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S Albers

Showing results (21-30 of 65) with videos related to

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Clinical Science (London, England : 1979)|June 1, 1989
Availability of amino acids supplied by constant intravenous infusion of synthetic dipeptides in healthy manS Albers, J Wernerman, P Stehle, et al.
Clinical Science (London, England : 1979)|November 1, 1988
Availability of amino acids supplied intravenously in healthy man as synthetic dipeptides: kinetic evaluation of L-alanyl-L-glutamine and glycyl-L-tyrosineS Albers, J Wernerman, P Stehle, et al.
Journal of Clinical Psychopharmacology|November 1, 1981
Extrapyramidal symptoms in patients with primary degenerative dementiaN Pomara, B Reisberg, S Albers, et al.
Brain Research|September 17, 2002
Stress-induced mitochondrial depolarization and oxidative damage in PSP cybridsJason W Chirichigno, Giovanni Manfredi, M Flint Beal, et al.
Experimental Neurology|December 4, 2002
Expression of MMP-2, MMP-9, and MMP-1 and their endogenous counterregulators TIMP-1 and TIMP-2 in postmortem brain tissue of Parkinson's diseaseStefan Lorenzl, David S Albers, Sabine Narr, et al.
Analytical Biochemistry|November 15, 1985
An ultra rapid and sensitive high-performance liquid chromatographic method for determination of tissue and plasma free amino acidsT A Graser, H G Godel, S Albers, et al.
Unfallchirurgie (Heidelberg, Germany)|May 26, 2025
[Focus on the shoulder : Precise diagnostics for complex pathological alterations]S Albers, M Zyskowski, P Zehnder, et al.
American Journal of Pharmaceutical Education|November 20, 2013
Educational and career goals of pharmacy students upon graduationMattia M Migliore, Ryan C Costantino, Nicholas A Campagna, et al.
Neuroscience|March 2, 1999
Immunohistochemical localization of N-methyl-D-aspartate and alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionate receptor subunits in the substantia nigra pars compacta of the ratD S Albers, S W Weiss, M J Iadarola, et al.
Journal of Inherited Metabolic Disease|August 7, 2001
Compound heterozygosity in four asymptomatic siblings with medium-chain acyl-CoA dehydrogenase deficiencyS Albers, H L Levy, M Irons, et al.
Pageof 7

Showing results (21-30 of 65) with videos related to

Sort By:
Pageof 7
Clinical Science (London, England : 1979)|June 1, 1989
Availability of amino acids supplied by constant intravenous infusion of synthetic dipeptides in healthy manS Albers, J Wernerman, P Stehle, et al.
Clinical Science (London, England : 1979)|November 1, 1988
Availability of amino acids supplied intravenously in healthy man as synthetic dipeptides: kinetic evaluation of L-alanyl-L-glutamine and glycyl-L-tyrosineS Albers, J Wernerman, P Stehle, et al.
Journal of Clinical Psychopharmacology|November 1, 1981
Extrapyramidal symptoms in patients with primary degenerative dementiaN Pomara, B Reisberg, S Albers, et al.
Brain Research|September 17, 2002
Stress-induced mitochondrial depolarization and oxidative damage in PSP cybridsJason W Chirichigno, Giovanni Manfredi, M Flint Beal, et al.
Experimental Neurology|December 4, 2002
Expression of MMP-2, MMP-9, and MMP-1 and their endogenous counterregulators TIMP-1 and TIMP-2 in postmortem brain tissue of Parkinson's diseaseStefan Lorenzl, David S Albers, Sabine Narr, et al.
Analytical Biochemistry|November 15, 1985
An ultra rapid and sensitive high-performance liquid chromatographic method for determination of tissue and plasma free amino acidsT A Graser, H G Godel, S Albers, et al.
Unfallchirurgie (Heidelberg, Germany)|May 26, 2025
[Focus on the shoulder : Precise diagnostics for complex pathological alterations]S Albers, M Zyskowski, P Zehnder, et al.
American Journal of Pharmaceutical Education|November 20, 2013
Educational and career goals of pharmacy students upon graduationMattia M Migliore, Ryan C Costantino, Nicholas A Campagna, et al.
Neuroscience|March 2, 1999
Immunohistochemical localization of N-methyl-D-aspartate and alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionate receptor subunits in the substantia nigra pars compacta of the ratD S Albers, S W Weiss, M J Iadarola, et al.
Journal of Inherited Metabolic Disease|August 7, 2001
Compound heterozygosity in four asymptomatic siblings with medium-chain acyl-CoA dehydrogenase deficiencyS Albers, H L Levy, M Irons, et al.
Pageof 7