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Results of search for 'au:"ROSENBLATT, D"', page 7 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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Languages
English
French
Your search returned 197 results.
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121.
Molecular analysis of a woman with late onset cystic fibrosis.
[electronic resource]
by
Levy, R D
Leith, W
Miller, S D
Rosenblatt, D S
Rozen, R
Producer:
19910426
In:
Clinical and investigative medicine. Medecine clinique et experimentale
vol. 13
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122.
In vitro and in vivo inactivation of transcobalamin II receptor by its antiserum.
[electronic resource]
by
Bose, S
Komorowski, R
Seetharam, S
Gilfix, B
Rosenblatt, D S
Seetharam, B
Producer:
19960621
In:
The Journal of biological chemistry
vol. 271
Online resources:
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123.
Polycystic kidney diseases in childhood.
[electronic resource]
by
Kaplan, B S
Kaplan, P
Rosenberg, H K
Lamothe, E
Rosenblatt, D S
Producer:
19900102
In:
The Journal of pediatrics
vol. 115
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124.
Folate-responsive homocystinuria and megaloblastic anaemia in a female patient with functional methionine synthase deficiency (cblE disease).
[electronic resource]
by
Fowler, B
Schutgens, R B
Rosenblatt, D S
Smit, G P
Lindemans, J
Producer:
19980218
In:
Journal of inherited metabolic disease
vol. 20
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125.
Policy statement concerning DNA banking and molecular genetic diagnosis. Canadian College of Medical Geneticists.
[electronic resource]
by
Hall, J
Hamerton, J
Hoar, D
Korneluk, R
Ray, P
Rosenblatt, D
Wood, S
Producer:
19920313
In:
Clinical and investigative medicine. Medecine clinique et experimentale
vol. 14
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126.
Vitamin B12 responsive homocystinuria and megaloblastic anemia: heterogeneity in methylcobalamin deficiency.
[electronic resource]
by
Rosenblatt, D S
Thomas, I T
Watkins, D
Cooper, B A
Erbe, R W
Producer:
19870318
In:
American journal of medical genetics
vol. 26
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127.
cblC disease: case report and monitoring of a pregnancy at risk by chorionic villus sampling.
[electronic resource]
by
Zammarchi, E
Lippi, A
Falorni, S
Pasquini, E
Cooper, B A
Rosenblatt, D S
Producer:
19900815
In:
Clinical and investigative medicine. Medecine clinique et experimentale
vol. 13
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128.
Influence of chemical structure on the rate of azo coupling and its significance in histochemical methodology.
[electronic resource]
by
NACHLAS, M M
GOLDSTEIN, T P
ROSENBLATT, D H
KIRSCH, M
SELIGMAN, A M
Producer:
20000701
In:
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society
vol. 7
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129.
Transcobalamin (TC) deficiency--potential cause of bone marrow failure in childhood.
[electronic resource]
by
Prasad, C
Rosenblatt, D S
Corley, K
Cairney, A E L
Rupar, C A
Producer:
20120111
In:
Journal of inherited metabolic disease
vol. 31 Suppl 2
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130.
New disorder of vitamin B12 metabolism (cobalamin F) presenting as methylmalonic aciduria.
[electronic resource]
by
Rosenblatt, D S
Laframboise, R
Pichette, J
Langevin, P
Cooper, B A
Costa, T
Producer:
19860811
In:
Pediatrics
vol. 78
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131.
Functional methionine synthase deficiency due to cblG disorder: a report of two patients and a review.
[electronic resource]
by
Harding, C O
Arnold, G
Barness, L A
Wolff, J A
Rosenblatt, D S
Producer:
19971007
In:
American journal of medical genetics
vol. 71
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132.
Synthesis of methotrexate polyglutamates in cultured human cells.
[electronic resource]
by
Rosenblatt, D S
Whitehead, V M
Dupont, M M
Vuchich, M J
Vera, N
Producer:
19780417
In:
Molecular pharmacology
vol. 14
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133.
Changes in cobalamin metabolism are associated with the altered methionine auxotrophy of highly growth autonomous human melanoma cells.
[electronic resource]
by
Liteplo, R G
Hipwell, S E
Rosenblatt, D S
Sillaots, S
Lue-Shing, H
Producer:
19920117
In:
Journal of cellular physiology
vol. 149
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134.
Genetic characterization of a MUT locus mutation discriminating heterogeneity in mut0 and mut- methylmalonic aciduria by interallelic complementation.
[electronic resource]
by
Raff, M L
Crane, A M
Jansen, R
Ledley, F D
Rosenblatt, D S
Producer:
19910201
In:
The Journal of clinical investigation
vol. 87
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135.
Light modulation with resonant grating-waveguide structures.
[electronic resource]
by
Sharon, A
Rosenblatt, D
Friesem, A A
Weber, H G
Engel, H
Steingrueber, R
Producer:
20121002
In:
Optics letters
vol. 21
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136.
Knowledge of nephrologists and patients about autosomal dominant polycystic kidney disease (ADPKD).
[electronic resource]
by
Rosenberg, E E
Tannenbaum, T N
Miller, S D
Lamothe, E M
Rosenblatt, D S
Producer:
19930114
In:
Clinical and investigative medicine. Medecine clinique et experimentale
vol. 15
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137.
Prolonged inhibition of DNA synthesis associated with the accumulation of methotrexate polyglutamates by cultured human cells.
[electronic resource]
by
Rosenblatt, D S
Whitehead, V M
Vera, N
Pottier, A
Dupont, M
Vuchich, M J
Producer:
19790324
In:
Molecular pharmacology
vol. 14
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138.
Identification of a protease inhibitor produced by astrocytes that is structurally and functionally homologous to human protease nexin-I.
[electronic resource]
by
Rosenblatt, D E
Cotman, C W
Nieto-Sampedro, M
Rowe, J W
Knauer, D J
Producer:
19871015
In:
Brain research
vol. 415
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139.
Altered vitamin B12 metabolism in fibroblasts from a patient with megaloblastic anemia and homocystinuria due to a new defect in methionine biosynthesis.
[electronic resource]
by
Rosenblatt, D S
Cooper, B A
Pottier, A
Lue-Shing, H
Matiaszuk, N
Grauer, K
Producer:
19850131
In:
The Journal of clinical investigation
vol. 74
Online resources:
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140.
Methylenetetrahydrofolate reductase deficiency in a patient with phenotypic findings of Angelman syndrome.
[electronic resource]
by
Arn, P H
Williams, C A
Zori, R T
Driscoll, D J
Rosenblatt, D S
Producer:
19980709
In:
American journal of medical genetics
vol. 77
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