戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1  (olfactory dysfunction, delayed puberty and hypogonadotropic hypogonadism).
2 elayed puberty, hypothalamic amenorrhea, and hypogonadotropic hypogonadism.
3 rized by anosmia and pubertal failure due to hypogonadotropic hypogonadism.
4 ithin the cell and if dysfunctional leads to Hypogonadotropic Hypogonadism.
5 ency, including the rare adult-onset form of hypogonadotropic hypogonadism.
6 lls are known to exhibit subfertility due to hypogonadotropic hypogonadism.
7  immune function, and delayed puberty due to hypogonadotropic hypogonadism.
8 on population in the hypothalamus as well as hypogonadotropic hypogonadism.
9 r characterized by adrenal insufficiency and hypogonadotropic hypogonadism.
10  features of hypomyelination, hypodontia and hypogonadotropic hypogonadism.
11 ism, hypoparathyroidism, hypoadrenalism, and hypogonadotropic hypogonadism.
12 ons include Kallmann syndrome and idiopathic hypogonadotropic hypogonadism.
13 hase (NOS1) activity underlies some forms of hypogonadotropic hypogonadism.
14 on mutations in six probands with congenital hypogonadotropic hypogonadism (2%), who displayed additi
15 at mutations in genes involved in idiopathic hypogonadotropic hypogonadism, a congenital form of GnRH
16 llular loop (IL2) of GPR54 causes idiopathic hypogonadotropic hypogonadism, a disorder characterized
17                                In congenital hypogonadotropic hypogonadism, a lack of gonadotropin ac
18 d prospectively among 50 men with idiopathic hypogonadotropic hypogonadism after a mean (+/-SD) durat
19 rome AHC, a disorder that is associated with hypogonadotropic hypogonadism also.
20 410K phenotype to include Kallmann syndrome (hypogonadotropic hypogonadism and anosmia), stereotyped
21 Lats1-/- mice are reminiscent of isolated LH-hypogonadotropic hypogonadism and corpus luteum insuffic
22 ate when adjusted for fat-free mass, partial hypogonadotropic hypogonadism and growth failure.
23 e (KS) is a genetic disease characterized by hypogonadotropic hypogonadism and impaired sense of smel
24  microRNA synthesis in GnRH neurons leads to hypogonadotropic hypogonadism and infertility in mice.
25 fic deletion of Kiss1r (Kiss1r(d/d)) display hypogonadotropic hypogonadism and infertility.
26 4 prevents the onset of puberty and leads to hypogonadotropic hypogonadism and infertility.
27 ve function, as mice lacking miR-7a2 develop hypogonadotropic hypogonadism and infertility.
28 ertal timing, including causes of idiopathic hypogonadotropic hypogonadism and Kallmann syndrome.
29 genital disorder characterized by idiopathic hypogonadotropic hypogonadism and olfactory dysfunction.
30 trophic Factor (NDNF) involved in congenital hypogonadotropic hypogonadism and several types of cance
31   Sustained reversal of normosmic idiopathic hypogonadotropic hypogonadism and the Kallmann syndrome
32 variants in genes associated with idiopathic hypogonadotropic hypogonadism are found in women with hy
33 e (GnRH) receptor mutants from patients with hypogonadotropic hypogonadism are frequently misrouted p
34 defined the sustained reversal of idiopathic hypogonadotropic hypogonadism as the presence of normal
35                              The syndrome of hypogonadotropic hypogonadism, ataxia, and dementia can
36 severe gynecomastia of prepubertal onset and hypogonadotropic hypogonadism caused by elevated estroge
37  in neurokinin B (NKB) and its receptor show hypogonadotropic hypogonadism characterised by failure t
38 (NKB) or its receptor, NK3 (NK3R), result in hypogonadotropic hypogonadism, characterized by an absen
39                                   Congenital hypogonadotropic hypogonadism (CHH) is a condition chara
40           Patients (n = 337) with congenital hypogonadotropic hypogonadism (CHH) showed enrichment of
41 ion of GnRH neurons, resulting in congenital hypogonadotropic hypogonadism (CHH), a heterogeneous dis
42 re reported to result in isolated congenital hypogonadotropic hypogonadism (CHH).
43 xpress LepR and inactivation of Kiss1 causes hypogonadotropic hypogonadism, Donato et al., in this is
44 his recessive mutation (GnRHR E(90)K) causes hypogonadotropic hypogonadism (failed puberty associated
45 xome sequencing in a patient with ataxia and hypogonadotropic hypogonadism, followed by targeted sequ
46 tral hypoadrenalism, central hypothyroidism, hypogonadotropic hypogonadism, growth hormone deficiency
47 opathy, bifid uvula, malignant hyperthermia, hypogonadotropic hypogonadism, growth retardation, hypog
48 lassic GnRH deficiency, men with adult-onset hypogonadotropic hypogonadism had larger mean (+/-SD) te
49 rism, with anterior pituitary hypoplasia and hypogonadotropic hypogonadism, has been reported in pati
50 nked, adrenal hypoplasia congenita (AHC) and hypogonadotropic hypogonadism (HH).
51 inked adrenal hypoplasia congenita (AHC) and hypogonadotropic hypogonadism (HH).
52                                              Hypogonadotropic hypogonadism (HHG) has been identified
53 erogeneous disorder consisting of idiopathic hypogonadotropic hypogonadism (IHH) and anosmia, and is
54 iss1-/-) replicate the phenotype of isolated hypogonadotropic hypogonadism (IHH) associated with vari
55                                   Idiopathic hypogonadotropic hypogonadism (IHH) due to defects of go
56                                   Idiopathic hypogonadotropic hypogonadism (IHH) is a condition chara
57                                     Isolated hypogonadotropic hypogonadism (IHH) is a rare disease wi
58                                     Isolated hypogonadotropic hypogonadism (IHH) is caused by defecti
59                                   Idiopathic hypogonadotropic hypogonadism (IHH) with anosmia (Kallma
60 erase 1 (HS6ST1) in families with idiopathic hypogonadotropic hypogonadism (IHH).
61 sequence of genes associated with idiopathic hypogonadotropic hypogonadism in 55 women with hypothala
62 r gene, cause autosomal recessive idiopathic hypogonadotropic hypogonadism in humans and mice, sugges
63 nction mutations in the FSHB/Fshb gene cause hypogonadotropic hypogonadism in humans and mice.
64 n, and mutations or deletions of GPR54 cause hypogonadotropic hypogonadism in humans and mice.
65 uggest a basis for adrenal insufficiency and hypogonadotropic hypogonadism in males affected by adren
66               The recognition of adult-onset hypogonadotropic hypogonadism in men as a distinct disor
67 compelling explanation for the occurrence of hypogonadotropic hypogonadism in patients with inactivat
68  hormonal therapy to assess reversibility of hypogonadotropic hypogonadism is reasonable.
69 uman presents either as normosmic idiopathic hypogonadotropic hypogonadism (nIHH) or with anosmia [Ka
70 rtion of 4H (Hypomyelination, Hypodontia and Hypogonadotropic Hypogonadism) or RNA polymerase III (PO
71        The Gpr54-deficient mice had isolated hypogonadotropic hypogonadism (small testes in male mice
72 e describe an adult-onset form of idiopathic hypogonadotropic hypogonadism that develops after pubert
73 1 knockout mice are a novel genetic model of hypogonadotropic hypogonadism that establishes essential
74 ifferences of sex development and congenital hypogonadotropic hypogonadism, the European Union has fu
75  on a cohort of 341 probands with congenital hypogonadotropic hypogonadism to identify ultrarare vari
76 ce suffering from adult onset of obesity and hypogonadotropic hypogonadism to study effects of gonado
77 54, and an unrelated proband with idiopathic hypogonadotropic hypogonadism was determined to have two
78                                   Idiopathic hypogonadotropic hypogonadism was previously thought to
79 nked adrenal hypoplasia congenita (AHC) with hypogonadotropic hypogonadism was recently shown to be c
80 scribe 15 men in whom reversal of idiopathic hypogonadotropic hypogonadism was sustained after discon
81  who lacked pubertal development (idiopathic hypogonadotropic hypogonadism) was examined for mutation
82                                   Idiopathic hypogonadotropic hypogonadism, which may be associated w
83 n the GNRHR and GPR54 genes cause idiopathic hypogonadotropic hypogonadism with normal olfaction (nIH
84 ompared with six patients who had idiopathic hypogonadotropic hypogonadism without GPR54 mutations.