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1 timum for bone health of adult patients with growth hormone deficiency.
2 hthalmia, hypogonadotrophic hypogonadism and growth hormone deficiency.
3 0.02) standard deviation scores in isolated growth hormone deficiency.
4 uate nutrition, insulin unresponsiveness, or growth hormone deficiency.
5 xperience with growth hormone replacement of growth hormone deficiency.
6 expanded beyond the realm of replacement for growth hormone deficiency.
8 wth hormone for the treatment of adults with growth hormone deficiency and conditions such as Turner'
9 h whole-genome resequencing in patients with growth hormone deficiency and maternally inherited gingi
10 crinology clinic where he was diagnosed with growth hormone deficiency and was started on replacement
11 with adrenocorticotropic hormone deficiency, growth hormone deficiency, and mild ectodermal dysplasia
12 mononeuropathies and mild distal neuropathy, growth hormone deficiency, and mild mental retardation w
13 he regulation of human growth, and show that growth hormone deficiency associated with maternally inh
14 hormone administered to men with adult-onset growth hormone deficiency at a dose adjusted according t
17 ciency syndrome include doubts about whether growth hormone deficiency causes increased morbidity and
19 es associated with the phenotype of isolated growth hormone deficiency, combined pituitary hormone de
20 to valvular aortic stenosis, acromegaly, or growth hormone deficiency, conditions associated with al
21 or older and had an established diagnosis of growth hormone deficiency, either alone or with multiple
23 treatment on fracture risk in patients with growth hormone deficiency from the international Hypopit
26 thyroid function and stimulation testing for growth hormone deficiency (GHD), and adrenocorticotropin
29 mpared with controls, children with isolated growth hormone deficiency had lower Full-Scale IQ (P < 0
30 Growth hormone as therapy for adults with growth hormone deficiency has not been universally accep
32 yroid cancer (HR, 9.2; 95% CI, 6.2 to 13.7), growth hormone deficiency (HR, 5.3; 95% CI, 4.3 to 6.4),
33 se in weight Z: score and the development of growth-hormone deficiency, hypothyroidism, hypogonadism,
34 e treatment are now required to confirm that growth hormone deficiency impacts significantly on brain
36 , the suggestion has emerged that endogenous growth-hormone deficiency might account for any excess m
39 ildren (mean 8.8 years of age) with isolated growth hormone deficiency [peak growth hormone <6.7 micr
40 se progressed, including diabetes insipidus, growth hormone deficiency, primary hypogonadism, adrenal
42 syndrome, coeliac disease, cystic fibrosis, growth hormone deficiency, renal tubular acidosis, and s
43 ocus, in a large family in which an isolated growth hormone deficiency segregates as an autosomal dom
45 cism about the use of growth hormone for the growth hormone deficiency syndrome include doubts about
46 expensive agents for certain aspects of the growth hormone deficiency syndrome, especially cardiovas
47 placement therapy for patients with definite growth hormone deficiency--that is, patients with sympto
48 he majority of mutations that cause isolated growth hormone deficiency type II are the result of aber
49 this prospective cohort study, patients with growth hormone deficiency were analysed from the HypoCCS
51 ive against fracture for adult patients with growth hormone deficiency without previously reported os
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