Childhood cystinuria in New South Wales. Results in children who were followed up after being detected by urinary screening in infancy.-Reference-Cited by-同舟云学术

Childhood cystinuria in New South Wales. Results in children who were followed up after being detected by urinary screening in infancy.

Published:1979-09-01 Issue:9 Volume:54 Page:676-681
ISSN:0003-9888
Container-title:Archives of Disease in Childhood
language:en
Short-container-title:Archives of Disease in Childhood

Author:

Smith A,Yu J S,Brown D A

Publisher

BMJ

Subject

Pediatrics, Perinatology and Child Health

Reference16 articles.

1. Cystinuria in Sweden. VII. Clinical, histo-pathological, and medicosocial aspects of the disease;Bostrom, H.; Hambraeus, L.;Acta medica Scandinavica,1964

2. Screening for inherited metabolic disease in Wales using urine-impregnated filter paper;Bradley, D.M.;Archives of Disease in Childhood,1975

3. Stature and nutrition in cystinuria and Hartnup disease;Colliss, J.E.; Levi, A.J.; Milne, M.D.;British Medical Journal,1963

4. Cystinuria and mental deficiency;Gold, R.J.M.; Dobrinski, M.J.; Gold, D.P.;Clinical Genetics,1977

5. Quantitative studies on the urinary cystine in patients with cystine stone formation and in their relatives;Harris, H.; Warren, F.L.;Annals of Eugenics,1953

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5. Reference values of urinary excretion of cystine and dibasic aminoacids: classification of patients with cystinuria in the Valencian Community, Spain;Clinical Biochemistry;1999-02