Lv32
300 积分 2024-09-15 加入
Molecular and clinical studies of Dents disease in Japan: biochemical examination and renal ultrasonography do not predict carrier state
11小时前
已完结
Dents disease: identification of a novel mutation in the renal chloride channel CLCN5
11小时前
求助中
[Bartter's syndrome: new classification, old therapy]
12小时前
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Familial hypomagnesemia-hypercalciuria in 2 siblings
12小时前
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[Familial hypophosphatemic rickets]
12小时前
求助中
Severe hypophosphatasia due to mutations in the tissue-nonspecific alkaline phosphatase (TNSALP) gene
12小时前
求助中
[Familial hypoparathyroidism due to activating mutations in the calcium-sensing receptor gene]
12小时前
求助中
[Dent's disease: hereditary nephrolithiasis related to defective tubular endocytosis processes]
12小时前
求助中
Renal abnormalities in congenital chloride diarrhea
12小时前
求助中
Genetic advances, biochemical and clinical features and critical approach to treatment of patients with X-linked hypophosphatemic rickets
12小时前
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