Lemonde, Hugh

Junior physician's use of Web 2.0 for information seeking and medical education: a qualitative study

Hughes, B., Joshi, I., Lemonde, H., & Wareham, J. (2009) · International Journal of Medical Informatics

Health Literacy and Information AccessibilitySocial Media in Health Education

Cited by 217

Peroxisomal d -hydroxyacyl-CoA dehydrogenase deficiency: Resolution of the enzyme defect and its molecular basis in bifunctional protein deficiency

van Grunsven, E. G., van Berkel, E., Ijlst, L., Vreken, P., de Klerk, J. B. C., Adamski, J., Lemonde, H., Clayton, P. T., Cuebas, D. A., & Wanders, R. J. A. (1998) · Proceedings of the National Academy of Sciences

Metabolism and Genetic DisordersNeurological diseases and metabolism

Cited by 152

Mutations in SRD5B1 ( AKR1D1 ), the gene encoding Δ 4 -3-oxosteroid 5β-reductase, in hepatitis and liver failure in infancy

Lemonde, H. A., Custard, E. J., Bouquet, J., Duran, M., Overmars, H., Scambler, P. J., & Clayton, P. T. (2003) · Gut

Pediatric Hepatobiliary Diseases and TreatmentsMetabolism and Genetic Disorders

Cited by 125