Zobrazeno 1 - 10
of 73
pro vyhledávání: '"D. P. Brenton"'
Autor:
D. P. Brenton
Publikováno v:
Developmental Medicine & Child Neurology. 11:519-521
Publikováno v:
European Journal of Pediatrics. 155:S93-S96
In our clinic the decision on whether to continue with dietary treatment of phenylketonuria or not is left to each adolescent and adult patient after the advantages and disadvantages, as discussed in this paper, of continuing diet have been presented
Autor:
D. P. Brenton
Publikováno v:
Journal of inherited metabolic disease. 23(3)
Adolescent and adult clinics for patients with inborn metabolic errors are needed first to provide care to patients who develop distinctive problems as their different disorders impinge on education, career and family life. The selection of patients
Publikováno v:
Lancet (London, England). 353(9152)
Publikováno v:
Postgraduate Medical Journal. 66:235-237
Summary A 52 year old man presented with myoglobinuria-induced acute renal failure requiring dialysis. Despite renal biopsy, the cause of the myoglobinuria was not established until he re-presented a year later with a milder episode. At this stage in
Autor:
M Lilburn, D P Brenton
Publikováno v:
European journal of pediatrics. 155
By November 1994, 39 pregnancies had been completed in phenylketonuric mothers. Dietary control was post-conception in 6 and 2 of these offspring died of congenital heart disease and 1 other needed surgery for coarctation. There were no heart defects
Autor:
I. Smith, D. P. Brenton
Publikováno v:
Inborn Metabolic Diseases ISBN: 9783662031490
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f95a980f8b8db09d22a6a588efe486e6
https://doi.org/10.1007/978-3-662-03147-6_12
https://doi.org/10.1007/978-3-662-03147-6_12
Autor:
D. P. Brenton
Publikováno v:
Human Genetics. 110:520-521
Autor:
D. P. Brenton, Sarah Tillotson, B. E. Kendall, Isabel M. Smith, Alan J. Thompson, Susan G. Moore
Publikováno v:
Brain : a journal of neurology. 116
Following the introduction 30 years ago of neonatal screening and early dietary treatment for phenylketonuria there has been a dramatic decrease in the severity of neurological dysfunction associated with this disorder. However, there is evidence tha
Publikováno v:
Clinical chemistry. 39(6)