期刊： PEDIATRICS INTERNATIONAL, 2021; 63 (8)
Background Wilson disease (WD) is an autosomal recessive disorder caused by mutations in the ATP7B gene. In 1984, Scheinberg and Sternlieb estimated t......
期刊： PEDIATRICS INTERNATIONAL, 2021; 63 (8)
Background: This study focused on comparing the applicability and efficacy of the World Health Organization (WHO) growth standards and the China growt......
期刊： PEDIATRICS INTERNATIONAL, 2021; 63 (7)
Background We aimed to assess the efficacy of different initial intravenous immunoglobulin (IVIG) regimens in Kawasaki disease (KD) patients to find m......
期刊： PEDIATRICS INTERNATIONAL, 2021; 63 (9)
Background Toll-interacting protein is a key factor in regulating innate immunity responses via gatekeeping Toll-like receptors. Genetic variance in i......
期刊： PEDIATRICS INTERNATIONAL, 2021; 63 (7)
Background Thiopurine methyltransferase (TPMT) polymorphism is one of the causes of the toxicity of thiopurines, but this is rarely seen in Asian popu......
期刊： PEDIATRICS INTERNATIONAL, ; ()
Background Fundamental movement skill proficiency and perceived physical competence have been shown to influence the physical activity of children. Ho......
期刊： PEDIATRICS INTERNATIONAL, 2021; 63 (2)
Background Interleukin-17A (IL-17A) and IL-17F are involved in the pathogenesis of asthma and allergy. Interleukin-17 receptor A (IL-17RA), encoded by......
期刊： PEDIATRICS INTERNATIONAL, 2020; 62 (2)
Background Urinary tract infection (UTI) is common in children. The purpose of this retrospective study was to determine the various risk factors that......
期刊： PEDIATRICS INTERNATIONAL, 2020; 62 (3)
Background Automatic lancets have been reported to be superior to manual lancets in terms of pain and treatment time. However, no studies have yet bee......
期刊： PEDIATRICS INTERNATIONAL, 2020; 62 (3)
Background There is no consensus about how to manage pulmonary metastasis in patients with hepatoblastoma. We reviewed a treatment with a combination ......
期刊： PEDIATRICS INTERNATIONAL, 2020; 62 (4)
Bartter syndrome (BS) and Gitelman syndrome (GS) are syndromes associated with congenital tubular dysfunction, characterized by hypokalemia and metabo......
