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Results of search for 'su:"Leukodystrophy, Metachromatic"', page 22 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
421.
Metachromatic leukodystrophy: multiple nonfunctional and pseudodeficiency alleles in a pedigree: problems with diagnosis and counseling.
[electronic resource]
by
Francis, G S
Bonni, A
Shen, N
Hechtman, P
Yamut, B
Carpenter, S
Karpati, G
Chang, P L
Producer:
19930826
In:
Annals of neurology
vol. 34
Online resources:
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422.
Nine-year-old girl presenting familial occurrence of progressive developmental abnormalities with the white matter lesions.
[electronic resource]
by
Hayashi, Masaharu
Producer:
20030402
In:
Neuropathology : official journal of the Japanese Society of Neuropathology
vol. 22
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423.
Quantification of plasma sulfatides by mass spectrometry: Utility for metachromatic leukodystrophy.
[electronic resource]
by
Saville, Jennifer T
Smith, Nicholas J C
Fletcher, Janice M
Fuller, Maria
Producer:
20180613
In:
Analytica chimica acta
vol. 955
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424.
A comparative study of myelin fractions from metachromatic and globoid leukodystrophies.
[electronic resource]
by
Malone, M J
Sakuragawa, N
Szoke, M
Producer:
19751204
In:
Neurology
vol. 25
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425.
First-trimester diagnosis of metachromatic leucodystrophy.
[electronic resource]
by
Fensom, A H
Marsh, J
Jackson, M
McGuire, V M
Vimal, C
Nicolaides, K
Sheridan, R
Producer:
19890111
In:
Clinical genetics
vol. 34
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426.
[Clinical and histological diagnosis of a case of familial adult metachromatic leucodystrophy (author's transl)].
[electronic resource]
by
Czmok, E
Regli, F
Bischoff, A
Harzer, K
Benz, H U
Producer:
19741219
In:
Journal of neurology
vol. 207
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427.
[Saposin C deficiency].
[electronic resource]
by
Sano, A
Producer:
19980925
In:
Ryoikibetsu shokogun shirizu
no. 19 Pt 2
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428.
Arylsulfatase A pseudodeficiency in healthy Brazilian individuals.
[electronic resource]
by
Pedron, C G
Gaspar, P A
Giugliani, R
Pereira, M L
Producer:
20000316
In:
Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas
vol. 32
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429.
Retrovirally expressed human arylsulfatase A corrects the metabolic defect of arylsulfatase A-deficient mouse cells.
[electronic resource]
by
Matzner, U
Habetha, M
Gieselmann, V
Producer:
20000614
In:
Gene therapy
vol. 7
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430.
Dopamine-deficiency-enhanced hyperthermia and rhabdomyolysis during a heat wave in a metachromatic leucodystrophy heterozygote with metabolic myopathy.
[electronic resource]
by
Finsterer, Josef
Reining-Festa, Alice
Stollbergr, Claudia
Voigtlander, Till
Producer:
20120320
In:
Acta neurologica Belgica
vol. 111
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431.
Developing therapeutic approaches for metachromatic leukodystrophy.
[electronic resource]
by
Patil, Shilpa A
Maegawa, Gustavo H B
Producer:
20131126
In:
Drug design, development and therapy
vol. 7
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432.
Studies in metachromatic leukodystrophy. XIV. Purification and subunit structure of human liver arylsulfatase A.
[electronic resource]
by
James, G T
Austin, J H
Producer:
19800124
In:
Clinica chimica acta; international journal of clinical chemistry
vol. 98
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433.
The relationship of the metachromatic leukodystrophies to neuropsychiatric disorders.
[electronic resource]
by
Fluharty, A L
Producer:
19910715
In:
Molecular and chemical neuropathology
vol. 13
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434.
Pseudodeficiency of arylsulfatase A: a counseling dilemma.
[electronic resource]
by
Baldinger, S
Pierpont, M E
Wenger, D A
Producer:
19870515
In:
Clinical genetics
vol. 31
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435.
[The adult form of metachromatic leukodystrophy with a predominantly psychotic manifestation].
[electronic resource]
by
Schäffer, S
Oepen, G
Ott, D
Producer:
19890301
In:
Der Nervenarzt
vol. 59
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436.
Correlation of the dispersion state of pyrene cerebroside sulfate and its uptake and degradation by cultured cells.
[electronic resource]
by
Viani, P
Marchesini, S
Cestaro, B
Gatt, S
Producer:
19890428
In:
Biochimica et biophysica acta
vol. 1002
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437.
Identification of a mutation in the arylsulfatase A gene of a patient with adult-type metachromatic leukodystrophy.
[electronic resource]
by
Kondo, R
Wakamatsu, N
Yoshino, H
Fukuhara, N
Miyatake, T
Tsuji, S
Producer:
19910523
In:
American journal of human genetics
vol. 48
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438.
Arylsulfatases A and B in leukocytes: a comparative statistical study of late infantile and juvenile forms of metachromatic leukodystrophy and controls.
[electronic resource]
by
Dubois, G
Turpin, J C
Georges, M C
Baumann, N
Producer:
19800712
In:
Biomedicine / [publiee pour l'A.A.I.C.I.G.]
vol. 33
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439.
Prenatal diagnosis of metachromatic leukodystrophy: a diagnosis with amniotic fluid by DEAE-Sepharose column chromatography and its confirmation by kidney lipid analysis.
[electronic resource]
by
Eto, Y
Tahara, T
Koda, N
Yamaguchi, S
Producer:
19830610
In:
Journal of inherited metabolic disease
vol. 5
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440.
Sphingolipidoses.
[electronic resource]
by
Sandhoff, K
Producer:
19840215
In:
Journal of clinical pathology. Supplement (Royal College of Pathologists)
vol. 8
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