Search


Start a new search
Add filters:

Use filters to refine the search results.


Results 2851-2860 of 2877 (Search time: 0.011 seconds).
Item hits:
PreviewIssue DateTitleAuthor(s)
2014Hypoxia-inducible factor-1α gene polymorphisms in early and late onset preeclampsia in Sinhalese womenAndraweera, P.; Dekker, G.; Thompson, S.; Dissanayake, V.; Jayasekara, R.; Roberts, C.
1996Pneumocystis carinii pneumonia in childhood systemic lupus erythematosusFoster, H.; Malleson, P.; Petty, R.; Roberton, D.; Cabral, D.
1998Enhanced in vivo airway gene transfer via transient modification of host barrier properties with a surface-active agentParsons, D.; Grubb, B.; Johnson, L.; Boucher, R.
2002The molecular basis of cystathionine b-synthase deficiency in Australian patients: Genotype-phenotype correlations and response to treatmentGaustadnes, M.; Wilcken, B.; Oliveriusova, J.; McGill, J.; Fletcher, J.; Kraus, J.; Wilcken, D.
2020Characteristics of paediatric frequent presenters at emergency departments: a whole-of-population studyProcter, A.M.; Gialamas, A.; Pilkington, R.M.; Montgomerie, A.; Chittleborough, C.R.; Smithers, L.G.; Lynch, J.W.
2004Potential immaturity of the T-cell and antigen-presenting cell interaction in cord blood with particular emphasis on the CD40-CD40 ligand costimulatory pathwayHan, P.; McDonald, T.; Hodge, G.
1995Substrate specificity of rat liver mitochondrial carnitine palmitoyl transferase I : Evidence against a-oxidation of phytanic acid in rat liver mitochondriaSingh, H.; Poulos, A.
2009Optimising coherence properties for phase contrast x-Ray imaging (PCXI) to reveal airway surface liquid (ASL) as an airway health measureMorgan, K.; Paganin, D.; Parsons, D.; Donnelley, M.; Yagi, N.; Uesugi, K.; Suzuki, Y.; Takeuchi, A.; Siu, K.; World Congress on Medical Physics and Biomedical Engineering (2009 : Munich, Germany)
2009Hyperchloraemic metabolic acidosis slows recovery in children with diabetic ketoacidosis: A retrospective auditMrozik, L.; Yung, M.
2020Evaluation of DNA methylation episignatures for diagnosis and phenotype correlations in 42 Mendelian neurodevelopmental disordersAref-Eshghi, E.; Kerkhof, J.; Pedro, V.; Barat-Houari, M.; Ruiz-Pallares, N.; Alders, M.; Mannens, M.; Henneman, P.; Hennekam, R.C.; Ciolfi, A.; Pizzi, S.; Tartaglia, M.; Campeau, P.M.; Rousseau, J.; Levy, M.A.; Brick, L.; Kozenko, M.; Balci, T.B.; Siu, V.M.; Stuart, A.; Kadour, M.; Masters, J.; Takano, K.; Kleefstra, T.; de Leeuw, N.; Field, M.; Shaw, M.; Gecz, J.; Merla, G.; Ainsworth, P.J.; Lin, H.; Rodenhiser, D.I.; Friez, M.J.; Tedder, M.; Lee, J.A.; DuPont, B.R.; Stevenson, R.E.; Skinner, S.A.; Schwartz, C.E.; Genevieve, D.; Sadikovic, B.; 53rd European Society of Human Genetics (ESHG) Conference (06 Jun 2020 - 09 Jun 2020 : Virtual Online)