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1  malformations include Kallmann syndrome and idiopathic hypogonadotropic hypogonadism.
2 thesized that mutations in genes involved in idiopathic hypogonadotropic hypogonadism, a congenital f
3 ond intracellular loop (IL2) of GPR54 causes idiopathic hypogonadotropic hypogonadism, a disorder cha
4 e identified prospectively among 50 men with idiopathic hypogonadotropic hypogonadism after a mean (+
5 ties in pubertal timing, including causes of idiopathic hypogonadotropic hypogonadism and Kallmann sy
6 S) is a congenital disorder characterized by idiopathic hypogonadotropic hypogonadism and olfactory d
7              Sustained reversal of normosmic idiopathic hypogonadotropic hypogonadism and the Kallman
8       Rare variants in genes associated with idiopathic hypogonadotropic hypogonadism are found in wo
9         We defined the sustained reversal of idiopathic hypogonadotropic hypogonadism as the presence
10 tically heterogeneous disorder consisting of idiopathic hypogonadotropic hypogonadism (IHH) and anosm
11                                              Idiopathic hypogonadotropic hypogonadism (IHH) due to de
12                                              Idiopathic hypogonadotropic hypogonadism (IHH) is a cond
13                                              Idiopathic hypogonadotropic hypogonadism (IHH) with anos
14 sulfotransferase 1 (HS6ST1) in families with idiopathic hypogonadotropic hypogonadism (IHH).
15 the coding sequence of genes associated with idiopathic hypogonadotropic hypogonadism in 55 women wit
16 led receptor gene, cause autosomal recessive idiopathic hypogonadotropic hypogonadism in humans and m
17 cy in the human presents either as normosmic idiopathic hypogonadotropic hypogonadism (nIHH) or with
18           We describe an adult-onset form of idiopathic hypogonadotropic hypogonadism that develops a
19 tion in GPR54, and an unrelated proband with idiopathic hypogonadotropic hypogonadism was determined
20                                              Idiopathic hypogonadotropic hypogonadism was previously
21       We describe 15 men in whom reversal of idiopathic hypogonadotropic hypogonadism was sustained a
22 ith members who lacked pubertal development (idiopathic hypogonadotropic hypogonadism) was examined f
23                                              Idiopathic hypogonadotropic hypogonadism, which may be a
24 mutations in the GNRHR and GPR54 genes cause idiopathic hypogonadotropic hypogonadism with normal olf
25 ormone as compared with six patients who had idiopathic hypogonadotropic hypogonadism without GPR54 m