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Results of search for 'au:"BEUTLER, E"', page 35 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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Gaucher Disease
Glucosephosphate Dehydrogenase
Glucosephosphate Dehydrogenase Deficiency
Glucosylceramidase
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681.
The treatment of chronic progressive multiple sclerosis with cladribine.
[electronic resource]
by
Beutler, E
Sipe, J C
Romine, J S
Koziol, J A
McMillan, R
Zyroff, J
Producer:
19960717
In:
Proceedings of the National Academy of Sciences of the United States of America
vol. 93
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682.
Development of cladribine treatment in multiple sclerosis.
[electronic resource]
by
Sipe, J C
Romine, J S
Koziol, J A
McMillan, R
Zyroff, J
Beutler, E
Producer:
19971212
In:
Multiple sclerosis (Houndmills, Basingstoke, England)
vol. 1
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683.
Cladribine.
[electronic resource]
by
Romine, J S
Sipe, J C
Koziol, J A
Zyroff, J
McMillan, R
Beutler, E
Producer:
20130422
In:
BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy
vol. 7
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684.
2-Chlorodeoxyadenosine chemotherapy triggers programmed cell death in normal and malignant lymphocytes.
[electronic resource]
by
Carrera, C J
Piro, L D
Saven, A
Beutler, E
Terai, C
Carson, D A
Producer:
19920323
In:
Advances in experimental medicine and biology
vol. 309A
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685.
Hazards of indiscriminate screening for sickling.
[electronic resource]
by
Beutler, E
Boggs, D R
Heller, P
Maurer, A
Motulsky, A G
Sheehy, T W
Producer:
19720202
In:
The New England journal of medicine
vol. 285
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686.
International Committee for Standardization in Haematology: recommended screening test for glucose-6-phosphate dehydrogenase (G-6-PD) deficiency.
[electronic resource]
by
Beutler, E
Blume, K G
Kaplan, J C
Löhr, G W
Ramot, B
Valentine, W N
Producer:
19800119
In:
British journal of haematology
vol. 43
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687.
Triosephosphate isomerase deficiency: repetitive occurrence of point mutation in amino acid 104 in multiple apparently unrelated families.
[electronic resource]
by
Schneider, A
Westwood, B
Yim, C
Prchal, J
Berkow, R
Labotka, R
Warrier, R
Beutler, E
Producer:
19951228
In:
American journal of hematology
vol. 50
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688.
Hemoglobin Pasadena,alpha 2 beta 275(E19)Leu leads to Arg. Identification by high performance liquid chromatography of a new unstable variant with increased oxygen affinity.
[electronic resource]
by
Johnson, C S
Moyes, D
Schroeder, W A
Shelton, J B
Shelton, J R
Beutler, E
Producer:
19801021
In:
Biochimica et biophysica acta
vol. 623
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689.
Downeast anemia (dea), a new mouse model of severe nonspherocytic hemolytic anemia caused by hexokinase (HK(1)) deficiency.
[electronic resource]
by
Peters, L L
Lane, P W
Andersen, S G
Gwynn, B
Barker, J E
Beutler, E
Producer:
20030417
In:
Blood cells, molecules & diseases
vol. 27
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690.
Molecular analysis of G6PD variants in northern Italy: a study on the population from the Ferrara district.
[electronic resource]
by
Ninfali, P
Baronciani, L
Ruzzo, A
Fortini, C
Amadori, E
Dall'ara, G
Magnani, M
Beutler, E
Producer:
19931012
In:
Human genetics
vol. 92
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691.
Microcytosis in Hodgkin disease associated with unbalanced globin chain synthesis.
[electronic resource]
by
Fahey, J L
Rahbar, S
Farbstein, M J
Forman, S J
Blume, K G
Beutler, E
Producer:
19861020
In:
American journal of hematology
vol. 23
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692.
Frequency of glucose-6-phosphate dehydrogenase (G6PD) mutations in Chinese, Filipinos, and Laotians from Hawaii.
[electronic resource]
by
Hsia, Y E
Miyakawa, F
Baltazar, J
Ching, N S
Yuen, J
Westwood, B
Beutler, E
Producer:
19940105
In:
Human genetics
vol. 92
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693.
Marrow suppression produced by repeated doses of cladribine.
[electronic resource]
by
Beutler, E
Koziol, J A
McMillan, R
Sipe, J C
Romine, J S
Carrera, C J
Producer:
19940601
In:
Acta haematologica
vol. 91
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694.
Natural history of Korean vivax malaria after deliberate inoculation of human volunteers.
[electronic resource]
by
ARNOLD, J
ALVING, A S
HOCKWALD, R S
CLAYMAN, C B
DERN, R J
BEUTLER, E
Producer:
20030501
In:
The Journal of laboratory and clinical medicine
vol. 44
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695.
A case of nonneurologic Gaucher's disease that biochemically resembles the neurologic types.
[electronic resource]
by
Glew, R H
Gopalan, V
Hubbell, C A
Beutler, E
Geil, J D
Lee, R E
Producer:
19910503
In:
Journal of neuropathology and experimental neurology
vol. 50
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696.
Continuous intravenous deferoxamine infusion. Treatment of secondary hemochromatosis in adults.
[electronic resource]
by
Blume, K G
Beutler, E
Chillar, R K
Fahey, J L
Sharkoff, D
Zia, P K
Producer:
19780628
In:
JAMA
vol. 239
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697.
G-6-PD Jalisco and G-6-PD Morelia: two new Mexican variants.
[electronic resource]
by
Vaca, G
Ibarra, B
García Cruz, D
Medina, C
Romero, F
Cantú, J M
Beutler, E
Producer:
19851017
In:
Human genetics
vol. 71
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698.
Coincidence of Gaucher's disease due to a private mutation and Ph' positive chronic myeloid leukemia.
[electronic resource]
by
Petrides, P E
leCoutre, P
Müller-Höcker, J
Magin, E
Harzer, K
Demina, A
Beutler, E
Producer:
19980922
In:
American journal of hematology
vol. 59
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699.
Coincidence of Gaucher's disease due to a 1226G/1448C mutation and of an immunoglobulin G lambda multiple myeloma with Bence-Jones proteinuria.
[electronic resource]
by
Harder, H
Eucker, J
Zang, C
Possinger, K
Müller-Höcker, J
Beutler, E
Petrides, P E
Producer:
20010104
In:
Annals of hematology
vol. 79
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700.
Hemolytic anemia due to pyrimidine-5'-nucleotidase deficiency: report of eight cases in six families.
[electronic resource]
by
Beutler, E
Baranko, P V
Feagler, J
Matsumoto, F
Miro-Quesdada, M
Selby, G
Singh, P
Producer:
19801024
In:
Blood
vol. 56
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