A BamHI RFLP in the human arylsulfatase A gene

le Polten, A., Gieselmann, V.
Foilsithe 1990

Hexosaminidase--pseudodeficiency?

le Kappler, J, Gieselmann, V, Propping, P
Foilsithe 1990

Multiple mutations in a specific gene in a small geographic area: a common phenomenon?

le Zlotogora, J., Gieselmann, V., Bach, G.
Foilsithe 1996

Antibody to mannose 6-phosphate specific receptor induces receptor deficiency in human fibroblasts.

le von Figura, K, Gieselmann, V, Hasilik, A
Foilsithe 1984

Mannose 6-phosphate-specific receptor is a transmembrane protein with a C-terminal extension oriented towards the cytosol.

le von Figura, K, Gieselmann, V, Hasilik, A
Foilsithe 1985

Multiple mutations are responsible for the high frequency of metachromatic leukodystrophy in a small geographic area.

le Heinisch, U, Zlotogora, J, Kafert, S, Gieselmann, V
Foilsithe 1995

Arylsulfatase A pseudodeficiency: loss of a polyadenylylation signal and N-glycosylation site.

le Gieselmann, V, Polten, A, Kreysing, J, von Figura, K
Foilsithe 1989

Recognition of human urine alpha-N-acetylglucosaminidase by rat hepatocytes. Involvement of receptors specific for galactose, mannose 6-phosphate and mannose.

le Ullrich, K, Basner, R, Gieselmann, V, Von Figura, K
Foilsithe 1979

Mutations in the arylsulfatase A pseudodeficiency allele causing metachromatic leukodystrophy.

le Gieselmann, V, Fluharty, A L, Tønnesen, T, Von Figura, K
Foilsithe 1991

Four monoclonal antibodies inhibit the recognition of arylsulphatase A by the lysosomal enzyme phosphotransferase.

le Sommerlade, H J, Hille-Rehfeld, A, von Figura, K, Gieselmann, V
Foilsithe 1994

Restoration of arylsulphatase A activity in human-metachromatic-leucodystrophy fibroblasts via retroviral-vector-mediated gene transfer.

le Rommerskirch, W, Fluharty, A L, Peters, C, von Figura, K, Gieselmann, V
Foilsithe 1991

Two new arylsulfatase A (ARSA) mutations in a juvenile metachromatic leukodystrophy (MLD) patient.

le Fluharty, A L, Fluharty, C B, Bohne, W, von Figura, K, Gieselmann, V
Foilsithe 1991

A single origin for the most frequent mutation causing late infantile metachromatic leucodystrophy.

le Zlotogora, J, Furman-Shaharabani, Y, Harris, A, Barth, M L, von Figura, K, Gieselmann, V
Foilsithe 1994

High residual arylsulfatase A (ARSA) activity in a patient with late-infantile metachromatic leukodystrophy.

le Kreysing, J, Bohne, W, Bösenberg, C, Marchesini, S, Turpin, J C, Baumann, N, von Figura, K, Gieselmann, V
Foilsithe 1993

Modest phenotypic improvements in ASA-deficient mice with only one UDP-galactose:ceramide-galactosyltransferase gene

le De Deyn PP, D'Hooge R, Mansson JE, Wittke D, Franken S, Lüllmann-Rauch R, Matzner U, Gieselmann V
Foilsithe 2006-08-01

Modest phenotypic improvements in ASA-deficient mice with only one UDP-galactose:ceramide-galactosyltransferase gene

le Franken, S, Wittke, D, Mansson, JE, D'Hooge, R, De Deyn, PP, Lüllmann-Rauch, R, Matzner, U, Gieselmann, V
Foilsithe 2006

Compound heterozygosity for metachromatic leukodystrophy and arylsulfatase A pseudodeficiency alleles is not associated with progressive neurological disease

le Penzien, J. M., Kappler, J., Herschkowitz, N., Schuknecht, B., Leinekugel, P., Propping, P., Tønnesen, T., Lou, H., Moser, H., Zierz, S., Conzelmann, E., Gieselmann, V.
Foilsithe 1993