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Journal of Inherited Metabolic Disease|January 1, 1989
Cholesterol and prostaglandin synthesis by cultured human skin fibroblasts in the Alagille syndrome involving paucity of interlobular bile ductsJ Dupont, J Raulin, M Gautier, et al.Journal of Inherited Metabolic Disease|January 1, 1989
The management of breast feeding among infants with phenylketonuriaL McCabe, A E Ernest, M R Neifert, et al.Journal of Inherited Metabolic Disease|September 3, 2014
Inborn errors of metabolism in the biosynthesis and remodelling of phospholipidsSaskia B Wortmann, Marc Espeel, Ligia Almeida, et al.Journal of Inherited Metabolic Disease|March 27, 2012
Living situation, occupation and health-related quality of life in adult patients with classic galactosemiaBjörn Hoffmann, Nico Dragano, Susanne Schweitzer-KrantzJournal of Inherited Metabolic Disease|March 27, 2012
In vivo catecholaminergic metabolism in the medial prefrontal cortex of ENU2 mice: an investigation of the cortical dopamine deficit in phenylketonuriaTiziana Pascucci, Giacomo Giacovazzo, Diego Andolina, et al.Journal of Inherited Metabolic Disease|March 29, 2012
Genetically modified pigs for biomedical researchYonglun Luo, Lin Lin, Lars Bolund, et al.Journal of Inherited Metabolic Disease|March 28, 2012
Lysosomal delivery of therapeutic enzymes in cell models of Fabry diseaseD Marchesan, T M Cox, P B DeeganJournal of Inherited Metabolic Disease|May 8, 2012
Fertility and pregnancy in women affected by glycogen storage disease type I, results of a multicenter Italian studyAnnalisa Sechi, Laura Deroma, Annunziata Lapolla, et al.Journal of Inherited Metabolic Disease|September 17, 2015
Nervous system involvement in Farber diseaseAlberto M Cappellari, Marta Torcoletti, Fabio Triulzi, et al.Journal of Inherited Metabolic Disease|June 9, 2016
Metabolite amyloids: a new paradigm for inborn error of metabolism disordersEhud GazitPageof 429