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Results of search for 'su:"Leukodystrophy, Metachromatic"', page 14 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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261.
Metachromatic leukodystrophy: a case of triplets with the late infantile variant and a systematic review of the literature.
[electronic resource]
by
Mahmood, Asif
Berry, Jay
Wenger, David A
Escolar, Maria
Sobeih, Magdi
Raymond, Gerald
Eichler, Florian S
Producer:
20100805
In:
Journal of child neurology
vol. 25
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262.
Determinants of health care use in a population-based leukodystrophy cohort.
[electronic resource]
by
Nelson, Clint
Mundorff, Michael B
Korgenski, E Kent
Brimley, Cameron J
Srivastava, Rajendu
Bonkowsky, Joshua L
Producer:
20130426
In:
The Journal of pediatrics
vol. 162
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263.
Infantile metachromatic leukodystrophy in an 18 month old girl.
[electronic resource]
by
Ali Mallick, Muhammad Saad
Godil, Ansab
Khetpal, Akash
Rizvi, Ather Hasan
Khan, Fahad
Producer:
20180820
In:
JPMA. The Journal of the Pakistan Medical Association
vol. 66
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264.
Juvenile onset metachromatic leucodystrophy. Failure of response on a low vitamin A diet.
[electronic resource]
by
Warner, J O
Producer:
19760114
In:
Archives of disease in childhood
vol. 50
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265.
Elevated sulfatide excretion in heterozygotes of metachromatic leukodystrophy: dependence on reduction of arylsulfatase A activity.
[electronic resource]
by
Molzer, B
Sundt-Heller, R
Kainz-Korschinsky, M
Zobel, M
Producer:
19921214
In:
American journal of medical genetics
vol. 44
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266.
The influence of low arylsulfatase A activity on neuropsychiatric morbidity: a large-scale screening in patients.
[electronic resource]
by
Propping, P
Friedl, W
Huschka, M
Schlör, K H
Reimer, F
Lee-Vaupel, M
Conzelmann, E
Sandhoff, K
Producer:
19870120
In:
Human genetics
vol. 74
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267.
[Metachromatic leukodystrophy in childhood. Description of a case].
[electronic resource]
by
Parenti, D
Ricci, R
Scoppetta, C
Segni, G
Producer:
19781220
In:
Minerva pediatrica
vol. 30
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268.
Very low arylsulfatase A and cerebroside sulfatase activities in leukocytes of healthy members of metachromatic leukodystrophy family.
[electronic resource]
by
Dubois, G
Harzer, K
Baumann, N
Producer:
19770520
In:
American journal of human genetics
vol. 29
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269.
[Enzyme studies of a patient suffering from metachromatic leukodystrophy and his family members].
[electronic resource]
by
László, A
Németh, I
Havass, Z
Producer:
19771130
In:
Kinderarztliche Praxis
vol. 45
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270.
Histopathological and ultrastructural study of a case of infantile metachromatic leukodystrophy.
[electronic resource]
by
Fenzi, F
Moretto, G
Maleci, A
Galiazzo Rizzuto, S
Dalla Bernardina, B
Bondavalli, S
Rizzuto, N
Producer:
19840608
In:
Italian journal of neurological sciences
vol. 4
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271.
[Use of electrophoresis for the detection of metachromatic leukodystrophy from human leukocytes].
[electronic resource]
by
Dubois, G
Turpin, J C
Baumann, N
Producer:
19741007
In:
Comptes rendus hebdomadaires des seances de l'Academie des sciences. Serie D: Sciences naturelles
vol. 278
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272.
Detection of donor lymphocytes in the cerebrospinal fluid of a patient with metachromatic leukodystrophy following bone marrow transplantation.
[electronic resource]
by
Yazaki, M
Ohno, T
Matsubayashi, T
Yamada, K
Osaka, Y
Yamamori, K
Ishikawa, T
Wada, Y
Sakuraba, H
Producer:
19950615
In:
Bone marrow transplantation
vol. 15
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273.
Gene symbol: ARSA. Disease: metachromatic leukodystrophy.
[electronic resource]
by
Berna, L
Gieselmann, V
Poupetova, H
Hrebicek, M
Elleder, M
Ledvinova, J
Producer:
20060321
In:
Human genetics
vol. 118
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274.
Gene symbol: ARSA.
[electronic resource]
by
Waye, J S
Eng, B
Producer:
20070502
In:
Human genetics
vol. 120
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275.
[Diagnostic strategy of metachromatic leukodystrophy in Tunisia].
[electronic resource]
by
Barboura, Ilhem
Chebel, Saber
Ferchichi, Salima
Ben Mansour, Rachida
Frih-Ayed, Mahbouba
Miled, Abdelhedi
Producer:
20111104
In:
Annales de biologie clinique
vol. 69
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276.
Mutation Frequency of Three Neurodegenerative Lysosomal Storage Diseases: From Screening to Treatment?
[electronic resource]
by
Duarte, Ana Joana
Ribeiro, Diogo
Oliveira, Pedro
Amaral, Olga
Producer:
20171023
In:
Archives of medical research
vol. 48
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277.
Is multiple sulphatase deficiency due to defective regulation of sulphohydrolase expression?
[electronic resource]
by
Fiddler, M B
Vine, D
Shapira, E
Nadler, H L
Producer:
19800119
In:
Nature
vol. 282
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278.
Letter: Genetic disorders in gypsies.
[electronic resource]
by
Harper, P S
Williams, E M
Producer:
19750826
In:
Lancet (London, England)
vol. 1
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279.
Diagnosis of arylsulfatase A deficiency in intact cultured cells using a fluorescent derivative of cerebroside sulfate.
[electronic resource]
by
Bach, G
Dagan, A
Herz, B
Gatt, S
Producer:
19870724
In:
Clinical genetics
vol. 31
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280.
Studies in metachromatic leukodystrophy. XIII. Purification of sulfatase A from normal human liver.
[electronic resource]
by
Collins, J
Yamada, W
Worth, W
Austin, J
Producer:
19760823
In:
Advances in experimental medicine and biology
vol. 68
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