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E Naughten

Showing results (1-10 of 21) with videos related to

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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 controlS Yap, E Naughten
Journal of Inherited Metabolic Disease|January 1, 1990
Maternal phenylketonuria--the Irish experienceE Naughten, I P Saul
Lancet (London, England)|October 8, 1977
Vitamin D and human lactationA 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 dietsG 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 chainM 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 delayS Yap, A A Monavari, P Thornton, et al.
Lancet (London, England)|October 31, 1981
Tuberculous meningitis in children. Recent experience in two English centresE Naughten, A M Weindling, R Newton, et al.
Lancet (London, England)|March 15, 1997
3-Methylglutaconic aciduria in pregnancyR Walsh, H Conway, G Roche, et al.
The British Journal of Ophthalmology|March 1, 1993
Ophthalmic findings in classical galactosaemia--prospective studyB Beigi, M O'Keefe, R Bowell, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 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 controlS Yap, E Naughten
Journal of Inherited Metabolic Disease|January 1, 1990
Maternal phenylketonuria--the Irish experienceE Naughten, I P Saul
Lancet (London, England)|October 8, 1977
Vitamin D and human lactationA 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 dietsG 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 chainM 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 delayS Yap, A A Monavari, P Thornton, et al.
Lancet (London, England)|October 31, 1981
Tuberculous meningitis in children. Recent experience in two English centresE Naughten, A M Weindling, R Newton, et al.
Lancet (London, England)|March 15, 1997
3-Methylglutaconic aciduria in pregnancyR Walsh, H Conway, G Roche, et al.
The British Journal of Ophthalmology|March 1, 1993
Ophthalmic findings in classical galactosaemia--prospective studyB Beigi, M O'Keefe, R Bowell, et al.
Pageof 3