Zobrazeno 1 - 10
of 75
pro vyhledávání: '"Shih Yao Liu"'
Autor:
Cheng-Ting Lee, Wen-Hao Tsai, Chien-Ching Chang, Pei-Chun Chen, Cathy Shen-Jang Fann, Hsueh-Kai Chang, Shih-Yao Liu, Mu-Zon Wu, Pao-Chin Chiu, Wen-Ming Hsu, Wei-Shiung Yang, Ling-Ping Lai, Wen-Yu Tsai, Shi-Bing Yang, Pei-Lung Chen
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
ObjectiveCongenital hyperinsulinism (CHI) is a group of clinically and genetically heterogeneous disorders characterized by dysregulated insulin secretion. The aim of the study was to elucidate genetic etiologies of Taiwanese children with the most s
Externí odkaz:
https://doaj.org/article/1245d9fc0f6545668f7be7e04ecc5a60
Publikováno v:
Journal of the Formosan Medical Association, Vol 121, Iss 11, Pp 2331-2337 (2022)
Hereditary cerebral cavernous malformations (CCMs) are characterized by clustered dilated capillary-like vessels in the brain. Autosomal dominant polycystic kidney disease (PKD) is characterized by renal cysts and extra-renal abnormalities. We report
Externí odkaz:
https://doaj.org/article/b91ed3e08a014a029aa359db7635c6c7
Autor:
Ju-Hao Lee, Feng-Jung Yang, Wen-Yu Tsai, Cheng-Ting Lee, Shih-Yao Liu, Wei-Shiung Yang, Yi-Ching Tung
Publikováno v:
Journal of the Formosan Medical Association, Vol 121, Iss 4, Pp 832-840 (2022)
Background/Purpose: Diabetic kidney disease (DKD) is a major complication in patients with type 1 diabetes (T1D). The aim of this study was to evaluate the role of serum neutrophil gelatinase-associated lipocalin (sNGAL) in the early detection of DKD
Externí odkaz:
https://doaj.org/article/9ba18a6359ac43ff91358b1f2e50e0dc
Autor:
Chih-Yi Cho, Wen-Yu Tsai, Cheng-Ting Lee, Shih-Yao Liu, Shu-Yuan Huang, Yin-Hsiu Chien, Wuh-Liang Hwu, Ni-Chung Lee, Yi-Ching Tung
Publikováno v:
Journal of the Formosan Medical Association, Vol 121, Iss 1, Pp 218-226 (2022)
Background: Idiopathic (isolated) hypogonadotropic hypogonadism (IHH) is a rare disease that can be classified as Kallmann syndrome (KS) or normosmic IHH (nIHH). This study investigated the phenotype and genotype of IHH in Taiwanese patients. Methods
Externí odkaz:
https://doaj.org/article/9708cb279a6441e1b956bdde12578078
Publikováno v:
BMC Pediatrics, Vol 21, Iss 1, Pp 1-7 (2021)
Abstract Background Stress hyperglycemia (SH) is considered a transient manifestation and routine diagnostic evaluation was thought to be unnecessary due to the lack of definite correlation with diabetes mellitus (DM). Although SH was usually benign
Externí odkaz:
https://doaj.org/article/2ff2f161eb8e472ca050b14f104aae30
Autor:
Han-Yi Lin, Wen-Yu Tsai, Yi-Ching Tung, Shih-Yao Liu, Ni-Chung Lee, Yin-Hsiu Chien, Wuh-Liang Hwu, Cheng-Ting Lee
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
BackgroundEndocrine disorders are common in patients with 22q11.2 deletion syndrome (22q11.2DS). This study aimed to elucidate the clinical manifestations of endocrine disorders, including parathyroid, thyroid and growth disorders, in Taiwanese patie
Externí odkaz:
https://doaj.org/article/b0ad21ab5a204421a4036a991b747163
Autor:
Yen-Chun Huang, Cheng-Ting Lee, Mu-Zon Wu, Shih-Yao Liu, Yi-Ching Tung, Hong-Nerng Ho, Wen-Yu Tsai
Publikováno v:
Journal of the Formosan Medical Association, Vol 118, Iss 1, Pp 450-456 (2019)
Background/Purpose: 45,X/46,XY mosaicism is a rare sex chromosome abnormality. Here, we present our experience in the management of 45,X/46,XY Taiwanese children. Patients and Methods: We enrolled 19 patients from January 1981 to September 2016. The
Externí odkaz:
https://doaj.org/article/4d067fe9003044adb7a6e035ec3aafb7
Autor:
Meng-Ju Melody Tsai, Wen-Yu Tsai, Cheng-Ting Lee, Shih-Yao Liu, Yin-Hsiu Chien, Yi-Ching Tung
Publikováno v:
Journal of the Formosan Medical Association. 122:106-112
Congenital adrenal hyperplasia attributable to 21-hydroxylase deficiency (21-OHD) is a disorder of adrenal steroidogenesis. Achievement of optimal growth by such patients is challenging. We evaluated the adult height of Taiwanese children with 21-OHD
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c99e7b4621e602ec623d26e732dab4f
https://doi.org/10.1016/j.jfma.2022.09.007
https://doi.org/10.1016/j.jfma.2022.09.007
Publikováno v:
Journal of International Medical Research, Vol 48 (2020)
Pelvic congestion syndrome (PCS) typically causes chronic non-cyclical abdominal pain with a considerable negative effect on the quality of life of women. However, pediatric cases with PCS are limited and non-invasive therapy for adolescent patients
Externí odkaz:
https://doaj.org/article/1c3e088d68234bd4bc2898a3f5b26623
Autor:
Yi-Ching Tung, Ni-Chung Lee, Wuh-Liang Hwu, Shih-Yao Liu, Cheng-Ting Lee, Yin-Hsiu Chien, Wen-Yu Tsai
Publikováno v:
Journal of the Formosan Medical Association, Vol 117, Iss 10, Pp 909-914 (2018)
Background: SHOX deficiency is a common cause of idiopathic short stature. The aim of this study was to describe the clinical characteristics and molecular findings of patients with SHOX deficiency in Taiwan. Methods: A phenotype scoring system was u
Externí odkaz:
https://doaj.org/article/d7a982c0a21b4f02892c8d7640dcbee2