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期刊名:Clinical pediatric endocrinology

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ISSN:0918-5739

e-ISSN:1347-7358

IF/分区:1.0/Q4

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Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Hiromi Hyodo,Yuichiro Tomita,Kohta Hirai et al. Hiromi Hyodo et al.
Turner syndrome is a chromosomal disease frequently associated with autoimmune disorders including diabetes mellitus, thyroid disease and inflammatory bowel disease (IBD). Although the etiology of IBD has not been fully elucidated, genetic ...
Mari Satoh,Keiko Aso,Sayaka Ogikubo et al. Mari Satoh et al.
About 30% of children with elevated TSH levels during neonatal screening have a transient form of disorder. On the other hand, it has been reported that subclinical hypothyroidism persists in late childhood in about 30% of children found to...
Kosei Hasegawa,Yoshiharu Nagaoka,Hidehiko Maruyama et al. Kosei Hasegawa et al.
Noonan syndrome is characterized by facial dysmorphology, congenital heart disease and growth failure. Although it is also accompanied by deranged lymph-vessel formation, protein-losing enteropathy (PLE) with Noonan syndrome is rarely repor...
Taichi Kitaoka,Noriyuki Namba,Ji Yoo Kim et al. Taichi Kitaoka et al.
We report a male infant with FATCO syndrome, an acronym for fibular aplasia, tibial campomelia, and oligosyndactyly. Courtens et al. reported an infant with oligosyndactyly of the left hand, complete absence of the right fibula, bowing of t...
Keiko Homma,Mariko Hida,Kazushige Ikeda et al. Keiko Homma et al.
Immunochemical measurement of serum 17α-hydroxyprogesterone (17OHP), the most important parameter for diagnosis of classical 21-hydroxylase deficiency (21OHD) in newborn infants, is known to be inaccurate due to the cross-reactivity of ant...