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Archives of Disease in Childhood
|
November 1, 1973
Familial selective malabsorption of vitamin B12
M Bell, J T Harries, O H Wolff, et al.
Archives of Disease in Childhood
|
June 1, 1970
Effects of short-term high-carbohydrate feeding on serum triglyceride of children with familial hypercholesterolaemia
M M Segall, I Tamir, A S Fosbrooke, et al.
Archives of Disease in Childhood
|
February 1, 1971
Low proline diet in type I hyperprolinaemia
J T Harries, A T Piesowicz, J W Seakins, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1978
Disordered intestinal function in glycogen storage disease
P J Milla, D A Atherton, J V Leonard, et al.
Archives of Disease in Childhood
|
January 1, 1979
Behavioural deviance in children with early treated phenylketonuria
J E Stevenson, J Hawcroft, M Lobascher, et al.
Clinical Pediatrics
|
July 1, 1986
The investigation of atypical psychosomatic illness. A team approach to diagnosis
D B Dunger, J Pritchard, S Hensman, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
June 18, 1981
Effects of delipidated serum and lipoprotein-deficient serum on sterol biosynthesis and efflux in cultured skin fibroblasts - a comparison of the behaviour of cells from a control with those from a heterozygote and homozygote for familial hypercholesterolaemia
P M Giles, B J Andrews, J Cheshire, et al.
British Medical Journal
|
September 9, 1978
Effect of stopping low-phenylalanine diet on intellectual progress of children with phenylketonuria
I Smith, M E Lobascher, J E Stevenson, et al.
Lancet (London, England)
|
January 6, 1979
Fetal damage despite low-phenylalanine diet after conception in a phenylketonuric woman
I Smith, M Erdohazi, F J Macartney, et al.
Page
of 5
Search research articles
Search
Showing results (41-50 of 49) with videos related to
Sort By:
Page
of 5
You have reached the last page of results.
This site can display upto 49 results.
Archives of Disease in Childhood
|
November 1, 1973
Familial selective malabsorption of vitamin B12
M Bell, J T Harries, O H Wolff, et al.
Archives of Disease in Childhood
|
June 1, 1970
Effects of short-term high-carbohydrate feeding on serum triglyceride of children with familial hypercholesterolaemia
M M Segall, I Tamir, A S Fosbrooke, et al.
Archives of Disease in Childhood
|
February 1, 1971
Low proline diet in type I hyperprolinaemia
J T Harries, A T Piesowicz, J W Seakins, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1978
Disordered intestinal function in glycogen storage disease
P J Milla, D A Atherton, J V Leonard, et al.
Archives of Disease in Childhood
|
January 1, 1979
Behavioural deviance in children with early treated phenylketonuria
J E Stevenson, J Hawcroft, M Lobascher, et al.
Clinical Pediatrics
|
July 1, 1986
The investigation of atypical psychosomatic illness. A team approach to diagnosis
D B Dunger, J Pritchard, S Hensman, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
June 18, 1981
Effects of delipidated serum and lipoprotein-deficient serum on sterol biosynthesis and efflux in cultured skin fibroblasts - a comparison of the behaviour of cells from a control with those from a heterozygote and homozygote for familial hypercholesterolaemia
P M Giles, B J Andrews, J Cheshire, et al.
British Medical Journal
|
September 9, 1978
Effect of stopping low-phenylalanine diet on intellectual progress of children with phenylketonuria
I Smith, M E Lobascher, J E Stevenson, et al.
Lancet (London, England)
|
January 6, 1979
Fetal damage despite low-phenylalanine diet after conception in a phenylketonuric woman
I Smith, M Erdohazi, F J Macartney, et al.
Page
of 5