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541601 to 541700 most common queries
List represents a sample of symptoms, diseases, and other queries. Updated weekly.
Catecholamine release in the newborn infant at birth.
Determinants of the increasing cesarean birth rate. Ontario data 1979 to 1982.
Maternal mortality and severe morbidity associated with low-risk planned cesarean delivery versus planned vaginal delivery at term.
Antecedents of cerebral palsy. Multivariate analysis of risk.
Planned caesarean section versus planned vaginal birth for breech presentation at term: a randomised multicentre trial. Term Breech Trial Collaborative Group.
Diarrhea, Hypertension, Tachycardia, blood in stool
Estimation of potential effects of improved community-based drug provision, to augment health-facility strengthening, on maternal mortality due to post-partum haemorrhage and sepsis in sub-Saharan Africa: an equity-effectiveness model.
Prophylactic use of oxytocin in the third stage of labour.
Active versus expectant management in the third stage of labour.
Maternal epilepsy and abnormalities of the fetus and newborn.
Placenta previa, placenta accreta, and vasa previa.
Investigation of an increase in postpartum haemorrhage in Canada.
The epidemiology of postpartum hemorrhage in a large, nationwide sample of deliveries.
Hemodynamically mediated glomerular injury and the progressive nature of kidney disease.
WHO multicentre randomised trial of misoprostol in the management of the third stage of labour.
A prospective key informant surveillance system to measure maternal mortality - findings from indigenous populations in Jharkhand and Orissa, India.
Trends in postpartum hemorrhage in high resource countries: a review and recommendations from the International Postpartum Hemorrhage Collaborative Group.
Induction of labour versus expectant monitoring for gestational hypertension or mild pre-eclampsia after 36 weeks' gestation (HYPITAT): a multicentre, open-label randomised controlled trial.
A behavioral intervention to improve obstetrical care.
Outcome of pregnancy in a woman with an increased body mass index.
Oral misoprostol in preventing postpartum haemorrhage in resource-poor communities: a randomised controlled trial.
Incidence and predictors of severe obstetric morbidity: case-control study.
Role of tissue factor in hemostasis, thrombosis, and vascular development.
Human fatty liver disease: old questions and new insights.
A simple noninvasive index can predict both significant fibrosis and cirrhosis in patients with chronic hepatitis C.
Risk of hepatocellular carcinoma across a biological gradient of serum hepatitis B virus DNA level.
Nonalcoholic fatty liver disease: a spectrum of clinical and pathological severity.
Hepatitis B virus epidemiology, disease burden, treatment, and current and emerging prevention and control measures.
Selective depletion of macrophages reveals distinct, opposing roles during liver injury and repair.
A model to predict survival in patients with end-stage liver disease.
Nonalcoholic fatty liver disease: from steatosis to cirrhosis.
Molecular regulation of hepatic fibrosis, an integrated cellular response to tissue injury.
The natural history of nonalcoholic fatty liver disease: a population-based cohort study.
Hepatic stellate cells: protean, multifunctional, and enigmatic cells of the liver.
Transforming growth factor beta in tissue fibrosis.
Mechanisms of hepatic fibrogenesis.
Liver transplantation for the treatment of small hepatocellular carcinomas in patients with cirrhosis.
Diagnosis, management, and treatment of hepatitis C: an update.
The L-arginine-nitric oxide pathway.
Acute Kidney Failure, Cold, Clammy Skin, Hypotension, Tachycardia, Tachypnea
Coxa Valga, Failure to Thrive, Obesity, Scoliosis, Short Stature in Children
Central Nervous System Disorder, Dehydration, Malaise
Georgios I Androutsos
Role of T cells, TNF alpha and IFN gamma in recall of immunity to oral challenge with virulent salmonellae in mice vaccinated with live attenuated aro- Salmonella vaccines.
Salmonella SirA is a global regulator of genes mediating enteropathogenesis.
Quinolone-resistant Salmonella typhi in Viet Nam: molecular basis of resistance and clinical response to treatment.
A study of typhoid fever in five Asian countries: disease burden and implications for controls.
Resistance of inbred mice to Salmonella typhimurium.
Evolutionary genetic relationships of clones of Salmonella serovars that cause human typhoid and other enteric fevers.
Typhoid and paratyphoid fever.
Intestinal inflammation allows Salmonella to use ethanolamine to compete with the microbiota.
Robust Salmonella metabolism limits possibilities for new antimicrobials.
Typhoid fever: pathogenesis and immunologic control.
Global trends in typhoid and paratyphoid Fever.
Salmonella typhi, the causative agent of typhoid fever, is approximately 50,000 years old.
Evolutionary history of Salmonella typhi.
Host-parasite relations in mouse typhoid.
Animal models of Salmonella infections: enteritis versus typhoid fever.
Mechanisms of acquired resistance in mouse typhoid.
Persistent bacterial infections: the interface of the pathogen and the host immune system.
High-throughput sequencing provides insights into genome variation and evolution in Salmonella Typhi.
The global burden of typhoid fever.
Daniel A Assad
A missense mutation disrupting a dibasic prohormone processing site in pro-opiomelanocortin (POMC) increases susceptibility to early-onset obesity through a novel molecular mechanism.
Meta-analysis: the effect of steroids on survival and shock during sepsis depends on the dose.
Inflammation, coagulopathy, and the pathogenesis of multiple organ dysfunction syndrome.
Adrenoleukodystrophy: evidence for X linkage, inactivation, and selection favoring the mutant allele in heterozygous cells.
Prophylaxis of early adrenal insufficiency to prevent bronchopulmonary dysplasia: a multicenter trial.
Measurements of serum free cortisol in critically ill patients.
Genetic variant of the scavenger receptor BI in humans.
DAX-1 inhibits SF-1-mediated transactivation via a carboxy-terminal domain that is deleted in adrenal hypoplasia congenita.
A RAPID TEST OF ADRENOCORTICAL FUNCTION.
Ipilimumab (anti-CTLA4 antibody) causes regression of metastatic renal cell cancer associated with enteritis and hypophysitis.
Clinical variation of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) in a series of 68 patients.
Corticosteroid insufficiency in acutely ill patients.
Recommendations for the diagnosis and management of corticosteroid insufficiency in critically ill adult patients: consensus statements from an international task force by the American College of Critical Care Medicine.
Clinical practice. Primary ovarian insufficiency.
Mutations in the DAX-1 gene give rise to both X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism.
A mutation in the gene encoding steroidogenic factor-1 causes XY sex reversal and adrenal failure in humans.
An unusual member of the nuclear hormone receptor superfamily responsible for X-linked adrenal hypoplasia congenita.
Severe early-onset obesity, adrenal insufficiency and red hair pigmentation caused by POMC mutations in humans.
Effect of treatment with low doses of hydrocortisone and fludrocortisone on mortality in patients with septic shock.
Establishment by an original single-cell cloning method and characterization of an immortal mouse melanoblast cell line (NCCmelb4).
Establishment of a kit-negative cell line of melanocyte precursors from mouse neural crest cells.
Meiotic recombination cold spots in chromosomal cohesion sites.
Spatiotemporal regulation of meiotic recombination by Liaisonin.
Oncrasin targets the JNK-NF-κB axis to sensitize glioma cells to TNFα-induced apoptosis.
Structural analysis of the complex between penta-EF-hand ALG-2 protein and Sec31A peptide reveals a novel target recognition mechanism of ALG-2.
β-defensin-3 negatively regulates TLR4-HMGB1 axis mediated HLA-G expression in IL-1β treated glioma cells.