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S Rust

Showing results (71-80 of 88) with videos related to

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Molecular Genetics and Metabolism|February 7, 2012
Congenital disorder of glycosylation type Ij (CDG-Ij, DPAGT1-CDG): extending the clinical and molecular spectrum of a rare diseaseA E Würde, J Reunert, S Rust, et al.
Developmental Medicine and Child Neurology|February 11, 2012
An unusual presentation of anti-Hu-associated paraneoplastic limbic encephalitisJennifer E Langer, M Beatriz S Lopes, Nathan B Fountain, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|July 17, 2012
Heterozygosity for lysosomal acid lipase E8SJM mutation and serum lipid concentrationsSa Muntoni, H Wiebusch, M Jansen-Rust, et al.
Gene|October 26, 2013
ALG1-CDG: a new case with early fatal outcomeA-K Rohlfing, S Rust, J Reunert, et al.
Plos One|November 6, 2014
Social determinants and the classification of disease: descriptive epidemiology of selected socially mediated disease constellationsRobert S Levine, Barbara A Kilbourne, George S Rust, et al.
Plos One|September 1, 2023
Machine learning to predict risk for community-onset Staphylococcus aureus infections in children living in southeastern United StatesXiting Lin, Ruijin Geng, Kurt Menke, et al.
The American Journal of Physiology|October 1, 1991
Evaluation of the role of cellular hypoxia in sepsis by the hypoxic marker [18F]fluoromisonidazoleR S Hotchkiss, R S Rust, C S Dence, et al.
American Journal of Public Health|September 1, 2007
Black-White mortality from HIV in the United States before and after introduction of highly active antiretroviral therapy in 1996Robert S Levine, Nathaniel C Briggs, Barbara S Kilbourne, et al.
Journal of Inherited Metabolic Disease|March 18, 2015
A new case of UDP-galactose transporter deficiency (SLC35A2-CDG): molecular basis, clinical phenotype, and therapeutic approachK Dörre, M Olczak, Y Wada, et al.
Nature Genetics|August 4, 1999
Tangier disease is caused by mutations in the gene encoding ATP-binding cassette transporter 1S Rust, M Rosier, H Funke, et al.
Pageof 9

Showing results (71-80 of 88) with videos related to

Sort By:
Pageof 9
Molecular Genetics and Metabolism|February 7, 2012
Congenital disorder of glycosylation type Ij (CDG-Ij, DPAGT1-CDG): extending the clinical and molecular spectrum of a rare diseaseA E Würde, J Reunert, S Rust, et al.
Developmental Medicine and Child Neurology|February 11, 2012
An unusual presentation of anti-Hu-associated paraneoplastic limbic encephalitisJennifer E Langer, M Beatriz S Lopes, Nathan B Fountain, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|July 17, 2012
Heterozygosity for lysosomal acid lipase E8SJM mutation and serum lipid concentrationsSa Muntoni, H Wiebusch, M Jansen-Rust, et al.
Gene|October 26, 2013
ALG1-CDG: a new case with early fatal outcomeA-K Rohlfing, S Rust, J Reunert, et al.
Plos One|November 6, 2014
Social determinants and the classification of disease: descriptive epidemiology of selected socially mediated disease constellationsRobert S Levine, Barbara A Kilbourne, George S Rust, et al.
Plos One|September 1, 2023
Machine learning to predict risk for community-onset Staphylococcus aureus infections in children living in southeastern United StatesXiting Lin, Ruijin Geng, Kurt Menke, et al.
The American Journal of Physiology|October 1, 1991
Evaluation of the role of cellular hypoxia in sepsis by the hypoxic marker [18F]fluoromisonidazoleR S Hotchkiss, R S Rust, C S Dence, et al.
American Journal of Public Health|September 1, 2007
Black-White mortality from HIV in the United States before and after introduction of highly active antiretroviral therapy in 1996Robert S Levine, Nathaniel C Briggs, Barbara S Kilbourne, et al.
Journal of Inherited Metabolic Disease|March 18, 2015
A new case of UDP-galactose transporter deficiency (SLC35A2-CDG): molecular basis, clinical phenotype, and therapeutic approachK Dörre, M Olczak, Y Wada, et al.
Nature Genetics|August 4, 1999
Tangier disease is caused by mutations in the gene encoding ATP-binding cassette transporter 1S Rust, M Rosier, H Funke, et al.
Pageof 9