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Results of search for 'au:"Orviský, E"'
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Authors
Bembi, B
Blazícková, S
Callahan, M
Capek, P
Cech, K
Krasnewich, D
Kéry, V
LaMarca, M E
Madike, V
Martin, B M
Orvisky, E
Orviský, E
Schiffmann, R
Sidransky, E
Stanciková, M
Stancíková, M
Stubblefield, B
Stubblefield, B K
Tayebi, N
Walker, J M
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Topics
Adult
Alleles
Animals
Arthritis, Experimental
Arthritis, Rheumatoid
Blotting, Southern
Chromatography, High Pressure Liquid
Female
Gaucher Disease
Glucosylceramidase
Heterozygote
Humans
Hyaluronic Acid
Infant
Male
Middle Aged
analysis
chemistry
genetics
metabolism
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English
Your search returned 15 results.
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1.
Specific high performance liquid chromatographic determination of the molecular weight and concentration of hyaluronic acid in complex mixtures by labelled hyaluronate binding proteins.
[electronic resource]
by
Orviský, E
Kéry, V
Stanciková, M
Producer:
19920207
In:
Biomedical chromatography : BMC
vol. 5
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2.
High-molecular-weight hyaluronan--a valuable tool in testing the antioxidative activity of amphiphilic drugs stobadine and vinpocetine.
[electronic resource]
by
Orviský, E
Soltés, L
Stancíková, M
Producer:
19980715
In:
Journal of pharmaceutical and biomedical analysis
vol. 16
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3.
Rapid determination of immobilized ConA lectin activity.
[electronic resource]
by
Orviský, E
Kéry, V
Vandáková, K
Stancíková, M
Producer:
19921106
In:
Applied biochemistry and biotechnology
vol. 32
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4.
Influence of various forms of dialyzable leukocyte extracts on rat adjuvant arthritis.
[electronic resource]
by
Stanciková, M
Rovenský, J
Pekárek, J
Orviský, E
Blazícková, S
Cech, K
Producer:
19951212
In:
Archivum immunologiae et therapiae experimentalis
vol. 42
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5.
Glucocerebrosidase gene mutations in patients with type 2 Gaucher disease.
[electronic resource]
by
Stone, D L
Tayebi, N
Orvisky, E
Stubblefield, B
Madike, V
Sidransky, E
Producer:
20000224
In:
Human mutation
vol. 15
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6.
Gustin from human parotid saliva is carbonic anhydrase VI.
[electronic resource]
by
Thatcher, B J
Doherty, A E
Orvisky, E
Martin, B M
Henkin, R I
Producer:
19981123
In:
Biochemical and biophysical research communications
vol. 250
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7.
Methyl-alpha-D-mannopyranoside, mannooligosaccharides and yeast mannans inhibit development of rat adjuvant arthritis.
[electronic resource]
by
Prokopová, A
Kéry, V
Stancíková, M
Grimová, J
Capek, P
Sandula, J
Orviský, E
Producer:
19930618
In:
The Journal of rheumatology
vol. 20
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8.
Phosphomannomutase activity in congenital disorders of glycosylation type Ia determined by direct analysis of the interconversion of mannose-1-phosphate to mannose-6-phosphate by high-pH anion-exchange chromatography with pulsed amperometric detection.
[electronic resource]
by
Orvisky, E
Stubblefield, B
Long, R T
Martin, B M
Sidransky, E
Krasnewich, D
Producer:
20040114
In:
Analytical biochemistry
vol. 317
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9.
Glucocerebrosidase mutation T369M appears to be another polymorphism.
[electronic resource]
by
Walker, J M
Lwin, A
Tayebi, N
LaMarca, M E
Orvisky, E
Sidransky, E
Producer:
20031112
In:
Clinical genetics
vol. 63
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10.
Divergent phenotypes in Gaucher disease implicate the role of modifiers.
[electronic resource]
by
Goker-Alpan, O
Hruska, K S
Orvisky, E
Kishnani, P S
Stubblefield, B K
Schiffmann, R
Sidransky, E
Producer:
20060502
In:
Journal of medical genetics
vol. 42
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11.
Gaucher disease and parkinsonism: a phenotypic and genotypic characterization.
[electronic resource]
by
Tayebi, N
Callahan, M
Madike, V
Stubblefield, B K
Orvisky, E
Krasnewich, D
Fillano, J J
Sidransky, E
Producer:
20011101
In:
Molecular genetics and metabolism
vol. 73
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12.
Gaucher disease with parkinsonian manifestations: does glucocerebrosidase deficiency contribute to a vulnerability to parkinsonism?
[electronic resource]
by
Tayebi, N
Walker, J
Stubblefield, B
Orvisky, E
LaMarca, M E
Wong, K
Rosenbaum, H
Schiffmann, R
Bembi, B
Sidransky, E
Producer:
20040204
In:
Molecular genetics and metabolism
vol. 79
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13.
Glucosylsphingosine accumulation in mice and patients with type 2 Gaucher disease begins early in gestation.
[electronic resource]
by
Orvisky, E
Sidransky, E
McKinney, C E
Lamarca, M E
Samimi, R
Krasnewich, D
Martin, B M
Ginns, E I
Producer:
20001120
In:
Pediatric research
vol. 48
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14.
The identification of eight novel glucocerebrosidase (GBA) mutations in patients with Gaucher disease.
[electronic resource]
by
Orvisky, E
Park, J K
Parker, A
Walker, J M
Martin, B M
Stubblefield, B K
Uyama, E
Tayebi, N
Sidransky, E
Producer:
20020830
In:
Human mutation
vol. 19
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15.
Dominant inheritance of sialuria, an inborn error of feedback inhibition.
[electronic resource]
by
Leroy, J G
Seppala, R
Huizing, M
Dacremont, G
De Simpel, H
Van Coster, R N
Orvisky, E
Krasnewich, D M
Gahl, W A
Producer:
20010705
In:
American journal of human genetics
vol. 68
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