Browsing by Author Rhead, William

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Issue DateTitleAuthor(s)Citation
2006'Classical' organic acidurias, propionic aciduria, methylmalonic aciduria and isovaleric aciduria: Long-term outcome and effects of expanded newborn screening using tandem mass spectrometry.Wilcken, Bridget; Deodato, Federica; Dionisi-Vici, Carlo; Rhead, William; Roschinger, Wulf; Children's Hospital Westmead: Paediatrics & Child Health'Classical' organic acidurias, propionic aciduria, methylmalonic aciduria and isovaleric aciduria: Long-term outcome and effects of expanded newborn screening using tandem mass spectrometry., Journal of inherited metabolic disease, vol.29,(2-3),2006,pp 383-389
2011Maternal Riboflavin Deficiency, Resulting in Transient Neonatal-Onset Glutaric Aciduria Type 2, Is Caused by a Microdeletion in the Riboflavin Transporter Gene GPR172BCarpenter, Kevin; Christodoulou, John; Ho, Gladys; Peters, Gregory; Inui, Ken-Ichi; Masuda, Satohiro; Mitchell, John J.; Olsen, R. K. J.; Rhead, William; Sim, K. G.; Yonezawa, Atsushi; Children's Hospital Westmead: Medicine; Children's Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Paediatrics & Child HealthMaternal Riboflavin Deficiency, Resulting in Transient Neonatal-Onset Glutaric Aciduria Type 2, Is Caused by a Microdeletion in the Riboflavin Transporter Gene GPR172B, Human Mutation, vol.32, 1, 2011,pp E1976-E1984