Smith I - Search Results

1

Demyelination and decreased S-adenosylmethionine in 5,10-methylenetetrahydrofolate reductase deficiency.

Hyland K, Smith I, Bottiglieri T, Perry J, Wendel U, Clayton PT, Leonard JV. Hyland K, et al. Among authors: smith i. Neurology. 1988 Mar;38(3):459-62. doi: 10.1212/wnl.38.3.459. Neurology. 1988. PMID: 3347350

2

Biopterins in arginase, dihydropteridine reductase and phenylalanine hydroxylase deficiency.

Hyland K, Smith I, Leonard JV. Hyland K, et al. Among authors: smith i. J Neurol Neurosurg Psychiatry. 1987 Feb;50(2):242. doi: 10.1136/jnnp.50.2.242. J Neurol Neurosurg Psychiatry. 1987. PMID: 3572445 Free PMC article. No abstract available.

3

Subacute combined degeneration of the cord, dementia and parkinsonism due to an inborn error of folate metabolism.

Clayton PT, Smith I, Harding B, Hyland K, Leonard JV, Leeming RJ. Clayton PT, et al. Among authors: smith i. J Neurol Neurosurg Psychiatry. 1986 Aug;49(8):920-7. doi: 10.1136/jnnp.49.8.920. J Neurol Neurosurg Psychiatry. 1986. PMID: 3755752 Free PMC article.

4

Cerebrospinal fluid concentrations of pterins and metabolites of serotonin and dopamine in a pediatric reference population.

Hyland K, Surtees RA, Heales SJ, Bowron A, Howells DW, Smith I. Hyland K, et al. Among authors: smith i. Pediatr Res. 1993 Jul;34(1):10-4. doi: 10.1203/00006450-199307000-00003. Pediatr Res. 1993. PMID: 7689195

5

Familial glucocorticoid deficiency with achalasia of the cardia associated with mixed neuropathy, long-tract degeneration and mild dementia.

Grant DB, Dunger DB, Smith I, Hyland K. Grant DB, et al. Among authors: smith i. Eur J Pediatr. 1992 Feb;151(2):85-9. doi: 10.1007/BF01958948. Eur J Pediatr. 1992. PMID: 1537368

6

Central-nervous-system methyl-group metabolism in children with neurological complications of HIV infection.

Surtees R, Hyland K, Smith I. Surtees R, et al. Among authors: smith i. Lancet. 1990 Mar 17;335(8690):619-21. doi: 10.1016/0140-6736(90)90409-x. Lancet. 1990. PMID: 1969014

7

Clinical role of pteridine therapy in tetrahydrobiopterin deficiency.

Smith I, Hyland K, Kendall B. Smith I, et al. J Inherit Metab Dis. 1985;8 Suppl 1:39-45. doi: 10.1007/BF01800658. J Inherit Metab Dis. 1985. PMID: 3930840

8

Tetrahydrobiopterin in dihydropteridine reductase deficiency.

Howells D, Smith I, Leonard J, Hyland K. Howells D, et al. Among authors: smith i. N Engl J Med. 1986 Feb 20;314(8):520-1. doi: 10.1056/nejm198602203140818. N Engl J Med. 1986. PMID: 3945285 No abstract available.

9

Impaired neurotransmitter amine metabolism in arginase deficiency.

Hyland K, Smith I, Clayton PT, Leonard JV. Hyland K, et al. Among authors: smith i. J Neurol Neurosurg Psychiatry. 1985 Nov;48(11):1188-9. doi: 10.1136/jnnp.48.11.1188-a. J Neurol Neurosurg Psychiatry. 1985. PMID: 4078590 Free PMC article. No abstract available.

10

Tryptophan and serotonin metabolism in familial erythrophagocytic lymphohistiocytosis.

Howells DW, Hyland K, Smith I, Strobel S. Howells DW, et al. Among authors: smith i. J Inherit Metab Dis. 1992;15(6):891-7. doi: 10.1007/BF01800228. J Inherit Metab Dis. 1992. PMID: 1284084

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