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Results of search for 'su:"Leukodystrophy, Metachromatic"', page 18 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
341.
Enzyme replacement in cultured fibroblasts from metachromatic leukodystrophy.
[electronic resource]
by
Kihara, H
Porter, M T
Fluharty, A L
Producer:
19750227
In:
Birth defects original article series
vol. 9
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342.
[Quantitative metachromasia with pseudoisocyanin: a new method for the determination of sulphatides, and for use in the diagnosis of metachromatic leucodystrophy (sulphatide lipidosis) (author's transl)].
[electronic resource]
by
Harzer, K
Benz, H U
Producer:
19750318
In:
Zeitschrift fur klinische Chemie und klinische Biochemie
vol. 11
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343.
Late juvenile metachromatic leukodystrophy (MLD) in three patients with a similar clinical course and identical mutation on one allele.
[electronic resource]
by
Tylki-Szymanska, A
Berger, J
Löschl, B
Lugowska, A
Molzer, B
Producer:
19970325
In:
Clinical genetics
vol. 50
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344.
Variable onset of metachromatic leukodystrophy in a Vietnamese family.
[electronic resource]
by
Arbour, L T
Silver, K
Hechtman, P
Treacy, E P
Coulter-Mackie, M B
Producer:
20001128
In:
Pediatric neurology
vol. 23
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345.
[Frontotemporal dementia in metachromatic leukodystrophy].
[electronic resource]
by
Kozian, R
Sieber, N
Thiergart, S
Producer:
20071029
In:
Fortschritte der Neurologie-Psychiatrie
vol. 75
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346.
[A clinicopathological study of young-onset dementia: report of 2 autopsied cases].
[electronic resource]
by
Ishihara, Kenji
Horibe, Yuzo
Ohno, Hideki
Sugie, Masayuki
Shiota, Jun'ichi
Nakano, Imaharu
Kawamura, Mitsuru
Producer:
20120104
In:
Brain and nerve = Shinkei kenkyu no shinpo
vol. 63
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347.
Isolated noradrenergic failure in adult-onset autosomal dominant leukodystrophy.
[electronic resource]
by
Guaraldi, Pietro
Donadio, Vincenzo
Capellari, Sabina
Contin, Manuela
Casadio, Maria Chiara
Montagna, Pasquale
Liguori, Rocco
Cortelli, Pietro
Producer:
20111110
In:
Autonomic neuroscience : basic & clinical
vol. 159
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348.
Saposin B-Deficient Metachromatic Leukodystrophy Mimicking Acute Flaccid Paralysis.
[electronic resource]
by
Madaan, Priyanka
Jauhari, Prashant
Chakrabarty, Biswaroop
Kumar, Atin
Gulati, Sheffali
Producer:
20200609
In:
Neuropediatrics
vol. 50
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349.
An adult onset metachromatic leukodystrophy with dominant inheritance and normal arylsulphatase A levels.
[electronic resource]
by
Wright, G D
Patel, M K
Mikel, J
Producer:
19890213
In:
Journal of the neurological sciences
vol. 87
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350.
Metachromatic leukodystrophy: conduct disorder progressing to dementia.
[electronic resource]
by
Fisher, N R
Cope, S J
Lishman, W A
Producer:
19870626
In:
Journal of neurology, neurosurgery, and psychiatry
vol. 50
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351.
[Metachromatic leukodystrophy].
[electronic resource]
by
Aracena, M
Valenzuela, E
Selman, E
Milos, C
Producer:
19850912
In:
Revista chilena de pediatria
vol. 55
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352.
Spinal cord and cauda equina MRI findings in metachromatic leukodystrophy: case report.
[electronic resource]
by
Toldo, Irene
Carollo, Carla
Battistella, Pier Antonio
Laverda, Anna Maria
Producer:
20051014
In:
Neuroradiology
vol. 47
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353.
Gallbladder polyposis in metachromatic leukodystrophy.
[electronic resource]
by
Agarwal, Aanchal
Shipman, Peter J
Producer:
20131211
In:
Pediatric radiology
vol. 43
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354.
Muscle fibrillation following thiopentone and pancuronium bromide. An association with metachromatic leucodystrophy.
[electronic resource]
by
Quader, M A
Healy, T E
Producer:
19771031
In:
Anaesthesia
vol. 32
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355.
Adult metachromatic leukodystrophy.
[electronic resource]
by
Goebel, H H
Argyrakis, A
Producer:
19791026
In:
American journal of ophthalmology
vol. 88
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356.
Metachromatic leukodystrophy: heterozygosity and psychopathology.
[electronic resource]
by
Fricchione, G L
Kahaner, K
Producer:
19890329
In:
Psychosomatics
vol. 29
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357.
Pseudo arylsulfatase-A deficiency in healthy individuals: genetic and biochemical relationship to metachromatic leukodystrophy.
[electronic resource]
by
Chang, P L
Davidson, R G
Producer:
19840127
In:
Proceedings of the National Academy of Sciences of the United States of America
vol. 80
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358.
Molecular genetics of metachromatic leukodystrophy.
[electronic resource]
by
Gieselmann, V
Zlotogora, J
Harris, A
Wenger, D A
Morris, C P
Producer:
19950329
In:
Human mutation
vol. 4
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359.
Alzheimer's original patient.
[electronic resource]
by
Amaducci, L
Producer:
19961031
In:
Science (New York, N.Y.)
vol. 274
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360.
Neuropathy of metachromatic leukodystrophy: improvement with immunomodulation.
[electronic resource]
by
Nevo, Y
Pestronk, A
Lopate, G
Carroll, S L
Producer:
19970320
In:
Pediatric neurology
vol. 15
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