Showing results (81-90 of 186) with videos related to
Sort By:
Pageof 19
European Journal of Pediatrics|July 1, 1987
Profound neurological illness, relieved by protein restriction, in a baby with a transient disturbance in the metabolism of ingested isoleucineG K Brown, S M Hunt, D K Mitchell, et al.Chemico-Biological Interactions|January 1, 1990
The effect of D-penicillamine on metallothionein mRNA levels and copper distribution in mouse hepatocytesH J McArdle, P Kyriakou, A Grimes, et al.Archives of Disease in Childhood|May 1, 1977
Studies of the aetiology of neonatal hepatitis and biliary atresiaD M Danks, P E Campbell, I Jack, et al.Archives of Disease in Childhood|September 1, 1976
Metaphyseal chondrodysplasia, neutropenia, and pancreatic insufficiency presenting with respiratory distress in the neonatal periodD M Danks, R Haslam, V Mayne, et al.Clinical Orthopaedics and Related Research|May 13, 1998
The genetics of fibrodysplasia ossificans progressivaM Delatycki, J G RogersThe Biochemical Journal|November 1, 1980
Isolation of phenylalanine hydroxylase-stimulating monoclonal antibody by rat-myeloma--rat-spleen-cell fusionK H Choo, J Myer, R G Cotton, et al.European Journal of Pediatrics|September 1, 1986
Difficulties in assessing the effect of strychnine on the outcome of non-ketotic hyperglycinaemia. Observations on sisters with a mild T-protein defectE A Haan, D M Kirby, K Tada, et al.Acta Neuropathologica|January 1, 1992
Autopsy findings in two siblings with infantile Refsum diseaseC W Chow, A Poulos, A J Fellenberg, et al.Acta Paediatrica Japonica : Overseas Edition|October 1, 1991
Williams syndrome in one dizygotic twinT Hokama, J G RogersBiochemical Genetics|February 1, 1980
Altered copper metabolism in cultured cells from human Menkes' syndrome and mottled mouse mutantsJ Camakaris, D M Danks, L Ackland, et al.Pageof 19