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Results of search for 'au:"BEUTLER, E"', page 28 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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Adult
Animals
Child
Erythrocytes
Female
Gaucher Disease
Glucosephosphate Dehydrogenase
Glucosephosphate Dehydrogenase Deficiency
Glucosylceramidase
Humans
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Middle Aged
Mutation
analysis
blood
drug effects
enzymology
genetics
metabolism
pharmacology
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541.
Electrophoresis of glucocerebrosidase from normal and Gaucher disease fibroblasts.
[electronic resource]
by
Dale, G L
Gudas, J
Woloszyn, W
Beutler, E
Producer:
19791128
In:
American journal of human genetics
vol. 31
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542.
Mutation analysis of the transferrin receptor-2 gene in patients with iron overload.
[electronic resource]
by
Lee, P L
Halloran, C
West, C
Beutler, E
Producer:
20011004
In:
Blood cells, molecules & diseases
vol. 27
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543.
Drug-induced haemolytic anaemias and the mechanism and significance of Heinz body formation in red blood cells.
[electronic resource]
by
BEUTLER, E
SASS-KORTSAK, A
THALME, B
ERNSTER, L
Producer:
19981101
In:
Nature
vol. 196
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544.
Erythrocyte glutathione S-transferase deficiency and hemolytic anemia.
[electronic resource]
by
Beutler, E
Dunning, D
Dabe, I B
Forman, L
Producer:
19880819
In:
Blood
vol. 72
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545.
Glucose-6-phosphate dehydrogenase variants in Hawaii.
[electronic resource]
by
Beutler, E
Westwood, B
Kuhl, W
Hsia, Y E
Producer:
19930114
In:
Human heredity
vol. 42
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546.
The subunits of human hexosaminidase A.
[electronic resource]
by
Beutler, E
Yoshida, A
Kuhl, W
Lee, J E
Producer:
19770224
In:
The Biochemical journal
vol. 159
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547.
Glycolytic enzymes of stored granulocytes.
[electronic resource]
by
Lane, T A
Beutler, E
West, C
Lamkin, G
Producer:
19840523
In:
Transfusion
vol. 24
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548.
Hexose-6-phosphate dehydrogenase found in human liver.
[electronic resource]
by
Ohno, S
Payne, H W
Morrison, M
Beutler, E
Producer:
19661223
In:
Science (New York, N.Y.)
vol. 153
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549.
GPI Mount Scopus--a variant of glucosephosphate isomerase deficiency.
[electronic resource]
by
Shalev, O
Shalev, R S
Forman, L
Beutler, E
Producer:
19931129
In:
Annals of hematology
vol. 67
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550.
CHROMOSOME-21 AND PAROXYSMAL NOCTURNAL HEMOGLOBINURIA.
[electronic resource]
by
BEUTLER, E
GOLDENBURG, E W
OHNO, S
YETTRA, M
Producer:
19961201
In:
Blood
vol. 24
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551.
The origin of glucose-6-phosphate-dehydrogenase (G6PD) polymorphisms in African-Americans.
[electronic resource]
by
Kay, A C
Kuhl, W
Prchal, J
Beutler, E
Producer:
19920304
In:
American journal of human genetics
vol. 50
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552.
Electrophoretic abnormality in triosephosphate isomerase deficiency.
[electronic resource]
by
Kaplan, J C
Teeple, L
Shore, N
Beutler, E
Producer:
19680925
In:
Biochemical and biophysical research communications
vol. 31
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553.
Molecular abnormality of a phosphoglycerate kinase variant (PGK-Alabama).
[electronic resource]
by
Yoshida, A
Twele, T W
Davé, V
Beutler, E
Producer:
19960815
In:
Blood cells, molecules & diseases
vol. 21
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554.
Neonatal jaundice in Saudi newborns with G6PD Aures.
[electronic resource]
by
Niazi, G A
Adeyokunnu, A
Westwood, B
Beutler, E
Producer:
19960926
In:
Annals of tropical paediatrics
vol. 16
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555.
Mutation analysis of glucose-6-phosphate dehydrogenase (G6PD) variants in Costa Rica.
[electronic resource]
by
Beutler, E
Kuhl, W
Sáenz, G F
Rodríguez, W
Producer:
19911002
In:
Human genetics
vol. 87
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556.
G-->T transition at cDNA nt 110 (K37Q) in the PKLR (pyruvate kinase) gene is the molecular basis of a case of hereditary increase of red blood cell ATP.
[electronic resource]
by
Beutler, E
Westwood, B
van Zwieten, R
Roos, D
Producer:
19970617
In:
Human mutation
vol. 9
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557.
A NEW GENETIC ABNORMALITY RESULTING IN GALACTOSE-1-PHOSPHATE URIDYLTRANSFERASE DEFICIENCY.
[electronic resource]
by
BEUTLER, E
BALUDA, M C
STURGEON, P
DAY, R
Producer:
19961201
In:
Lancet (London, England)
vol. 1
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558.
A chimeric mouse model of Gaucher disease.
[electronic resource]
by
Beutler, E
West, C
Torbett, B E
Deguchi, H
Producer:
20030409
In:
Molecular medicine (Cambridge, Mass.)
vol. 8
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559.
Overweight and obesity associated with a missense polymorphism in fatty acid amide hydrolase (FAAH).
[electronic resource]
by
Sipe, J C
Waalen, J
Gerber, A
Beutler, E
Producer:
20051003
In:
International journal of obesity (2005)
vol. 29
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560.
Gamma-glutamylcysteine synthetase deficiency and hemolytic anemia.
[electronic resource]
by
Beutler, E
Moroose, R
Kramer, L
Gelbart, T
Forman, L
Producer:
19900209
In:
Blood
vol. 75
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