Recent Publications Filtered rss feed from: US National Library of Medicine | National Institutes of Health We are actively engaged in a broad range of clinical and biomedical research activities that focus on advancing the care of our patients. Our department has particular strengths in the fields of genetics, medical education and neurosciences. Variations and similarities in clinical management of neonatal abstinence syndrome: Findings of a Canadian survey.Posted on 2018-02-27 Trends in incidence of neonatal abstinence syndrome in Canada and associated healthcare resource utilization.Posted on 2018-02-28 [Selective left mainstem bronchial intubation in the neonatal intensive care unit].Posted on 2018-04-17 Clinical spectrum of KIAA2022 pathogenic variants in males: Case report of two boys with kiaa2022 pathogenic variants and review of the literature.Posted on 2018-04-26 Primary care providers' lived experiences of genetics in practice.Posted on 2018-04-28 Interpregnancy Interval and Congenital Anomalies: A Record-Linkage Study Using the Manitoba Population Research Data Repository.Posted on 2018-05-09 Determinants of Successful Direct Breastfeeding at Hospital Discharge in High-Risk Premature Infants.Posted on 2018-05-11 Pediatric Investigators Collaborative Network on Infections in Canada (PICNIC) Study of Respiratory Syncytial Virus-Associated Deaths in Pediatric Patients in Canada: 2003 to 2013.Posted on 2018-05-23 Noncompaction cardiomyopathy in an infant with Walker-Warburg syndrome.Posted on 2018-06-06 HLX is a candidate gene for a pattern of anomalies associated with congenital diaphragmatic hernia, short bowel, and asplenia.Posted on 2018-06-06 Pagination Current page 1 Page 2 Next page Next › Last page Last »
