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Preview	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	Haemolytic-uraemic syndrome outbreak caused by Escherichia coli O111:H-: clinical outcomes	Henning, P.; Tham, E.; Martin, A.; Beare, T.; Jureidini, K.
	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	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.
	1998	Autosomal dominant Klippel-Feil anomaly with cleft palate	Thompson, E.; Haan, E.; Sheffield, L.
	1998	Bowel dysfunction in cystic fibrosis: importance of breath testing	Lewindon, P.; Robb, T.; Moore, D.; Davidson, G.; Martin, A.
	1998	IgG subclass antibodies to glutamic acid decarboxylase and risk for progression to clinical insulin-dependent diabetes	Couper, J.; Harrison, L.; Aldis, J.; Colman, P.; Honeyman, M.; Ferrante, A.
	1998	What constitutes cerebral palsy?	Badawi, N.; Watson, L.; Petterson, B.; Blair, E.; Slee, J.; Haan, E.; Stanley, F.