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Results of search for 'su:"Leukodystrophy, Metachromatic"', page 25 of 63
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Authors
Bach, G
Baumann, N
Berger, J
Biffi, Alessandra
Conzelmann, E
Eto, Y
Fluharty, A L
Gieselmann, V
Gieselmann, Volkmar
Goebel, H H
Harzer, K
Kihara, H
Krivit, W
Matzner, Ulrich
Moser, H W
Naldini, Luigi
Turpin, J C
Wenger, D A
Zlotogora, J
von Figura, K
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Topics
Adolescent
Adult
Animals
Brain
Cerebroside-Sulfatase
Child
Child, Preschool
Female
Humans
Infant
Leukodystrophy, Metachromatic
Male
Sulfatases
Sulfoglycosphingolipids
deficiency
diagnosis
enzymology
genetics
metabolism
pathology
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481.
The first Alzheimer disease case: a metachromatic leukodystrophy?
[electronic resource]
by
Amaducci, L
Sorbi, S
Piacentini, S
Bick, K L
Producer:
19920709
In:
Developmental neuroscience
vol. 13
Online resources:
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482.
Metabolism of cerebroside sulphate and subcellular distribution of its metabolites in cultured skin fibroblasts derived from controls, metachromatic leukodystrophy, globoid cell leukodystrophy and Farber disease.
[electronic resource]
by
Inui, K
Furukawa, M
Nishimoto, J
Okada, S
Yabuuchi, H
Producer:
19880229
In:
Journal of inherited metabolic disease
vol. 10
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483.
Probable metachromatic leukodystrophy/pseudodeficiency compound heterozygote at the arylsulfatase A locus with neurological and psychiatric symptomatology.
[electronic resource]
by
Hohenschutz, C
Friedl, W
Schlör, K H
Waheed, A
Conzelmann, E
Sandhoff, K
Propping, P
Producer:
19890323
In:
American journal of medical genetics
vol. 31
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484.
Prenatal diagnosis of metachromatic leukodystrophy in a family with pseudo arylsulfatase A deficiency by the cerebroside sulfate loading test.
[electronic resource]
by
Kihara, H
Ho, C K
Fluharty, A L
Tsay, K K
Hartlage, P L
Producer:
19800825
In:
Pediatric research
vol. 14
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485.
[Activator protein for the enzymic hydrolysis of sphingolipids and their relationships to sphingolipidosis. Special reference to the catabolism of GM2 ganglioside].
[electronic resource]
by
Hirabayashi, Y
Li, Y T
Li, S C
Producer:
19830623
In:
Seikagaku. The Journal of Japanese Biochemical Society
vol. 55
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486.
Structural characterization of variant forms of arylsulfatase A that associate with alcoholism.
[electronic resource]
by
Park, D S
Manowitz, P
Stein, S
Poretz, R D
Producer:
19961002
In:
Alcoholism, clinical and experimental research
vol. 20
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487.
Late juvenile metachromatic leukodystrophy treated with bone marrow transplantation; a 4-year follow-up study.
[electronic resource]
by
Navarro, C
Fernández, J M
Domínguez, C
Fachal, C
Alvarez, M
Producer:
19960223
In:
Neurology
vol. 46
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488.
Epileptic seizures and electroencephalographic evolution in genetic leukodystrophies.
[electronic resource]
by
Wang, P J
Hwu, W L
Shen, Y Z
Producer:
20010802
In:
Journal of clinical neurophysiology : official publication of the American Electroencephalographic Society
vol. 18
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489.
[Recent advances in the diagnosis and treatment of lysosomal storage diseases].
[electronic resource]
by
Wu, Xi-ru
Bao, Xin-hua
Producer:
20061212
In:
Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences
vol. 37
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490.
Increased concentration of the CSF Tau protein and its phosphorylated form in the late juvenile metachromatic leukodystrophy form: a case report.
[electronic resource]
by
Tarasiuk, Joanna
Kapica-Topczewska, Katarzyna
Kułakowska, Alina
Halicka, Dorota
Drozdowski, Wiesław
Kornhuber, Johannes
Lewczuk, Piotr
Producer:
20121106
In:
Journal of neural transmission (Vienna, Austria : 1996)
vol. 119
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491.
4H leukodystrophy caused by a homozygous POLR3B mutation: Further delineation of the phenotype.
[electronic resource]
by
Verberne, Eline A
Dalen Meurs, Lotje
Wolf, Nicole I
van Haelst, Mieke M
Producer:
20210428
In:
American journal of medical genetics. Part A
vol. 182
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492.
Clinical and biochemical pathophysiology of ataxia in the sphingolipidoses.
[electronic resource]
by
Philippart, M
Producer:
19790324
In:
Advances in neurology
vol. 21
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493.
[Do psychodynamic considerations still play a role in degenerative brain processes?].
[electronic resource]
by
de Lorme, I
Producer:
19900904
In:
Praxis der Kinderpsychologie und Kinderpsychiatrie
vol. 39
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494.
An assay for the rapid detection of the arylsulfatase A pseudodeficiency allele facilitates diagnosis and genetic counseling for metachromatic leukodystrophy.
[electronic resource]
by
Gieselmann, V
Producer:
19910402
In:
Human genetics
vol. 86
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495.
Restoration of arylsulphatase A activity in human-metachromatic-leucodystrophy fibroblasts via retroviral-vector-mediated gene transfer.
[electronic resource]
by
Rommerskirch, W
Fluharty, A L
Peters, C
von Figura, K
Gieselmann, V
Producer:
19920115
In:
The Biochemical journal
vol. 280 ( Pt 2)
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496.
[Adult metachromatic leukodystrophy manifested as schizophrenic psychosis (author's transl)].
[electronic resource]
by
Kothbauer, P
Jellinger, K
Gross, H
Molzer, B
Bernheimer, H
Producer:
19780417
In:
Archiv fur Psychiatrie und Nervenkrankheiten
vol. 224
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497.
Differential assay of arylsulfatase A and B activities: a sensitive method for cultured human cells.
[electronic resource]
by
Chang, P L
Rosa, N E
Davidson, R G
Producer:
19820313
In:
Analytical biochemistry
vol. 117
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498.
Adult metachromatic leukodystrophy. IV. Ultrastructural studies on the central and peripheral nervous system.
[electronic resource]
by
Goebel, H H
Argyrakis, A
Shimokawa, K
Seidel, D
Heipertz, R
Producer:
19801021
In:
European neurology
vol. 19
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499.
Metachromatic leukodystrophy caused by a partial cerebroside sulfatase.
[electronic resource]
by
Kihara, H
Fluharty, A L
O'Brien, J S
Fish, C H
Producer:
19821021
In:
Clinical genetics
vol. 21
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500.
Problems in genetic counseling.
[electronic resource]
by
Cohen, T
Producer:
19830415
In:
Progress in clinical and biological research
vol. 103 Pt B
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