Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
Failure to confirm abnormal copper utilization in crinkler (cr) mice.
Biological trace element research·2013
Mutations in the 4-hydroxyphenylpyruvic acid dioxygenase gene are responsible for tyrosinemia type III and hawkinsinuria.
Molecular genetics and metabolism·2000
Analysis of the distribution of Cu, Fe and Zn and other elements in brindled mouse kidney using a scanning proton microprobe.
Journal of inorganic biochemistry·1998
Mutations of the flavin-containing monooxygenase gene (FMO3) cause trimethylaminuria, a defect in detoxication.
Human molecular genetics·1998
Early treatment of Menkes disease with parenteral copper-histidine: long-term follow-up of four treated patients.
American journal of medical genetics·1998
Systemic candidiasis with DIC and candida endophthalmitis in a postoperative neonate.
Australian paediatric journal·1989
Urinary tract calculi in aboriginal children.
Australian paediatric journal·1989
Fetal echocardiography in the diagnosis of congenital heart disease.
Australian paediatric journal·1989
Congenital tuberculosis.
Australian paediatric journal·1989
Radiological and clinical features of basal ganglia infarction in tuberculous meningitis.
Australian paediatric journal·1989
Faecal incontinence in childhood: a multidisciplinary approach including biofeedback.
Australian paediatric journal·1989
Intracavitary electrocardiography for 1‑Fr epicutaneous‑cava catheter tip location in neonates: 6‑Year retrospective study.
The journal of vascular access·2026