Results 111 to 120 of about 22,159 (250)

Yield of Whole Genome Sequencing for Pathogenic Single Nucleotide Variants in Congenital Heart Disease: A Systematic Review and Meta‐Analysis

open access: yesPrenatal Diagnosis, Volume 46, Issue 5-6, Page 780-818, May 2026.
ABSTRACT Objective This systematic review and meta‐analysis aimed to assess the diagnostic yield of pathogenic or likely pathogenic (P/LP) single nucleotide variants (SNVs) using whole genome sequencing (WGS) in congenital heart disease (CHD). Methods A systematic search of three databases (2000–2024) was conducted, and two reviewers independently ...
Hiba J. Mustafa   +7 more
wiley   +1 more source

Atresia in the esophagus

open access: yesMedisur, 2005
Esophageal atresia is the congenital lack of continuity of the esophagus with or without communication to the airway. Incidence is estimateed in 1 by 3000 to 4500 alive newborns. Cases in brothers are found and children of parents with atresia esophagus,
Crisanto Abad Celuria   +2 more
doaj   +2 more sources

The EUROmediCAT Network and Databases: A Resource for Pharmacovigilance in Pregnancy

open access: yesPharmacoepidemiology and Drug Safety, Volume 35, Issue 5, May 2026.
ABSTRACT Background The evidence gap relating to the risk of congenital anomalies (CA) associated with first trimester medication exposure in pregnancy is well recognized. Aims We describe the EUROmediCAT network and databases, and the methodological approach to pregnancy pharmacovigilance.
Helen Dolk   +27 more
wiley   +1 more source

Biliary atresia

open access: yesMedisur, 2005
Biliary atresia is an obstructive and progressive process of unknown etiology that affects intra and/or extrahepatics biliary tracts and cause neonatal jaundice by serious obstruction of the biliary flow.
Miurkis Endis Miranda   +2 more
doaj   +2 more sources

Pediatric liver transplantation. Part II. Diagnostic imaging in postoperative management [PDF]

open access: yes, 1985
Bron, KM   +6 more
core   +1 more source

“Prevalencia de malformaciones congénitas gastrointestinales en el Hospital Materno Perinatal Mónica Pretelini Sáenz durante el periodo de 2010 a 2015” [PDF]

open access: yes, 2017
I. RESUMEN INTRODUCCIÓN: Las malformaciones congénitas suelen ser causadas por alteraciones en el desarrollo morfológico, estructural, funcional o molecular del embrión, generando repercusiones tanto estéticas como funcionales con alteraciones ...
GONZÁLEZ OCAMPO, NURI   +2 more
core  

Surgical correction of a double congenital hernia in a veal calf

open access: yesVeterinary Record Case Reports, Volume 14, Issue 2, May 2026.
Abstract This clinical case report describes the rare occurrence and successful surgical management of two simultaneous congenital hernias, umbilical and perineal, in a crossbred veal calf. At 5 days of age, the animal, weighing approximately 40 kg, showed visible swelling in the umbilical and perineal regions together with a congenital tail ...
Andrea Spadaro   +4 more
wiley   +1 more source

Fibroblast growth factors in gastrointestinal development, homeostasis and injury

open access: yes, 2010
Fibroblast growth factors (FGFs) and their receptors (FGFRs) are essential for controlling cell growth and proliferation, angiogenesis, wound healing and tumourigenesis.
Ding, Su Sin, Ding, Su Sin
core   +1 more source

Women with PCOS have a later menopausal transition and a lower prevalence of menopausal symptoms at age 46: A population‐based birth cohort study

open access: yesActa Obstetricia et Gynecologica Scandinavica, Volume 105, Issue 5, Page 836-846, May 2026.
Findings from a population‐based cohort study indicate that late peri−/postmenopausal status, as well as menopausal symptoms, were less prevalent in women with PCOS at age 46, supporting the hypothesis of prolonged ovarian function and a delayed menopausal transition with this condition. Created in https://BioRender.com.
Johanna Lavi   +6 more
wiley   +1 more source

Clinical liver transplantation [PDF]

open access: yes, 1969
Brettschneider, L   +5 more
core   +1 more source

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