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Issue Date
Title
Author(s)
1998
Transcranial correction of orbital neurofibromatosis
Snyder, B.
;
Hanieh, A.
;
Trott, J.
;
David, D.
2009
ASPREN surveillance system for influenza-like illness: a comparison with FluTracking and the National Notifiable Diseases Surveillance System
Parrella, A.
;
Dalton, C.B.
;
Pearce, R.
;
Litt, J.C.B.
;
Stocks, N.
1998
Identification of a common mutation (R245h) in Sanfilippo A patients from the Netherlands
Weber, B.
;
Vandekamp, J.
;
Kleijer, W.
;
Guo, X.H.
;
Blanch, L.
;
van Diggelen, O.
;
Wevers, R.
;
Poorthuis, B.
;
Hopwood, J.
1995
Immunoglobulin M capture immunoassay in investigation of coxsackie B5 and B6 outbreaks in South Australia
Goldwater, P.
2018
Maternal smoking during pregnancy and offspring overweight: is there a dose-response relationship? An individual patient data meta-analysis
Albers, L.
;
Sobotzki, C.
;
Kuß, O.
;
Ajslev, T.
;
Batista, R.
;
Bettiol, H.
;
Brabin, B.
;
Buka, S.
;
Cardoso, V.
;
Clifton, V.
;
Devereux, G.
;
Gilman, S.
;
Grzeskowiak, L.
;
Heinrich, J.
;
Hummel, S.
;
Jacobsen, G.
;
Jones, G.
;
Koshy, G.
;
Morgen, C.
;
Oken, E.
;
et al.
2015
Novel IL1RAPL1 mutations associated with intellectual disability impair synaptogenesis
Ramos-Brossier, M.
;
Montani, C.
;
Lebrun, N.
;
Gritti, L.
;
Martin, C.
;
Seminatore-Nole, C.
;
Toussaint, A.
;
Moreno, S.
;
Poirier, K.
;
Dorseuil, O.
;
Chelly, J.
;
Hackett, A.
;
Gecz, J.
;
Bieth, E.
;
Faudet, A.
;
Heron, D.
;
Kooy, R.
;
Loeys, B.
;
Humeau, Y.
;
Sala, C.
;
et al.
1996
Characterisation of four novel fibrillin-1 mutations in the Marfan syndrome
Ades, L.
;
Haan, E.
;
Colley, A.
;
Richards, R.
2005
Threshold effect of urinary glycosaminoglycans and the walk test as indicators of disease progression in a survey of subjects with mucopolysaccharidosis VI (Maroteaux-Lamy syndrome)
Swiedler, S.
;
Beck, M.
;
Bajbouj, M.
;
Giugliani, R.
;
Schwartz, I.
;
Harmatz, P.
;
Wraith, J.
;
Roberts, J.
;
Ketteridge, D.
;
Hopwood, J.
;
Guffon, N.
;
Miranda, C.
;
Teles, E.
;
Berger, K.
;
Piscia-Nichols, C.
2002
The molecular basis of cystathionine b-synthase deficiency in Australian patients: Genotype-phenotype correlations and response to treatment
Gaustadnes, M.
;
Wilcken, B.
;
Oliveriusova, J.
;
McGill, J.
;
Fletcher, J.
;
Kraus, J.
;
Wilcken, D.
1998
Familial partial epilepsy with variable foci: A new partial epilepsy syndrome with suggestion of linkage to chromosome 2
Scheffer, I.
;
Phillips, H.
;
O'Brien, C.
;
Saling, M.
;
Wrennall, J.
;
Wallace, R.
;
Mulley, J.
;
Berkovic, S.
Discover
Author
6
Haan, E.
5
et al.
3
Gecz, J.
3
Hopwood, J.
2
Ades, L.
2
Baghurst, P.
2
Beck, M.
2
Davidson, G.
2
Fletcher, J.
2
Giugliani, R.
.
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Subject
33
Male
26
Adolescent
17
Middle Aged
14
Infant
10
Infant, Newborn
7
Mutation
7
Pedigree
6
Aged
5
Follow-Up Studies
5
Intellectual Disability
.
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Date issued
7
2010 - 2018
15
2000 - 2009
12
1995 - 1999