Results 171 to 180 of about 17,405 (343)
Aplasia cutis congenita in surviving co-twin after propylthiouracil exposure in utero [PDF]
Aim: Aplasia cutis congenita (ACC) has been observed after fetal exposure to the antithyroid drug methimazole (MMI), but not reported after propylthiouracil (PTU), the current antithyroid drug of choice during pregnancy.
Calza, Anne-Marie+3 more
core
Teratogen-Induced, Dietary and Genetic Models of Congenital Diaphragmatic Hernia Share a Common Mechanism of Pathogenesis [PDF]
Robin D. Clugston+6 more
openalex +1 more source
Abstract Objective This study aimed to explore genetic etiologies of conotruncal defects (CTDs) in fetuses by analyzing the results of different genetic tests and to assess pregnancy outcomes of fetuses with CTD in a Chinese prenatal cohort. Methods A total of 146 fetuses that underwent invasive prenatal genetic testing for CTD at the prenatal ...
Min Li+5 more
wiley +1 more source
FIGO guideline on liver disease and pregnancy
Abstract The number of women entering pregnancy with chronic liver disease is rising. Gestational liver disorders affect 3% of the pregnant population. Both can be associated with significant maternal and fetal morbidity and mortality. European guidance has recently been published to inform management.
Melanie Nana+24 more
wiley +1 more source
Gene‐teratogen interaction in insulin‐induced mouse exencephaly
Wendy A. Cole, Daphne G. Trasler
openalex +2 more sources
Genetic Differences in Sensitivity to Alterations of Mandible Structure Caused by the Teratogen 2,3,7,8-Tetrachlorodibenzo-p-Dioxin [PDF]
James M. Keller+3 more
openalex +1 more source
Abstract BACKGROUND The heterogeneous photo‐Fenton process demands stable and efficient materials as catalysts to decompose hydrogen peroxide and generate reactive oxygen species to promote the degradation of organic contaminants in wastewater. In this study, the catalytic activity of an iron mining residue (IMR) was investigated for the heterogeneous ...
Nayara de M Costa‐Serge+4 more
wiley +1 more source
ABSTRACT Background Cleft palate (CP) is a congenital defect characterized by an opening in the palate. Two crossbred paternal half‐sibs with a complex syndrome including CP were identified. Hypothesis/Objectives Characterize disease phenotype and evaluate the genetic cause of the observed syndrome.
Marilena Bolcato+5 more
wiley +1 more source
2-1) SENSITIVE PHASES FOR TERATOGEN-INDUCED DEVELOPMENTAL DEFECTS IN THE BRAIN
Y Kameyama
openalex +2 more sources
En el desarrollo del sistema osteomioarticular desempeñan una función determinante los mecanismos morfogenéticos básicos: inducción, migración, proliferación, diferenciación y apoptosis, los cuales son detectados por la acción de diversos agentes ...
Alexi Domínguez Fabars+4 more
doaj