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K Harzer

Showing results (61-70 of 126) with videos related to

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Human Genetics|July 1, 1992
Metabolism of GM1 ganglioside in cultured skin fibroblasts: anomalies in gangliosidoses, sialidoses, and sphingolipid activator protein (SAP, saposin) 1 and prosaposin deficient disordersB Schmid, B C Paton, K Sandhoff, et al.
American Journal of Medical Genetics|June 5, 1995
Significance of lipopigments with fingerprint profiles in eccrine sweat gland epithelial cellsH H Goebel, I Warlo, T Klockgether, et al.
Pediatric Research|January 1, 1989
B1 variant of GM2 gangliosidosis in a 12-year-old patientH H Goebel, G Stolte, B Kustermann-Kuhn, et al.
Virchows Archiv. A, Pathological Anatomy and Histology|April 17, 1978
An unusual case of phospholipidosisM Elleder, A Jirásek, F Smíd, et al.
Deutsche Medizinische Wochenschrift (1946)|April 25, 1975
[Prenatal diagnosis of a case of metachromatic leucodystrophy (author's transl)]K Harzer, V Zahn, S Stengel-Rutkowski, et al.
European Journal of Cell Biology|February 1, 1990
Immunocytochemical localization of sphingolipid activator protein 2 (SAP-2) in normal and SAP-deficient fibroblastsB C Paton, J L Hughes, K Harzer, et al.
Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie. Albrecht Von Graefe'S Archive for Clinical and Experimental Ophthalmology|May 2, 1978
[Niemann-Pick disease type B: An enzymatically confirmed case with unexpected retinal involvement (author's transl)]K Harzer, K W Ruprecht, D Seuffer-Schulze, et al.
Acta Neuropathologica|January 1, 1993
Unusual orthochromatic leukodystrophy with epitheloid cells (Norman-Gullotta): increase of very long chain fatty acids in brain discloses a peroxisomal disorderB Molzer, F Gullotta, K Harzer, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 30, 1996
Neuraminidase assay in cultured human fibroblasts: in situ versus in vitro proceduresM Beck, E Scheuring, H U Voelter, et al.
Geburtshilfe Und Frauenheilkunde|May 1, 1990
[Gaucher disease and pregnancy]M Menton, M Frauz, K Harzer, et al.
Pageof 13

Showing results (61-70 of 126) with videos related to

Sort By:
Pageof 13
Human Genetics|July 1, 1992
Metabolism of GM1 ganglioside in cultured skin fibroblasts: anomalies in gangliosidoses, sialidoses, and sphingolipid activator protein (SAP, saposin) 1 and prosaposin deficient disordersB Schmid, B C Paton, K Sandhoff, et al.
American Journal of Medical Genetics|June 5, 1995
Significance of lipopigments with fingerprint profiles in eccrine sweat gland epithelial cellsH H Goebel, I Warlo, T Klockgether, et al.
Pediatric Research|January 1, 1989
B1 variant of GM2 gangliosidosis in a 12-year-old patientH H Goebel, G Stolte, B Kustermann-Kuhn, et al.
Virchows Archiv. A, Pathological Anatomy and Histology|April 17, 1978
An unusual case of phospholipidosisM Elleder, A Jirásek, F Smíd, et al.
Deutsche Medizinische Wochenschrift (1946)|April 25, 1975
[Prenatal diagnosis of a case of metachromatic leucodystrophy (author's transl)]K Harzer, V Zahn, S Stengel-Rutkowski, et al.
European Journal of Cell Biology|February 1, 1990
Immunocytochemical localization of sphingolipid activator protein 2 (SAP-2) in normal and SAP-deficient fibroblastsB C Paton, J L Hughes, K Harzer, et al.
Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie. Albrecht Von Graefe'S Archive for Clinical and Experimental Ophthalmology|May 2, 1978
[Niemann-Pick disease type B: An enzymatically confirmed case with unexpected retinal involvement (author's transl)]K Harzer, K W Ruprecht, D Seuffer-Schulze, et al.
Acta Neuropathologica|January 1, 1993
Unusual orthochromatic leukodystrophy with epitheloid cells (Norman-Gullotta): increase of very long chain fatty acids in brain discloses a peroxisomal disorderB Molzer, F Gullotta, K Harzer, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 30, 1996
Neuraminidase assay in cultured human fibroblasts: in situ versus in vitro proceduresM Beck, E Scheuring, H U Voelter, et al.
Geburtshilfe Und Frauenheilkunde|May 1, 1990
[Gaucher disease and pregnancy]M Menton, M Frauz, K Harzer, et al.
Pageof 13