| 5 | -- | 22 | Louise R. Guillaume, Peter A. Bath. The Impact of Health Scares on Parents Information Needs and Preferred Information Sources: A Case Study of the MMR Vaccine Scare |
| 23 | -- | 36 | Leonidas Orfanidis, Panagiotis D. Bamidis, Barry Eaglestone. Data Quality Issues in Electronic Health Records: An Adaptation Framework for the Greek Health System |
| 37 | -- | 48 | Lars Höglund, Elena Maceviciute, T. D. Wilson. Trust in Healthcare: An Information Perspective |
| 49 | -- | 69 | Mark Hepworth, Janet Harrison. A Survey of the Information Needs of People with Multiple Sclerosis |
| 71 | -- | 75 | Lars Andersson, Greta Petersen, Per Johnson, Fredrik Ståhl. Finding Genes Contributing to the Arthritis Phenotype by Comparing Rat and Human Genome Data |
| 77 | -- | 82 | Y. W. Chow, T. Treasure, S. Gallivan. Can the Internet Be Used to Collect Clinical Data for Research? |
| 83 | -- | 88 | Lennart Magnusson, Elizabeth Hanson. Working with Older People and Their Carers to Research and Develop Responsive ICT Support Services |