Results 121 to 130 of about 13,108 (240)

Maternal Fish Intake in the Year Prior to Conception and Birth Defects, National Birth Defects Prevention Study, 1997–2011

Birth Defects Research, Volume 118, Issue 5, May 2026.
ABSTRACT Background Epidemiologic data on the association between maternal fish intake and birth defects are sparse. Our objective was to assess associations between maternal fish intake and 52 different birth defects, most of which have not been assessed previously.
Dorothy Kim Waller, Zeyu Miao, Renata H. Benjamin, Richard Finnell, Nithya Lakshmi Mohan Dass, Eirini Nestoridi, Marcia C. de Oliveira Otto, Julie Peterson, Tunu Ramadhani, Mark A. Canfield, the National Birth Defects Prevention Study   +10 more
wiley   +1 more source

Influence of advanced maternal age (≥35 years) on maternal and neonatal outcomes in vaginally intended breech deliveries at term—A FRABAT study

International Journal of Gynecology &Obstetrics, Volume 173, Issue 2, Page 889-896, May 2026.
Abstract Objective To examine maternal and neonatal outcomes in women aged 35 years and older compared with those under 35 years following planned vaginal breech deliveries. Methods This study encompassed all vaginally intended breech deliveries at the Department of Obstetrics and Perinatal Medicine at Goethe University Hospital in Frankfurt from ...
Bilal Alemi, Tatjana Nobs, Samira Catharina Hoock, Eileen Deuster, Anna Elisabeth Hentrich, Anne Kristina Kämpf, Wiebke Schaarschmidt, Frank Louwen, Lukas Jennewein   +8 more
wiley   +1 more source

Intermembraneous polyhydramnios in a pregnancy with separated membranes

Acta Obstetricia et Gynecologica Scandinavica, 1997
Soren Krue, Kjeld Leisgaard Rasmussen
doaj   +1 more source

Amniotic Band [PDF]

Proceedings of the Royal Society of Medicine, 1935
openaire   +2 more sources

Impact of organic pollutants on phenotype and gene expression in human breast cancer cells

Journal of Applied Toxicology, Volume 46, Issue 5, Page 1487-1505, May 2026.
ABSTRACT Human exposure to industrial chemical compounds is widespread and, although often beneficial, prolonged contact may contribute to disease development, including cancer. While many studies have shown organic pollutants (OP) are cytotoxic, few have explored how long‐term exposure alters cell phenotype.
Camila Confortin, Heloisa Amancio, Jessica Zablocki da Luz, Aliciane de Almeida Roque, Tugstênio Lima de Souza, José Eduardo Vargas, Ciro Alberto de Oliveira Ribeiro, Francisco Filipak Neto   +7 more
wiley   +1 more source

The Fetus as Our Patient: The Confluence of Faith and Science in The Care of the Unborn [PDF]

, 2005
Calhoun, Byron C.
core   +2 more sources

Flow Cytometric Detection of Biomarker Changes in CFDA‐SE‐Labelled Plasma Extracellular Vesicles Using a Rodent Pregnancy Model of Prenatal Diagnostics

Journal of Extracellular Biology, Volume 5, Issue 5, May 2026.
ABSTRACT Circulating extracellular vesicles (EVs) offer a promising source of non‐invasive biomarkers for congenital disease diagnostics but robust assays for their detection are lacking. We used a rodent pregnancy model as a proxy for a prenatal diagnostics assay to test whether we could detect a difference in EV tetraspanin display between pregnant ...
Petra Adamova, Lesley Sloan, Andrew K. Powell, Iain M. Dykes   +3 more
wiley   +1 more source

RNA Modifications: Current Understandings and Future Perspectives

MedComm, Volume 7, Issue 5, May 2026.
Types of RNA modification. We have summarized the currently common types of RNA modifications, including ac4C, m6A, m1A, m5C, m3C, m7G, and ψ, and visually characterized their features through structural formulas. The characteristic structures are marked with a background color different from the background color.
Shiyu Xiao, Tingwen Xiang, Chuan Yang, Xiaohua Wang, Gang Huang, Fei Luo, Zhao Xie, Yueqi Chen   +7 more
wiley   +1 more source

Carrier screening in the reproductive setting—Are there medical implications for the heterozygote?—A guide for clinicians

Pregnancy, Volume 2, Issue 3, May 2026.
Abstract Carrier screening for genetic conditions performed preconception or during pregnancy allows identification of fetal risk for inherited autosomal recessive and X‐linked conditions. The goal is to identify at‐risk patients/couples and offer them reproductive options such as preimplantation genetic diagnosis, prenatal testing, or targeted newborn
Emily B. Rosenfeld, Nicole Kasatkin, Bi Liu Yu, Milen Velinov, Justin S. Brandt, Elena Ashkinadze   +5 more
wiley   +1 more source

Prenatal diagnosis of a skeletal disorder characterized by rhizomelic shortening of limbs caused by compound heterozygous variants in the PKDCC gene: Case report and literature review

Molecular Genetics & Genomic Medicine
Background The protein kinase domain containing cytoplasmic (PKDCC) gene (OMIM#618821) is associated with bone development. Biallelic variants in the PKDCC gene can cause rhizomelic limb shortening with dysmorphic features.
Jing Wang, Huijun Yu, Xiaoying Zhang, Xiuyun Zhou, Ya Tan, Zhi Li, Ying Gu, Li Lin   +7 more
doaj   +1 more source