S Ziyeh|K Harzer - JoVE Visualize

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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.

Acta Neurologica Scandinavica|April 12, 2005

FDG-PET and MRI in potassium channel antibody-associated non-paraneoplastic limbic encephalitis: correlation with clinical course and neuropsychologyS Fauser, J Talazko, K Wagner, et al.

European Radiology|March 10, 2004

Parkes Weber or Klippel-Trenaunay syndrome? Non-invasive diagnosis with MR projection angiographyS Ziyeh, J Spreer, J Rössler, 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.

European Journal of Pediatrics|October 1, 1979

Oculo-neural involvement in an enzymatically proven case of Niemann-Pick disease type BG Hammersen, H C Oppermann, E Harms, et al.

European Journal of Pediatrics|February 14, 1998

Early-lethal pulmonary form of Niemann-Pick type C disease belonging to a second, rare genetic complementation groupO Schofer, B Mischo, W Püschel, et al.

Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|October 1, 1992

[Response criteria for enzyme substitution in Gaucher disease]F Berthold, H Sieverts, G Benz-Bohm, et al.

Human Genetics|January 1, 1984

Pyruvate dehydrogenase activity is not deficient in the brain of three autopsied cases with Leigh disease (subacute necrotizing encephalomyelopathy, SNE)B Kustermann-Kuhn, K Harzer, R Schröder, et al.

Neuropadiatrie|August 1, 1975

Cytosome morphology and distribution of generalized ceroidlipofuscinosis in a twenty-eight month old boy with normal myeloperoxidase activityA P Anzil, K Blinzinger, K Harzer, et al.

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Showing results (51-60 of 108) with videos related to

Sort By:

Pageof 11

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.

Acta Neurologica Scandinavica|April 12, 2005

FDG-PET and MRI in potassium channel antibody-associated non-paraneoplastic limbic encephalitis: correlation with clinical course and neuropsychologyS Fauser, J Talazko, K Wagner, et al.

European Radiology|March 10, 2004

Parkes Weber or Klippel-Trenaunay syndrome? Non-invasive diagnosis with MR projection angiographyS Ziyeh, J Spreer, J Rössler, 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.

European Journal of Pediatrics|October 1, 1979

Oculo-neural involvement in an enzymatically proven case of Niemann-Pick disease type BG Hammersen, H C Oppermann, E Harms, et al.

European Journal of Pediatrics|February 14, 1998

Early-lethal pulmonary form of Niemann-Pick type C disease belonging to a second, rare genetic complementation groupO Schofer, B Mischo, W Püschel, et al.

Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|October 1, 1992

[Response criteria for enzyme substitution in Gaucher disease]F Berthold, H Sieverts, G Benz-Bohm, et al.

Human Genetics|January 1, 1984

Pyruvate dehydrogenase activity is not deficient in the brain of three autopsied cases with Leigh disease (subacute necrotizing encephalomyelopathy, SNE)B Kustermann-Kuhn, K Harzer, R Schröder, et al.

Neuropadiatrie|August 1, 1975

Cytosome morphology and distribution of generalized ceroidlipofuscinosis in a twenty-eight month old boy with normal myeloperoxidase activityA P Anzil, K Blinzinger, K Harzer, et al.

Pageof 11