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1 nction, delayed puberty and hypogonadotropic hypogonadism).
2 f the hypothalamic-pituitary unit (secondary hypogonadism).
3 ads to a strong meiotic phenotype and severe hypogonadism.
4 tigate the pathogenesis of hypogonadotrophic hypogonadism.
5 unctions absent in patients with hypogonadal hypogonadism.
6 um criteria necessary to identify late-onset hypogonadism.
7 exhibit subfertility due to hypogonadotropic hypogonadism.
8 g recognized in males and is associated with hypogonadism.
9 erlapping features of impaired olfaction and hypogonadism.
10 he rare adult-onset form of hypogonadotropic hypogonadism.
11 ransplant recipients should be evaluated for hypogonadism.
12  and delayed puberty due to hypogonadotropic hypogonadism.
13 germ cells to progress through meiosis I and hypogonadism.
14 ced effect on the prostate in a rat model of hypogonadism.
15 the hypothalamus as well as hypogonadotropic hypogonadism.
16 SHR) null mice have bone loss despite severe hypogonadism.
17 ivation therapy (ADT), resulting in profound hypogonadism.
18 loss of sense of smell and hypogonadotrophic hypogonadism.
19 y adrenal insufficiency and hypogonadotropic hypogonadism.
20 hormone replacement therapy as indicated for hypogonadism.
21 lative effect of estrogen status compared to hypogonadism.
22 d primary hypogonadism and two had secondary hypogonadism.
23 sk of prostate cancer in men with late-onset hypogonadism.
24  beta gene, which causes Q54 to be R, causes hypogonadism.
25 roduce less testosterone, leading to primary hypogonadism.
26 e intervention in older men with obesity and hypogonadism.
27 upted vaginal cycling, and hypergonadotropic hypogonadism.
28 myelination, hypodontia and hypogonadotropic hypogonadism.
29 oidism, hypoadrenalism, and hypogonadotropic hypogonadism.
30 me a promising prospect for treating primary hypogonadism.
31 ed body mass, reduced physical activity, and hypogonadism.
32 d if dysfunctional leads to Hypogonadotropic Hypogonadism.
33 y, intellectual disability, polydactyly, and hypogonadism.
34 ase, although it is often in part related to hypogonadism.
35 ann syndrome and idiopathic hypogonadotropic hypogonadism.
36 oportionate short stature, microcephaly, and hypogonadism.
37 ypothalamic amenorrhea, and hypogonadotropic hypogonadism.
38 rrhea, hypothyroidism, and hypergonadotropic hypogonadism.
39 a, uterine hypoplasia, and hypergonadotropic hypogonadism.
40  health in relation to testosterone and male hypogonadism.
41 aracterized by anosmia and hypogonadotrophic hypogonadism.
42 ctions, such as potency and libido, to avoid hypogonadism.
43 cts of the medications as opposed to chronic hypogonadism.
44 sk of prostate cancer in men with late-onset hypogonadism.
45 and pubertal failure due to hypogonadotropic hypogonadism.
46  range and reported no increased symptoms of hypogonadism.
47 g ADT and in elderly men with age-associated hypogonadism.
48 steoporosis caused by chronic opioid-induced hypogonadism.
49 hs, that underlies typical hypogonadotrophic hypogonadism.
50 rophin deficiency known as hypogonadotrophic hypogonadism.
51 unction of the reproductive axis and causing hypogonadism.(1-4) Thirteen-lined ground squirrels (Icti
52 sterone deficiency (30%-50%) and symptomatic hypogonadism (15%) in men with HF is significant.
53 bnormal reproductive hormones: 4 had primary hypogonadism, 2 had secondary hypogonadism, and 1 develo
54 D] body mass index, 33.5 [7.3]), 116 men had hypogonadism, 427 had eugonadism, and 180 were receiving
55 ta suggest that in aging men with late-onset hypogonadism, 6 months of TRT normalizes serum androgen
56 enes involved in idiopathic hypogonadotropic hypogonadism, a congenital form of GnRH deficiency, are
57  of GPR54 causes idiopathic hypogonadotropic hypogonadism, a disorder characterized by delayed pubert
58               In congenital hypogonadotropic hypogonadism, a lack of gonadotropin activity results pr
59  hormonal changes were simulated by inducing hypogonadism, adding back estradiol (E2) and progesteron
60 nsipidus, growth hormone deficiency, primary hypogonadism, adrenal insufficiency, and hypothyroidism.
61           Reduced serum testosterone (T), or hypogonadism, affects millions of men and is associated
62 infertility accompanied by hypergonadotropic hypogonadism after 30 weeks of age.
63 mong 50 men with idiopathic hypogonadotropic hypogonadism after a mean (+/-SD) duration of treatment
64 y hyperphagia, obesity and hypogonadotrophic hypogonadism, all highly suggestive of hypothalamic dysf
65 der that is associated with hypogonadotropic hypogonadism also.
66                               In conclusion, hypogonadism, although common among men older than 54 ye
67                                              Hypogonadism, an acquired endocrine deficiency state cha
68 adotropes is delayed, resulting in transient hypogonadism and a delay in the onset of puberty.
69            In middle-aged and older men with hypogonadism and anemia, TRT was more efficacious than p
70  include Kallmann syndrome (hypogonadotropic hypogonadism and anosmia), stereotyped midface hypoplasi
71 drome, a condition characterized by obesity, hypogonadism and behavioral abnormalities, the expressio
72            POF presents as hypergonadotropic hypogonadism and can be part of a syndrome or occur in i
73 e disease characterized by hypogonadotrophic hypogonadism and cardiomyopathy.
74      Although the bidirectional link between hypogonadism and cardiovascular disease has been clarifi
75 mild of form of FA-like phenotypes including hypogonadism and cellular sensitivity to the crosslinker
76  reminiscent of isolated LH-hypogonadotropic hypogonadism and corpus luteum insufficiency in humans.
77 pectrum of endocrine abnormalities including hypogonadism and feminization, with elevated serum estra
78 ncy results in stunted growth, skin lesions, hypogonadism and frequent infections in humans.
79 , as well as severe germline defects such as hypogonadism and germ cell depletion.
80  for fat-free mass, partial hypogonadotropic hypogonadism and growth failure.
81 al bilateral anophthalmia, hypogonadotrophic hypogonadism and growth hormone deficiency.
82 ascular disease and who reported symptoms of hypogonadism and had two fasting testosterone levels of
83  formation leading to high bone mass despite hypogonadism and hypercortisolism.
84 ent approaches that should be considered for hypogonadism and hypoadrenalism.
85 ic disease characterized by hypogonadotropic hypogonadism and impaired sense of smell.
86 ic hypogonadism (IHH) is a rare disease with hypogonadism and infertility caused by the defects in em
87 is in GnRH neurons leads to hypogonadotropic hypogonadism and infertility in mice.
88 treatment of CFRD, CFBD, growth and puberty, hypogonadism and infertility, iatrogenic adrenal insuffi
89 set of puberty and leads to hypogonadotropic hypogonadism and infertility.
90 ice lacking miR-7a2 develop hypogonadotropic hypogonadism and infertility.
91 ecocious germline differentiation leading to hypogonadism and infertility.
92 iss1r (Kiss1r(d/d)) display hypogonadotropic hypogonadism and infertility.
93 cross-sectional study examines prevalence of hypogonadism and its correlation with QoL and sexual dys
94 luding causes of idiopathic hypogonadotropic hypogonadism and Kallmann syndrome.
95                                         Both hypogonadism and low estrogen levels adversely affect bo
96                       MSG treatments induced hypogonadism and obesity, retain-->and markedly reduced
97 ess, and the use of testosterone in men with hypogonadism and obesity.
98 characterized by idiopathic hypogonadotropic hypogonadism and olfactory dysfunction.
99 astatic prostate cancer are at risk for both hypogonadism and osteoporosis.
100  in an individual with hyperphagia, obesity, hypogonadism and other features associated with PWS, whi
101                                  In men with hypogonadism and preexisting or a high risk of cardiovas
102  metabolic syndrome, cardiovascular disease, hypogonadism and psychosocial issues, and might yield gr
103             Treatment with GnRH reversed the hypogonadism and restored fertility in each of the five
104 ssive loss of male fertility, accompanied by hypogonadism and seminal vesicle agenesis/hypodysplasia.
105 DNF) involved in congenital hypogonadotropic hypogonadism and several types of cancer.
106 y syndrome associated with hypergonadotropic hypogonadism and short stature.
107 ith CSF measures of androsterone during both hypogonadism and testosterone replacement (r = -0.76 and
108 sal of normosmic idiopathic hypogonadotropic hypogonadism and the Kallmann syndrome was noted after d
109 ression models to examine the association of hypogonadism and time to depression diagnosis, adjusting
110 e of hypogonadism pre-PTX: three had primary hypogonadism and two had secondary hypogonadism.
111  4 had primary hypogonadism, 2 had secondary hypogonadism, and 1 developed hyperestrogenemia with ele
112 rain anomalies, heart defects, macrocephaly, hypogonadism, and additional features with variable expr
113 g resolution of type 2 diabetes mellitus and hypogonadism, and beneficial effects on ingestive and no
114  published studies relating to testosterone, hypogonadism, and HF and provide practical clinical info
115 e molecular mechanisms of vascular injury in hypogonadism, and identify hypospadias as a cardiovascul
116  which includes hyperphagia, severe obesity, hypogonadism, and impaired immunity, has provided insigh
117 y, congenital malformations of the skeleton, hypogonadism, and increased risk of leukemia.
118 gies, including hyperphagia-induced obesity, hypogonadism, and learning and memory deficits.
119  phenotypes are hyperphagic obesity, central hypogonadism, and low growth hormone (GH).
120 ignificantly more growth hormone deficiency, hypogonadism, and neuropathy than controls.
121 one parameters, menstrual cycle, symptoms of hypogonadism, and offspring were evaluated.
122 /134; 9.0%]) and mostly included withdrawal, hypogonadism, and overdose.
123 oxicity, neurotoxicity, decreased fertility, hypogonadism, and psychosocial problems.
124 ally reduced mating frequency and fertility, hypogonadism, and reduced serum testosterone.
125 tional risk factors such as low body weight, hypogonadism, and smoking, as well as direct effects of
126 te, testicular, or male breast cancer; known hypogonadism; and HIV.
127 diovascular disease; one or more symptoms of hypogonadism; and two morning testosterone concentration
128                             Both obesity and hypogonadism are common in older men which could additiv
129  associated with idiopathic hypogonadotropic hypogonadism are found in women with hypothalamic amenor
130  mutants from patients with hypogonadotropic hypogonadism are frequently misrouted proteins that exer
131                                         Male hypogonadism, arising from a range of etiologies includi
132 g body of evidence suggests the role of male hypogonadism as a possible harbinger for poor clinical o
133 ciency, central diabetes insipidus, and male hypogonadism as new features of PCSK1 insufficiency.
134 ined reversal of idiopathic hypogonadotropic hypogonadism as the presence of normal adult testosteron
135 palatal abnormalities, ventriculomegaly, and hypogonadism as well as additional findings such as bone
136 e randomly assigned 1199 men with primary or hypogonadism-associated osteoporosis who were 50 to 85 y
137 , placebo-controlled trial included men with hypogonadism at 316 US sites enrolled between May 2018 a
138             The syndrome of hypogonadotropic hypogonadism, ataxia, and dementia can be caused by inac
139                   An alternate definition of hypogonadism based only on a mean testosterone level les
140  of 12,779 men who were newly diagnosed with hypogonadism between January 1, 1995, and August 31, 201
141 ted PRL may not only improve infertility and hypogonadism but also have a positive effect on the meta
142                                   Late-onset hypogonadism can be defined by the presence of at least
143 population of middle-aged and older men with hypogonadism, carefully evaluated to exclude those at hi
144 ia of prepubertal onset and hypogonadotropic hypogonadism caused by elevated estrogen levels.
145 (NKB) and its receptor show hypogonadotropic hypogonadism characterised by failure to progress throug
146 ptor, NK3 (NK3R), result in hypogonadotropic hypogonadism, characterized by an absence of pubertal de
147                  Congenital hypogonadotropic hypogonadism (CHH) is a condition characterized by absen
148 s (n = 337) with congenital hypogonadotropic hypogonadism (CHH) showed enrichment of rare variants in
149 ns, resulting in congenital hypogonadotropic hypogonadism (CHH), a heterogeneous disease characterize
150 thus raising the hypothesis that ADT-induced hypogonadism could potentially lead to acute kidney inju
151 eficient in PC1 display hyperphagic obesity, hypogonadism, decreased GH, and hypoinsulinemic diabetes
152 mple, patients exhibit obesity, polydactyly, hypogonadism, developmental delay and skeletal abnormali
153                                   Short-term hypogonadism did not affect VLDL triglyceride (TG) secre
154                    We recently reported that hypogonadism does not affect respiratory muscle performa
155                               In conclusion, hypogonadism does not decrease respiratory or limb muscl
156 nactivation of Kiss1 causes hypogonadotropic hypogonadism, Donato et al., in this issue of the JCI, a
157        However, the cardiovascular impact of hypogonadism during development is unknown.
158 rogeneous and manifests as hypergonadotropic hypogonadism either as part of a syndrome or in isolatio
159 ale fertility are multifactorial and include hypogonadism, erectile dysfunction, sperm abnormalities,
160 dy androgen receptor (AR)-knockout mice with hypogonadism exhibit insulin resistance.
161 ation (GnRHR E(90)K) causes hypogonadotropic hypogonadism (failed puberty associated with low or apul
162 n a patient with ataxia and hypogonadotropic hypogonadism, followed by targeted sequencing of candida
163                                              Hypogonadism, found in about one-third of patients with
164 sm, central hypothyroidism, hypogonadotropic hypogonadism, growth hormone deficiency, or arginine vas
165 la, malignant hyperthermia, hypogonadotropic hypogonadism, growth retardation, hypoglycemia, myopathy
166 eterogeneous, frequently have not adhered to hypogonadism guidelines, and suffer from many intrinsic
167 sufficiency and associated hypogonadotrophic hypogonadism had a measurable response to gonadotropin-r
168     After multivariable adjustment, men with hypogonadism had higher odds than men with eugonadism of
169 iency, men with adult-onset hypogonadotropic hypogonadism had larger mean (+/-SD) testicular volumes
170 or pituitary hypoplasia and hypogonadotropic hypogonadism, has been reported in patients carrying SOX
171 oplasia congenita (AHC) and hypogonadotropic hypogonadism (HH).
172 oplasia congenita (AHC) and hypogonadotropic hypogonadism (HH).
173                             Hypogonadotropic hypogonadism (HHG) has been identified as a component of
174 ilar to patients with AS, including obesity, hypogonadism, hyperinsulinemia, retinal dysfunction and
175 splay growth deficiencies as adolescents and hypogonadism, hyperphagia, and obesity as adults.
176 ormal glucose homeostasis, hypogonadotrophic hypogonadism, hypocortisolism and elevated plasma proins
177 nally observed include acanthosis nigricans, hypogonadism, hypothyroidism, alopecia, short stature an
178 rweight or obesity, bone mineral deficiency, hypogonadism, hypothyroidism, and adrenal insufficiency,
179                      The crude prevalence of hypogonadism (ie, TT < 300 ng/dL) was 48%, and mean TT i
180 er consisting of idiopathic hypogonadotropic hypogonadism (IHH) and anosmia, and is most commonly due
181 e the phenotype of isolated hypogonadotropic hypogonadism (IHH) associated with variants of these gen
182                  Idiopathic hypogonadotropic hypogonadism (IHH) due to defects of gonadotropin-releas
183                  Idiopathic hypogonadotropic hypogonadism (IHH) is a condition characterized by failu
184                    Isolated hypogonadotropic hypogonadism (IHH) is a rare disease with hypogonadism a
185                    Isolated hypogonadotropic hypogonadism (IHH) is caused by defective gonadotropin-r
186                  Idiopathic hypogonadotropic hypogonadism (IHH) with anosmia (Kallmann syndrome; KS)
187 in families with idiopathic hypogonadotropic hypogonadism (IHH).
188  associated with idiopathic hypogonadotropic hypogonadism in 55 women with hypothalamic amenorrhea an
189  and could be used to treat men with primary hypogonadism in a more specific and personalized approac
190 hypogonadal state were simulated by inducing hypogonadism in euthymic women-eight with and eight with
191  short-term estradiol withdrawal and induced hypogonadism in healthy premenopausal women.
192 t to describe the effects on mood of induced hypogonadism in healthy young men, suggest that short-te
193 osomal recessive idiopathic hypogonadotropic hypogonadism in humans and mice, suggesting that this re
194 or deletions of GPR54 cause hypogonadotropic hypogonadism in humans and mice.
195 in the FSHB/Fshb gene cause hypogonadotropic hypogonadism in humans and mice.
196                The prevalence of symptomatic hypogonadism in male patients with cancer exceeds that f
197 r adrenal insufficiency and hypogonadotropic hypogonadism in males affected by adrenal hypoplasia con
198                   Obesity is associated with hypogonadism in males, characterized by low testosterone
199 strophy, deafness, mandibular hypoplasia and hypogonadism in males.
200  recognition of adult-onset hypogonadotropic hypogonadism in men as a distinct disorder expands the s
201 lated testosterone deficiency and late-onset hypogonadism in men remains a controversial concept.
202 short-term treatment of symptoms of clinical hypogonadism in men with symptomatic human immunodeficie
203 l testosterone, free testosterone, SHBG, and hypogonadism in men within the Million Veteran Program (
204 the approach to evaluation and management of hypogonadism in men.
205 , and acute treatment substantially corrects hypogonadism in mice starved for 2 d without affecting b
206 on on proper diagnosis and treatment of male hypogonadism in patients with HF.
207 ation for the occurrence of hypogonadotropic hypogonadism in patients with inactivating mutations in
208                            However, treating hypogonadism in the aging male has resulted in discrepan
209 ce-based criteria for identifying late-onset hypogonadism in the general population on the basis of a
210 tients had hypothyroidism, hypergonadotropic hypogonadism (in men), pulmonary insufficiency, swallowi
211 ry, and swallowing function; muscle atrophy; hypogonadism (in men); retinopathy; vascular and cerebra
212 vere obesity, mild learning difficulties and hypogonadism, in whom diagnostic tests for Prader-Willi
213 f growth-hormone deficiency, hypothyroidism, hypogonadism, infertility, and cataracts.
214  adenomas are prolactinomas, which can cause hypogonadism, infertility, and/or galactorrhea.
215  including kyphosis, uncoordinated movement, hypogonadism, infertility, severe skeletal muscle wastin
216 st neonatal hypotonia, feeding difficulties, hypogonadism, intellectual disability and sleep apnea.
217                                   Late-onset hypogonadism is a clinical condition in the ageing male
218                                         Male hypogonadism is a clinical syndrome that results from fa
219                                              Hypogonadism is a major risk factor.
220                                 Because male hypogonadism is a risk factor for metabolic syndrome and
221                                              Hypogonadism is associated with cardiovascular disease.
222                Although a high prevalence of hypogonadism is associated with opioid use, HIV and tran
223                                         Male hypogonadism is defined as low circulating testosterone
224                    The clinical diagnosis of hypogonadism is made on the basis of signs and symptoms
225  to assess reversibility of hypogonadotropic hypogonadism is reasonable.
226 n healthy young men, suggest that short-term hypogonadism is sufficient to precipitate depressive sym
227                                              Hypogonadism is the most well recognised consequence of
228 cancer, diabetes mellitus, hypogonadotrophic hypogonadism, joint disease, and cardiomyopathy.
229                                              Hypogonadism may arise from testicular disease (primary
230  of hospitalization differs between men with hypogonadism, men with eugonadism, and those receiving t
231 nia, childhood obesity, dysmorphic features, hypogonadism, mental retardation, and behavioral problem
232 oly/syn/brachydactyly, retinal degeneration, hypogonadism, mental retardation, obesity, diabetes, and
233 Testosterone therapy for congenital forms of hypogonadism must be lifelong, whereas testosterone trea
234  = 2), myelodysplastic syndrome (n = 2), and hypogonadism (n = 4).
235        Screening and appropriate therapy for hypogonadism need to be evaluated as a strategy to preve
236 nd whether specific symptoms associated with hypogonadism (nighttime hot flushes and disturbed sleep)
237 her as normosmic idiopathic hypogonadotropic hypogonadism (nIHH) or with anosmia [Kallmann syndrome (
238  for osteoporotic fracture, the influence of hypogonadism on bone mineral density remains unclear, as
239 ngly, we determined prevalence and impact of hypogonadism on health-related quality of life in men wi
240 larly if high index of clinical suspicion of hypogonadism or hypoadrenalism) and evaluation of bone h
241 on (OR, 1.70, 95% CI, 1.19-2.44; AF, 11.5%), hypogonadism (OR, 3.27, 95% CI, 2.35-4.55; AF, 25.1%), g
242 m may arise from testicular disease (primary hypogonadism) or dysfunction of the hypothalamic-pituita
243 myelination, Hypodontia and Hypogonadotropic Hypogonadism) or RNA polymerase III (POLR3)-related leuk
244 , including kyphosis, severe muscle wasting, hypogonadism, osteopenia, emphysema, uncoordinated movem
245 tion in TACR3 for idiopathic hypogonatrophic hypogonadism (p.W275X) is associated with 1.25-year-late
246 erone levels were significantly lower during hypogonadism (P=.002, .04, and .046, respectively), but
247 f opioids rather than chronic opioid-induced hypogonadism play a key role in fracture risk.
248                        Two men had secondary hypogonadism pre-PTX with resolution in one and persiste
249        Five of the ten women had evidence of hypogonadism pre-PTX: three had primary hypogonadism and
250 ogen receptors; and (2) such alcohol-induced hypogonadism precedes changes in hepatic sex hormone hom
251 30 days of alcohol exposure, suggesting that hypogonadism precedes liver feminization.
252 scular calcification, severe muscle wasting, hypogonadism, pulmonary emphysema, distention of intesti
253  levels between testosterone replacement and hypogonadism (r = -0.68; P<.05).
254                              In elderly men, hypogonadism related to aging has little influence on bo
255 ce, a syndrome emerged with delayed puberty, hypogonadism, relative macrocephaly, moderate short stat
256              Controlling for all covariates, hypogonadism remained significantly associated with depr
257 whereas testosterone treatment of late-onset hypogonadism remains a matter of debate because of uncle
258  by retinal dystrophy, polydactyly, obesity, hypogonadism, renal abnormalities, and mental retardatio
259 besity, pigmentary retinopathy, polydactyly, hypogonadism, renal and cardiac abnormalities, and cogni
260 y, hepatic dysfunction, hypothyroidism, male hypogonadism, short stature and mild to moderate develop
261 deficient mice had isolated hypogonadotropic hypogonadism (small testes in male mice and a delay in v
262 ing, is characterized by neonatal hypotonia, hypogonadism, small hands and feet, hyperphagia and obes
263                               Age-associated hypogonadism (testosterone deficit) occurs in 30% of men
264 stablished medical conditions known to cause hypogonadism, testosterone therapy may provide small imp
265         Among middle-aged and older men with hypogonadism, testosterone treatment did not result in a
266                        No cases of secondary hypogonadism that developed or resolved post-PTX were re
267 lt-onset form of idiopathic hypogonadotropic hypogonadism that develops after puberty.
268 re a novel genetic model of hypogonadotropic hypogonadism that establishes essential role(s) of SF1 i
269           When it comes to managing men with hypogonadism, the benefit of testosterone replacement th
270  development and congenital hypogonadotropic hypogonadism, the European Union has funded a number of
271 nverse energy, such as inducing hypothalamic hypogonadism to prevent fertilization.
272  adult onset of obesity and hypogonadotropic hypogonadism to study effects of gonadotropin releasing
273             Among older men with symptomatic hypogonadism, treatment with testosterone gel for 1 year
274 ssors and the development of obesity-induced hypogonadism, underscoring the physiological and patholo
275 -producing cells that could be used to treat hypogonadism via transplantation and reestablishment of
276  unadjusted hazard ratio for depression with hypogonadism was 3.5 (95% confidence interval, 1.3-9.4)
277                Relative to baseline, induced hypogonadism was associated with significantly decreased
278                                              Hypogonadism was defined as a mean testosterone level le
279                                              Hypogonadism was defined as a total testosterone concent
280 ted proband with idiopathic hypogonadotropic hypogonadism was determined to have two separate mutatio
281                The combination of ataxia and hypogonadism was first described more than a century ago
282                  Idiopathic hypogonadotropic hypogonadism was previously thought to require lifelong
283 plasia congenita (AHC) with hypogonadotropic hypogonadism was recently shown to be caused by mutation
284                                  ADT-induced hypogonadism was reported to have the potential to lead
285                            Among those whose hypogonadism was reversed, the mean serum level of endog
286 whom reversal of idiopathic hypogonadotropic hypogonadism was sustained after discontinuation of horm
287                            The prevalence of hypogonadism was unexpectedly high.
288                                              Hypogonadism was untreated in 50% of men and 20% of wome
289            A similar model that adjusted for hypogonadism was used to examine the association of estr
290 tal development (idiopathic hypogonadotropic hypogonadism) was examined for mutations in a candidate
291  treatment in middle-aged and older men with hypogonadism, we examined the risk of clinical fracture
292                                     Men with hypogonadism were more likely than men with eugonadism t
293 P > 0.2), even when alternate definitions of hypogonadism were used.
294                  Idiopathic hypogonadotropic hypogonadism, which may be associated with anosmia (the
295  to testosterone) and symptoms suggestive of hypogonadism who were enrolled in the Testosterone Trial
296                           The association of hypogonadism with bone mineral density was examined with
297 sing hormone (GnRH) that is characterized by hypogonadism with delayed or absent puberty and dysfunct
298 PR54 genes cause idiopathic hypogonadotropic hypogonadism with normal olfaction (nIHH).
299 patients who had idiopathic hypogonadotropic hypogonadism without GPR54 mutations.
300 ed with improved IIEF score in patients with hypogonadism (WMD, 1.61; 95% CI, 0.99-2.23; I2 = 0%), mo

 
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