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Klaus Harzer

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Biological Chemistry|May 22, 2015
High β-glucosidase (GBA) activity not attributable to GBA1 and GBA2 in live normal and enzyme-deficient fibroblasts may emphasise the role of additional GBAsKlaus Harzer, Yildiz Yildiz
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|June 21, 2013
Gangliosides and gangliosidoses: principles of molecular and metabolic pathogenesisKonrad Sandhoff, Klaus Harzer
Der Pathologe|August 29, 2015
[Lysosomal storage diseases: A brief summary]A Bornemann, Klaus Harzer
FEBS Letters|February 28, 2003
Concurrent increase of cholesterol, sphingomyelin and glucosylceramide in the spleen from non-neurologic Niemann-Pick type C patients but also patients possibly affected with other lipid trafficking disordersKlaus Harzer, Gero Massenkeil, Eckhart Fröhlich
Acta Neuropathologica|October 7, 2006
Neurolysosomal pathology in human prosaposin deficiency suggests essential neurotrophic function of prosaposinJakub Sikora, Klaus Harzer, Milan Elleder
Biological Chemistry|March 14, 2019
Assay of β-glucosidase 2 (GBA2) activity using lithocholic acid β-3-O-glucoside substrate for cultured fibroblasts and glucosylceramide for brain tissueKlaus Harzer, Yildiz Yildiz, Stefanie Beck-Wödl
JIMD Reports|July 4, 2013
Niemann-pick disease type C: new aspects in a long published family - partial manifestations in heterozygotesKlaus Harzer, Stefanie Beck-Wödl, Peter Bauer
Journal of Cutaneous Pathology|October 21, 2021
Angiokeratoma corporis diffusum with severe acroparesthesia, an endothelial abnormality, and inconspicuous genetic findingsKlaus Harzer, Stefanie Beck-Wödl, Tobias B Haack
Biochemical and Biophysical Research Communications|April 25, 2006
Reduced brain cholesterol content in arylsulfatase A-deficient miceDieter Lütjohann, Klaus Harzer, Volkmar Gieselmann, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|January 30, 2002
Residual galactosylsphingosine (psychosine) beta-galactosidase activities and associated GALC mutations in late and very late onset Krabbe diseaseKlaus Harzer, Rupert Knoblich, Arndt Rolfs, et al.
Pageof 3

Showing results (1-10 of 30) with videos related to

Sort By:
Pageof 3
Biological Chemistry|May 22, 2015
High β-glucosidase (GBA) activity not attributable to GBA1 and GBA2 in live normal and enzyme-deficient fibroblasts may emphasise the role of additional GBAsKlaus Harzer, Yildiz Yildiz
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|June 21, 2013
Gangliosides and gangliosidoses: principles of molecular and metabolic pathogenesisKonrad Sandhoff, Klaus Harzer
Der Pathologe|August 29, 2015
[Lysosomal storage diseases: A brief summary]A Bornemann, Klaus Harzer
FEBS Letters|February 28, 2003
Concurrent increase of cholesterol, sphingomyelin and glucosylceramide in the spleen from non-neurologic Niemann-Pick type C patients but also patients possibly affected with other lipid trafficking disordersKlaus Harzer, Gero Massenkeil, Eckhart Fröhlich
Acta Neuropathologica|October 7, 2006
Neurolysosomal pathology in human prosaposin deficiency suggests essential neurotrophic function of prosaposinJakub Sikora, Klaus Harzer, Milan Elleder
Biological Chemistry|March 14, 2019
Assay of β-glucosidase 2 (GBA2) activity using lithocholic acid β-3-O-glucoside substrate for cultured fibroblasts and glucosylceramide for brain tissueKlaus Harzer, Yildiz Yildiz, Stefanie Beck-Wödl
JIMD Reports|July 4, 2013
Niemann-pick disease type C: new aspects in a long published family - partial manifestations in heterozygotesKlaus Harzer, Stefanie Beck-Wödl, Peter Bauer
Journal of Cutaneous Pathology|October 21, 2021
Angiokeratoma corporis diffusum with severe acroparesthesia, an endothelial abnormality, and inconspicuous genetic findingsKlaus Harzer, Stefanie Beck-Wödl, Tobias B Haack
Biochemical and Biophysical Research Communications|April 25, 2006
Reduced brain cholesterol content in arylsulfatase A-deficient miceDieter Lütjohann, Klaus Harzer, Volkmar Gieselmann, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|January 30, 2002
Residual galactosylsphingosine (psychosine) beta-galactosidase activities and associated GALC mutations in late and very late onset Krabbe diseaseKlaus Harzer, Rupert Knoblich, Arndt Rolfs, et al.
Pageof 3