Xueyan Wu

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Familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC) is an autosomal recessive disorder caused by mutations in the CLDN16 or CLDN19 genes, encoding claudin-16 and claudin-19 in the thick ascending limb of Henle’s loop. In patients with claudin-19 mutations, severe ocular involvement (macular coloboma, pigmentary retinitis, nystagmus, or(More)
Gonadotropin induces masculinization and spermatogenesis in men with congenital hypogonadotropic hypogonadism (CHH). However, large cohort studies for the efficacy and reliable predictors of this therapy need to be conducted. The aim of this study was to investigate the efficacy of gonadotropin treatment in a large cohort of male CHH patients and analyze(More)
Tea category classification is of vital importance to industrial applications. We developed a tea-category identification system based on machine learning and computer vision with the aim of classifying different tea types automatically and accurately. 75 photos of three categories of tea were obtained with 3-CCD digital camera, they are green, black, and(More)
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