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Results of search for 'au:"ROSENBLATT, D"', page 5 of 10
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Authors
Aune, D
BELKIN, M
Beaulieu, D
Chan, D S M
Christensen, B
Cooper, B A
Goyette, P
Ledley, F D
Matiaszuk, N V
Norat, T
ROSENBLATT, D
Rosenblatt, D
Rosenblatt, D E
Rosenblatt, D H
Rosenblatt, D S
Rozen, R
Vieira, A R
Vuchich, M J
Watkins, D
Whitehead, V M
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Topics
5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase
Adult
Cells, Cultured
Child
Female
Fibroblasts
Folic Acid
Homocystinuria
Humans
Infant
Infant, Newborn
Male
Metabolism, Inborn Errors
Methylmalonic Acid
Mutation
Vitamin B 12
blood
deficiency
genetics
metabolism
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English
French
Your search returned 197 results.
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81.
Reporting mistreatment of older adults: the role of physicians.
[electronic resource]
by
Rosenblatt, D E
Cho, K H
Durance, P W
Producer:
19960208
In:
Journal of the American Geriatrics Society
vol. 44
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82.
MOTHERS' UTILIZATION OF THE CHILD HEALTH STATION AND EVALUATION OF THE CHILD HEALTH CONFERENCE.
[electronic resource]
by
BELKIN, M
SUCHMAN, E A
ROSENBLATT, D
JACOBZINER, H
Producer:
19961201
In:
American journal of public health and the nation's health
vol. 54
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83.
EFFECT OF PHYSICIAN TRAINING IN MENTAL HEALTH PRINCIPLES ON MOTHERS' APPRAISAL OF CHILD HEALTH CONFERENCES.
[electronic resource]
by
BELKIN, M
SUCHMAN, E A
ROSENBLATT, D
JACOBZINER, H
Producer:
19961201
In:
Mental hygiene
vol. 49
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84.
Mitochondrial vitamin B12-binding proteins in patients with inborn errors of cobalamin metabolism.
[electronic resource]
by
Moras, E
Hosack, A
Watkins, D
Rosenblatt, D S
Producer:
20070329
In:
Molecular genetics and metabolism
vol. 90
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85.
Molecular basis for methionine synthase reductase deficiency in patients belonging to the cblE complementation group of disorders in folate/cobalamin metabolism.
[electronic resource]
by
Wilson, A
Leclerc, D
Rosenblatt, D S
Gravel, R A
Producer:
19991216
In:
Human molecular genetics
vol. 8
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86.
Hereditary defect of cobalamin metabolism (cblG mutation) presenting as a neurologic disorder in adulthood.
[electronic resource]
by
Carmel, R
Watkins, D
Goodman, S I
Rosenblatt, D S
Producer:
19880714
In:
The New England journal of medicine
vol. 318
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87.
Protease nexin-1 activity in cultured Schwann cells.
[electronic resource]
by
Mulligan, L P
Rosenblatt, D E
Toms, R
Johnson, D
Producer:
19911105
In:
Neuroscience letters
vol. 128
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88.
Detection of heterozygotes for recessive alleles. Homocyst(e)inemia: paradigm of pitfalls in phenotypes.
[electronic resource]
by
McGill, J J
Mettler, G
Rosenblatt, D S
Scriver, C R
Producer:
19900604
In:
American journal of medical genetics
vol. 36
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89.
Deletional beta-thalassemia with high Hb A2.
[electronic resource]
by
Kendall, A G
Popovich, B W
Rosenblatt, D S
Nishioka, Y
Producer:
19890216
In:
Hemoglobin
vol. 12
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90.
Tubulointerstitial nephritis in methylmalonic acidemia.
[electronic resource]
by
Rutledge, S L
Geraghty, M
Mroczek, E
Rosenblatt, D
Kohout, E
Producer:
19930329
In:
Pediatric nephrology (Berlin, Germany)
vol. 7
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91.
Clinical correlates of subnormal vitamin B12 levels in patients infected with the human immunodeficiency virus.
[electronic resource]
by
Paltiel, O
Falutz, J
Veilleux, M
Rosenblatt, D S
Gordon, K
Producer:
19950914
In:
American journal of hematology
vol. 49
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92.
Reversible dementia in an adolescent with cblC disease: clinical heterogeneity within the same family.
[electronic resource]
by
Augoustides-Savvopoulou, P
Mylonas, I
Sewell, A C
Rosenblatt, D S
Producer:
19991004
In:
Journal of inherited metabolic disease
vol. 22
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93.
Transcobalamin (TC) deficiency and newborn screening.
[electronic resource]
by
Prasad, Chitra
Cairney, A E
Rosenblatt, D S
Rupar, C A
Producer:
20130205
In:
Journal of inherited metabolic disease
vol. 35
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94.
Lysosomal cobalamin accumulation in fibroblasts from a patient with an inborn error of cobalamin metabolism (cblF complementation group): visualization by electron microscope radioautography.
[electronic resource]
by
Vassiliadis, A
Rosenblatt, D S
Cooper, B A
Bergeron, J J
Producer:
19910819
In:
Experimental cell research
vol. 195
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95.
Transcobalamin II deficiency with methylmalonic aciduria in three sisters.
[electronic resource]
by
Bibi, H
Gelman-Kohan, Z
Baumgartner, E R
Rosenblatt, D S
Producer:
19991221
In:
Journal of inherited metabolic disease
vol. 22
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96.
CHILD HEALTH STATION PERSONNEL: A PROFILE.
[electronic resource]
by
GOLDMAN, M
BELKIN, M
SUCHMAN, E A
ROSENBLATT, D
JACOBZINER, H
Producer:
19961201
In:
American journal of public health and the nation's health
vol. 54
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97.
Molecular characterization of an atypical beta-thalassemia caused by a large deletion in the 5' beta-globin gene region.
[electronic resource]
by
Popovich, B W
Rosenblatt, D S
Kendall, A G
Nishioka, Y
Producer:
19870127
In:
American journal of human genetics
vol. 39
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98.
Effect of methionine and nitrous oxide on homocysteine export and remethylation in fibroblasts from cystathionine synthase-deficient, cb1G, and cb1E patients.
[electronic resource]
by
Christensen, B
Rosenblatt, D S
Chu, R C
Ueland, P M
Producer:
19940415
In:
Pediatric research
vol. 35
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99.
EVALUATION OF HEARING TESTING PROGRAM IN NEW YORK CITY ELEMENTARY SCHOOLS.
[electronic resource]
by
BELKIN, M
SUCHMAN, E A
BERGMAN, M
ROSENBLATT, D
JACOBZINER, H
Producer:
19961201
In:
Public health reports (Washington, D.C. : 1896)
vol. 78
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100.
Heterogeneity in cblG: differential retention of cobalamin on methionine synthase.
[electronic resource]
by
Sillaots, S L
Hall, C A
Hurteloup, V
Rosenblatt, D S
Producer:
19920814
In:
Biochemical medicine and metabolic biology
vol. 47
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