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Enzo A. Palombo

Researcher at Swinburne University of Technology

Publications -  215
Citations -  8343

Enzo A. Palombo is an academic researcher from Swinburne University of Technology. The author has contributed to research in topics: Rotavirus & Gene. The author has an hindex of 43, co-authored 205 publications receiving 7130 citations. Previous affiliations of Enzo A. Palombo include La Trobe University & Royal Children's Hospital.

Papers
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Journal ArticleDOI

Structure Analysis of Solid Lipid Nanoparticles for Drug Delivery: A Combined USANS/SANS Study

Rohan M. Shah, +9 more
- 01 Jan 2019 - 
Journal Article

Characterisation of rearranged NSP5 gene of a human rotavirus.

Enzo A. Palombo, +2 more
- 01 Feb 1998 - 
TL;DR: An atypical human rotavirus strain Z10262, isolated from a chronically infected immunodeficient child, displayed an unusual genomic RNA electrophoretic pattern and was derived from a genetic rearrangement which involved a partial duplication of the open reading frame encoding the non-structural protein NSP5.
Journal ArticleDOI

Comparative degradation of hydrothermal pretreated winery grape wastes by various fungi

Avinash V. Karpe, +2 more
- 01 Aug 2014 - 
TL;DR: In this paper, the results suggest that successive hydrothermal and fungal treatments produce greater lignocellulose degradation than regular fermentation, and they also show that successive hyperedgelating produces greater cellulase and xylanase activity.
Journal ArticleDOI

Sequence conservation within neutralization epitope regions of VP 7 and VP 4 proteins of human serotype G 4 rotavirus isolates

Enzo A. Palombo, +2 more
- 01 Jan 1993 - 
TL;DR: The characteristic periodicity of occurrence of serotype G 4 isolates causing severe diarrhoea in Melbourne children is unlikely to be due to changes in neutralization epitopes located on the outer capsid proteins, VP 7 or VP 4.
Journal ArticleDOI

Determination of Ancylostoma caninum ova viability using metabolic profiling.

Pradip Gyawali, +8 more
- 28 May 2016 - 
TL;DR: It is demonstrated that metabolic profiling using GC-MS methods can be used to determine the viability of canine hookworm ova, and the major compounds observed in viable and non-viable hook worm ova were tetradecanoic acid and dodecanoic acid.