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Journal of Inherited Metabolic Disease
|
November 20, 1998
Homocystinuria due to cystathionine beta-synthase deficiency in Ireland: 25 years' experience of a newborn screened and treated population with reference to clinical outcome and biochemical control
S Yap, E Naughten
Journal of Inherited Metabolic Disease
|
January 1, 1990
Maternal phenylketonuria--the Irish experience
E Naughten, I P Saul
Lancet (London, England)
|
October 8, 1977
Vitamin D and human lactation
A Fairney, E Naughten, T E Oppé
American Journal of Diseases of Children (1960)
|
August 1, 1982
At what age do diabetic children give their own injections?
E Naughten, M A Smith, J D Baum
Journal of Inherited Metabolic Disease
|
January 1, 1992
Serum selenium levels in individuals on PKU diets
G Darling, P Mathias, M O'Regan, et al.
Metabolic, Pediatric, and Systemic Ophthalmology (New York, N.Y. : 1985)
|
January 1, 1996
Two cases of hereditary optic atrophy associated with an enzymatic defect of the respiratory chain
M Cahill, A Monavari, E Naughten, et al.
Journal of Inherited Metabolic Disease
|
May 19, 1998
Late-infantile 3-methylcrotonyl-CoA carboxylase deficiency presenting as global developmental delay
S Yap, A A Monavari, P Thornton, et al.
Lancet (London, England)
|
October 31, 1981
Tuberculous meningitis in children. Recent experience in two English centres
E Naughten, A M Weindling, R Newton, et al.
Lancet (London, England)
|
March 15, 1997
3-Methylglutaconic aciduria in pregnancy
R Walsh, H Conway, G Roche, et al.
The British Journal of Ophthalmology
|
March 1, 1993
Ophthalmic findings in classical galactosaemia--prospective study
B Beigi, M O'Keefe, R Bowell, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 21) with videos related to
Sort By:
Page
of 3
Journal of Inherited Metabolic Disease
|
November 20, 1998
Homocystinuria due to cystathionine beta-synthase deficiency in Ireland: 25 years' experience of a newborn screened and treated population with reference to clinical outcome and biochemical control
S Yap, E Naughten
Journal of Inherited Metabolic Disease
|
January 1, 1990
Maternal phenylketonuria--the Irish experience
E Naughten, I P Saul
Lancet (London, England)
|
October 8, 1977
Vitamin D and human lactation
A Fairney, E Naughten, T E Oppé
American Journal of Diseases of Children (1960)
|
August 1, 1982
At what age do diabetic children give their own injections?
E Naughten, M A Smith, J D Baum
Journal of Inherited Metabolic Disease
|
January 1, 1992
Serum selenium levels in individuals on PKU diets
G Darling, P Mathias, M O'Regan, et al.
Metabolic, Pediatric, and Systemic Ophthalmology (New York, N.Y. : 1985)
|
January 1, 1996
Two cases of hereditary optic atrophy associated with an enzymatic defect of the respiratory chain
M Cahill, A Monavari, E Naughten, et al.
Journal of Inherited Metabolic Disease
|
May 19, 1998
Late-infantile 3-methylcrotonyl-CoA carboxylase deficiency presenting as global developmental delay
S Yap, A A Monavari, P Thornton, et al.
Lancet (London, England)
|
October 31, 1981
Tuberculous meningitis in children. Recent experience in two English centres
E Naughten, A M Weindling, R Newton, et al.
Lancet (London, England)
|
March 15, 1997
3-Methylglutaconic aciduria in pregnancy
R Walsh, H Conway, G Roche, et al.
The British Journal of Ophthalmology
|
March 1, 1993
Ophthalmic findings in classical galactosaemia--prospective study
B Beigi, M O'Keefe, R Bowell, et al.
Page
of 3