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Tissue & Cell|May 7, 2002
Hydroxyl free radicals induce cell differentiation in SK-N-MC neuroblastoma cellsK Oravecz, D Kalka, F Jeney, et al.
Enzyme|January 1, 1987
Lysosomal sialidase deficiency: increased ganglioside content in autopsy tissues of a sialidosis patientB Ulrich-Bott, B Klem, R Kaiser, et al.
Zeitschrift Fur Geburtshilfe Und Neonatologie|October 23, 1998
[Intravenous immunoglobulins (IVIG) in treatment of an antiphospholipid syndrome in pregnancy]L Heilmann, C Berg, G F von Tempelhoff, et al.
The Journal of Biological Chemistry|June 6, 1998
Galectin-1 is a major receptor for ganglioside GM1, a product of the growth-controlling activity of a cell surface ganglioside sialidase, on human neuroblastoma cells in cultureJ Kopitz, C von Reitzenstein, M Burchert, et al.
American Journal of Medical Genetics|May 3, 1996
Methylamine accumulation in cultured cells as a measure of the aqueous storage compartment in the laboratory diagnosis of genetic lysosomal diseasesJ Kopitz, K Harzer, A Kohlschütter, et al.
Fetal Diagnosis and Therapy|March 1, 1996
Nonimmune hydrops fetalis with galactosialidosis: consequences for family planningF Haverkamp, D Jacobs, M Cantz, et al.
Experimental Cell Research|December 1, 1984
Pattern of collagen synthesis and chemotactic response of fibroblasts derived from mucopolysaccharidosis patientsB F Pontz, A Albini, H Mensing, et al.
Neuropediatrics|May 1, 1985
Familial lysosomal storage disease with generalized vacuolization and sialic aciduria. Sporadic Salla diseaseK Wolburg-Buchholz, W Schlote, J Baumkötter, et al.
Virchows Archiv. A, Pathological Anatomy and Histopathology|January 1, 1983
Liver pathology in transient neonatal hyperammonemiaA Zimmermann, C Bachmann, I Högger, et al.
FEBS Letters|July 27, 2001
Splice donor site mutation in the lysosomal neuraminidase gene causing exon skipping and complete loss of enzyme activity in a sialidosis patientR Penzel, J Uhl, J Kopitz, et al.
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