Rosenblatt DS - Search Results

1

Clinical heterogeneity in cobalamin C variant of combined homocystinuria and methylmalonic aciduria.

Mitchell GA, Watkins D, Melançon SB, Rosenblatt DS, Geoffroy G, Orquin J, Homsy MB, Dallaire L. Mitchell GA, et al. Among authors: rosenblatt ds. J Pediatr. 1986 Mar;108(3):410-5. doi: 10.1016/s0022-3476(86)80882-4. J Pediatr. 1986. PMID: 3950820

2

Vitamin B12-responsive megaloblastic anemia, homocystinuria, and transient methylmalonic aciduria in cb1E disease.

Tuchman M, Kelly P, Watkins D, Rosenblatt DS. Tuchman M, et al. Among authors: rosenblatt ds. J Pediatr. 1988 Dec;113(6):1052-6. doi: 10.1016/s0022-3476(88)80582-1. J Pediatr. 1988. PMID: 3193313 No abstract available.

3

Clinical and molecular heterogeneity in patients with the cblD inborn error of cobalamin metabolism.

Miousse IR, Watkins D, Coelho D, Rupar T, Crombez EA, Vilain E, Bernstein JA, Cowan T, Lee-Messer C, Enns GM, Fowler B, Rosenblatt DS. Miousse IR, et al. Among authors: rosenblatt ds. J Pediatr. 2009 Apr;154(4):551-6. doi: 10.1016/j.jpeds.2008.10.043. Epub 2008 Dec 5. J Pediatr. 2009. PMID: 19058814

4

Methylmalonic aciduria due to a new defect in adenosylcobalamin accumulation by cells.

Cooper BA, Rosenblatt DS, Watkins D. Cooper BA, et al. Among authors: rosenblatt ds. Am J Hematol. 1990 Jun;34(2):115-20. doi: 10.1002/ajh.2830340207. Am J Hematol. 1990. PMID: 2339678

5

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.

6

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

7

Inherited defects of cobalamin metabolism.

Watkins D, Rosenblatt DS. Watkins D, et al. Among authors: rosenblatt ds. Vitam Horm. 2022;119:355-376. doi: 10.1016/bs.vh.2022.01.010. Epub 2022 Feb 21. Vitam Horm. 2022. PMID: 35337626

8

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.

9

Genetic heterogeneity among patients with methylcobalamin deficiency. Definition of two complementation groups, cblE and cblG.

Watkins D, Rosenblatt DS. Watkins D, et al. Among authors: rosenblatt ds. J Clin Invest. 1988 Jun;81(6):1690-4. doi: 10.1172/JCI113507. J Clin Invest. 1988. PMID: 3384945 Free PMC article.

10

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

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