Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

M L Barth

Showing results (11-20 of 22) with videos related to

Pageof 3
Sort By:
Environmental Health Perspectives|June 1, 1975
Experimental toxicology of pyrolysis and combustion hazardsH H Cornish, K J Hahn, M L Barth
Journal of Medical Genetics|September 1, 1994
Frequency of arylsulphatase A pseudodeficiency associated mutations in a healthy populationM L Barth, C Ward, A Harris, et al.
Developments in Toxicology and Environmental Science|January 1, 1980
Inhibitor characteristics of native, solubilized, and lipid-reconstituted neurotoxic esteraseC S Davis, M L Barth, B R Dudek, et al.
Journal of Medical Genetics|April 1, 1993
Gaucher's disease in the United Kingdom: screening non-Jewish patients for the two common mutationsA J Walley, M L Barth, I Ellis, et al.
Journal of Toxicology and Environmental Health. Part A|July 15, 1999
Comparison of neurotoxic effects and potential risks from oral administration or ingestion of tricresyl phosphate and jet engine oil containing tricresyl phosphateC R Mackerer, M L Barth, A J Krueger, et al.
Journal of Medical Genetics|September 1, 1994
A single origin for the most frequent mutation causing late infantile metachromatic leucodystrophyJ Zlotogora, Y Furman-Shaharabani, A Harris, et al.
Food and Cosmetics Toxicology|December 1, 1971
Correlation between serum enzymes, isozyme patterns and histologically detectable organ damageH C Grice, M L Barth, H H Cornish, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Seven-year experience of a reference laboratory for detection of inborn errors of metabolism in BrazilR Giugliani, J C Dutra, M L Barth, et al.
Journal of Medical Genetics|August 1, 1990
Very low levels of high density lipoprotein cholesterol in four sibs of a family with non-neuropathic Niemann-Pick disease and sea-blue histiocytosisM B Viana, R Giugliani, V H Leite, et al.
American Journal of Medical Genetics|December 1, 1990
Application of a flowchart for the detection of lysosomal storage diseases in 105 high-risk Brazilian patientsM L Barth, R Giugliani, S L Goldenfum, et al.
Pageof 3

Showing results (11-20 of 22) with videos related to

Sort By:
Pageof 3
Environmental Health Perspectives|June 1, 1975
Experimental toxicology of pyrolysis and combustion hazardsH H Cornish, K J Hahn, M L Barth
Journal of Medical Genetics|September 1, 1994
Frequency of arylsulphatase A pseudodeficiency associated mutations in a healthy populationM L Barth, C Ward, A Harris, et al.
Developments in Toxicology and Environmental Science|January 1, 1980
Inhibitor characteristics of native, solubilized, and lipid-reconstituted neurotoxic esteraseC S Davis, M L Barth, B R Dudek, et al.
Journal of Medical Genetics|April 1, 1993
Gaucher's disease in the United Kingdom: screening non-Jewish patients for the two common mutationsA J Walley, M L Barth, I Ellis, et al.
Journal of Toxicology and Environmental Health. Part A|July 15, 1999
Comparison of neurotoxic effects and potential risks from oral administration or ingestion of tricresyl phosphate and jet engine oil containing tricresyl phosphateC R Mackerer, M L Barth, A J Krueger, et al.
Journal of Medical Genetics|September 1, 1994
A single origin for the most frequent mutation causing late infantile metachromatic leucodystrophyJ Zlotogora, Y Furman-Shaharabani, A Harris, et al.
Food and Cosmetics Toxicology|December 1, 1971
Correlation between serum enzymes, isozyme patterns and histologically detectable organ damageH C Grice, M L Barth, H H Cornish, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Seven-year experience of a reference laboratory for detection of inborn errors of metabolism in BrazilR Giugliani, J C Dutra, M L Barth, et al.
Journal of Medical Genetics|August 1, 1990
Very low levels of high density lipoprotein cholesterol in four sibs of a family with non-neuropathic Niemann-Pick disease and sea-blue histiocytosisM B Viana, R Giugliani, V H Leite, et al.
American Journal of Medical Genetics|December 1, 1990
Application of a flowchart for the detection of lysosomal storage diseases in 105 high-risk Brazilian patientsM L Barth, R Giugliani, S L Goldenfum, et al.
Pageof 3