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Barbara Tavazzi

Showing results (21-30 of 97) with videos related to

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Clinical Biochemistry|September 17, 2013
New T530C mutation in the aspartoacylase gene caused Canavan disease with no correlation between severity and N-acetylaspartate excretionValentina Di Pietro, Ugo Cavallari, Angela M Amorini, et al.
Neurobiology of Disease|November 25, 2022
Acute restraint stress impairs histamine type 2 receptor ability to increase the excitability of medium spiny neurons in the nucleus accumbensGiuseppe Aceto, Luca Nardella, Giacomo Lazzarino, et al.
Journal of Chromatography. A|November 7, 2017
Single-step preparation of selected biological fluids for the high performance liquid chromatographic analysis of fat-soluble vitamins and antioxidantsGiacomo Lazzarino, Salvatore Longo, Angela Maria Amorini, et al.
Molecular Genetics and Metabolism Reports|August 31, 2019
Broadening phenotype of adenylosuccinate lyase deficiency: A novel clinical pattern resembling neuronal ceroid lipofuscinosisMario Mastrangelo, Chiara Alfonsi, Isabella Screpanti, et al.
Clinical Chemistry and Laboratory Medicine|April 3, 2023
Improved diagnostics of purine and pyrimidine metabolism disorders using LC-MS/MS and its clinical applicationAlessio Cremonesi, David Meili, Anahita Rassi, et al.
Blood Transfusion = Trasfusione Del Sangue|June 12, 2012
Glucose ameliorates the metabolic profile and mitochondrial function of platelet concentrates during storage in autologous plasmaAngela M Amorini, Michele Tuttobene, Flora M Tomasello, et al.
Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences|February 28, 2007
Comparison of nitrite/nitrate concentration in human plasma and serum samples measured by the enzymatic batch Griess assay, ion-pairing HPLC and ion-trap GC-MS: the importance of a correct removal of proteins in the Griess assayFederica Romitelli, Stefano Angelo Santini, Eleonora Chierici, et al.
Clinical Biochemistry|November 28, 2006
Clinical, biochemical and molecular diagnosis of a compound homozygote for the 254 bp deletion-8 bp insertion of the APRT gene suffering from severe renal failureValentina Di Pietro, Italia Perruzza, Angela Maria Amorini, et al.
NDT Plus|May 19, 2015
Is adenine phophorybosiltransferase deficiency a still underdiagnosed cause of urolithiasis and chronic renal failure? A report of two cases in a family with an uncommon novel mutationItalia Perruzza, Valentina Di Pietro, Barbara Tavazzi, et al.
Clinical Biochemistry|February 19, 2008
A new T677C mutation of the aspartoacylase gene encodes for a protein with no enzymatic activityValentina Di Pietro, Alessandra Gambacurta, Angela Maria Amorini, et al.
Pageof 10

Showing results (21-30 of 97) with videos related to

Sort By:
Pageof 10
Clinical Biochemistry|September 17, 2013
New T530C mutation in the aspartoacylase gene caused Canavan disease with no correlation between severity and N-acetylaspartate excretionValentina Di Pietro, Ugo Cavallari, Angela M Amorini, et al.
Neurobiology of Disease|November 25, 2022
Acute restraint stress impairs histamine type 2 receptor ability to increase the excitability of medium spiny neurons in the nucleus accumbensGiuseppe Aceto, Luca Nardella, Giacomo Lazzarino, et al.
Journal of Chromatography. A|November 7, 2017
Single-step preparation of selected biological fluids for the high performance liquid chromatographic analysis of fat-soluble vitamins and antioxidantsGiacomo Lazzarino, Salvatore Longo, Angela Maria Amorini, et al.
Molecular Genetics and Metabolism Reports|August 31, 2019
Broadening phenotype of adenylosuccinate lyase deficiency: A novel clinical pattern resembling neuronal ceroid lipofuscinosisMario Mastrangelo, Chiara Alfonsi, Isabella Screpanti, et al.
Clinical Chemistry and Laboratory Medicine|April 3, 2023
Improved diagnostics of purine and pyrimidine metabolism disorders using LC-MS/MS and its clinical applicationAlessio Cremonesi, David Meili, Anahita Rassi, et al.
Blood Transfusion = Trasfusione Del Sangue|June 12, 2012
Glucose ameliorates the metabolic profile and mitochondrial function of platelet concentrates during storage in autologous plasmaAngela M Amorini, Michele Tuttobene, Flora M Tomasello, et al.
Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences|February 28, 2007
Comparison of nitrite/nitrate concentration in human plasma and serum samples measured by the enzymatic batch Griess assay, ion-pairing HPLC and ion-trap GC-MS: the importance of a correct removal of proteins in the Griess assayFederica Romitelli, Stefano Angelo Santini, Eleonora Chierici, et al.
Clinical Biochemistry|November 28, 2006
Clinical, biochemical and molecular diagnosis of a compound homozygote for the 254 bp deletion-8 bp insertion of the APRT gene suffering from severe renal failureValentina Di Pietro, Italia Perruzza, Angela Maria Amorini, et al.
NDT Plus|May 19, 2015
Is adenine phophorybosiltransferase deficiency a still underdiagnosed cause of urolithiasis and chronic renal failure? A report of two cases in a family with an uncommon novel mutationItalia Perruzza, Valentina Di Pietro, Barbara Tavazzi, et al.
Clinical Biochemistry|February 19, 2008
A new T677C mutation of the aspartoacylase gene encodes for a protein with no enzymatic activityValentina Di Pietro, Alessandra Gambacurta, Angela Maria Amorini, et al.
Pageof 10