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C Sewell

Showing results (181-190 of 198) with videos related to

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Human Genetics|November 1, 1986
Normomorphic sialidosis in two female adults with severe neurologic disease and without sialyl oligosacchariduriaK Harzer, M Cantz, A C Sewell, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Liver transplantation in two cases of propionic acidaemiaJ S Schlenzig, F Poggi-Travert, J Laurent, et al.
The American Journal of Physiology|October 1, 1995
Regulation of hexokinase II and glycogen synthase mRNA, protein, and activity in human muscleL J Mandarino, R L Printz, K A Cusi, et al.
The Journal of Pediatrics|May 16, 2018
Methicillin-Resistant Staphylococcus aureus: The Effects Are More Than Skin DeepCarol E Muenks, Whitney C Sewell, Patrick G Hogan, et al.
Journal of Alzheimer'S Disease : JAD|June 7, 2021
Research Attitudes and Interest Among Elderly Latinxs: The Impact of a Collaborative Video and Community PeersMargaret C Sewell, Judith Neugroschl, Mari Umpierre, et al.
Neuropediatrics|August 23, 2007
Ethylmalonic encephalopathy: clinical and biochemical observationsD I Zafeiriou, P Augoustides-Savvopoulou, D Haas, et al.
Journal of Inherited Metabolic Disease|March 28, 2002
Selective screening for inborn errors of metabolism: the primary care-based model in rural CreteA Evangeliou, C Lionis, H Michailidou, et al.
Molecular Neurodegeneration|February 4, 2014
A consecutive case series experience with [18 F] florbetapir PET imaging in an urban dementia center: impact on quality of life, decision making, and dispositionEffie M Mitsis, Heidi A Bender, Lale Kostakoglu, et al.
G3 (Bethesda, Md.)|March 2, 2018
A Nonsense Variant in the <i>ACADVL</i> Gene in German Hunting Terriers with Exercise Induced Metabolic MyopathyVincent Lepori, Franziska Mühlhause, Adrian C Sewell, et al.
Journal of Inherited Metabolic Disease|July 23, 2003
Recurrent vomiting and ethylmalonic aciduria associated with rare mutations of the short-chain acyl-CoA dehydrogenase geneJ Seidel, S Streck, K Bellstedt, et al.
Pageof 20

Showing results (181-190 of 198) with videos related to

Sort By:
Pageof 20
Human Genetics|November 1, 1986
Normomorphic sialidosis in two female adults with severe neurologic disease and without sialyl oligosacchariduriaK Harzer, M Cantz, A C Sewell, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Liver transplantation in two cases of propionic acidaemiaJ S Schlenzig, F Poggi-Travert, J Laurent, et al.
The American Journal of Physiology|October 1, 1995
Regulation of hexokinase II and glycogen synthase mRNA, protein, and activity in human muscleL J Mandarino, R L Printz, K A Cusi, et al.
The Journal of Pediatrics|May 16, 2018
Methicillin-Resistant Staphylococcus aureus: The Effects Are More Than Skin DeepCarol E Muenks, Whitney C Sewell, Patrick G Hogan, et al.
Journal of Alzheimer'S Disease : JAD|June 7, 2021
Research Attitudes and Interest Among Elderly Latinxs: The Impact of a Collaborative Video and Community PeersMargaret C Sewell, Judith Neugroschl, Mari Umpierre, et al.
Neuropediatrics|August 23, 2007
Ethylmalonic encephalopathy: clinical and biochemical observationsD I Zafeiriou, P Augoustides-Savvopoulou, D Haas, et al.
Journal of Inherited Metabolic Disease|March 28, 2002
Selective screening for inborn errors of metabolism: the primary care-based model in rural CreteA Evangeliou, C Lionis, H Michailidou, et al.
Molecular Neurodegeneration|February 4, 2014
A consecutive case series experience with [18 F] florbetapir PET imaging in an urban dementia center: impact on quality of life, decision making, and dispositionEffie M Mitsis, Heidi A Bender, Lale Kostakoglu, et al.
G3 (Bethesda, Md.)|March 2, 2018
A Nonsense Variant in the <i>ACADVL</i> Gene in German Hunting Terriers with Exercise Induced Metabolic MyopathyVincent Lepori, Franziska Mühlhause, Adrian C Sewell, et al.
Journal of Inherited Metabolic Disease|July 23, 2003
Recurrent vomiting and ethylmalonic aciduria associated with rare mutations of the short-chain acyl-CoA dehydrogenase geneJ Seidel, S Streck, K Bellstedt, et al.
Pageof 20