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Issue Date
Title
Author(s)
2007
Polysomnography in Australia-trends in provision
Marshall, N.
;
Wilsmore, B.
;
McEvoy, R.
;
Wheatley, J.
;
Dodd, M.
;
Grunstein, R.
2002
Sodium-channel defects in benign familial neonatal-infantile seizures
Heron, S.
;
Crossland, K.
;
Andermann, E.
;
Phillips, H.
;
Hall, A.
;
Bleasel, A.
;
Shevell, M.
;
Mercho, S.
;
Seni, M.
;
Guiot, M.
;
Mulley, J.
;
Berkovic, S.
;
Scheffer, I.
2005
A community-based intervention to reduce antibiotic use for upper respiratory tract infections in regional South Australia
Dollman, W.
;
LeBlanc, V.
;
Stevens, L.
;
O'Connor, P.
;
Turnidge, J.
2019
GJB2 and GJB6 mutations in hereditary recessive non-syndromic hearing impairment in Cameroon
Tingang Wonkam, E.
;
Chimusa, E.
;
Noubiap, J.J.
;
Adadey, S.M.
;
F Fokouo, J.V.
;
Wonkam, A.
2013
Rare variants in single-minded 1 (SIM1) are associated with severe obesity
Ramachandrappa, S.
;
Raimondo, A.
;
Cali, A.
;
Keogh, J.
;
Henning, E.
;
Saeed, S.
;
Thompson, A.
;
Garg, S.
;
Bochukova, E.
;
Brage, S.
;
Trowse, V.
;
Wheeler, E.
;
Sullivan, A.
;
Dattani, M.
;
Clayton, P.
;
Datta, V.
;
Bruning, J.
;
Wareham, N.
;
O'Rahilly, S.
;
Peet, D.
;
et al.
2004
Benign familial neonatal-infantile seizures: Characterization of a new sodium channelopathy
Berkovic, S.
;
Heron, S.
;
Giordano, L.
;
Marini, C.
;
Guerrini, R.
;
Kaplan, R.
;
Gambardella, A.
;
Steinlein, O.
;
Grinton, B.
;
Dean, J.
;
Bordo, L.
;
Hodgson, B.
;
Yamamoto, T.
;
Mulley, J.
;
Zara, F.
;
Scheffer, I.
2011
MLVA and phage typing as complementary tools in the epidemiological investigation of Salmonella enterica serovar typhimurium clusters
Ross, I.
;
Davos, D.
;
Mwanri, L.
;
Raupach, J.
;
Heuzenroeder, M.
2013
Mutations in DEPDC5 cause familial focal epilepsy with variable foci
Dibbens, L.
;
de Vries, B.
;
Donatello, S.
;
Heron, S.
;
Hodgson, B.
;
Chintawar, S.
;
Crompton, D.
;
Hughes, J.
;
Bellows, S.
;
Klein, K.
;
Callenbach, P.
;
Corbett, M.
;
Gardner, A.
;
Kivity, S.
;
Iona, X.
;
Regan, B.
;
Weller, C.
;
Crimmins, D.
;
O'Brien, T.
;
Guerrero-Lopez, R.
;
et al.
2007
Temporal lobe epilepsy and GEFS(+) phenotypes associated with SCN1B mutations
Scheffer, I.
;
Harkin, L.
;
Grinton, B.
;
Dibbens, L.
;
Turner, S.
;
Zielinski, M.
;
Xu, R.
;
Jackson, G.
;
Adams, J.
;
Connellan, M.
;
Petrou, S.
;
Wellard, R.
;
Briellmann, R.
;
Wallace, R.
;
Mulley, J.
;
Berkovic, S.
2008
Treatment of scedosporiosis with Voriconazole: Clinical experience with 107 patients
Troke, P.
;
Aguirrebengoa, K.
;
Arteaga, C.
;
Ellis, D.
;
Heath, C.
;
Lutsar, I.
;
Rovira, M.
;
Nguyen, Q.
;
Slavin, M.
;
Chen, S.
Discover
Author
3
Berkovic, S.
3
Heron, S.
3
Mulley, J.
3
Scheffer, I.
2
Davos, D.
2
Dibbens, L.
2
et al.
2
Grinton, B.
2
Heuzenroeder, M.
2
Hodgson, B.
.
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Subject
12
Child
11
Adult
11
Child, Preschool
8
Middle Aged
6
Pedigree
5
Aged
4
Australia
3
Case-Control Studies
3
DNA Mutational Analysis
3
Genotype
.
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Date issued
4
2010 - 2019
8
2002 - 2009