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Acta Neuropathologica|January 1, 1994
Leptomeningeal lipid storage patterns in Fabry diseaseM Elleder, H Christomanou, B Kustermann-Kuhn, et al.Biochemical and Molecular Medicine|August 1, 1995
Deficient ferritin immunoreactivity in visceral organs from four patients with Niemann-Pick disease type CH Christomanou, J Kellermann, R P Linke, et al.Der Nervenarzt|October 11, 2003
[Niemann-Pick disease type C--a neurometabolic disease through disturbed intracellular lipid transport]A J Grau, M Weisbrod, E Hund, et al.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.Pageof 11