Quality of Life for Youth Scale: A psychometric testing in Taiwanese adolescents with type 1 diabetes

OBJECTIVE To test the psychometric properties of the short form of the Chinese version Diabetes Quality of Life for Youth scale (C-DQOLY-SF).

Association of Cytotoxic T-Lymphocyte-Associated Protein 4 (CTLA4) Gene Polymorphisms with Autoimmune Thyroid Disease in Children and Adults: Case-Control Study

Autoimmune thyroid disease (AITD), including Graves disease (GD) and Hashimoto disease (HD), is an organ-specific autoimmune disease with a strong genetic component. Although the cytotoxic T-lymphocyte-associated protein 4 (CTLA4) polymorphism has been reported to be associated with AITD in adults, few studies have focused on children. The aim of our study was to investigate...

Mutations in Pseudohypoparathyroidism 1a and Pseudopseudohypoparathyroidism in Ethnic Chinese

An inactivating mutation in the GNAS gene causes either pseudohypoparathyroidism 1a (PHP1A) when it is maternally inherited or pseudopseudohypoparathyroidism (PPHP) when it is paternally inherited. We investigated clinical manifestations and mutations of the GNAS gene in ethnic Chinese patients with PHP1A or PPHP. Seven patients from 5 families including 4 girls and 2 boys with...