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Issue Date
Title
Author(s)
1996
Children with hyperimmunoglobulinemia D and periodic fever syndrome
Grose, C.
;
Schnetzer, J.
;
Ferrante, A.
;
Vladutiu, A.
1998
Coexistence of Gaucher-Disease Type 1 and Joubert-Syndrome
Van Royen-Kerkhof, A.
;
Pollthe, B.
;
Kleijer, W.
;
van Diggelen, O.
;
Aerts, J.
;
Hopwood, J.
;
Beemer, F.
1996
Identification, expression, and biochemical characterization of N-acetylgalactosamine-4-sulfatase mutations and relationship with clinical phenotype in MPS-VI patients
Litjens, T.
;
Brooks, D.
;
Peters, C.
;
Gibson, G.
;
Hopwood, J.
2005
Gastro-oesophageal reflux disease in infants and children: New insights, developments and old chestnuts
Omari, T.
2003
Two further cases of Ohdo syndrome delineate the phenotypic variability of the condition
White, S.
;
Ades, L.
;
Amor, D.
;
Liebelt, J.
;
Bankier, A.
;
Baker, E.
;
Wilson, M.
;
Savarirayan, R.
1995
Haemolytic uraemic syndrome due to a Shiga-like toxin-producing Escherichia coli 048: H21 in South Australia
Goldwater, P.
;
Bettelheim, K.
2007
Annual report on surveillance of adverse events following immunisation in Australia 2006
Lawrence, G.
;
Aratchige, P.
;
Boyd, I.
;
McIntyre, P.
;
Gold, M.
2003
Local reactions after the fourth-dose of acellular pertussis vaccine in South Australia
Gold, M.
;
Noonan, S.
;
Osbourn, M.
;
Precepa, S.
;
Kempe, A.
1998
Transcranial correction of orbital neurofibromatosis
Snyder, B.
;
Hanieh, A.
;
Trott, J.
;
David, D.
1995
Adverse outcomes of bacterial meningitis in school aged survivors
Grimwood, K.
;
Anderson, V.
;
Bond, L.
;
Catroppa, C.
;
Hore, R.
;
Keir, E.
;
Nolan, T.
;
Roberton, D.
Discover
Author
18
Hopwood, J.
15
Davidson, G.
14
et al.
13
Gecz, J.
13
Haan, E.
10
Gold, M.
10
Makrides, M.
10
Omari, T.
9
Anderson, P.J.
8
Baghurst, P.
.
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Subject
27
Mutation
23
Middle Aged
20
Prospective Studies
19
Follow-Up Studies
18
Pedigree
14
Phenotype
13
Cohort Studies
13
Retrospective Studies
12
Case-Control Studies
12
DNA Mutational Analysis
.
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