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Carlos R Ferreira

Showing results (1-10 of 143) with videos related to

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American Journal of Medical Genetics. Part A|December 21, 2018
The human phenotype of ornithine decarboxylase superactivity: A new syndromeCarlos R Ferreira
Molecular Genetics and Metabolism Reports|January 28, 2017
Prevalence of adenylosuccinate lyase deficiency based on aggregated exome dataCarlos R Ferreira
American Journal of Medical Genetics. Part A|March 14, 2019
Corrigendum to "The human phenotype of ornithine decarboxylase superactivity: a new syndrome"Carlos R Ferreira
American Journal of Medical Genetics. Part A|March 19, 2019
The burden of rare diseasesCarlos R Ferreira
Molecular Genetics and Metabolism|January 3, 2021
Clinical and biochemical footprints of inherited metabolic diseases. IV. Metabolic cardiovascular diseaseCarlos R Ferreira, Nenad Blau
Molecular Genetics and Metabolism|January 19, 2025
Rare disorders, big challenges: Special issue on congenital disorders of glycosylationPeter Witters, Carlos R Ferreira
JIMD Reports|April 13, 2016
Spurious Elevation of Multiple Urine Amino Acids by Ion-Exchange Chromatography in Patients with Prolidase DeficiencyCarlos R Ferreira, Kristina Cusmano-Ozog
Translational Science of Rare Diseases|January 23, 2018
Disorders of metal metabolismCarlos R Ferreira, William A Gahl
Translational Science of Rare Diseases|November 21, 2017
Lysosomal storage diseasesCarlos R Ferreira, William A Gahl
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 17, 2021
Response to Stern et alShira G Ziegler, Carlos R Ferreira
Pageof 15

Showing results (1-10 of 143) with videos related to

Sort By:
Pageof 15
American Journal of Medical Genetics. Part A|December 21, 2018
The human phenotype of ornithine decarboxylase superactivity: A new syndromeCarlos R Ferreira
Molecular Genetics and Metabolism Reports|January 28, 2017
Prevalence of adenylosuccinate lyase deficiency based on aggregated exome dataCarlos R Ferreira
American Journal of Medical Genetics. Part A|March 14, 2019
Corrigendum to "The human phenotype of ornithine decarboxylase superactivity: a new syndrome"Carlos R Ferreira
American Journal of Medical Genetics. Part A|March 19, 2019
The burden of rare diseasesCarlos R Ferreira
Molecular Genetics and Metabolism|January 3, 2021
Clinical and biochemical footprints of inherited metabolic diseases. IV. Metabolic cardiovascular diseaseCarlos R Ferreira, Nenad Blau
Molecular Genetics and Metabolism|January 19, 2025
Rare disorders, big challenges: Special issue on congenital disorders of glycosylationPeter Witters, Carlos R Ferreira
JIMD Reports|April 13, 2016
Spurious Elevation of Multiple Urine Amino Acids by Ion-Exchange Chromatography in Patients with Prolidase DeficiencyCarlos R Ferreira, Kristina Cusmano-Ozog
Translational Science of Rare Diseases|January 23, 2018
Disorders of metal metabolismCarlos R Ferreira, William A Gahl
Translational Science of Rare Diseases|November 21, 2017
Lysosomal storage diseasesCarlos R Ferreira, William A Gahl
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 17, 2021
Response to Stern et alShira G Ziegler, Carlos R Ferreira
Pageof 15