Search results for "Neonatal diseases"

showing 5 items of 345 documents

Prenatal air pollution exposure and growth and cardio-metabolic risk in preschoolers

2020

Objectives: We investigated the association between outdoor air pollutants exposure in the first trimester of pregnancy, and growth and cardio-metabolic risk at four years of age, and evaluated the mediating role of birth weight. Methods: We included mother-child pairs (N = 1,724) from the Spanish INMA birth cohort established in 2003-2008. First trimester of pregnancy nitrogen dioxide (NO2) and fine particles (PM2.5) exposure levels were estimated. Height, weight, waist circumference, blood pressure, and lipids were measured at four years of age. Body mass index (BMI) trajectories from birth to four years were identified. Results: Increased PM2.5 exposure in the first trimester of pregnanc…

obesity010504 meteorology & atmospheric sciencesair pollutionprenatal exposureuse regression-models010501 environmental sciencesMalalties neonatals01 natural sciencesPregnancyInterquartile rangePrenatal exposureChildhood obesityChildlcsh:Environmental sciencesGeneral Environmental Sciencelcsh:GE1-3502. Zero hungerAir Pollutants*Childhood obesityObstetrics*Prenatal exposureChildhood growthhealthtraffic pollutionfetalPollutionMaternal ExposureChild PreschoolContaminaciómaternal smokingFemaleNeonatal diseaseschildhood obesitypregnant-womenmedicine.medical_specialtyWaistBirth weightNitrogen DioxideAir pollutioncomplex mixturesChildhood obesity*Air pollutionchildhood growthearly-childhoodmedicineHumansmediation analysis0105 earth and related environmental sciencesparticulate matterFetusPregnancybusiness.industrymedicine.disease*Particulate matterObesity*Childhood growthbusinessParticulate matterBody mass index
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Testing for Lynch Syndrome in Endometrial Carcinoma: From Universal to Age-Selective MLH1 Methylation Analysis

2022

Simple Summary International guidelines recommend universal screening of endometrial carcinoma patients for Lynch syndrome, a hereditary cancer predisposition syndrome. Screening is based on mismatch repair protein immunohistochemistry and reflex MLH1 methylation analysis to exclude the likely sporadic cases of MMR deficiency. As sporadic MLH1 protein loss is common in endometrial carcinoma, the ability to target methylation testing would save efforts and costs. We discovered that limiting methylation testing to patients under 65 years would have significantly reduced the testing effort while maintaining a low false negative rate for MLH1-LS detection (0% and 3% in our clinic and registry-b…

perinnölliset tauditcongenital hereditary and neonatal diseases and abnormalitiesCancer Researchseulontatutkimusendometrial carcinoma; Lynch syndrome screening; MLH1 immunohistochemistry; <i>MLH1</i> methylation analysisMICROSATELLITE INSTABILITYMUTATIONS3122 Cancersikäryhmätnutritional and metabolic diseasesendometrial carcinomaCANCERdigestive system diseasesREGIONDNA-metylaatioMLH1 methylation analysiskohdunrungon syöpäOncologyLynch syndrome screeningMLH1 immunohistochemistryLynchin oireyhtymäCancers
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Race in Young Adult Speculative Fiction by Gilbert-Hickey and Gren-Barteet - books in review

2022

Race in Young Adult Speculative Fiction by Gilbert-Hickey and Gren-Barteet - books in review

stomatognathic diseasescongenital hereditary and neonatal diseases and abnormalitiesCiència-ficciónutritional and metabolic diseaseseye diseaseshumanities
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Oral manifestations of Cowden?s disease : presentation of a clinical case

2006

Cowden?s disease, or multiple hamartoma syndrome, is an autosomal dominant genodermatosis, characterized by the presence of multiple cutaneous hamartomas, oral fibromas and benign acral keratosis. It affects multiple organs (breast, thyroids, stomach, colon), with the strong possibility of malignant neoplasia developing in these organs. We present a case of this rare syndrome, highlighting the presentation of some clinical characteristics that, in suspected cases, can help to establish an early diagnosis of this disease, this being of great importance given the high frequency of tumors in people with this clinical picture.

stomatognathic diseasescongenital hereditary and neonatal diseases and abnormalitiesUNESCO::CIENCIAS MÉDICAS:CIENCIAS MÉDICAS [UNESCO]
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Interaction of the n-terminal domain of human t1r2 taste receptor with brazzein, a sweet-tasting protein

2015

Brazzein is a small (6.5 kDa) sweet-tasting protein originating from the fruit of Pentadiplandra brazzeana, a plant found in West Africa. Brazzein like all classes of sweet compounds is perceived through the activation of the T1R2/T1R3 heterodimeric sweet-taste receptor. T1R2 and T1R3 subunits are members of the small family of class C G-protein coupled receptors (GPCRs). Class C GPCRs possess a large N-terminal domain (NTD) linked to seven transmembrane domain by a cysteine rich domain (CRD). The NTD of T1R2 (T1R2-NTD) has been shown to contain the primary binding site for most of the sweet ligands. However, brazzein has been shown to require CRD of human T1R3 for receptor activation [1]. …

taste[SDV.AEN] Life Sciences [q-bio]/Food and Nutritioncongenital hereditary and neonatal diseases and abnormalities[ SDV.AEN ] Life Sciences [q-bio]/Food and Nutritionreceptor[SDV.IDA]Life Sciences [q-bio]/Food engineering[ SDV.IDA ] Life Sciences [q-bio]/Food engineering[SDV.IDA] Life Sciences [q-bio]/Food engineering[SDV.AEN]Life Sciences [q-bio]/Food and Nutritionsweet tasting protein
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