Results 51 to 60 of about 7,715 (213)
Background Anorectal malformations (ARM) represent a wide spectrum of defects. Caudal and genitourinary malformations can associate with anorectal malformations. Genetic factors may play role in the development of anorectal malformations. Perineal masses
Ayca Kocaaga +2 more
doaj +1 more source
THE PREVALENCE OF BIRTH DEFECTS AMONG NON-HISPANIC ASIANS AND AMERICAN INDIANS/ALASKA NATIVES IN TEXAS, 1999-2015 [PDF]
Background: Birth defects are disproportionately higher among certain race/ethnic groups. We examined how birth defects prevalence differs among the less studied non-Hispanic (NH) Asian and any American Indian/Alaska Native (AI/AN) populations, relative ...
LE, VAN
core +1 more source
Clinical assessment of epidural analgesia induced by xylazine-lidocaine combination accompanied by xylazine sedation in calves [PDF]
The aim of the present study was to investigate whether epidural administration of a xylazine-lidocaine combination accompanied by xylazine sedation would provide satisfactory analgesia for some surgical procedures on 10 calves admitted to the Department
Alkan Kamiloglu +4 more
core +2 more sources
Membranous variety of rectal atresia - primary management in a neonate
Rectal atresia is a rare form of anorectal malformation, with reported incidence of 1 to 2% and membranous variety of rectal atresia is even rarer. Most reported cases have been dealt with a staged procedure which includes sigmoid colostomy.
Jayaswal Shalika +4 more
doaj
Abstract Purpose To establish the first DRLs for contrast‐enhanced diagnostic pediatric fluoroscopic procedures in Brazil, stratified by body weight, based on data collected in a single tertiary referral public hospital of Rio de Janeiro city. Methods This descriptive, cross‐sectional study included 928 diagnostic fluoroscopy examinations performed in ...
Claudia M. C. Ribeiro +6 more
wiley +1 more source
Introduction: Concurrent esophageal atresia with tracheoesophageal fistula and Hirschsprung disease is a rare combination of congenital anomalies, with only four cases reported to date in full-term neonates.
Yidnekachew Getachew +4 more
doaj +1 more source
ABSTRACT Background No consistent genetic etiology has been found for a group of six different conditions in humans with multiple malformations called “recurrent constellations of embryonic malformations” (RCEM). Recent studies indicate hypoxia/reoxygenation and generation Reactive Oxygen Species (ROS) as an underlying mechanism for RCEM with the ...
Aaron P. Adam +3 more
wiley +1 more source
Human Cyclophilins—An Emerging Class of Drug Targets
ABSTRACT Cyclophilins are a family of enzymes with peptidyl‐prolyl isomerase activity found in all cells of all organisms. To date, 17 cyclophilin isoforms have been identified in the human body, participating in diverse biological processes. Consequently, cyclophilins have emerged as promising targets for drug development to address a wide array of ...
Katarina Jurkova +3 more
wiley +1 more source
Esophageal atresia in newborns: a wide spectrum from the isolated forms to a full VACTERL phenotype? [PDF]
Background: VATER association was first described in 1972 by Quan and Smith as an acronym which identifies a non-random co-occurrence of Vertebral anomalies, Anal atresia, Tracheoesophageal fistula and/or Esophageal atresia, Radial dysplasia.
Antona, V +9 more
core +4 more sources
Study on Sedation with Local Analgesia in Calves [PDF]
. The effect of sedatives and analgesics on heart rate, respiration rate and rectal temperature were observed. Heart rate and respiration rate significantly decreased during sedation with xylazine hydrochloride plus 2% lignocaine hydrochloride or 0.5 ...
Hashim, M. (MA) +3 more
core +2 more sources

