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M Rimoldi

Showing results (61-70 of 245) with videos related to

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Drug Metabolism and Disposition: the Biological Fate of Chemicals|August 3, 2006
Synthesis of substituted phenyl diaziridines and characterization as mechanism-based inactivators of human cytochrome P450 2B6Chitra Sridar, Yoshimasa Kobayashi, Holly Brevig, et al.
Neurology|May 26, 2004
L-2-hydroxyglutaric aciduria and brain malignant tumors: a predisposing condition?I Moroni, M Bugiani, L D'Incerti, et al.
Italian Journal of Neurological Sciences|August 1, 1987
Needle biopsy for muscle diagnosis and research: an Italian experienceF Dworzak, L Morandi, S Daniel, et al.
Behavioural Pharmacology|March 21, 2009
Antidepressant efficacy screening of novel targets in the chick anxiety-depression modelKenneth J Sufka, Jason E Warnick, Cassan N Pulaski, et al.
Neuromuscular Disorders : NMD|May 5, 1998
Very-long-chain acyl-coenzyme A dehydrogenase deficiency in a child with recurrent myoglobinuriaC Minetti, B Garavaglia, M Bado, et al.
Journal of Inherited Metabolic Disease|September 3, 1999
Medium-chain triglyceride loading test in carnitine-acylcarnitine translocase deficiency: insights on treatmentR Parini, F Invernizzi, F Menni, et al.
Journal of the Neurological Sciences|April 1, 1996
Autosomal dominant limb girdle myopathy with ragged-red fibers and cardiomyopathy. A pedigree study by in vivo 31P-MR spectroscopy indicating a multisystem mitochondrial defectG M Fabrizi, R Lodi, M D'Ettorre, et al.
Biochemical and Biophysical Research Communications|December 21, 2010
Highly selective hydrolysis of kinins by recombinant prolylcarboxypeptidaseS M Chajkowski, J Mallela, D E Watson, et al.
Neuromuscular Disorders : NMD|May 1, 1994
Lysosomal glycogen storage with normal acid maltase: a familial study with successful heart transplantF Dworzak, F Casazza, M Mora, et al.
Journal of Natural Products|September 27, 2012
Marine proteomics: a critical assessment of an emerging technologyMarc Slattery, Sridevi Ankisetty, Jone Corrales, et al.
Pageof 25

Showing results (61-70 of 245) with videos related to

Sort By:
Pageof 25
Drug Metabolism and Disposition: the Biological Fate of Chemicals|August 3, 2006
Synthesis of substituted phenyl diaziridines and characterization as mechanism-based inactivators of human cytochrome P450 2B6Chitra Sridar, Yoshimasa Kobayashi, Holly Brevig, et al.
Neurology|May 26, 2004
L-2-hydroxyglutaric aciduria and brain malignant tumors: a predisposing condition?I Moroni, M Bugiani, L D'Incerti, et al.
Italian Journal of Neurological Sciences|August 1, 1987
Needle biopsy for muscle diagnosis and research: an Italian experienceF Dworzak, L Morandi, S Daniel, et al.
Behavioural Pharmacology|March 21, 2009
Antidepressant efficacy screening of novel targets in the chick anxiety-depression modelKenneth J Sufka, Jason E Warnick, Cassan N Pulaski, et al.
Neuromuscular Disorders : NMD|May 5, 1998
Very-long-chain acyl-coenzyme A dehydrogenase deficiency in a child with recurrent myoglobinuriaC Minetti, B Garavaglia, M Bado, et al.
Journal of Inherited Metabolic Disease|September 3, 1999
Medium-chain triglyceride loading test in carnitine-acylcarnitine translocase deficiency: insights on treatmentR Parini, F Invernizzi, F Menni, et al.
Journal of the Neurological Sciences|April 1, 1996
Autosomal dominant limb girdle myopathy with ragged-red fibers and cardiomyopathy. A pedigree study by in vivo 31P-MR spectroscopy indicating a multisystem mitochondrial defectG M Fabrizi, R Lodi, M D'Ettorre, et al.
Biochemical and Biophysical Research Communications|December 21, 2010
Highly selective hydrolysis of kinins by recombinant prolylcarboxypeptidaseS M Chajkowski, J Mallela, D E Watson, et al.
Neuromuscular Disorders : NMD|May 1, 1994
Lysosomal glycogen storage with normal acid maltase: a familial study with successful heart transplantF Dworzak, F Casazza, M Mora, et al.
Journal of Natural Products|September 27, 2012
Marine proteomics: a critical assessment of an emerging technologyMarc Slattery, Sridevi Ankisetty, Jone Corrales, et al.
Pageof 25