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Results of search for 'su:"Leukodystrophy, Metachromatic"', page 39 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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Results
761.
Long-term stabilization after bone marrow transplantation in juvenile metachromatic leukodystrophy.
[electronic resource]
by
Kidd, D
Nelson, J
Jones, F
Dusoir, H
Wallace, I
McKinstry, S
Patterson, V
Producer:
19980206
In:
Archives of neurology
vol. 55
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762.
DNA-based diagnosis of arylsulfatase A deficiencies as a supplement to enzyme assay: a case in point.
[electronic resource]
by
Coulter-Mackie, M B
Applegarth, D A
Toone, J
Vallance, H
Producer:
19970529
In:
Clinical biochemistry
vol. 30
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763.
Improved peripheral nerve conduction, EEG and verbal IQ after bone marrow transplantation for adult metachromatic leukodystrophy.
[electronic resource]
by
Solders, G
Celsing, G
Hagenfeldt, L
Ljungman, P
Isberg, B
Ringdén, O
Producer:
19990325
In:
Bone marrow transplantation
vol. 22
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764.
ARSA gene mutations in five Chinese metachromatic leukodystrophy patients.
[electronic resource]
by
Wang, Jingmin
Zhang, Weimin
Pan, Hong
Bao, Xinhua
Wu, Ye
Wu, Xiru
Jiang, Yuwu
Producer:
20070827
In:
Pediatric neurology
vol. 36
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765.
Chromosomal deletion unmasking a recessive disease: 22q13 deletion syndrome and metachromatic leukodystrophy.
[electronic resource]
by
Bisgaard, A-M
Kirchhoff, M
Nielsen, J E
Kibaek, M
Lund, A
Schwartz, M
Christensen, E
Producer:
20090416
In:
Clinical genetics
vol. 75
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766.
The pseudo-Hurler syndromes.
[electronic resource]
by
Gordon, N
Producer:
19780915
In:
Developmental medicine and child neurology
vol. 20
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767.
Ultrastructural findings of peripheral nerve in a preclinical case of adult metachromatic leukodystrophy.
[electronic resource]
by
Argyrakis, A
Pilz, H
Goebel, H H
Müller, D
Producer:
19770922
In:
Journal of neuropathology and experimental neurology
vol. 36
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768.
Above-normal urinary excretion of urinary ceramides in Farber's disease, and characterization of their components by high-performance liquid chromatography.
[electronic resource]
by
Iwamori, M
Moser, H W
Producer:
19750701
In:
Clinical chemistry
vol. 21
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769.
Recurrent seizures in metachromatic leukodystrophy.
[electronic resource]
by
Balslev, T
Cortez, M A
Blaser, S I
Haslam, R H
Producer:
19971231
In:
Pediatric neurology
vol. 17
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770.
Disease-causing mutations in cis with the common arylsulfatase A pseudodeficiency allele compound the difficulties in accurately identifying patients and carriers of metachromatic leukodystrophy.
[electronic resource]
by
Rafi, Mohammad A
Coppola, Stephanie
Liu, Shu Ling
Rao, Han Zhi
Wenger, David A
Producer:
20040204
In:
Molecular genetics and metabolism
vol. 79
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771.
Development and reliability of a classification system for gross motor function in children with metachromatic leucodystrophy.
[electronic resource]
by
Kehrer, Christiane
Blumenstock, Gunnar
Raabe, Christa
Krägeloh-Mann, Ingeborg
Producer:
20110218
In:
Developmental medicine and child neurology
vol. 53
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772.
Hematopoietic SCT: a useful treatment for late metachromatic leukodystrophy.
[electronic resource]
by
Solders, M
Martin, D A
Andersson, C
Remberger, M
Andersson, T
Ringdén, O
Solders, G
Producer:
20150330
In:
Bone marrow transplantation
vol. 49
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773.
Metachromatic leukodystrophy: Disease spectrum and approaches for treatment.
[electronic resource]
by
van Rappard, Diane F
Boelens, Jaap Jan
Wolf, Nicole I
Producer:
20160209
In:
Best practice & research. Clinical endocrinology & metabolism
vol. 29
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774.
Alpha-L-fucosidase in cultured bone marrow fibroblasts from fucosidosis patients.
[electronic resource]
by
Beratis, N G
Hirschhorn, K
Producer:
19840717
In:
American journal of medical genetics
vol. 2
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775.
Arylsulphatases A and B in human diploid fibroblasts: differential assay with 4-methylumbelliferylsulphate and AgNO3.
[electronic resource]
by
Mercelis, R
Van Elsen, A F
Leroy, J G
Producer:
19790716
In:
Clinica chimica acta; international journal of clinical chemistry
vol. 93
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776.
Detection of a point mutation in sphingolipid activator protein-1 mRNA in patients with a variant form of metachromatic leukodystrophy.
[electronic resource]
by
Rafi, M A
Zhang, X L
DeGala, G
Wenger, D A
Producer:
19900305
In:
Biochemical and biophysical research communications
vol. 166
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777.
Multimodal evoked potential studies in leukodystrophies of children.
[electronic resource]
by
De Meirleir, L J
Taylor, M J
Logan, W J
Producer:
19880421
In:
The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques
vol. 15
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778.
Accumulation of lysosulfatide (sulfogalactosylsphingosine) in tissues of a boy with metachromatic leukodystrophy.
[electronic resource]
by
Toda, K
Kobayashi, T
Goto, I
Kurokawa, T
Ogomori, K
Producer:
19890425
In:
Biochemical and biophysical research communications
vol. 159
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779.
Partial enzyme deficiencies: residual activities and the development of neurological disorders.
[electronic resource]
by
Conzelmann, E
Sandhoff, K
Producer:
19840406
In:
Developmental neuroscience
vol. 6
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780.
Hereditary metabolic myelin diseases in humans.
[electronic resource]
by
Martin, J J
Producer:
19840626
In:
Bulletin de la Societe belge d'ophtalmologie
vol. 208 Pt 1
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