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Results of search for 'au:"Gal, A E"', page 2 of 2
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Authors
AVAKIAN, S
Barranger, J A
Bhagavan, N V
Bradley, R M
Brady, R O
Dekaban, A S
Fash, F J
Fouks, J
Furbish, F S
Gal, A E
Hibbert, S R
Johnson, W G
Kampine, J P
Kanfer, J N
Omodeo-Sale, F
Pentchev, P G
Quirk, J M
Shapiro, D
Tallman, J F
Tokoro, T
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Topics
Adult
Animals
Brain
Cerebrosides
Chromatography, Thin Layer
Female
Gaucher Disease
Glucosidases
Glucosylceramidase
Glucosylceramides
Glycolipids
Humans
Hydrogen-Ion Concentration
Liver
Male
Placenta
Rats
analysis
enzymology
metabolism
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English
Your search returned 40 results.
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21.
Diagnosis of adult Gaucher disease: use of a new chromogenic substrate, 2-hexadecanoylamino-4-nitrophenyl-beta-D-glucopyranoside, in cultured skin fibroblasts.
[electronic resource]
by
Johnson, W G
Gal, A E
Miranda, A F
Pentchev, P G
Producer:
19800923
In:
Clinica chimica acta; international journal of clinical chemistry
vol. 102
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22.
Sphingolipid hydrolases in brain tissue of patients with generalized gangliodosis.
[electronic resource]
by
Brady, R O
O'Brien, J S
Bradley, R M
Gal, A E
Producer:
19701027
In:
Biochimica et biophysica acta
vol. 210
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23.
Animal and cellular models of sphingolipid storage disorders of humans.
[electronic resource]
by
Gal, A E
Weis, A L
Quirk, J M
Tokoro, T
Brady, R O
Producer:
19870430
In:
Chemistry and physics of lipids
vol. 42
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24.
Isolation and relationship of human hexosaminidases.
[electronic resource]
by
Tallman, J F
Brady, R O
Quirk, J M
Villalba, M
Gal, A E
Producer:
19740726
In:
The Journal of biological chemistry
vol. 249
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25.
Isolation and characterization of glucocerebrosidase from human placental tissue.
[electronic resource]
by
Pentchev, P G
Brady, R O
Hibbert, S R
Gal, A E
Shapiro, D
Producer:
19740305
In:
The Journal of biological chemistry
vol. 248
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26.
Normolipemic subcutaneous xanthomatosis.
[electronic resource]
by
Fleischmajer, R
Schaefer, E J
Gal, A E
Pentchev, P G
Tint, G S
Producer:
19840107
In:
The American journal of medicine
vol. 75
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27.
Status of enzyme replacement therapy for Gaucher disease.
[electronic resource]
by
Brady, R O
Barranger, J A
Gal, A E
Pentchev, P G
Furbish, F S
Producer:
19810317
In:
Birth defects original article series
vol. 16
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28.
The distribution of glucocerebroside in the liver of patients with Gaucher's disease.
[electronic resource]
by
Gal, A E
Pentchev, P G
Barranger, J A
Dambrosia, J M
Brady, R O
Producer:
19791218
In:
Analytical biochemistry
vol. 95
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29.
Response of sphingolipid hydrolases in spleen and liver to increased erythrocytorhexis.
[electronic resource]
by
Kampine, J P
Kanfer, J N
Gal, A E
Bradley, R M
Brady, R O
Producer:
19670925
In:
Biochimica et biophysica acta
vol. 137
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30.
Replacement therapy for inherited enzyme deficiency. Use of purified glucocerebrosidase in Gaucher's disease.
[electronic resource]
by
Brady, R O
Pentchev, P G
Gal, A E
Hibbert, S R
Dekaban, A S
Producer:
19741219
In:
The New England journal of medicine
vol. 291
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31.
Enzymatic defect in Fabry's disease. Ceramidetrihexosidase deficiency.
[electronic resource]
by
Brady, R O
Gal, A E
Bradley, R M
Martensson, E
Warshaw, A L
Laster, L
Producer:
19670623
In:
The New England journal of medicine
vol. 276
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32.
Sphingolipid metabolism in leukemic leukocytes.
[electronic resource]
by
Kampine, J P
Brady, R O
Yankee, R A
Kanfer, J N
Shapiro, D
Gal, A E
Producer:
19900524
In:
Cancer research
vol. 27
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33.
Amygdalin (Laetrile) and prunasin beta-glucosidases: distribution in germ-free rat and in human tumor tissue.
[electronic resource]
by
Newmark, J
Brady, R O
Grimley, P M
Gal, A E
Waller, S G
Thistlethwaite, J R
Producer:
19820212
In:
Proceedings of the National Academy of Sciences of the United States of America
vol. 78
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34.
A lysosomal storage disorder in mice characterized by the accumulation of several sphingolipids.
[electronic resource]
by
Pentchev, P G
Gal, A E
Boothe, A D
Fouks, J
Omodeo-Sale, F
Brady, R O
Producer:
19810317
In:
Birth defects original article series
vol. 16
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35.
Nephrotic syndrome and renal failure associated with a novel glycolipid storage disorder.
[electronic resource]
by
Newsom, G D
Stanbaugh, G H
Kurtzman, N A
Brady, R O
Gal, A E
Vorstad, J
Producer:
19881212
In:
American journal of nephrology
vol. 8
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36.
A practical chromogenic procedure for the diagnosis of Krabbe's disease.
[electronic resource]
by
Gal, A E
Brady, R O
Pentchev, P G
Furbish, F S
Suzuki, K
Tanaka, H
Schneider, E L
Producer:
19770825
In:
Clinica chimica acta; international journal of clinical chemistry
vol. 77
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37.
Replacement therapy for inherited enzyme deficiency. Use of purified ceramidetrihexosidase in Fabry's disease.
[electronic resource]
by
Brady, R O
Tallman, J F
Johnson, W G
Gal, A E
Leahy, W R
Quirk, J M
Dekaban, A S
Producer:
19730806
In:
The New England journal of medicine
vol. 289
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38.
Biliary excretion of glycolipid in induced or inherited glucosylceramide lipidosis.
[electronic resource]
by
Pentchev, P G
Gal, A E
Wong, R
Morrone, S
Neumeyer, B
Massey, J
Kanter, R
Sawitsky, A
Brady, R O
Producer:
19820120
In:
Biochimica et biophysica acta
vol. 665
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39.
A lysosomal storage disorder in mice characterized by a dual deficiency of sphingomyelinase and glucocerebrosidase.
[electronic resource]
by
Pentchev, P G
Gal, A E
Booth, A D
Omodeo-Sale, F
Fouks, J
Neumeyer, B A
Quirk, J M
Dawson, G
Brady, R O
Producer:
19810413
In:
Biochimica et biophysica acta
vol. 619
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40.
Enzyme replacement therapy for the sphingolipidoses.
[electronic resource]
by
Brady, R O
Pentchev, P G
Gal, A E
Hibbert, S R
Quirk, J M
Mook, G E
Kusiak, J W
Tallman, J F
Dekaban, A S
Producer:
19760823
In:
Advances in experimental medicine and biology
vol. 68
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