Search


Current filters:




Start a new search
Add filters:

Use filters to refine the search results.


Results 31-40 of 40 (Search time: 0.003 seconds).
Item hits:
PreviewIssue DateTitleAuthor(s)
2005The Australasian Triage Scale applied in a tertiary care hospital in NepalKhanal, B.; Lewis, O.; Lewis, M.; Newbury, J.; Malla, G.
2008Treatment of scedosporiosis with Voriconazole: Clinical experience with 107 patientsTroke, P.; Aguirrebengoa, K.; Arteaga, C.; Ellis, D.; Heath, C.; Lutsar, I.; Rovira, M.; Nguyen, Q.; Slavin, M.; Chen, S.
2009Prevalence and causes of visual impairment in a Brazilian population: The Botucatu Eye StudySchellini, S.; Durkin, S.; Hoyama, E.; Hirai, F.; Cordeiro, R.; Casson, R.; Selva-Nayagam, D.; Padovani, C.
2009Cutaneous melanoma is related to immune suppression in kidney transplant recipientsVajdic, C.; van Leeuwen, M.; Webster, A.; McCredie, M.; Stewart, J.; Chapman, J.; Amin, J.; McDonald, S.; Grulich, A.
2009SPRED1 mutations (Legius syndrome): another clinically useful genotype for dissecting the neurofibromatosis type 1 phenotypeSpurlock, G.; Bennett, E.; Chuzhanova, N.; Thomas, N.; H-Ping, J.; Side, L.; Davies, S.; Haan, E.; Kerr, B.; Huson, S.; Upadhyaya, M.
2004Autosomal dominant congenital non-progressive ataxia overlaps with the SCA15 locusDudding, T.; Friend, K.; Schofield, P.; Lee, S.; Wilkinson, I.; Richards, R.
2002X-linked myoclonic epilepsy with spasticity and intellectual disability - Mutation in the homeobox gene ARXScheffer, I.; Wallace, R.; Phillips, F.; Hewson, P.; Reardon, K.; Parasivam, G.; Stromme, P.; Berkovic, S.; Gecz, J.; Mulley, J.
2001Medicine may be reducing the human capacity to surviveStephan, C.; Henneberg, M.
2003Fresh garlic: a possible vehicle for Salmonella VirchowBennett, C.; Dalton, C.; Beers-Deeble, M.; Milazzo, A.; Kraa, E.; Davos, D.; Puech, M.; Tan, A.; Heuzenroeder, M.
2003Craniopharyngioma: a review of long-term visual outcomeChen, C.; Okera, S.; Davies, P.; Selva-Nayagam, D.; Crompton, J.