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Results 1-10 of 25 (Search time: 0.003 seconds).
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Issue Date
Title
Author(s)
2008
Tuberculosis: the dis-ease that didn't dis-appear
Bastian, I.
;
Krause, V.
2007
Polysomnography in Australia-trends in provision
Marshall, N.
;
Wilsmore, B.
;
McEvoy, R.
;
Wheatley, J.
;
Dodd, M.
;
Grunstein, R.
2002
A mutation in the gene TNFRSF11B encoding osteoprotegerin causes an idiopathic hyperphosphatasia phenotype
Cundy, T.
;
Hegde, M.
;
Naot, D.
;
Chong, B.
;
King, A.
;
Wallace, R.
;
Mulley, J.
;
Love, D.
;
Seidel, J.
;
Fawkner, M.
;
Banovic, T.
;
Callon, K.
;
Grey, A.
;
Reid, I.
;
Middleton-Hardie, C.
;
Cornish, J.
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
Erythrocyte-binding antigens of Plasmodium falciparum are targets of human inhibitory antibodies and function to evade naturally acquired immunity
Persson, K.
;
Fowkes, F.
;
McCallum, F.
;
Gicheru, N.
;
Reiling, L.
;
Richards, J.
;
Wilson, D.
;
Lopaticki, S.
;
Cowman, A.
;
Marsh, K.
;
Beeson, J.
2023
The effects of age and biological sex on the association between I-wave recruitment and the response to cTBS: an exploratory study
Van Dam, J.M.
;
Graetz, L.
;
Pitcher, J.B.
;
Goldsworthy, M.R.
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.
Discover
Author
6
Mulley, J.
4
Berkovic, S.
4
Scheffer, I.
3
et al.
3
Heron, S.
2
Beeson, J.
2
Butler, R.
2
Cowman, A.
2
Davidson, G.
2
Davos, D.
.
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18
Adult
17
Child, Preschool
14
Middle Aged
12
Infant
10
Aged
9
Pedigree
5
Australia
5
Mutation
4
Aged, 80 and over
4
Case-Control Studies
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Date issued
1
2020 - 2023
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2010 - 2019
14
2000 - 2009
2
1995 - 1999