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V Gieselmann

Showing results (1-10 of 87) with videos related to

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International Journal of Clinical Pharmacology and Therapeutics|December 4, 2009
Maximizing the therapeutic potential of enzyme replacement therapy for lysosomal storage diseasesV Gieselmann
Biochimica Et Biophysica Acta|April 24, 1995
Lysosomal storage diseasesV Gieselmann
Acta Paediatrica (Oslo, Norway : 1992). Supplement|May 18, 2005
What can cell biology tell us about heterogeneity in lysosomal storage diseases?V Gieselmann
Human Genetics|January 1, 1991
An assay for the rapid detection of the arylsulfatase A pseudodeficiency allele facilitates diagnosis and genetic counseling for metachromatic leukodystrophyV Gieselmann
Gene Therapy|August 9, 2003
Specific hammerhead ribozymes reduce synthesis of cation-independent mannose 6-phosphate receptor mRNA and proteinA Yaghootfam, V Gieselmann
Nucleic Acids Research|November 25, 1990
A BamHI RFLP in the human arylsulfatase A geneA Polten, V Gieselmann
Journal of Inherited Metabolic Disease|January 1, 1990
Advances in the molecular genetics of metachromatic leukodystrophyV Gieselmann, K von Figura
Neuropediatrics|June 24, 2010
Metachromatic leukodystrophy--an updateV Gieselmann, I Krägeloh-Mann
International Journal of Clinical Pharmacology and Therapeutics|December 31, 2009
Disease pathogenesis--basic scienceV Gieselmann, G Pintos-Morell
Gene Therapy|May 24, 2000
Retrovirally expressed human arylsulfatase A corrects the metabolic defect of arylsulfatase A-deficient mouse cellsU Matzner, M Habetha, V Gieselmann
Pageof 9

Showing results (1-10 of 87) with videos related to

Sort By:
Pageof 9
International Journal of Clinical Pharmacology and Therapeutics|December 4, 2009
Maximizing the therapeutic potential of enzyme replacement therapy for lysosomal storage diseasesV Gieselmann
Biochimica Et Biophysica Acta|April 24, 1995
Lysosomal storage diseasesV Gieselmann
Acta Paediatrica (Oslo, Norway : 1992). Supplement|May 18, 2005
What can cell biology tell us about heterogeneity in lysosomal storage diseases?V Gieselmann
Human Genetics|January 1, 1991
An assay for the rapid detection of the arylsulfatase A pseudodeficiency allele facilitates diagnosis and genetic counseling for metachromatic leukodystrophyV Gieselmann
Gene Therapy|August 9, 2003
Specific hammerhead ribozymes reduce synthesis of cation-independent mannose 6-phosphate receptor mRNA and proteinA Yaghootfam, V Gieselmann
Nucleic Acids Research|November 25, 1990
A BamHI RFLP in the human arylsulfatase A geneA Polten, V Gieselmann
Journal of Inherited Metabolic Disease|January 1, 1990
Advances in the molecular genetics of metachromatic leukodystrophyV Gieselmann, K von Figura
Neuropediatrics|June 24, 2010
Metachromatic leukodystrophy--an updateV Gieselmann, I Krägeloh-Mann
International Journal of Clinical Pharmacology and Therapeutics|December 31, 2009
Disease pathogenesis--basic scienceV Gieselmann, G Pintos-Morell
Gene Therapy|May 24, 2000
Retrovirally expressed human arylsulfatase A corrects the metabolic defect of arylsulfatase A-deficient mouse cellsU Matzner, M Habetha, V Gieselmann
Pageof 9