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The Journal of Pediatrics
|
June 1, 1994
Carnitine palmitoyltransferase II deficiency: a new cause of recurrent pancreatitis
I Tein, J Christodoulou, E Donner, et al.
Molecular Biology & Medicine
|
February 1, 1991
Histidase and histidinemia. Clinical and molecular considerations
R G Taylor, H L Levy, R R McInnes
Acta Neuropathologica
|
January 1, 1992
"Reducing body"-like inclusions in skeletal muscle in childhood-onset acid maltase deficiency
V Jay, J Christodoulou, A Mercer-Connolly, et al.
Transactions of the American Ophthalmological Society
|
January 1, 1980
Treatment of gyrate atrophy of the choroid and retina with low arginine diet
R R McInnes, S A Arshinoff, L Bell, et al.
Journal of the Canadian Dietetic Association
|
September 8, 1982
Use and design of low protein diets for children with inborn metabolic disorders
L Bell, L Chan, W G Sherwood, et al.
The Journal of Pediatrics
|
March 1, 1993
Ornithine transcarbamylase deficiency presenting with strokelike episodes
J Christodoulou, I A Qureshi, R R McInnes, et al.
Human Molecular Genetics
|
July 1, 1994
Identical genotypes in siblings with different homocystinuric phenotypes: identification of three mutations in cystathionine beta-synthase using an improved bacterial expression system
R de Franchis, V Kozich, R R McInnes, et al.
Journal of Medical Genetics
|
March 1, 1995
A mutation causing DHPR deficiency results in a frameshift and a secondary splicing defect
P M Smooker, J Christodoulou, R R McInnes, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 19, 1997
Human argininosuccinate lyase: a structural basis for intragenic complementation
M A Turner, A Simpson, R R McInnes, et al.
Journal of the American Dietetic Association
|
August 1, 1981
Dietary treatment of hyperornithinemia in gyrate atrophy
L Bell, R R McInnes, S A Arshinoff, et al.
Page
of 8
Search research articles
Search
Showing results (21-30 of 74) with videos related to
Sort By:
Page
of 8
The Journal of Pediatrics
|
June 1, 1994
Carnitine palmitoyltransferase II deficiency: a new cause of recurrent pancreatitis
I Tein, J Christodoulou, E Donner, et al.
Molecular Biology & Medicine
|
February 1, 1991
Histidase and histidinemia. Clinical and molecular considerations
R G Taylor, H L Levy, R R McInnes
Acta Neuropathologica
|
January 1, 1992
"Reducing body"-like inclusions in skeletal muscle in childhood-onset acid maltase deficiency
V Jay, J Christodoulou, A Mercer-Connolly, et al.
Transactions of the American Ophthalmological Society
|
January 1, 1980
Treatment of gyrate atrophy of the choroid and retina with low arginine diet
R R McInnes, S A Arshinoff, L Bell, et al.
Journal of the Canadian Dietetic Association
|
September 8, 1982
Use and design of low protein diets for children with inborn metabolic disorders
L Bell, L Chan, W G Sherwood, et al.
The Journal of Pediatrics
|
March 1, 1993
Ornithine transcarbamylase deficiency presenting with strokelike episodes
J Christodoulou, I A Qureshi, R R McInnes, et al.
Human Molecular Genetics
|
July 1, 1994
Identical genotypes in siblings with different homocystinuric phenotypes: identification of three mutations in cystathionine beta-synthase using an improved bacterial expression system
R de Franchis, V Kozich, R R McInnes, et al.
Journal of Medical Genetics
|
March 1, 1995
A mutation causing DHPR deficiency results in a frameshift and a secondary splicing defect
P M Smooker, J Christodoulou, R R McInnes, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 19, 1997
Human argininosuccinate lyase: a structural basis for intragenic complementation
M A Turner, A Simpson, R R McInnes, et al.
Journal of the American Dietetic Association
|
August 1, 1981
Dietary treatment of hyperornithinemia in gyrate atrophy
L Bell, R R McInnes, S A Arshinoff, et al.
Page
of 8