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Results of search for 'su:"Leukodystrophy, Metachromatic"', page 63 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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1241.
Transplantation in relation to the treatment of inherited disease.
[electronic resource]
by
Groth, C G
Ringdén, O
Producer:
19841126
In:
Transplantation
vol. 38
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1242.
Nitric oxide mediates glial-induced neurodegeneration in Alexander disease.
[electronic resource]
by
Wang, Liqun
Hagemann, Tracy L
Kalwa, Hermann
Michel, Thomas
Messing, Albee
Feany, Mel B
Producer:
20160524
In:
Nature communications
vol. 6
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1243.
Development and maturation of invariant NKT cells in the presence of lysosomal engulfment.
[electronic resource]
by
Plati, Tiziana
Visigalli, Ilaria
Capotondo, Alessia
Buono, Mario
Naldini, Luigi
Cosma, Maria Pia
Biffi, Alessandra
Producer:
20091116
In:
European journal of immunology
vol. 39
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