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Results 1-10 of 18 (Search time: 0.002 seconds).
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Issue Date
Title
Author(s)
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.
1998
Transcranial correction of orbital neurofibromatosis
Snyder, B.
;
Hanieh, A.
;
Trott, J.
;
David, D.
1998
Service provision trends between 1983-84 and 1993-94 in Australian private general practice
Brennan, D.
;
Spencer, A.
;
Szuster, F.
1998
Haemolytic-uraemic syndrome outbreak caused by Escherichia coli O111:H-: clinical outcomes
Henning, P.
;
Tham, E.
;
Martin, A.
;
Beare, T.
;
Jureidini, K.
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.
1998
Evaluation of the lysosome-associated membrane protein LAMP-2 as a marker for lysosomal storage disorders
Hua, C.
;
Hopwood, J.
;
Carlsson, S.
;
Harris, R.
;
Meikle, P.
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.
1998
Loss to follow-up of preterm and very preterm babies
Turnbull, D.
1998
Acute appendicitis in childhood: Did mother know best? A pathological analysis of 1409 cases
Byard, R.
;
Manton, N.
;
Burnell, R.
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
3
Hopwood, J.
2
Haan, E.
2
Henning, P.
2
Jureidini, K.
2
Kleijer, W.
2
Martin, A.
2
Spencer, A.
2
van Diggelen, O.
1
Aerts, J.
1
Aldis, J.
.
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Subject
3
Australia
3
Infant, Newborn
3
Pedigree
3
South Australia
3
Syndrome
2
Follow-Up Studies
2
Prospective Studies
2
Tomography, X-Ray Computed
2
Treatment Outcome
1
Age Factors
.
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