Search research articles
Contact Us
Filters
Showing results (1-10 of 9) with videos related to
Page
of 1
Sort By:
Journal of Inherited Metabolic Disease
|
September 20, 2007
Biochemistry and bioenergetics of glutaryl-CoA dehydrogenase deficiency
S W Sauer
Annals of Emergency Medicine
|
June 1, 2001
Hydroxocobalamin: improved public health readiness for cyanide disasters
S W Sauer, M E Keim
Journal of Inherited Metabolic Disease
|
October 17, 2006
The aetiology of neurological complications of organic acidaemias--a role for the blood-brain barrier
S Kölker, S W Sauer, R A H Surtees, et al.
Journal of Inherited Metabolic Disease
|
October 10, 2009
Long-term exposure of human proximal tubule cells to hydroxycobalamin[c-lactam] as a possible model to study renal disease in methylmalonic acidurias
S W Sauer, S Opp, A Haarmann, et al.
Journal of Inherited Metabolic Disease
|
April 9, 2008
Pathogenesis of CNS involvement in disorders of amino and organic acid metabolism
S Kölker, S W Sauer, G F Hoffmann, et al.
Human Molecular Genetics
|
October 1, 2015
Molecular and biochemical alterations in tubular epithelial cells of patients with isolated methylmalonic aciduria
T Ruppert, A Schumann, H J Gröne, et al.
Journal of Inherited Metabolic Disease
|
September 12, 2007
Neurodegeneration and chronic renal failure in methylmalonic aciduria--a pathophysiological approach
M A Morath, J G Okun, I B Müller, et al.
FEBS Letters
|
December 10, 2013
TNF-α mediates mitochondrial uncoupling and enhances ROS-dependent cell migration via NF-κB activation in liver cells
L Kastl, S W Sauer, T Ruppert, et al.
Neurochemistry International
|
February 17, 2007
Enzymatic and metabolic evidence for a region specific mitochondrial dysfunction in brains of murine succinic semialdehyde dehydrogenase deficiency (Aldh5a1-/- mice)
S W Sauer, S Kölker, G F Hoffmann, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 9) with videos related to
Sort By:
Page
of 1
Journal of Inherited Metabolic Disease
|
September 20, 2007
Biochemistry and bioenergetics of glutaryl-CoA dehydrogenase deficiency
S W Sauer
Annals of Emergency Medicine
|
June 1, 2001
Hydroxocobalamin: improved public health readiness for cyanide disasters
S W Sauer, M E Keim
Journal of Inherited Metabolic Disease
|
October 17, 2006
The aetiology of neurological complications of organic acidaemias--a role for the blood-brain barrier
S Kölker, S W Sauer, R A H Surtees, et al.
Journal of Inherited Metabolic Disease
|
October 10, 2009
Long-term exposure of human proximal tubule cells to hydroxycobalamin[c-lactam] as a possible model to study renal disease in methylmalonic acidurias
S W Sauer, S Opp, A Haarmann, et al.
Journal of Inherited Metabolic Disease
|
April 9, 2008
Pathogenesis of CNS involvement in disorders of amino and organic acid metabolism
S Kölker, S W Sauer, G F Hoffmann, et al.
Human Molecular Genetics
|
October 1, 2015
Molecular and biochemical alterations in tubular epithelial cells of patients with isolated methylmalonic aciduria
T Ruppert, A Schumann, H J Gröne, et al.
Journal of Inherited Metabolic Disease
|
September 12, 2007
Neurodegeneration and chronic renal failure in methylmalonic aciduria--a pathophysiological approach
M A Morath, J G Okun, I B Müller, et al.
FEBS Letters
|
December 10, 2013
TNF-α mediates mitochondrial uncoupling and enhances ROS-dependent cell migration via NF-κB activation in liver cells
L Kastl, S W Sauer, T Ruppert, et al.
Neurochemistry International
|
February 17, 2007
Enzymatic and metabolic evidence for a region specific mitochondrial dysfunction in brains of murine succinic semialdehyde dehydrogenase deficiency (Aldh5a1-/- mice)
S W Sauer, S Kölker, G F Hoffmann, et al.
Page
of 1