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1 ttings, especially for HIV-positive women in reproductive age.
2 follicles and defective oocytes at advanced reproductive age.
3 hological problems, particularly in women of reproductive age.
4 osomiasis affects nearly 40 million women of reproductive age.
5 oids) are the most common tumors in women of reproductive age.
6 ontribute to obesity development in women of reproductive age.
7 e articles relevant to both men and women of reproductive age.
8 f T4 bound to TTR (T4-TTR) in Inuit women of reproductive age.
9 utplanted juveniles for 4 months, halfway to reproductive age.
10 ) in connection with cancer treatment during reproductive age.
11 ulation compared with that of other women of reproductive age.
12 workers compared with that for all women of reproductive age.
13 Hypertension occurs in about 8% of women of reproductive age.
14 increasing burden of obesity among women of reproductive age.
15 sion of a large number of cells at a defined reproductive age.
16 increased educational attainment in women of reproductive age.
17 nce of the metabolic syndrome among women of reproductive age.
18 ary 2008 on bariatric surgery among women of reproductive age.
19 d reproductive potential among women of late reproductive age.
20 lower genital tract syndrome among women of reproductive age.
21 e past 10 years, particularly among women of reproductive age.
22 factor in cognitive performance in women of reproductive age.
23 order affecting 6%-10% of all women in their reproductive age.
24 counseling of affected individuals who reach reproductive age.
25 omata are the most common tumors in women of reproductive age.
26 e most common endocrine disorder in women of reproductive age.
27 an incidence rate as high as 70% in women of reproductive age.
28 agnitude) was observed only among females of reproductive age.
29 D among African American and white women of reproductive age.
30 s regarding improved iron status in women of reproductive age.
31 refugees worldwide, 25% of whom are women of reproductive age.
32 disorder that occurs in 4% to 7% of women of reproductive age.
33 r of population vitamin A status in women of reproductive age.
34 ion was examined in 88 asymptomatic women of reproductive age.
35 mental surfaces in females, predominantly of reproductive age.
36 ine disorder affecting up to 10% of women of reproductive age.
37 ory of induced abortion among young women of reproductive age.
38 supported offering CF screening to women of reproductive age.
39 ed to an increasing number of obese women of reproductive age.
40 r Xa inhibitors in a case series of women of reproductive age.
41 percent were male, and 73% of women were of reproductive age.
42 nce was 1.0 case (0.3-2.4) per 1000 women of reproductive age.
43 se substitutions tend to go up with paternal reproductive age.
44 on and overweight and obesity among women of reproductive age.
45 credible interval 1.3-5.5) per 1000 women of reproductive age.
46 wide leading vaginal disorder among women of reproductive age.
47 <5 y old, school-aged children, and women of reproductive age.
48 s a significant number of women during their reproductive ages.
49 respiratory health often deteriorates during reproductive aging.
50 ted women, hepatic fibrosis accelerates with reproductive aging.
51 ory health might deteriorate in women during reproductive aging.
52 d rate of reproduction and an early onset of reproductive aging.
58 from under- to overnutrition) among women of reproductive age (15-49 y) is becoming increasingly comm
62 did a retrospective cohort study of women of reproductive age (15-49 years) who died between March 21
67 he global burden of tuberculosis in women of reproductive age; (2) how pregnancy and the postpartum p
68 concentration >300 mug/L) in HEIRS women of reproductive age (25-44 y).The HEIRS Study was a cross-s
70 ternal mortality rate (1.7 per 1000 women of reproductive age, 95% CI 1.3-2.1 in Ragh vs 0.2, 0.1-0.3
72 ransgender women compared with all adults of reproductive age across the 15 countries was 48.8 (95% C
74 ivities related to HIV infection in women of reproductive age affects the amount of ODA received by p
75 d reducing conditions prevail throughout the reproductive age, after which age-accompanied protein ox
76 elevated iron stores are present in women of reproductive age and are influenced by ethnicity and HFE
77 re the most common pelvic tumors in women of reproductive age and are the primary indication for hyst
80 pausal age was elevated by 34% compared with reproductive age and by 16% compared with menopause (mul
83 is affects approximately 40 million women of reproductive age and has been linked to elevated levels
84 intake in nonpregnant, nonlactating women of reproductive age and in nonbreastfed children 1-3 y old
85 eficiency is most commonly found in women of reproductive age and infants worldwide, but the influenc
86 is a relatively common condition in women of reproductive age and is associated with considerable mor
89 nterventions for schistosomiasis in women of reproductive age and preschool-age children, and the nee
90 Differences were not exclusively related to reproductive age and thus cannot be attributed to sex ho
93 ive aging, including the correlation between reproductive aging and declining oocyte quality and mech
94 pecific signaling events, the progression of reproductive aging and somatic aging is systemically coo
95 ical condition reported by 5-10% of women of reproductive age, and in turn, because up to half of wom
97 relating WHR to BMI for white UK females of reproductive age, and used this function to statisticall
98 es are increasingly targeted toward women of reproductive age, and vaccines to prevent influenza and
102 re than 20,000 children and young persons of reproductive age are exposed to known mutagens in the fo
103 es of female gonadal function in patients of reproductive age are recognized, however, pathological a
106 g., using exposures estimated among women of reproductive age as a proxy for maternal exposures, or e
107 for association with seven traits related to reproductive (age at natural menopause, number of childr
108 sed rates of fibrosis compared with women of reproductive age because they have lost the protective e
109 ase menstrual bleeding intensity in women of reproductive age, but the extent of this effect is unkno
110 beverages are widely consumed among women of reproductive age, but their association with reproductiv
111 Insulin/IGF-1 signaling regulate C. elegans reproductive aging by modulating multiple aspects of the
113 pread development of carcinogenesis at early reproductive ages, compromised spermatogenesis, and feta
115 the modelled rates in subgroups of women of reproductive age defined by their marital status and con
116 In a population of 90 816, 357 women of reproductive age died; 154 deaths were related to compli
121 had higher sputum %neutrophils than nonobese reproductive-aged females (45.4 +/- 24.3% vs 27.5 +/- 17
124 associated with lower sputum %neutrophils in reproductive-aged females warrants further investigation
126 al measures of glucocorticoid metabolites in reproductive-aged females, which peak during heavy workl
129 Approximately 20-35% of European women of reproductive age had sufficient iron stores (SF concentr
130 n humans, it is well known that the parental reproductive age has a strong influence on mutations tra
131 contrast, it is unknown whether the parental reproductive age has an effect on somatic mutation rates
139 the third leading cause of death in women of reproductive age in Kabul, and the leading cause in Ragh
141 , and 25-DCP were higher than among women of reproductive age in the US general population, while con
144 gonadal steroid secretion that occurs during reproductive aging in female, but not male, mammals.
148 C. elegans and humans share many aspects of reproductive aging, including the correlation between re
149 15, 2015, from expanded carrier screening in reproductive-aged individuals without known indication f
150 rs commonly in vulnerable groups of women of reproductive age, infants, and children, less is known a
151 ention of overweight and obesity in women of reproductive age is important to improve perinatal healt
159 eeding, is a common complication in women of reproductive age on direct oral factor Xa inhibitor ther
160 mesh herniorrhaphy, men, especially of young reproductive age or with a solitary testicle, need to be
161 ver, little is known about genes that affect reproductive aging or aging of specific somatic tissues.
164 f maternal deaths among deaths of females of reproductive age (PMDF) for each 5-year age group from 1
165 the most prevalent pelvic tumors in women of reproductive age, pose a major public health problem giv
166 rdial infarction is a rare event in women of reproductive age, pregnancy increases the risk 3- to 4-f
168 se burden caused by malnutrition in women of reproductive age, pregnancy, and children in the first 2
170 protein conjugate vaccines given to women of reproductive age proved to be highly immunogenic and wel
171 omen are limited, and thus, data on women of reproductive age provide useful background information i
172 ndergoes many more cell divisions across the reproductive age range, copy errors taking place in the
174 or its precursor (betacarotene) in women of reproductive age reduced pregnancy-related mortality by
175 ,256) consisted of births to male workers of reproductive age reported to the New York State Heavy Me
177 s. 1.46 and 1.21 transfers per 1000 women of reproductive age, respectively; P<0.001) and more transf
179 success), which was most pronounced at early reproductive ages (RR 2.92 [95% CI 1.18-7.20], p=0.020,
180 ngitudinal analyses of fibrosis rates across reproductive age should be conducted in non-HCV-related
181 d not smoke while pregnant, and all women of reproductive age should be warned that smoking increases
182 d not smoke while pregnant, and all women of reproductive age should be warned that smoking increases
183 diopathic constipation is higher in women of reproductive age than postmenopausal women or men, sugge
184 n in-hospital mortality in women with CHD of reproductive age that did not correlate with increased m
185 (PCOS) is a hormonal disorder of females of reproductive age that impacts their oral and systemic he
187 obin concentration <12 g/dL) Indian women of reproductive age.The Let's be Well Red study was a 90-d,
188 f prospectively collected data from women of reproductive age treated with direct oral factor Xa inhi
189 CV), we assessed fibrosis progression across reproductive age, using validated serum fibrosis markers
191 mated prevalence of hypertension in women of reproductive age was 7.7% (95% confidence interval (CI):
193 eveloping active tuberculosis among women of reproductive age was investigated in Santo Domingo.
195 uestions applicable to both men and women of reproductive age were considered; studies were excluded
197 ided by prevention of obesity among women of reproductive age, which should be viewed as a global pub
198 level, Asia has seen the mCPR among women of reproductive age who are married or in a union grow from
199 dern methods of contraception among women of reproductive age who are married or in a union in the fo
201 Between 2012 and 2017 the number of women of reproductive age who are married or in a union who use m
202 of additional users up to 2017 for women of reproductive age who are married or in a union would sug
207 stpartum women, and 137 nonpregnant women of reproductive age who were hospitalized with 2009 H1N1 in
209 esign to generate a representative sample of reproductive age women from the Central Zone of Tigray,
214 lycystic ovary syndrome (PCOS) affects 5% of reproductive aged women and is the leading cause of anov
217 ough August 11, 2009, for all H1N1-infected, reproductive-age women who were hospitalized or died--no
218 iladelphia County, Pennsylvania, of 203 late-reproductive-age women who were premenopausal at baselin
220 ased follicle-stimulating hormone values for reproductive-age women, and/or treatment with hormone re
221 eiomyomata (UL), the most common neoplasm in reproductive-age women, are classified into distinct gen
222 tional analysis of death certificate data of reproductive-age women, live birth and fetal death recor
236 infection reported to the NNDSS; 2.1 million reproductive-aged women and 56 684 children who had HCV
237 s and Quest laboratory data regarding unique reproductive-aged women and children who were tested for
238 est a recent increase in HCV infection among reproductive-aged women and may inform deliberations reg
239 drugs, but the extent of this epidemic among reproductive-aged women and their children is unknown.
243 The factors that predispose one-tenth of reproductive-aged women to endometriosis are poorly unde
245 suggest that, in Europe, the iron status of reproductive-aged women varies by region and worsens in
246 cation, however, only an estimated 29% of US reproductive-aged women were taking a supplement contain
248 mate numbers and describe characteristics of reproductive-aged women with HCV infection and of their
249 ew-onset depression in 2 populations of late-reproductive-aged women with no Diagnostic and Statistic
250 k-skinned individuals, infants, adolescents, reproductive-aged women, and pregnant and lactating wome
252 eproductive tract, occurring in up to 77% of reproductive-aged women, yet molecular pathogenesis rema
256 perimenopausal age group, meeting Stages of Reproductive Aging Workshop criteria for perimenopause,
257 asingly high rates of obesity among women of reproductive age worldwide and the importance of breastf
258 dren (PSC) (age range: 6-59 mo) and women of reproductive age (WRA) (age range: 15-49 y) and investig
259 dren (PSC) (age range: 6-59 mo) and women of reproductive age (WRA) (age range: 15-49 y) and investig
260 dren (PSC) (age range: 6-59 mo) and women of reproductive age (WRA) (age range: 15-49 y) and to inves
262 dren (PSC) (age range: 6-59 mo) and women of reproductive age (WRA) (age range: 15-49 y).Cross-sectio
263 dren (PSC) (age range: 6-59 mo) and women of reproductive age (WRA) (age range: 15-49 y).Cross-sectio
264 and from 10 surveys for nonpregnant women of reproductive age (WRA) (n = 25,731) from the Biomarkers
265 mia in preschool children (PSC) and women of reproductive age (WRA).The BRINDA database inclusion cri
266 stic x-rays are performed commonly on men of reproductive age, yet little is known about the potentia
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