Zobrazeno 1 - 10
of 107
pro vyhledávání: '"Ji Nan Sheu"'
Publikováno v:
Pediatrics and Neonatology, Vol 64, Iss 4, Pp 491-492 (2023)
Externí odkaz:
https://doaj.org/article/7068ef53c9434c6da0fb09e39b80d17d
Publikováno v:
Frontiers in Psychology, Vol 13 (2022)
BackgroundMost tuberous sclerosis complex (TSC) patients have neurological disorders and are at high risk of academic difficulties. Among academic skills, reading ability is the most important academic skill. The study applied the Chinese character f
Externí odkaz:
https://doaj.org/article/3fdfa15866c046cab0c6c98ed13a4c07
Autor:
Yi-Jie Wu, Wei-Fong Wu, Chia-Wei Hung, Ming-Shiu Ku, Pei-Fen Liao, Hai-Lun Sun, Ko-Hsiu Lu, Ji-Nan Sheu, Ko-Huang Lue
Publikováno v:
Journal of Microbiology, Immunology and Infection, Vol 50, Iss 5, Pp 684-692 (2017)
Objective: The main objective of this study was to evaluate the efficacy and safety of Lactobacillus rhamnosus in children aged 4–48 months with atopic dermatitis. Methods: The design of this study was a two-center, double-blind, randomized, and pl
Externí odkaz:
https://doaj.org/article/b7a475b93601441d82a2718b422e6ecb
Publikováno v:
Pediatrics and Neonatology, Vol 57, Iss 2, Pp 113-119 (2016)
This study was designed to examine the capability of renal ultrasonography (US) for predicting vesicoureteral reflux (VUR) and renal scarring (RS), and to assess, using initial US, the significant urologic abnormalities that impact on management of c
Externí odkaz:
https://doaj.org/article/926a6eb0006a4ea38c6f8256c1edb984
Autor:
You-Cheng Lin, Ji-Nan Sheu, Wen-Hung Chung, Ren-You Pan, Chu-Ju Hung, Jen-Jung Cheng, Yu-Ping Hsiao
Publikováno v:
Frontiers in Pediatrics, Vol 6 (2018)
Stevens-Johnson syndrome (SJS) is a life-threatening disease, which is mainly ascribed to drugs, such as sulfonamides and psychoepileptics. In this article, we present a pediatric case of vancomycin-induced SJS and an alternative diagnostic algorithm
Externí odkaz:
https://doaj.org/article/fd81a3f51a5d4318a8594add04efadd7
Autor:
Sung-Hsi Wei, Pesus Chou, Lei-Ron Tseng, Hung-Chih Lin, Jen-Hsien Wang, Ji-Nan Sheu, Ming-Tsan Liu, Fang-Ching Liu, Hoa-Hsin Wu, Min-Cheng Lin, Ching-Fen Ko, Hsiang-Yu Lin, Pei-Hsiu Kao, Kao-Pin Hwang, Yu-Lung Hsu, Tsung-Lin Kuo, Chuen-Sheue Chiang
Publikováno v:
Emerging Infectious Diseases, Vol 20, Iss 11, Pp 1922-1925 (2014)
We report 2 cases of neonatal Legionella infection associated with aspiration of contaminated water used in hospitals to make infant formula. The molecular profiles of Legionella strains isolated from samples from the infants and from water dispenser
Externí odkaz:
https://doaj.org/article/c785b7009fe843baad36cc887a1f2244
Publikováno v:
Pediatrics and Neonatology, Vol 55, Iss 4, Pp 312-315 (2014)
Deficiency of hypoxanthine phosphoribosyltransferase activity is a rare inborn error of purine metabolism with subsequent uric acid overproduction and neurologic presentations. The diagnosis of Lesch–Nyhan syndrome (LNS) is frequently delayed until
Externí odkaz:
https://doaj.org/article/a9f3077c1919406bb09becbe767faf05
Publikováno v:
Pediatrics and Neonatology, Vol 55, Iss 2, Pp 120-126 (2014)
Rotavirus and norovirus are the most common known causes of viral gastroenteritis in children. This study examined the association between serum interleukin 6 (IL-6) and interleukin 8 (IL-8) levels and disease severity in the acute phase of rotavirus
Externí odkaz:
https://doaj.org/article/9d2a98da18e9480095866ae01ca49551
Publikováno v:
American Journal of Perinatology. 38:1244-1253
Objective This study aimed to determine whether neonatal hyperbilirubinemia is associated with a risk of autism spectrum disorder (ASD) using a large population-based cohort.Study Design This retrospective cohort study used data from the children's d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::42418aff96453e8e0e468810e348924d
https://doi.org/10.1055/s-0040-1708033
https://doi.org/10.1055/s-0040-1708033
Publikováno v:
Pediatrics and Neonatology, Vol 52, Iss 4, Pp 227-231 (2011)
Multicystic dysplastic kidney (MCDK) is a congenital maldevelopment in which the renal cortex is characteristically replaced by numerous cysts of multiple sizes. MCDK presenting as a single predominant large cyst in morphology is less common. We repo
Externí odkaz:
https://doaj.org/article/e86c375d74544f8c96dc46c44867eaed