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Results of search for 'au:"Paschke, E"', page 1 of 3
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Authors
Barrera, L A
Beck, M
Braun, F
Breier, F
Böck, A
Cooper, A
Deutsch, J
Erwa, W
Fang-Kircher, S
Glössl, J
Gutierrez, M A
Hoefler, G
Jurecka, W
Kircher, S G
Kresse, H
Paschke, E
Paul, K
Plecko, B
Stöckler, S
von Figura, K
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Topics
Adolescent
Adult
Cells, Cultured
Child
Child, Preschool
Female
Fibroblasts
Glycosaminoglycans
Humans
Infant
Infant, Newborn
Male
Mucopolysaccharidoses
Phenotype
analysis
complications
diagnosis
enzymology
genetics
metabolism
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English
German
Your search returned 55 results.
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1.
Morquio disease, type B: activation of GM1-beta-galactosidase by GM1-activator protein.
[electronic resource]
by
Paschke, E
Kresse, H
Producer:
19830225
In:
Biochemical and biophysical research communications
vol. 109
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2.
[Strategies for the diagnosis of lysosomal storage diseases: symptoms, methods and samples].
[electronic resource]
by
Paschke, E
Stöckler, S
Producer:
19930201
In:
Wiener klinische Wochenschrift
vol. 104
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3.
[New aspects in diagnosis and therapy of hereditary diseases of the nervous and skeletal systems].
[electronic resource]
by
Plecko, B
Paschke, E
Producer:
19970507
In:
Wiener klinische Wochenschrift
vol. 109
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4.
Multiple forms of 2-deoxy-D-glucoside-2-sulphamate sulphohydrolase from human placenta.
[electronic resource]
by
Paschke, E
Kresse, H
Producer:
19800226
In:
The Biochemical journal
vol. 181
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5.
Studies on a distinct fraction of bovine vitreous body collagen.
[electronic resource]
by
Schmut, O
Mallinger, R
Paschke, E
Producer:
19841120
In:
Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie
vol. 221
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6.
Infantile sialic acid storage disease: the fate of biosynthetically labeled N-acetyl-(3H)-neuraminic acid in cultured human fibroblasts.
[electronic resource]
by
Paschke, E
Höfler, G
Roscher, A
Producer:
19860922
In:
Pediatric research
vol. 20
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7.
A simple, one-step synthesis of N-acetyl-9-O-acetylneuraminic acid by enzymic transesterification mediated by porcine pancreas lipase in pyridine.
[electronic resource]
by
Forstner, M
Freytag, K
Paschke, E
Producer:
19900309
In:
Carbohydrate research
vol. 193
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8.
The effect of D-(+)-glucosamine on levels of free N-acetylneuraminic acid and UDP-N-acetylhexosamines in infantile sialic acid storage disease (ISSD) fibroblasts.
[electronic resource]
by
Paschke, E
Höfler, G
Roscher, A
Producer:
19870605
In:
Journal of inherited metabolic disease
vol. 10
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9.
[Congenital metabolic diseases as a cause of acute illnesses in the neonatal period].
[electronic resource]
by
Stöckler, S
Ipsiroglu, O S
Paschke, E
Producer:
19891122
In:
Klinische Padiatrie
vol. 201
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10.
New phenotype of adult alpha-L-iduronidase deficiency (mucopolysaccharidosis I) masquerading as Friedreich's ataxia with cardiopathy.
[electronic resource]
by
Jellinger, K
Paulus, W
Grisold, W
Paschke, E
Producer:
19901211
In:
Clinical neuropathology
vol. 9
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11.
Storage material from urine and tissues in the nephropathic phenotype of infantile sialic acid storage disease.
[electronic resource]
by
Paschke, E
Gruber, W
Ring, E
Sperl, W
Producer:
19920617
In:
Journal of inherited metabolic disease
vol. 15
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12.
Degradation of keratan sulphate by beta-N-acetylhexosaminidases A and B.
[electronic resource]
by
Ludolph, T
Paschke, E
Glössl, J
Kresse, H
Producer:
19820109
In:
The Biochemical journal
vol. 193
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13.
Aggregation properties of beta-galactosidase of human urine and degradation of its natural substrates by a purified preparation of the enzyme.
[electronic resource]
by
Paschke, E
Niemann, R
Strecker, G
Kresse, H
Producer:
19820924
In:
Biochimica et biophysica acta
vol. 704
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14.
Mucopolysaccharidosis I and intracranial tumor in a patient with high-pressure hydrocephalus.
[electronic resource]
by
Stöckler, S
Kleinert, R
Ebner, F
Paschke, E
Producer:
19931207
In:
Pediatric radiology
vol. 23
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15.
Accumulation of sialic acid in endocytic compartments interferes with the formation of mature lysosomes. Impaired proteolytic processing of cathepsin B in fibroblasts of patients with lysosomal sialic acid storage disease.
[electronic resource]
by
Schmid, J A
Mach, L
Paschke, E
Glössl, J
Producer:
19990727
In:
The Journal of biological chemistry
vol. 274
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16.
Sanfilippo's disease type A: sulfamidase activity in peripheral leukocytes of normal, heterozygous and homozygous individuals.
[electronic resource]
by
Schmidt, R
Von Figura, K
Paschke, E
Kresse, H
Producer:
19771130
In:
Clinica chimica acta; international journal of clinical chemistry
vol. 80
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17.
A novel 6 bp insertion in exon 7 associated with an unusual phenotype in a family with Fabry disease.
[electronic resource]
by
Kroepfl, Th
Paul, K
Kotanko, P
Plecko, B
Paschke, E
Producer:
20031021
In:
Journal of inherited metabolic disease
vol. 25
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18.
Uptake of fluorescent plasmalogen analogs by cultured human skin fibroblasts deficient in plasmalogen.
[electronic resource]
by
Loidl, J
Schwabe, G
Paschke, E
Paltauf, F
Hermetter, A
Producer:
19901219
In:
Biochimica et biophysica acta
vol. 1029
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19.
The frequency of common mutations among patients with mucopolysaccharidosis types I, II and IIIA diagnosed in Austria over the last 17 years.
[electronic resource]
by
Kroepfl, T
Milos, I
Paul, K
Plecko, B
Paschke, E
Producer:
20020508
In:
Clinical genetics
vol. 60
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20.
Plasma concentrations of glucose, corticosterone, glucagon and insulin and liver content of metabolic substrates and enzymes during starvation and additional hypoxia in the rat.
[electronic resource]
by
Mlekusch, W
Paletta, B
Truppe, W
Paschke, E
Grimus, R
Producer:
19820222
In:
Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme
vol. 13
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