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Bruno Maranda

Showing results (51-60 of 63) with videos related to

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Nature Communications|June 25, 2025
Metabolic reprogramming of the neovascular niche promotes regenerative angiogenesis in proliferative retinopathyGael Cagnone, Sheetal Pundir, Charlotte Betus, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|December 5, 2016
Acid Ceramidase Deficiency is characterized by a unique plasma cytokine and ceramide profile that is altered by therapyShaalee Dworski, Ping Lu, Aneal Khan, et al.
JIMD Reports|February 27, 2015
Metabolic Clinic Atlas: Organization of Care for Children with Inherited Metabolic Disease in CanadaMonica F Lamoureux, Kylie Tingley, Jonathan B Kronick, et al.
American Journal of Human Genetics|March 8, 2011
Excess of de novo deleterious mutations in genes associated with glutamatergic systems in nonsyndromic intellectual disabilityFadi F Hamdan, Julie Gauthier, Yoichi Araki, et al.
Nature Medicine|March 15, 2016
Retinal lipid and glucose metabolism dictates angiogenesis through the lipid sensor Ffar1Jean-Sébastien Joyal, Ye Sun, Marin L Gantner, et al.
Molecular Genetics and Metabolism|November 26, 2013
Guanidinoacetate methyltransferase (GAMT) deficiency: outcomes in 48 individuals and recommendations for diagnosis, treatment and monitoringSylvia Stockler-Ipsiroglu, Clara van Karnebeek, Nicola Longo, et al.
Nature Medicine|June 9, 2016
Corrigendum: Retinal lipid and glucose metabolism dictates angiogenesis through the lipid sensor Ffar1Jean-Sébastien Joyal, Ye Sun, Marin L Gantner, et al.
American Journal of Human Genetics|October 20, 2015
Joubert Syndrome in French Canadians and Identification of Mutations in CEP104Myriam Srour, Fadi F Hamdan, Dianalee McKnight, et al.
Orphanet Journal of Rare Diseases|January 16, 2020
Outcomes in pediatric studies of medium-chain acyl-coA dehydrogenase (MCAD) deficiency and phenylketonuria (PKU): a reviewMichael Pugliese, Kylie Tingley, Andrea Chow, et al.
Pediatrics|July 16, 2021
Core Outcome Sets for Medium-Chain Acyl-CoA Dehydrogenase Deficiency and PhenylketonuriaMichael Pugliese, Kylie Tingley, Andrea Chow, et al.
Pageof 7

Showing results (51-60 of 63) with videos related to

Sort By:
Pageof 7
Nature Communications|June 25, 2025
Metabolic reprogramming of the neovascular niche promotes regenerative angiogenesis in proliferative retinopathyGael Cagnone, Sheetal Pundir, Charlotte Betus, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|December 5, 2016
Acid Ceramidase Deficiency is characterized by a unique plasma cytokine and ceramide profile that is altered by therapyShaalee Dworski, Ping Lu, Aneal Khan, et al.
JIMD Reports|February 27, 2015
Metabolic Clinic Atlas: Organization of Care for Children with Inherited Metabolic Disease in CanadaMonica F Lamoureux, Kylie Tingley, Jonathan B Kronick, et al.
American Journal of Human Genetics|March 8, 2011
Excess of de novo deleterious mutations in genes associated with glutamatergic systems in nonsyndromic intellectual disabilityFadi F Hamdan, Julie Gauthier, Yoichi Araki, et al.
Nature Medicine|March 15, 2016
Retinal lipid and glucose metabolism dictates angiogenesis through the lipid sensor Ffar1Jean-Sébastien Joyal, Ye Sun, Marin L Gantner, et al.
Molecular Genetics and Metabolism|November 26, 2013
Guanidinoacetate methyltransferase (GAMT) deficiency: outcomes in 48 individuals and recommendations for diagnosis, treatment and monitoringSylvia Stockler-Ipsiroglu, Clara van Karnebeek, Nicola Longo, et al.
Nature Medicine|June 9, 2016
Corrigendum: Retinal lipid and glucose metabolism dictates angiogenesis through the lipid sensor Ffar1Jean-Sébastien Joyal, Ye Sun, Marin L Gantner, et al.
American Journal of Human Genetics|October 20, 2015
Joubert Syndrome in French Canadians and Identification of Mutations in CEP104Myriam Srour, Fadi F Hamdan, Dianalee McKnight, et al.
Orphanet Journal of Rare Diseases|January 16, 2020
Outcomes in pediatric studies of medium-chain acyl-coA dehydrogenase (MCAD) deficiency and phenylketonuria (PKU): a reviewMichael Pugliese, Kylie Tingley, Andrea Chow, et al.
Pediatrics|July 16, 2021
Core Outcome Sets for Medium-Chain Acyl-CoA Dehydrogenase Deficiency and PhenylketonuriaMichael Pugliese, Kylie Tingley, Andrea Chow, et al.
Pageof 7