Search PubMed⌕ Search

Biomedical subjects

M Ismail

Publications and source records attributed to M Ismail.

149 records · Page 9Linked to original sources
PubMedDate not supplied

Studies and observations on the use of isoelectric focusing in ultra-thin polyacrylamide gels as a method of typing human red cell phosphoglucomutase.

The technique of isoelectric focusing in ultra-thin polyacrylamide gels as a method of typing human red cell phosphoglucomutase (PGM1) has been studied. Typing was possible without the samples attaining true equilibrium focusing conditions. The isozyme patterns so obtained were clearly defined and free from distortion. The importance of assessing relative band intensities when interpreting the isozyme patterns is discussed. Our experience of using the technique to analyse casework material is described.

Acrylic Resins↗
PubMedDate not supplied

Lactate dehydrogenase isozymes in vaginal swab extracts: a problem for the identification of menstrual blood.

Extracts of vaginal swabs free of both blood and semen, collected from three donors throughout several menstrual cycles, have been examined by cellulose acetate membrane electrophoresis for the presence of lactate dehydrogenase (LDH) isozymes. LDH activity, predominantly in the form of LDH-5 was detected in some extracts. Mixtures of these particular extracts with peripheral blood gave LDH patterns similar to those observed for menstrual blood. The results indicate that LDH isozyme patterns cannot be used to differentiate between stains of menstrual blood and bloodstains that have become mixed or contaminated with vaginal secretions.

Adult↗
PubMedDate not supplied

Group B streptococcus: to culture or not to culture?

OBJECTIVE: To determine if universal Group B Streptococcus (GBS) culturing and antibiotic prophylaxis of obstetric patients decreased the incidence of neonatal early-onset GBS sepsis and mortality and maternal chorioamnionitis. STUDY DESIGN: A time series observational study was conducted to compare the cohort of all obstetric patients delivering at the University of Chicago neonatal center from January 1989 through December 1993, before a GBS surveillance policy existed, with the cohort delivering January 1994 through December 1996, after initiation of a GBS policy. Included in the policy were universal GBS cultures at 28 weeks' gestation, antibiotic prophylaxis at the time of labor for all those with positive cultures and for all with risk factors of preterm delivery, preterm premature rupture of membranes, prolonged rupture of membranes greater than 18 hours, and a previous child affected by GBS or maternal fever in labor. Predictor variables were GBS culturing and antibiotic usage; outcome variables were incidence of GBS sepsis and mortality in the neonates and maternal chorioamnionitis. chi-squared and Fisher exact analyses were used with p < 0.05 being significant. RESULTS: Before the GBS policy, there were 16,272 deliveries with a 2.24/1000 deliveries rate of early-onset GBS sepsis (n = 35); after initiating the GBS policy, 9130 deliveries occurred with an early-onset GBS sepsis rate of 2.29/1000 (n = 20). Early-onset GBS sepsis case fatality rates before and after initiation of the policy were 14.3% and 0%, respectively (p = 0.09). Antibiotic use almost doubled (relative risk = 1.84; confidence interval, 1.74 to 1.93, p < 0.001) over the two time periods, and the relative risk of chorioamnionitis decreased to 0.95 (confidence interval, 0.73 to 0.99, p = 0.04). CONCLUSION: Despite universal GBS culturing and very liberal use of antibiotics in labor, we were unable to effect a statistically significant change in the rate of early-onset GBS sepsis or mortality, and there was only a slightly decreased chorioamnionitis rate.

Anti-Bacterial Agents↗
PubMedDate not supplied

Craniofacial alterations in adult rats after acute prenatal alcohol exposure.

BACKGROUND: Exposure during pregnancy to alcohol (ethanol) produces a number of adverse effects. One of them is fetal alcohol syndrome. The hallmark of fetal alcohol syndrome (FAS) is craniofacial dysmorphism and the changes in craniofacial measurement are dependent on the alcoholic dose and its time of exposure. Since prenatal ethanol exposure can alter craniofacial development in rodents and reliably produce long-term behavioral effect in them, the present study was designed to extend the same changes in the Sprague Dawley species. METHODS: The albino rat was studied to determine whether gestational exposure to alcohol (Ethanol) produces permanent craniofacial effect. On gestational day (GD7-10) 25% ethanol was injected intraperitoneally to pregnant rats. Various dimensions for skull and face of adult male rats were taken. RESULTS: Both vertical and coronal dimensions were altered in the exposed animals. CONCLUSIONS: This study demonstrates that exposure to ethanol on a critical gestational period produces permanent craniofacial defects.

Animals↗