Finkelstein JD - Search Results

1

Folate-responsive homocystinuria and "schizophrenia". A defect in methylation due to deficient 5,10-methylenetetrahydrofolate reductase activity.

Freeman JM, Finkelstein JD, Mudd SH. Freeman JM, et al. Among authors: finkelstein jd. N Engl J Med. 1975 Mar 6;292(10):491-6. doi: 10.1056/NEJM197503062921001. N Engl J Med. 1975. PMID: 1117892

2

HOMOCYSTINURIA: AN ENZYMATIC DEFECT.

MUDD SH, FINKELSTEIN JD, IRREVERRE F, LASTER L. MUDD SH, et al. Among authors: finkelstein jd. Science. 1964 Mar 27;143(3613):1443-5. doi: 10.1126/science.143.3613.1443. Science. 1964. PMID: 14107447

3

HOMOCYSTINURIA DUE TO CYSTATHIONINE SYNTHETASE DEFICIENCY: THE MODE OF INHERITANCE.

FINKELSTEIN JD, MUDD SH, IRREVERRE F, LASTER L. FINKELSTEIN JD, et al. Science. 1964 Nov 6;146(3645):785-7. doi: 10.1126/science.146.3645.785. Science. 1964. PMID: 14197572

4

Homocystinuria associated with decreased methylenetetrahydrofolate reductase activity.

Mudd SH, Uhlendorf BW, Freeman JM, Finkelstein JD, Shih VE. Mudd SH, et al. Among authors: finkelstein jd. Biochem Biophys Res Commun. 1972 Jan 31;46(2):905-12. doi: 10.1016/s0006-291x(72)80227-4. Biochem Biophys Res Commun. 1972. PMID: 5057914 No abstract available.

5

Trans-sulfuration in mammals. The methionine-sparing effect of cystine.

Finkelstein JD, Mudd SH. Finkelstein JD, et al. J Biol Chem. 1967 Mar 10;242(5):873-80. J Biol Chem. 1967. PMID: 6067003 Free article. No abstract available.

6

Persistent hypermethioninaemia with dominant inheritance.

Blom HJ, Davidson AJ, Finkelstein JD, Luder AS, Bernardini I, Martin JJ, Tangerman A, Trijbels JM, Mudd SH, Goodman SI, et al. Blom HJ, et al. Among authors: finkelstein jd. J Inherit Metab Dis. 1992;15(2):188-97. doi: 10.1007/BF01799629. J Inherit Metab Dis. 1992. PMID: 1527987

7

Transsulfuration in an adult with hepatic methionine adenosyltransferase deficiency.

Gahl WA, Bernardini I, Finkelstein JD, Tangerman A, Martin JJ, Blom HJ, Mullen KD, Mudd SH. Gahl WA, et al. Among authors: finkelstein jd. J Clin Invest. 1988 Feb;81(2):390-7. doi: 10.1172/JCI113331. J Clin Invest. 1988. PMID: 3339126 Free PMC article.

8

Hepatic methionine adenosyltransferase deficiency in a 31-year-old man.

Gahl WA, Finkelstein JD, Mullen KD, Bernardini I, Martin JJ, Backlund P, Ishak KG, Hoofnagle JH, Mudd SH. Gahl WA, et al. Among authors: finkelstein jd. Am J Hum Genet. 1987 Jan;40(1):39-49. Am J Hum Genet. 1987. PMID: 3812486 Free PMC article.

9

Homocystinuria due to cystathionine synthase deficiency: the metabolism of L-methionine.

Laster L, Mudd SH, Finkelstein JD, Irreverre F. Laster L, et al. Among authors: finkelstein jd. J Clin Invest. 1965 Oct;44(10):1708-19. doi: 10.1172/JCI105278. J Clin Invest. 1965. PMID: 5840537 Free PMC article. No abstract available.

10

Deficiencies of cystathionase and homoserine dehydratase activities in cystathioninuria.

Finkelstein JD, Mudd SH, Irreverre F, Laster L. Finkelstein JD, et al. Proc Natl Acad Sci U S A. 1966 Apr;55(4):865-72. doi: 10.1073/pnas.55.4.865. Proc Natl Acad Sci U S A. 1966. PMID: 5219695 Free PMC article. No abstract available.

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