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Nature Communications
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June 25, 2025
Metabolic reprogramming of the neovascular niche promotes regenerative angiogenesis in proliferative retinopathy
Gael 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 therapy
Shaalee 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 Canada
Monica 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 disability
Fadi F Hamdan, Julie Gauthier, Yoichi Araki, et al.
Nature Medicine
|
March 15, 2016
Retinal lipid and glucose metabolism dictates angiogenesis through the lipid sensor Ffar1
Jean-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 monitoring
Sylvia 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 Ffar1
Jean-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 CEP104
Myriam 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 review
Michael Pugliese, Kylie Tingley, Andrea Chow, et al.
Pediatrics
|
July 16, 2021
Core Outcome Sets for Medium-Chain Acyl-CoA Dehydrogenase Deficiency and Phenylketonuria
Michael Pugliese, Kylie Tingley, Andrea Chow, et al.
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of 7
Search research articles
Search
Showing results (51-60 of 63) with videos related to
Sort By:
Page
of 7
Nature Communications
|
June 25, 2025
Metabolic reprogramming of the neovascular niche promotes regenerative angiogenesis in proliferative retinopathy
Gael 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 therapy
Shaalee 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 Canada
Monica 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 disability
Fadi F Hamdan, Julie Gauthier, Yoichi Araki, et al.
Nature Medicine
|
March 15, 2016
Retinal lipid and glucose metabolism dictates angiogenesis through the lipid sensor Ffar1
Jean-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 monitoring
Sylvia 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 Ffar1
Jean-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 CEP104
Myriam 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 review
Michael Pugliese, Kylie Tingley, Andrea Chow, et al.
Pediatrics
|
July 16, 2021
Core Outcome Sets for Medium-Chain Acyl-CoA Dehydrogenase Deficiency and Phenylketonuria
Michael Pugliese, Kylie Tingley, Andrea Chow, et al.
Page
of 7