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1 ations in maternal serum (1669 +/- 568 nM in late pregnancy).
2 entrations in maternal serum (1669 568 nM in late pregnancy).
3 for increased cervical distensibility during late pregnancy.
4 teine concentration that otherwise occurs in late pregnancy.
5 ws the substantial demand for choline during late pregnancy.
6 n in women who develop COVID-19 pneumonia in late pregnancy.
7 etal proteins in the maternal bloodstream in late pregnancy.
8 fetal growth acceleration or deceleration in late pregnancy.
9  increased overall NF-kappaB activity during late pregnancy.
10  is associated with exposure to SSRIs during late pregnancy.
11 ng concentrations of 25(OH)-vitamin D during late pregnancy.
12 id not correlate with insulin sensitivity in late pregnancy.
13  as a result of impaired mammogenesis during late pregnancy.
14 rapy with either raltegravir or efavirenz in late pregnancy.
15 pregnancy and regulate the onset of labor in late pregnancy.
16 dual RMRs increased from 456 to 3389 kJ/d by late pregnancy.
17 the four-compartment model in both early and late pregnancy.
18 response to the stress of chronic hypoxia in late pregnancy.
19 sin-1 underwent unscheduled apoptosis during late pregnancy.
20 ut transcripts decreased dramatically during late pregnancy.
21  on the nondominant wrist in early, mid, and late pregnancy.
22 malization of maternal adiponectin levels in late pregnancy.
23  exposed to higher UFP concentrations during late pregnancy.
24 roximal triggers of labor onset generated in late pregnancy.
25 , early to late pregnancy, and conception to late pregnancy.
26  and not early pregnancy, and both early and late pregnancy.
27 on of the feto-placental microvasculature in late pregnancy.
28 a cohort of 20 individuals vaccinated during late pregnancy.
29 o the establishment of insulin resistance in late pregnancy.
30 oxyvitamin D [25(OH)D] measured in early and late pregnancy.
31 kisspeptin excites oxytocin neurones only in late pregnancy.
32        Maternal infection with SARS-CoV-2 in late pregnancy.
33 etabolites were measured at early, mid-, and late pregnancy.
34 ymptoms during interviews in early, mid, and late pregnancy.
35 d by murine gestational and fetal tissues in late pregnancy.
36 eveloped markers of vitamin B6 deficiency in late pregnancy.
37 cifically activated T-cells increased during late pregnancy.
38 of fatty acids (FA) and accumulate lipids in late pregnancy.
39 l T-cell changes were most pronounced during late pregnancy.
40 -D (25(OH)D) level was measured in early and late pregnancy.
41 entrations increasing from early to mid- and late pregnancy.
42 ncy, but this adaptation was insufficient in late pregnancy.
43  was quantified serially in early, mid-, and late pregnancy.
44 ed distribution of the higher percentiles in late pregnancy.
45 ed glucose intolerance and hyperlipidemia in late pregnancy.
46 ine exposure is substantially lowered during late pregnancy.
47 mg once daily in HIV-1-infected women during late pregnancy.
48  of neutrophils in the blood of women during late pregnancy.
49 rses the metabolic changes seen in hearts in late pregnancy.
50  was used to reconstitute adiponectin during late pregnancy.
51 rnal FM across a spectrum of body weights in late pregnancy.
52 l resource allocation to fetal growth during late pregnancy.
53 nal exposure to influenza circulation during late pregnancy.
54 entration in the maternal circulation during late pregnancy.
55 vere fetal sequelae observed in early versus late pregnancy.
56 n with pregestational type 2 diabetes during late pregnancy.
57 egnancy (P < 0.001), but was restored during late pregnancy.
58 PHN associated with maternal use of SSRIs in late pregnancy.
59 women had 25(OH)D measured in both early and late pregnancy.
60                                           In late pregnancy, 11,272 were exposed to buprenorphine and
61 gnancy (early pregnancy, 94.7+/-15.9 mg/min; late pregnancy, 122.7+/-9.3 mg/min; P = 0.003).
62         LV strain decreased significantly in late pregnancy (-19.5+/-2% to -17.6+/-1.6%, P<0.001) and
63 ancy (6-17 wk gestation) and 16 women during late pregnancy (21-37 wk gestation).
64 ight gain, increased skinfold thicknesses in late pregnancy (28 wk) and early postpartum (4-6 wk), an
65  white), and 1,275 exposed in both early and late pregnancy (29 years; 75% white).
66 sistance in nine obese women with GDM during late pregnancy (30-36 weeks) and 1 year postpartum.
67  markedly lower in Asians than Caucasians in late pregnancy (31 +/- 6 vs. 49 +/- 3 bursts min(-1) at
68  isotope dilution in early (13-16 weeks) and late pregnancy (35-37 weeks).
69 s had a higher rate of smoking abstinence in late pregnancy (456 individuals [50.8%] vs 67 individual
70  ultra-performance LC tandem MS at early and late pregnancy, 6 mo postpartum, and in cord blood.
71 ce supporting the inadequacy of oral iron in late pregnancy, a critical period of iron need for norma
72 ased rates of bone calcium deposition during late pregnancy, a finding that was particularly evident
73 luate whether this panel can be also used in late pregnancy, a retrospective cohort study was conduct
74                                           In late pregnancy, activity of the allopregnanolone-synthes
75 56%) of 545 assigned to usual care smoked at late pregnancy (adjusted odds ratio [AOR] 0.90, 97.5% CI
76 efined as development of hypertension during late pregnancy affecting other organ systems (proteinuri
77                                           In late pregnancy, although there was an overall increase i
78 ctivity increased by approximately 2-fold in late pregnancy and after estrogen treatment.
79 tance) is a hallmark of normal physiology in late pregnancy and also underlies gestational diabetes m
80 ns between exposure to certain phthalates in late pregnancy and behavioral problems in boys.
81                               For periods in late pregnancy and childhood, we estimated spatially and
82 es, in urine samples from early, middle, and late pregnancy and created a subject-specific average to
83 , and estimated fetal weight from middle and late pregnancy and delivery measures were converted to s
84 ancer contributes to gene expression only in late pregnancy and early lactation, possibly by interact
85 ssessed 88 first-time gestational mothers in late pregnancy and early postpartum and 30 nulliparous c
86  the tracking of serum 25(OH)D from early to late pregnancy and factors that influence this.
87 zation of XOR in the non-secretory states of late pregnancy and induced involution compared with the
88 d maternal serum bile acid levels, occurs in late pregnancy and is often associated with poor perinat
89      Remarkably, defects are reverted during late pregnancy and lactation but return upon involution
90 y pregnancy with impaired development during late pregnancy and lactation followed by delayed postlac
91 cifically in mammary epithelial cells during late pregnancy and lactation resulted in efficient delet
92 ted protein 5 (Lrp5) that are induced during late pregnancy and lactation via use of the whey acidic
93 paraventricular nucleus are activated during late pregnancy and lactation, as measured by an increase
94 ammary gland, with maximum expression during late pregnancy and lactation.
95 ssion is significantly down-regulated during late pregnancy and lactation.
96 ssed microRNA declined precipitously between late pregnancy and lactation.
97 acid and glucose kinetics are altered during late pregnancy and might suggest a mechanism for higher
98 inol and beta-carotene concentrations during late pregnancy and offspring bone mineralization assesse
99 n the ST(dl), DA turnover was highest during late pregnancy and on the day of parturition, while no c
100 ry in gray matter (GM) volume, which dips in late pregnancy and partially recovers during postpartum.
101 structural and functional differentiation at late pregnancy and parturition to produce and secrete mi
102  status from preconception through early and late pregnancy and postpartum have been inferred from cr
103 mes, the hypercoaguable state that occurs in late pregnancy and postpartum, and the progressively dec
104 g was obtained in healthy women at early and late pregnancy and postwean.
105 ciation between the maternal use of SSRIs in late pregnancy and PPHN in the offspring; further study
106 conclusion, PBDEs may impair fetal growth in late pregnancy and reduce birth size.
107 n from the intestine to the mammary gland in late pregnancy and shared TCR clonotypes between intesti
108 onsumption of gluten-containing foods during late pregnancy and subsequent risk of celiac disease in
109 d exposure to ultraviolet B radiation during late pregnancy and the maternal use of vitamin D supplem
110      Expression of all four Cxs peaks during late pregnancy and throughout lactation suggesting essen
111  (HPA) axis is known to be attenuated during late pregnancy and throughout lactation.
112 protein-3 (IGFBP-3) to mammary tissue during late pregnancy and throughout lactation.
113 ows: conception to early pregnancy, early to late pregnancy, and conception to late pregnancy.
114 the developing CNS, adult testes, breasts in late pregnancy, and germinal centers of secondary B cell
115 Little is yet known about zinc absorption in late pregnancy, and no information on absorption from th
116  doses are higher in early pregnancy than in late pregnancy, and there can be considerable intersubje
117 l administration of L. salivarius PS2 during late pregnancy appears to be an efficient method to prev
118 sure in early pregnancy and DNOP exposure in late pregnancy are associated with lower nonverbal IQ sc
119  Pharmacokinetic changes for dolutegravir in late pregnancy are not clinically relevant and support t
120 tions of UBF during the follicular phase and late pregnancy are partially mediated by ER-dependent me
121                       Circulating factors in late pregnancy are thought to contribute to both disease
122 tudy measured insulin sensitivity in mice in late pregnancy at day 16 (D16) and near term at D19.
123    CRP concentration decreased from early to late pregnancy (B = -0.06, SE = 0.01, p < 0.001).
124 d self-reported tobacco use by the mother at late pregnancy, birthweight of the baby, the proportion
125          Each 5-unit increase in of maternal late-pregnancy BMI (mean [SD], 27.2 [3.8]) was associate
126 , channel mRNA and total protein increase in late pregnancy, but current density decreases as in rats
127 ep-disordered breathing are common in mid-to-late pregnancy, but most cases go undetected.
128  subjects had low insulin sensitivity during late pregnancy, but neither glucose clamp nor minimal mo
129   Higher maternal systolic blood pressure in late pregnancy, but not in middle pregnancy, was associa
130 d oxidation remained similar between mid and late pregnancy, but there was wide variation between the
131 e and N1-methylnicotinamide were measured in late pregnancy by mass spectrometry (n = 497) and relate
132                SnoN expression is induced at late pregnancy by the coordinated actions of TGF-beta an
133 isspeptin might activate oxytocin neurons in late pregnancy by transiently increasing oxytocin neuron
134 ggests that consumption of a high LA diet in late pregnancy can enhance placental PG production and m
135 vir disoproxil fumarate (TDF) therapy during late pregnancy can reduce mother-to-infant transmission
136 while more limited deficiency during mid- to late pregnancy causes deficits in hippocampal plasticity
137 e PCR and Western blots demonstrate that, in late pregnancy, channel transcript quantities and total
138  >/=30 ng/ml) was observed in both early and late pregnancy compared with insufficient levels (25OHD
139 to oxidative metabolism has been observed in late pregnancy compared with pregravid states.
140 utoreactive T cells from mice induced during late pregnancy compared with virgin controls.
141 eproductive failure linking subfertility and late pregnancy complications and has allowed us to rejec
142                                              Late pregnancy complications include gestational diabete
143 t heparin effectively prevents recurrence of late pregnancy complications, 135 women with previous hi
144 erapies, in particular better prophylaxis of late pregnancy complications, are urgently needed for ob
145 eight heparin in the prevention of recurrent late pregnancy complications.
146 ry outcomes included the live-birth rate and late pregnancy complications.
147             Thus, nadroparin did not prevent late-pregnancy complications in women at risk of recurre
148 Primary outcome was a composite end point of late-pregnancy complications.
149 hydroxyvitamin D2+3 [s-25(OH)D] in early and late pregnancy, cord blood, and at 5 y age, and the asso
150 5; however, development recovered by mid- to late pregnancy (d14.5).
151 r drinking water for 5 day periods in mid to late pregnancy (day, D, 11-16 or D14-19).
152 posed to 30 min immobilisation stress during late pregnancy (days 19-21), early lactation (days 3-4)
153                                       GWG in late pregnancy (defined as 28 weeks onward on the basis
154 autocrine prolactin or activate Stat5 during late pregnancy despite normal levels of circulating seru
155 also observed an inverse association between late pregnancy di-n-octyl phthalate (DNOP) exposure and
156 wth restriction (FGR) by examining early and late pregnancy differences in non-targeted urinary metab
157 ogical stages: virgin, early pregnancy (e7), late pregnancy (e20), lactating (day 4), involuting day
158                                              Late pregnancy elevated C-reactive protein (> or = 12 mi
159 coupled from the circadian clock, whereas in late pregnancy, energy availability is mediated by coord
160 ers with high concentrations of androgens in late pregnancy exhibit higher rates of aggression and mo
161 o early pregnancy exposure and middle and/or late pregnancy exposure for analysis of the association
162 ts and 2) the relative effects of early- and late-pregnancy exposure to tobacco on infant birth weigh
163 remained unchanged when adjusted for mid and late pregnancy exposures.
164                         In Malawian women in late pregnancy, FCM effectively and safely reduced anemi
165                                       During late pregnancy, female mice show no evidence of chronic
166                                           In late pregnancy, fetal weight in the folate deficient gro
167 epartures from trend lines in maternal FM in late pregnancy for any of the methods.
168                           LdT and LAM use in late pregnancy for highly viremic mothers was equally ef
169 telbivudine (LdT) or lamivudine (LAM) use in late pregnancy for preventing hepatitis B mother-to-chil
170 uropean ancestry; 85 [41.3%] primiparous) in late pregnancy from December 19, 2012, through March 17,
171 and inflammatory biomarkers during early and late pregnancy from participants enrolled in the Atlanta
172 om weeks 14-17, and positively associated in late pregnancy, from weeks 31-36.
173                                       During late pregnancy, full-length CDP levels decline, and a 15
174 uring early, gestational days (GD) 2-GD9, or late pregnancy, GD10-GD17.
175 rly pregnancy (through gestational week 19), late pregnancy (gestational week 20 through the day befo
176                                       In the late-pregnancy group, 3-HIA excretion decreased (P < 0.0
177                             Midpregnancy and late pregnancy GWGs were associated with fat-free mass.
178                        Women who smoked into late pregnancy had a much higher risk for schizophrenia
179 e mother was switched from MMF to SRL during late pregnancy had cleft lip and palate and microtia) an
180 parison with NPNL control subjects, women in late pregnancy had higher energy intakes and BMRs.
181 is of cervical hyaluronan (HA) from early to late pregnancy has long been proposed to play an essenti
182                    In conclusion, serum from late pregnancy has the capacity to down-regulate T cell
183                                           In late pregnancy, hearts show eccentric hypertrophy, as ex
184 ffspring of rats exposed to dexamethasone in late pregnancy, hepatic expression of glucocorticoid rec
185 ng perturbed maternal insulin sensitivity in late pregnancy; hepatic insulin sensitivity was higher,
186                                           In late pregnancy, HPA axis responses to stressors, includi
187 cence with the senolytic compound fisetin in late pregnancy improved cardiac function in these animal
188 red using a radioimmunoassay on samples from late pregnancy in 109 women delivering a child who devel
189 ravid, insulin resistance was evident during late pregnancy in all women (12.4 +/- 1.2 vs. 8.1 +/- 0.
190 glucose tolerance and insulin sensitivity in late pregnancy in association with dysregulated lipid an
191 e steroid hormones that play a vital role in late pregnancy in maturing fetal organs, including the h
192 inistration of a synthetic glucocorticoid in late pregnancy in mice downregulates the glucocorticoid
193 prevented by managing glycaemia in early and late pregnancy in some, but not all women with gestation
194 nd composition were observed during early to late pregnancy in the pandemic group, including lower re
195 sma leptin was analyzed in maternal blood in late pregnancy, in cord blood, and at 8, 16, and 52 wk i
196 tions occur in normal fetal membranes during late pregnancy, in preparation for labor.
197 ; inhibition of bone growth following use in late pregnancy, infancy, or childhood up to 8 years of a
198                                           In late pregnancy, inhibition of 5alpha-reductase (an allop
199            Maternal supine sleep position in late pregnancy is associated with an increased risk of s
200                  These results indicate that late pregnancy is associated with decreased ubiquitin-pr
201         Thus, the extreme hyperleptinemia of late pregnancy is attributable to binding of the leptin
202 usual increase in insulin resistance seen in late pregnancy is enhanced in obese mothers, causing mar
203 nd hence the HPA axis, following IL-1beta in late pregnancy is explained by presynaptic inhibition of
204 of gluten-containing food consumption during late pregnancy is not associated with risk of celiac dis
205 g-positive mothers, antiviral therapy during late pregnancy is permitted to prevent Mother-to-child t
206 (95% CI: 10.4, 19.9 mg . kg-1 . d-1); during late pregnancy, it was determined to be 21 mg . kg-1 . d
207                                           In late pregnancy, kisspeptin expression increases in rat p
208 diomyocytes and that elevated PDK4 levels in late pregnancy lead to inhibition of PDH (pyruvate dehyd
209               We hypothesized that IH during late pregnancy (LG-IH) may increase the propensity for m
210 ly pregnancy (EP; weeks 10-12 of gestation), late pregnancy (LP; weeks 34-36 of gestation), and early
211                                           In late pregnancy, many women consuming contemporary Wester
212                                       Higher late pregnancy maternal BMI was also associated with mor
213                                           In late pregnancy maternal hypothalamo-pituitary-adrenal (H
214  neonatal APPs and maternal infection during late pregnancy, maternal anemia, and maternal psychiatri
215                                           In late pregnancy, maternal insulin resistance occurs to su
216                                           In late pregnancy, maternal serum retinol and beta-carotene
217 at antibiotics taken during early life or in late pregnancy may be associated with childhood asthma.
218                    The risk of stillbirth in late pregnancy may be determined by placental function i
219 concentration of ADAMTS13 that occurs during late pregnancy may combine to increase the risk for occu
220 did not significantly differ in terms of the late-pregnancy NT-proBNP levels.
221 ious effect of malaria during both early and late pregnancy on fetal growth.
222 y only (28 years; 67% white), 556 exposed in late pregnancy only (27 years; 60% white), and 1,275 exp
223                      BNT161b2 vaccination in late pregnancy or lactation enhances systemic immunity t
224 y (tenofovir-unexposed) were enrolled during late pregnancy or within 72 hours of birth.
225 R(adj) 2.37, 95% CI [1.99-2.83]), smoking at late pregnancy (OR(adj) 2.04, 95% CI [1.60-2.59]), previ
226 etter improvement of migraine attacks during late pregnancy (OR, 5.10; 95% CI, 2.17-14.00), and faste
227 mation, which is given to pregnant people in late pregnancy, or by using a long-acting monoclonal ant
228 men living in the affected communities whose late pregnancy overlapped with the blowout.
229 ive hormones, and fat mass were increased in late pregnancy (P < 0.001).
230         For women immunized with Tdap during late pregnancy, pertussis-specific immunoglobulin G leve
231  ERG-encoded K(+) channels as a precursor to late pregnancy physiological activity.
232                    The data also explain how late pregnancy poses a threat to cardiac homeostasis, an
233 irected metabolic imprinting once set during late pregnancy prior to the first parturition persistent
234                Maternal social stress during late pregnancy programs hypothalamo-pituitary-adrenal (H
235 ta indicate that the hormonal environment of late pregnancy promotes metabolic remodeling in the hear
236 dels, and early pregnancy, midpregnancy, and late pregnancy rates of GWG (0-17, 17-27, and 27 wk to d
237           Early pregnancy, midpregnancy, and late pregnancy rates of GWG were independently associate
238                  Maternal supine position in late pregnancy reduces maternal cardiac output and uteri
239 d at birth (Guthrie card), age 18, early and late pregnancy respectively, and fathers' DNAm was measu
240 es in HbA1c over the entire pregnancy and in late pregnancy, respectively.
241 - 5 vs. 30 +/- 3 bursts min(-1) in early and late pregnancy, respectively; P = 0.023).
242 ciated with greater smoking cessation during late pregnancy (RR, 1.35 [95% CI, 1.23-1.48]), compared
243  seasonal variation in 25(OH)D for early and late pregnancy separately, and the difference between th
244 ized decrease in miRNAs, such as miR-150, at late pregnancy serves to allow translation of targets cr
245 f wild-type and ERBB4-null mammary glands at late pregnancy showed that ERBB4 expression was required
246 IAAO methods provided similar breakpoints in late pregnancy, showing that the DAAO method was appropr
247                                            A late pregnancy-specific, selective activation of the Liv
248 , with the most associations observed during late pregnancy (T(3)).
249  virus (HIV) infection who took tenofovir in late pregnancy (tenofovir-exposed) or no tenofovir durin
250 f all live births and stillbirths (including late-pregnancy terminations) delivered at >/=20 weeks' g
251 r requirement (40%) for phenylalanine during late pregnancy than during early pregnancy.
252 piratory quotient is significantly higher in late pregnancy than postpartum.
253 r enzymes, and low platelets), a disorder of late pregnancy that involves the liver as one of the tar
254 blood pressure (BP) with end organ damage in late pregnancy that is associated with high circulating
255 found evidence for a serum factor present in late pregnancy that suppresses T cell activation.
256                                    Except in late pregnancy, the doses estimated with realistic voxel
257           We found that during the period of late pregnancy there is protection against paralysis, du
258                                In middle and late pregnancy, there also is a four-fold increase in va
259                                       During late pregnancy, TNF-alpha was inversely correlated with
260 elopment of microbiomes and metabolomes from late pregnancy to 1 year of age using longitudinal multi
261  frequency questionnaire was administered in late pregnancy to 19,160 pregnant participants in the Ji
262 n supraoptic and paraventricular nuclei from late pregnancy to late lactation may reflect the functio
263 is condition when orally administered during late pregnancy to women who had experienced infectious m
264 r conditions of marked insulin resistance in late pregnancy, to predict abnormalities of glucose tole
265 omen failed to upregulate iron absorption in late pregnancy, transferred less iron to their fetus, an
266        According to our estimates, universal late pregnancy ultrasound in nulliparous women (1) would
267 hat, compared to current practice, universal late-pregnancy ultrasound would identify around 14,826 o
268     Serum samples collected during early and late pregnancy underwent untargeted metabolomic profilin
269 n inverse relation of child nonverbal IQ and late pregnancy urinary DAPs, but the estimated associati
270 takes (5.5-30.5 mg . kg-1 . d-1 in early and late pregnancy using DAAO, and 2.5-30.5 mg . kg-1 . d-1
271  using DAAO, and 2.5-30.5 mg . kg-1 . d-1 in late pregnancy using IAAO) for a total of 76 study days.
272 l group, 54.2% of participants developed low late-pregnancy vitamin B6 concentrations (pyridoxal 5-ph
273 as significantly decreased in the HFHS/OP at late pregnancy (vs.
274  between PI use and lower increase in BMI in late pregnancy warrants further study.
275                    Malaria both in early and late pregnancy was associated with a reduction in fetal
276              Higher oily fish consumption in late pregnancy was associated with lower childhood aorti
277             Higher maternal serum retinol in late pregnancy was associated with lower offspring total
278 ration of 25(OH)-vitamin D in mothers during late pregnancy was associated with reduced whole-body (r
279      A questionnaire on the mother's diet in late pregnancy was completed by 3-4.5 mo postpartum.
280  vitamin D insufficiency (<50 nmol/L) during late pregnancy was lower in the intervention group (35.1
281 auterine growth retardation, and exposure in late pregnancy was necessary to the association.
282 r confounders, reported maternal drinking in late pregnancy was negatively associated with childhood
283            Anaemia (haemoglobin <11 g/dL) in late pregnancy was negatively associated with forced vit
284 unlike cigarette use, e-cigarette use during late pregnancy was not statistically significantly assoc
285 y, the change in TNF-alpha from pregravid to late pregnancy was the only significant predictor of the
286  apoptosis when expressed ectopically during late pregnancy, we found that during post-lactational in
287               Moderate and heavy drinkers in late pregnancy were also more likely to have an SGA birt
288 era of patients and comparison subjects from late pregnancy were assayed by enzyme-linked immunosorbe
289  of 30 ng/ml or higher at trial entry and in late pregnancy were associated with a lower risk of pree
290           Blood TCM concentrations in mid to late pregnancy were associated with an increased risk of
291 ternal serum beta-carotene concentrations in late pregnancy were associated with greater total body B
292                       Results of exposure in late pregnancy were consistent with results of exposure
293                         Current densities in late pregnancy were lower than in female controls.
294                 Exposures to PM2.5 and BC in late pregnancy were positively associated with newborn S
295 cluded increasing or peak maternal stress in late pregnancy were related to stronger neonatal amygdal
296 al contractility is drastically increased in late pregnancy when compared to non-pregnant conditions.
297 ncy had a similar smoking abstinence rate in late pregnancy when compared with NRT users (10 users [2
298 ons of riboflavin declined through early and late pregnancy, whereas concentrations of 25-hydroxyvita
299                         SSRI exposure during late pregnancy-whether a causal factor or not-might iden
300 ll and in early pregnancy, midpregnancy, and late pregnancy with neonatal adiposity.

 
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