Rosenblatt DS - Search Results

1

Defective lysosomal release of vitamin B12 (cb1F): a hereditary cobalamin metabolic disorder associated with sudden death.

Shih VE, Axel SM, Tewksbury JC, Watkins D, Cooper BA, Rosenblatt DS. Shih VE, et al. Among authors: rosenblatt ds. Am J Med Genet. 1989 Aug;33(4):555-63. doi: 10.1002/ajmg.1320330431. Am J Med Genet. 1989. PMID: 2596518

2

Vitamin B12 responsive homocystinuria and megaloblastic anemia: heterogeneity in methylcobalamin deficiency.

Rosenblatt DS, Thomas IT, Watkins D, Cooper BA, Erbe RW. Rosenblatt DS, et al. Am J Med Genet. 1987 Feb;26(2):377-83. doi: 10.1002/ajmg.1320260216. Am J Med Genet. 1987. PMID: 3812589

3

Inborn errors of cobalamin absorption and metabolism.

Watkins D, Rosenblatt DS. Watkins D, et al. Among authors: rosenblatt ds. Am J Med Genet C Semin Med Genet. 2011 Feb 15;157C(1):33-44. doi: 10.1002/ajmg.c.30288. Epub 2011 Feb 10. Am J Med Genet C Semin Med Genet. 2011. PMID: 21312325

4

Inherited disorders of vitamin B12 utilization.

Rosenblatt DS, Cooper BA. Rosenblatt DS, et al. Bioessays. 1990 Jul;12(7):331-4. doi: 10.1002/bies.950120705. Bioessays. 1990. PMID: 2203337 Review.

5

Functional methionine synthase deficiency (cblE and cblG): clinical and biochemical heterogeneity.

Watkins D, Rosenblatt DS. Watkins D, et al. Among authors: rosenblatt ds. Am J Med Genet. 1989 Nov;34(3):427-34. doi: 10.1002/ajmg.1320340320. Am J Med Genet. 1989. PMID: 2688421 Review.

6

Inherited disorders of vitamin B12 metabolism.

Rosenblatt DS, Cooper BA. Rosenblatt DS, et al. Blood Rev. 1987 Sep;1(3):177-82. doi: 10.1016/0268-960x(87)90033-6. Blood Rev. 1987. PMID: 3332101 Review.

7

Failure of lysosomal release of vitamin B12: a new complementation group causing methylmalonic aciduria (cblF).

Watkins D, Rosenblatt DS. Watkins D, et al. Among authors: rosenblatt ds. Am J Hum Genet. 1986 Sep;39(3):404-8. Am J Hum Genet. 1986. PMID: 3766542 Free PMC article.

8

Complementation studies in the cblA class of inborn error of cobalamin metabolism: evidence for interallelic complementation and for a new complementation class (cblH).

Watkins D, Matiaszuk N, Rosenblatt DS. Watkins D, et al. Among authors: rosenblatt ds. J Med Genet. 2000 Jul;37(7):510-3. doi: 10.1136/jmg.37.7.510. J Med Genet. 2000. PMID: 10882753 Free PMC article.

9

Lessons in biology from patients with inborn errors of vitamin B12 metabolism.

Watkins D, Rosenblatt DS. Watkins D, et al. Among authors: rosenblatt ds. Biochimie. 2013 May;95(5):1019-22. doi: 10.1016/j.biochi.2013.01.013. Epub 2013 Feb 10. Biochimie. 2013. PMID: 23402785 Review.

10

Lysosomal cobalamin accumulation in fibroblasts from a patient with an inborn error of cobalamin metabolism (cblF complementation group): visualization by electron microscope radioautography.

Vassiliadis A, Rosenblatt DS, Cooper BA, Bergeron JJ. Vassiliadis A, et al. Among authors: rosenblatt ds. Exp Cell Res. 1991 Aug;195(2):295-302. doi: 10.1016/0014-4827(91)90376-6. Exp Cell Res. 1991. PMID: 2070814

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