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Results 1-10 of 79 (Search time: 0.004 seconds).
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Issue Date
Title
Author(s)
1995
Central nervous system imaging in Crouzon Syndrome
Proudman, T.
;
Clark, B.
;
Moore, M.
;
Abbott, A.
;
David, D.
1996
Munchausen Syndrome by Proxy: Child Abuse in the Medical System
Donald, T.
;
Jureidini, J.
2007
Improving patient satisfaction through information provision
Billing, K.
;
Newland, H.
;
Selva-Nayagam, D.
2000
Open invitation from the International Poverty and Health Network to all healthcare professionals
Heath, I.
;
Haines, A.
;
Glover, J.
;
Hetzel, D.
2016
TBC1D24 genotype-phenotype correlation
Balestrini, S.
;
Milh, M.
;
Castiglioni, C.
;
Lüthy, K.
;
Finelli, M.
;
Verstreken, P.
;
Cardon, A.
;
Stražišar, B.
;
Holder, J.
;
Lesca, G.
;
Mancardi, M.
;
Poulat, A.
;
Repetto, G.
;
Banka, S.
;
Bilo, L.
;
Birkeland, L.
;
Bosch, F.
;
Brockmann, K.
;
Cross, J.
;
Doummar, D.
;
et al.
1998
Declining blood lead levels and changes in cognitive function during childhood - The Port Pirie Cohort Study
Tong, S.
;
Baghurst, P.
;
Sawyer, M.
;
Burns, J.
;
McMichael, A.
2020
Contemporary Incidence and Prevalence of Rheumatic Fever and Rheumatic Heart Disease in Australia Using Linked Data: The Case for Policy Change
Katzenellenbogen, J.M.
;
Bond-Smith, D.
;
Seth, R.J.
;
Dempsey, K.
;
Cannon, J.
;
Stacey, I.
;
Wade, V.
;
de Klerk, N.
;
Greenland, M.
;
Sanfilippo, F.M.
;
Brown, A.
;
Carapetis, J.R.
;
Wyber, R.
;
Nedkoff, L.
;
Hung, J.
;
Bessarab, D.
;
Ralph, A.P.
2019
Pathogenic abnormal splicing due to intronic deletions that induce biophysical space constraint for spliceosome assembly
Bryen, S.J.
;
Joshi, H.
;
Evesson, F.J.
;
Girard, C.
;
Ghaoui, R.
;
Waddell, L.B.
;
Testa, A.C.
;
Cummings, B.
;
Arbuckle, S.
;
Graf, N.
;
Webster, R.
;
MacArthur, D.G.
;
Laing, N.G.
;
Davis, M.R.
;
Lührmann, R.
;
Cooper, S.T.
2021
Diet quality trajectories and cardiovascular phenotypes/metabolic syndrome risk by 11-12 years
Kerr, J.A.
;
Liu, R.S.
;
Gasser, C.E.
;
Mensah, F.K.
;
Burgner, D.
;
Lycett, K.
;
Gillespie, A.N.
;
Juonala, M.
;
Clifford, S.A.
;
Olds, T.
;
Saffery, R.
;
Gold, L.
;
Liu, M.
;
Azzopardi, P.
;
Edwards, B.
;
Dwyer, T.
;
Wake, M.
2019
Bi-allelic loss-of-function CACNA1B mutations in progressive epilepsy-dyskinesia
Gorman, K.M.
;
Meyer, E.
;
Grozeva, D.
;
Spinelli, E.
;
McTague, A.
;
Sanchis-Juan, A.
;
Carss, K.J.
;
Bryant, E.
;
Reich, A.
;
Schneider, A.L.
;
Pressler, R.M.
;
Simpson, M.A.
;
Debelle, G.D.
;
Wassmer, E.
;
Morton, J.
;
Sieciechowicz, D.
;
Jan-Kamsteeg, E.
;
Paciorkowski, A.R.
;
King, M.D.
;
Cross, J.H.
;
et al.
Discover
Author
18
et al.
6
David, D.
5
Makrides, M.
5
Selva-Nayagam, D.
4
Revesz, T.
3
Bond-Smith, D.
3
Gibson, R.A.
3
Gould, J.F.
3
Katzenellenbogen, J.M.
3
Law, T.
.
next >
Subject
7
Pregnancy
7
Registries
6
Case-Control Studies
6
Follow-Up Studies
6
Treatment Outcome
5
Incidence
5
Longitudinal Studies
5
Surveys and Questionnaires
5
Survival Rate
4
Age Distribution
.
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Date issued
23
2020 - 2023
36
2010 - 2019
14
2000 - 2009
6
1995 - 1999