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Acta Paediatrica (Oslo, Norway : 1992). Supplement|May 18, 2005
What can cell biology tell us about heterogeneity in lysosomal storage diseases?V GieselmannJournal of Child Neurology|October 24, 2003
Metachromatic leukodystrophy: recent research developmentsVolkmar GieselmannActa Paediatrica (Oslo, Norway : 1992)|May 28, 2008
Metachromatic leukodystrophy: genetics, pathogenesis and therapeutic optionsVolkmar GieselmannActa Paediatrica (Oslo, Norway : 1992). Supplement|May 25, 2006
Reversibility of cellular and organ pathology in enzyme replacement trials in animal models of lysosomal storage diseasesVolkmar GieselmannHuman Genetics|January 1, 1991
An assay for the rapid detection of the arylsulfatase A pseudodeficiency allele facilitates diagnosis and genetic counseling for metachromatic leukodystrophyV GieselmannFEBS Letters|February 24, 1992
ASP-56, a new actin sequestering protein from pig platelets with homology to CAP, an adenylate cyclase-associated protein from yeastR Gieselmann, K MannBiochimica Et Biophysica Acta|December 30, 2008
Lysosomal disorders: from storage to cellular damageAndrea Ballabio, Volkmar GieselmannDer Nervenarzt|February 21, 2020
[A palliative concept for psychiatry? Conceptional considerations on advantages and limits of a close cooperation between palliative care and psychiatry]Astrid Gieselmann, Jochen VollmannGene Therapy|August 9, 2003
Specific hammerhead ribozymes reduce synthesis of cation-independent mannose 6-phosphate receptor mRNA and proteinA Yaghootfam, V GieselmannExpert Opinion on Biological Therapy|February 16, 2005
Gene therapy of metachromatic leukodystrophyUlrich Matzner, Volkmar GieselmannPageof 32