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1 and that animals deficient in Prok2 would be hypogonadotropic.
2           Adult female GRIC-ERKdko mice were hypogonadotropic and anovulatory.
3 perprolactinemia is the most common cause of hypogonadotropic anovulation and is one of the leading c
4 d luteinizing hormone (LH) clearly separated hypogonadotropic from normal adult males.
5 ns, disruption of the GnRH-1 system leads to hypogonadotropic gonadism and Kallmann syndrome.
6 on mutations in six probands with congenital hypogonadotropic hypogonadism (2%), who displayed additi
7                                   Congenital hypogonadotropic hypogonadism (CHH) is a condition chara
8           Patients (n = 337) with congenital hypogonadotropic hypogonadism (CHH) showed enrichment of
9 ion of GnRH neurons, resulting in congenital hypogonadotropic hypogonadism (CHH), a heterogeneous dis
10 re reported to result in isolated congenital hypogonadotropic hypogonadism (CHH).
11 his recessive mutation (GnRHR E(90)K) causes hypogonadotropic hypogonadism (failed puberty associated
12 nked, adrenal hypoplasia congenita (AHC) and hypogonadotropic hypogonadism (HH).
13 inked adrenal hypoplasia congenita (AHC) and hypogonadotropic hypogonadism (HH).
14                                              Hypogonadotropic hypogonadism (HHG) has been identified
15 erogeneous disorder consisting of idiopathic hypogonadotropic hypogonadism (IHH) and anosmia, and is
16 iss1-/-) replicate the phenotype of isolated hypogonadotropic hypogonadism (IHH) associated with vari
17                                   Idiopathic hypogonadotropic hypogonadism (IHH) due to defects of go
18                                   Idiopathic hypogonadotropic hypogonadism (IHH) is a condition chara
19                                     Isolated hypogonadotropic hypogonadism (IHH) is a rare disease wi
20                                     Isolated hypogonadotropic hypogonadism (IHH) is caused by defecti
21                                   Idiopathic hypogonadotropic hypogonadism (IHH) with anosmia (Kallma
22 erase 1 (HS6ST1) in families with idiopathic hypogonadotropic hypogonadism (IHH).
23 uman presents either as normosmic idiopathic hypogonadotropic hypogonadism (nIHH) or with anosmia [Ka
24        The Gpr54-deficient mice had isolated hypogonadotropic hypogonadism (small testes in male mice
25 d prospectively among 50 men with idiopathic hypogonadotropic hypogonadism after a mean (+/-SD) durat
26 rome AHC, a disorder that is associated with hypogonadotropic hypogonadism also.
27 410K phenotype to include Kallmann syndrome (hypogonadotropic hypogonadism and anosmia), stereotyped
28 Lats1-/- mice are reminiscent of isolated LH-hypogonadotropic hypogonadism and corpus luteum insuffic
29 ate when adjusted for fat-free mass, partial hypogonadotropic hypogonadism and growth failure.
30 e (KS) is a genetic disease characterized by hypogonadotropic hypogonadism and impaired sense of smel
31  microRNA synthesis in GnRH neurons leads to hypogonadotropic hypogonadism and infertility in mice.
32 fic deletion of Kiss1r (Kiss1r(d/d)) display hypogonadotropic hypogonadism and infertility.
33 4 prevents the onset of puberty and leads to hypogonadotropic hypogonadism and infertility.
34 ve function, as mice lacking miR-7a2 develop hypogonadotropic hypogonadism and infertility.
35 ertal timing, including causes of idiopathic hypogonadotropic hypogonadism and Kallmann syndrome.
36 genital disorder characterized by idiopathic hypogonadotropic hypogonadism and olfactory dysfunction.
37 trophic Factor (NDNF) involved in congenital hypogonadotropic hypogonadism and several types of cance
38   Sustained reversal of normosmic idiopathic hypogonadotropic hypogonadism and the Kallmann syndrome
39 variants in genes associated with idiopathic hypogonadotropic hypogonadism are found in women with hy
40 e (GnRH) receptor mutants from patients with hypogonadotropic hypogonadism are frequently misrouted p
41 defined the sustained reversal of idiopathic hypogonadotropic hypogonadism as the presence of normal
42 severe gynecomastia of prepubertal onset and hypogonadotropic hypogonadism caused by elevated estroge
43  in neurokinin B (NKB) and its receptor show hypogonadotropic hypogonadism characterised by failure t
44 lassic GnRH deficiency, men with adult-onset hypogonadotropic hypogonadism had larger mean (+/-SD) te
45 sequence of genes associated with idiopathic hypogonadotropic hypogonadism in 55 women with hypothala
46 r gene, cause autosomal recessive idiopathic hypogonadotropic hypogonadism in humans and mice, sugges
47 nction mutations in the FSHB/Fshb gene cause hypogonadotropic hypogonadism in humans and mice.
48 n, and mutations or deletions of GPR54 cause hypogonadotropic hypogonadism in humans and mice.
49 uggest a basis for adrenal insufficiency and hypogonadotropic hypogonadism in males affected by adren
50               The recognition of adult-onset hypogonadotropic hypogonadism in men as a distinct disor
51 compelling explanation for the occurrence of hypogonadotropic hypogonadism in patients with inactivat
52  hormonal therapy to assess reversibility of hypogonadotropic hypogonadism is reasonable.
53 e describe an adult-onset form of idiopathic hypogonadotropic hypogonadism that develops after pubert
54 1 knockout mice are a novel genetic model of hypogonadotropic hypogonadism that establishes essential
55  on a cohort of 341 probands with congenital hypogonadotropic hypogonadism to identify ultrarare vari
56 ce suffering from adult onset of obesity and hypogonadotropic hypogonadism to study effects of gonado
57 54, and an unrelated proband with idiopathic hypogonadotropic hypogonadism was determined to have two
58                                   Idiopathic hypogonadotropic hypogonadism was previously thought to
59 nked adrenal hypoplasia congenita (AHC) with hypogonadotropic hypogonadism was recently shown to be c
60 scribe 15 men in whom reversal of idiopathic hypogonadotropic hypogonadism was sustained after discon
61 n the GNRHR and GPR54 genes cause idiopathic hypogonadotropic hypogonadism with normal olfaction (nIH
62 ompared with six patients who had idiopathic hypogonadotropic hypogonadism without GPR54 mutations.
63 rtion of 4H (Hypomyelination, Hypodontia and Hypogonadotropic Hypogonadism) or RNA polymerase III (PO
64  who lacked pubertal development (idiopathic hypogonadotropic hypogonadism) was examined for mutation
65  (olfactory dysfunction, delayed puberty and hypogonadotropic hypogonadism).
66 at mutations in genes involved in idiopathic hypogonadotropic hypogonadism, a congenital form of GnRH
67 llular loop (IL2) of GPR54 causes idiopathic hypogonadotropic hypogonadism, a disorder characterized
68                                In congenital hypogonadotropic hypogonadism, a lack of gonadotropin ac
69                              The syndrome of hypogonadotropic hypogonadism, ataxia, and dementia can
70 (NKB) or its receptor, NK3 (NK3R), result in hypogonadotropic hypogonadism, characterized by an absen
71 xpress LepR and inactivation of Kiss1 causes hypogonadotropic hypogonadism, Donato et al., in this is
72 xome sequencing in a patient with ataxia and hypogonadotropic hypogonadism, followed by targeted sequ
73 tral hypoadrenalism, central hypothyroidism, hypogonadotropic hypogonadism, growth hormone deficiency
74 opathy, bifid uvula, malignant hyperthermia, hypogonadotropic hypogonadism, growth retardation, hypog
75 rism, with anterior pituitary hypoplasia and hypogonadotropic hypogonadism, has been reported in pati
76 ifferences of sex development and congenital hypogonadotropic hypogonadism, the European Union has fu
77                                   Idiopathic hypogonadotropic hypogonadism, which may be associated w
78 elayed puberty, hypothalamic amenorrhea, and hypogonadotropic hypogonadism.
79 rized by anosmia and pubertal failure due to hypogonadotropic hypogonadism.
80 ithin the cell and if dysfunctional leads to Hypogonadotropic Hypogonadism.
81 ency, including the rare adult-onset form of hypogonadotropic hypogonadism.
82  immune function, and delayed puberty due to hypogonadotropic hypogonadism.
83 on population in the hypothalamus as well as hypogonadotropic hypogonadism.
84 lls are known to exhibit subfertility due to hypogonadotropic hypogonadism.
85 r characterized by adrenal insufficiency and hypogonadotropic hypogonadism.
86  features of hypomyelination, hypodontia and hypogonadotropic hypogonadism.
87 ism, hypoparathyroidism, hypoadrenalism, and hypogonadotropic hypogonadism.
88 hase (NOS1) activity underlies some forms of hypogonadotropic hypogonadism.
89 ons include Kallmann syndrome and idiopathic hypogonadotropic hypogonadism.