J. Bronte-Stewart

发表

Vitamin A deficiency in Crohn's disease.

R. Russell, A. Shenkin, P. Mills, 1983, Gut.

Primary pathogenic mtDNA mutations in multigeneration pedigrees with Leber hereditary optic neuropathy.

D. Mackey, T. Rosenberg, A. Harding, 1996, American journal of human genetics.

COLOUR VISION IN TOBACCO AMBLYOPIA

J. Bronte-Stewart, I. A. Chisholm, E. O. Awduche, 1970, Acta ophthalmologica.

Effects of raised intra-ocular pressure on hue discrimination.

W. Foulds, J. Bronte-Stewart, I. A. Chisholm, 1974, Modern problems in ophthalmology.

Colour Vision in Young Diabetics

J. Bronte-Stewart, J. Craig, J. Cant, 1984 .

Hydroxocobalamin versus cyanocobalamin in the treatment of tobacco amblyopia.

W. Foulds, J. Bronte-Stewart, I. A. Chisholm, 1967, Lancet.

Serum Thiocyanate Concentrations in Tobacco Amblyopia

W. Foulds, J. Bronte-Stewart, I. A. Chisholm, 1968, Nature.

Vitanin A deficiency in Crohn ' s disease

P. Mills, J. Bronte-Stewart, A. Mclelland, 2006 .

Analysis of mitochondrial DNA in Leber's hereditary optic neuropathy.

M. Deadman, J. Poulton, W. Foulds, 1991, Journal of medical genetics.

Cyanide induced optic neuropathy.

W. Foulds, J. Bronte-Stewart, I. A. Chisholm, 1969, Ophthalmologica. Journal international d'ophtalmologie. International journal of ophthalmology. Zeitschrift fur Augenheilkunde.

The investigation and therapy of the toxic amblyopias.

W. Foulds, J. Bronte-Stewart, Chisholm, 1970, Transactions of the ophthalmological societies of the United Kingdom.

Hydroxocobalamin in the treatment of Leber's hereditary optic atrophy.

J. Wilson, W. Foulds, J. Bronte-Stewart, 1968, Lancet.

Clinical and biochemical findings in Leber's hereditary optic atrophy.

W. Foulds, E. Mcclure, J. Bronte-Stewart, 1983, Transactions of the ophthalmological societies of the United Kingdom.

Vitamin B 12 absorption in tobacco amblyopia.

W. Foulds, J. Bronte-Stewart, I. A. Chisholm, 1969, The British journal of ophthalmology.