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Results of search for 'au:"BEUTLER, E"', page 34 of 37
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Authors
ALVING, A S
BEUTLER, E
Beutler, E
Blume, K G
Carrera, C J
Carson, D A
DERN, R J
Dale, G L
Forman, L
Gelbart, T
Koziol, J A
Kuhl, W
Matsumoto, F
McMillan, R
Piro, L D
Saven, A
Srivastava, S K
West, C
Westwood, B
Zimran, A
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Topics
Adult
Animals
Child
Erythrocytes
Female
Gaucher Disease
Glucosephosphate Dehydrogenase
Glucosephosphate Dehydrogenase Deficiency
Glucosylceramidase
Humans
Male
Middle Aged
Mutation
analysis
blood
drug effects
enzymology
genetics
metabolism
pharmacology
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661.
Cataracts, galactosuria and hypergalactosemia due to galactokinase deficiency in a child. Studies of a kindred.
[electronic resource]
by
Monteleone, J A
Beutler, E
Monteleone, P L
Utz, C L
Casey, E C
Producer:
19710608
In:
The American journal of medicine
vol. 50
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662.
Metabolic compensation for profound erythrocyte adenylate kinase deficiency. A hereditary enzyme defect without hemolytic anemia.
[electronic resource]
by
Beutler, E
Carson, D
Dannawi, H
Forman, L
Kuhl, W
West, C
Westwood, B
Producer:
19830920
In:
The Journal of clinical investigation
vol. 72
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663.
The relationship of the -5, -8, and -24 variant alleles in African Americans to triosephosphate isomerase (TPI) enzyme activity and to TPI deficiency.
[electronic resource]
by
Schneider, A
Forman, L
Westwood, B
Yim, C
Lin, J
Singh, S
Beutler, E
Producer:
19981109
In:
Blood
vol. 92
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664.
Gaucher disease. Clinical, laboratory, radiologic, and genetic features of 53 patients.
[electronic resource]
by
Zimran, A
Kay, A
Gelbart, T
Garver, P
Thurston, D
Saven, A
Beutler, E
Producer:
19921215
In:
Medicine
vol. 71
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665.
New glucose-6-phosphate dehydrogenase mutations from various ethnic groups.
[electronic resource]
by
Beutler, E
Westwood, B
Prchal, J T
Vaca, G
Bartsocas, C S
Baronciani, L
Producer:
19920729
In:
Blood
vol. 80
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666.
The clinical course of treated and untreated Gaucher disease. A study of 45 patients.
[electronic resource]
by
Beutler, E
Demina, A
Laubscher, K
Garver, P
Gelbart, T
Balicki, D
Vaughan, L
Producer:
19961024
In:
Blood cells, molecules & diseases
vol. 21
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667.
Characterization of heteropolymeric hexosaminidase A in human X mouse hybrid cells.
[electronic resource]
by
Chern, J
Beutler, E
Kuhl, W
Gilbert, F
Mellman, W J
Croce, C M
Producer:
19761230
In:
Proceedings of the National Academy of Sciences of the United States of America
vol. 73
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668.
Galactokinase deficiency as a cause of cataracts.
[electronic resource]
by
Beutler, E
Matsumoto, F
Kuhl, W
Krill, A
Levy, N
Sparkes, R
Degnan, M
Producer:
19730625
In:
The New England journal of medicine
vol. 288
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669.
Molecular characterization of a case of atransferrinemia.
[electronic resource]
by
Beutler, E
Gelbart, T
Lee, P
Trevino, R
Fernandez, M A
Fairbanks, V F
Producer:
20010118
In:
Blood
vol. 96
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670.
Toxicity studies of pyrimethamine (daraprim).
[electronic resource]
by
DERN, R J
BEUTLER, E
ARNOLD, J
LORINCZ, A
BLOCK, M
ALVING, A S
Producer:
20030501
In:
The American journal of tropical medicine and hygiene
vol. 4
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671.
Enzyme replacement therapy for Gaucher disease.
[electronic resource]
by
Beutler, E
Kay, A
Saven, A
Garver, P
Thurston, D
Dawson, A
Rosenbloom, B
Producer:
19910927
In:
Blood
vol. 78
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672.
Activity of 2-chloro-2'-deoxyadenosine in chronic lymphocytic leukemia, hairy cell leukemia, and autoimmune hemolytic anemia.
[electronic resource]
by
Carson, D A
Piro, L D
Wasson, D B
Carrera, C J
Beutler, E
Producer:
19900320
In:
Advances in experimental medicine and biology
vol. 253A
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673.
Field test of galactosemia screening methods in newborn infants.
[electronic resource]
by
Beutler, E
Irwin, H R
Blumenfeld, C M
Goldenburg, E W
Day, R W
Producer:
19670422
In:
JAMA
vol. 199
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674.
Familial sea-blue histiocytes with acid phosphatemia. A syndrome resembling Gaucher disease: the Lewis variant.
[electronic resource]
by
Blankenship, R M
Greenburg, B R
Lucas, R N
Reynolds, R D
Beutler, E
Producer:
19730828
In:
JAMA
vol. 225
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675.
Triosephosphate isomerase deficiency with elevated sweat chloride test: report of a case.
[electronic resource]
by
Yenicesu, I
Kalayci, O
Semizel, E
Kavak, U
Gümrük, F
Ferec, C
Beutler, E
Producer:
20010215
In:
The Turkish journal of pediatrics
vol. 42
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676.
Inherited phosphofructokinase deficiency in dogs with hyperventilation-induced hemolysis: increased in vitro and in vivo alkaline fragility of erythrocytes.
[electronic resource]
by
Giger, U
Harvey, J W
Yamaguchi, R A
McNulty, P K
Chiapella, A
Beutler, E
Producer:
19850313
In:
Blood
vol. 65
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677.
Glucose-6 phosphate dehydrogenase mutations and haplotypes in various ethnic groups.
[electronic resource]
by
Xu, W
Westwood, B
Bartsocas, C S
Malcorra-Azpiazu, J J
Indrák, K
Beutler, E
Producer:
19950202
In:
Blood
vol. 85
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678.
Home treatment with intravenous enzyme replacement therapy for Gaucher disease: an international collaborative study of 33 patients.
[electronic resource]
by
Zimran, A
Hollak, C E
Abrahamov, A
van Oers, M H
Kelly, M
Beutler, E
Producer:
19930917
In:
Blood
vol. 82
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679.
Cladribine in treatment of chronic progressive multiple sclerosis.
[electronic resource]
by
Sipe, J C
Romine, J S
Koziol, J A
McMillan, R
Zyroff, J
Beutler, E
Producer:
19940728
In:
Lancet (London, England)
vol. 344
Online resources:
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680.
Enzyme replacement therapy in type I Gaucher disease.
[electronic resource]
by
Kay, A C
Saven, A
Garver, P
Thurston, D W
Rosenbloom, B F
Beutler, E
Producer:
19930701
In:
Transactions of the Association of American Physicians
vol. 104
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