1. Adelaide Research & Scholarship

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Results 1-10 of 22 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
2012Paternal education status significantly influences infants’ measles vaccination uptake, independent of maternal education statusRammohan, A.; Awofeso, N.; Fernandez, R.
2012BRIDGE Study warrants critiqueAllen, D.; Parry, P.; Purssey, R.; Spielmans, G.; Jureidini, J.; Rosenlicht, N.; Healy, D.; Feinberg, I.
2012KCNQ2 encephalopathy: Emerging phenotype of a neonatal epileptic encephalopathyWeckhuysen, S.; Mandelstam, S.; Suls, A.; Audenaert, D.; Deconinck, T.; Claes, L.; Deprez, L.; Smets, K.; Hristova, D.; Yordanova, I.; Jordanova, A.; Ceulemans, B.; Jansen, A.; Hasaerts, D.; Roelens, F.; Lagae, L.; Yendle, S.; Stanley, T.; Heron, S.; Mulley, J.; et al.
2012A noncoding, regulatory mutation implicates HCFC1 in nonsyndromic intellectual disabilityHuang, L.; Jolly, L.; Willis-Owen, S.; Gardner, A.; Sharma, R.; Douglas, E.; Shoubridge, C.; Wieczorek, D.; Tzschach, A.; Cohen, M.; Hackett, A.; Field, M.; Froyen, G.; Hu, H.; Haas, S.; Ropers, H.; Kalscheuer, V.; Corbett, M.; Gecz, J.
2012A possible murine model for investigation of pathogenesis of Sudden Infant Death SyndromeBettelheim, K.; Luke, R.; Johnston, N.; Pearce, J.; Goldwater, P.
2012Neonatal gene therapy with a gamma retroviral vector in mucopolysaccharidosis VI catsPonder, K.; O'Malley, T.; Wang, P.; O'Donnell, P.; Traas, A.; Knox, V.; Aguirre, G.; Ellinwood, N.; Metcalf, J.; Wang, B.; Parkinson-Lawrence, E.; Sleeper, M.; Brooks, D.; Hopwood, J.; Haskins, M.
2012Hypoglycemia, but Not Glucose Variability, Relates to Vascular Function in Children with Type 1 DiabetesPena Vargas, A.; Couper, J.; Harrington, J.; Gent, R.; Fairchild, J.; Tham, E.; Baghurst, P.
2012Neonatal screening for lysosomal storage disordersFletcher, J.; Wilcken, B.
2012Comparison of intraabdominal abscess formation after laparoscopic and open appendicectomies in childrenNataraja, R.; Teague, W.; Galea, J.; Moore, L.; Haddad, M.; Tsang, T.; Khurana, S.; Clarke, S.
2012New mutations and sporadic intellectual disabilityGecz, J.; Haan, E.

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