Functional methionine synthase deficiency (cblE and cblG): clinical and biochemical heterogeneityWATKINS, D; ROSENBLATT, D. S.American journal of medical genetics. 1989, Vol 34, Num 3, pp 427-434, issn 0148-7299Article

Failure of lysosomal release of vitamin B₁₂: a new complementation group causing methylmalonic aciduria (cblF)WATKINS, D; ROSENBLATT, D. S.American journal of human genetics. 1986, Vol 39, Num 3, pp 404-408, issn 0002-9297Article

Genetic heterogeneity among patients with methylcobalamin deficiency: definition of two complementation groups, cblE and cblGWATKINS, D; ROSENBLATT, D. S.The Journal of clinical investigation. 1988, Vol 81, Num 6, pp 1690-1694, issn 0021-9738, 5 p.Article

Metabolic cooperation among cell lines from patients with inborn errors of vitamin B₁₂ metabolism : differential response of cbIC and cbIDBYCK, S; ROSENBLATT, D. S.Clinical and investigative medicine. 1991, Vol 14, Num 2, pp 153-159, issn 0147-958XArticle

Cobalamin and folate deficiency : Acquired and hereditary disorders in childrenROSENBLATT, D. S; WHITEHEAD, V. M.Seminars in hematology. 1999, Vol 36, Num 1, pp 19-34, issn 0037-1963Article

Effects of folate deficiency on embryonic developmentCHRISTENSEN, B; ROSENBLATT, D. S.Baillière's clinical haematology. 1995, Vol 8, Num 3, pp 617-637, issn 0950-3536Article

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, D. S et al.Journal of medical genetics. 2000, Vol 37, Num 7, pp 510-513, issn 0022-2593Article

Mechanisms of teratogenesis : folic acid and antiepileptic therapyDANSKY, L. V; ROSENBLATT, D. S; ANDERMANN, E et al.Neurology. 1992, Vol 42, Num 4, pp 32-42, issn 0028-3878, SUP5Article

Methylmalonic aciduria due to a new defect in adenosylcobalamin accumulation by cellsCOOPER, B. A; ROSENBLATT, D. S; WATKINS, D et al.American journal of hematology. 1990, Vol 34, Num 2, pp 115-120, issn 0361-8609, 6 p.Article

Expression of transcobalamin II by amniocytesROSENBLATT, D. S; HOSACK, A; MATIASZUK, N et al.Prenatal diagnosis. 1987, Vol 7, Num 1, pp 35-39, issn 0197-3851Article

Inherited defects of vitamin B₁₂ metabolismCOOPER, B. A; ROSENBLATT, D. S.Annual review of nutrition. 1987, Vol 7, pp 291-320, issn 0199-9885Article

The neurology of cobalaminSHEVELL, M. I; ROSENBLATT, D. S.Canadian journal of neurological sciences. 1992, Vol 19, Num 4, pp 472-486, issn 0317-1671Article

Glycine N-methyltransferase deficiency: A novel inborn error causing persistent isolated hypermethioninaemiaMUDD, S. H; CERONE, R; SCHWAHN, B et al.Journal of inherited metabolic disease. 2001, Vol 24, Num 4, pp 448-464, issn 0141-8955Article

Reversible dementia in an adolescent with cblC disease : Clinical heterogeneity within the same familyAUGOUSTIDES-SAVVOPOULOU, P; MYLONAS, I; SEWELL, A. C et al.Journal of inherited metabolic disease. 1999, Vol 22, Num 6, pp 756-758, issn 0141-8955Article

Methylenetetrahydrofolate reductase deficiency in a patient with phenotypic findings of Angelman syndromeARN, P. H; WILLIAMS, C. A; ZORI, R. T et al.American journal of medical genetics. 1998, Vol 77, Num 3, pp 198-200, issn 0148-7299Article

Correlation of a common mutation in the methylenetetrahydrofolate reductase gene with plasma homocysteine in patients with premature coronary artery diseaseCHRISTENSEN, B; FROSST, P; LUSSIER-CACAN, S et al.Arteriosclerosis, thrombosis, and vascular biology. 1997, Vol 17, Num 3, pp 569-573, issn 1079-5642Article

Expression of transcobalamin II mRNA in human tissues and cultured fibroblasts from normal and transcobalamin II-deficient patientsNING LI; SHAKUNTLA SEETHRAM; ROSENBLATT, D. S et al.Biochemical journal (London. 1984). 1994, Vol 301, pp 585-590, issn 0264-6021, 2Article

Identification of two mutant alleles of transcobalamin II in an affected familyLI, N; ROSENBLATT, D. S; KAMEN, B. A et al.Human molecular genetics (Print). 1994, Vol 3, Num 10, pp 1835-1840, issn 0964-6906Article

Cobalamin C defect associated with hemolytic-uremic syndromeGERAGHTY, M. T; PERLMAN, E. J; MARTIN, L. S et al.The Journal of pediatrics. 1992, Vol 120, Num 6, pp 934-937, issn 0022-3476Article

Knowledge of nephrologists and patients about autosomal dominant polycystic kidney disease (ADPKD)ROSNBERG, E. E; TANNENBAUM, T. N; MILLER, S. D et al.Clinical and investigative medicine. 1992, Vol 15, Num 5, pp 440-444, issn 0147-958XArticle

New disorder of vitamin B₁₂ metabolism (cobalamin F) presenting as methylmalonic aciduriaROSENBLATT, D. S; LAFRAMBOISE, R; PICHETTE, J et al.Pediatrics (Evanston). 1986, Vol 78, Num 1, pp 51-54, issn 0031-4005Article

The evolution of medicine : a geneticist's point of view. DiscussionROSENBLATT, D. S; EVANS, J; ROSENBLATT, D et al.Clinical and investigative medicine. 2000, Vol 23, Num 1, pp 59-63, issn 0147-958XConference Paper

Clinical correlates of subnormal vitamin B12 levels in patients infected with the human immunodeficiency virusPALTIEL, O; FALUTZ, J; VEILLEUX, M et al.American journal of hematology. 1995, Vol 49, Num 4, pp 318-322, issn 0361-8609Article

Methylenetetrahydrofolate reductase (MR) deficiency : thermolability of residual MR activity, methionine synthase activity, and methylcobalamin levels in cultured fibroblastsROSENBLATT, D. S; LUE-SHING, H; ARZOUMANIAN, A et al.Biochemical medicine and metabolic biology. 1992, Vol 47, Num 3, pp 221-225, issn 0885-4505Article

Changes in cobalamin metabolism are associated with the altered methionine auxotrophy of highly growth autonomous human melanoma cellsLITEPLO, R. G; HIPWELL, S. E; ROSENBLATT, D. S et al.Journal of cellular physiology. 1991, Vol 149, Num 2, pp 332-338, issn 0021-9541Article