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W Moser

Showing results (281-290 of 466) with videos related to

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Neurology|August 1, 1985
Familial spastic paraparesis: an adrenoleukodystrophy phenotype?B P O'Neill, J W Swanson, F R Brown, et al.
Journal of Lipid Research|May 1, 1974
High performance liquid chromatography of ceramides: application to analysis in human tissues and demonstration of ceramide excess in Farber's diseaseM Sugita, M Iwamori, J Evans, et al.
Journal of Environmental Radioactivity|July 17, 2022
Retrospective determination of U and Pu isotopes and atom ratios in lung samples from Vienna, AustriaG Wallner, P Zima, W Moser, et al.
Journal of the Neurological Sciences|December 1, 1995
Neurodegenerative course in ceramidase deficiency (Farber disease) correlates with the residual lysosomal ceramide turnover in cultured living patient cellsT Levade, H W Moser, A H Fensom, et al.
AJNR. American Journal of Neuroradiology|May 18, 2000
X-linked adrenoleukodystrophy: the role of contrast-enhanced MR imaging in predicting disease progressionE R Melhem, D J Loes, C S Georgiades, et al.
Human Mutation|March 29, 2000
Determination of 30 X-linked adrenoleukodystrophy mutations, including 15 not previously describedM B Lachtermacher, H N Seuánez, A B Moser, et al.
Anatomischer Anzeiger|January 1, 1975
[Experience with the written examination (multiple choice test) in the teaching of anatomy]M F Lischka, E B Krammer, R Mayr, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 15, 1993
Chromosomal rearrangement segregating with adrenoleukodystrophy: associated changes in color visionM Alpern, G H Sack, D H Krantz, et al.
Birth Defects Original Article Series|January 1, 1980
Therapeutic trial of plasmapheresis in Refsum disease and in Fabry diseaseH W Moser, H Braine, R E Pyeritz, et al.
Circulation|September 12, 2007
Radiation dose to patients from cardiac diagnostic imagingAndrew J Einstein, Kevin W Moser, Randall C Thompson, et al.
Pageof 47

Showing results (281-290 of 466) with videos related to

Sort By:
Pageof 47
Neurology|August 1, 1985
Familial spastic paraparesis: an adrenoleukodystrophy phenotype?B P O'Neill, J W Swanson, F R Brown, et al.
Journal of Lipid Research|May 1, 1974
High performance liquid chromatography of ceramides: application to analysis in human tissues and demonstration of ceramide excess in Farber's diseaseM Sugita, M Iwamori, J Evans, et al.
Journal of Environmental Radioactivity|July 17, 2022
Retrospective determination of U and Pu isotopes and atom ratios in lung samples from Vienna, AustriaG Wallner, P Zima, W Moser, et al.
Journal of the Neurological Sciences|December 1, 1995
Neurodegenerative course in ceramidase deficiency (Farber disease) correlates with the residual lysosomal ceramide turnover in cultured living patient cellsT Levade, H W Moser, A H Fensom, et al.
AJNR. American Journal of Neuroradiology|May 18, 2000
X-linked adrenoleukodystrophy: the role of contrast-enhanced MR imaging in predicting disease progressionE R Melhem, D J Loes, C S Georgiades, et al.
Human Mutation|March 29, 2000
Determination of 30 X-linked adrenoleukodystrophy mutations, including 15 not previously describedM B Lachtermacher, H N Seuánez, A B Moser, et al.
Anatomischer Anzeiger|January 1, 1975
[Experience with the written examination (multiple choice test) in the teaching of anatomy]M F Lischka, E B Krammer, R Mayr, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 15, 1993
Chromosomal rearrangement segregating with adrenoleukodystrophy: associated changes in color visionM Alpern, G H Sack, D H Krantz, et al.
Birth Defects Original Article Series|January 1, 1980
Therapeutic trial of plasmapheresis in Refsum disease and in Fabry diseaseH W Moser, H Braine, R E Pyeritz, et al.
Circulation|September 12, 2007
Radiation dose to patients from cardiac diagnostic imagingAndrew J Einstein, Kevin W Moser, Randall C Thompson, et al.
Pageof 47