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Nicholas Ah Mew

Showing results (11-20 of 56) with videos related to

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Advances in Neonatal Care : Official Journal of the National Association of Neonatal Nurses|July 31, 2015
Deconstructing Black Swans: An Introductory Approach to Inherited Metabolic Disorders in the NeonateNicholas Ah Mew, Sarah Viall, Brian Kirmse, et al.
Molecular Genetics and Metabolism|May 29, 2020
A pandemic will not stop metabolic innovationErin MacLeod, Danielle Starin, Nicholas Ah Mew, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 21, 2009
A new capillary zone electrophoresis method for the screening of congenital disorders of glycosylation (CDG)Fabienne Parente, Nicholas Ah Mew, Jaak Jaeken, et al.
Molecular Genetics and Metabolism|May 30, 2026
Resources and care structures for management of urea cycle disorders in Japan and the United States: A system-level comparisonYoko Nakajima, Erin MacLeod, Konomi Hirano, et al.
Molecular Genetics and Metabolism|November 6, 2017
"Mild" hyperphenylalaninemia? A case series of seven treated patients following newborn screeningSarah Viall, Omar Ayyub, Matthew Rasberry, et al.
The Journal of Pediatrics|August 21, 2012
Clinical outcomes of neonatal onset proximal versus distal urea cycle disorders do not differNicholas Ah Mew, Lauren Krivitzky, Robert McCarter, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 9, 2017
Time-dependent negative bias in plasma ammonia samples in a clinical settingOmar B Ayyub, Sean Hofherr, Kristina Cusmano-Ozog, et al.
Molecular Genetics and Metabolism|November 13, 2025
Propionic acidemia and methylmalonic aciduria: A portrait of the first 3 years-Admissions and complicationsKimberly A Chapman, Nicholas Ah Mew, Nina Mickle, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 26, 2017
Do the data really support ordering fragile X testing as a first-tier test without clinical features?Veronique Weinstein, Pranoot Tanpaiboon, Kimberly A Chapman, et al.
Molecular Genetics and Metabolism|June 28, 2021
Prospective diagnosis of MT-ATP6-related mitochondrial disease by newborn screeningRyan H Peretz, Nicholas Ah Mew, Hilary J Vernon, et al.
Pageof 6

Showing results (11-20 of 56) with videos related to

Sort By:
Pageof 6
Advances in Neonatal Care : Official Journal of the National Association of Neonatal Nurses|July 31, 2015
Deconstructing Black Swans: An Introductory Approach to Inherited Metabolic Disorders in the NeonateNicholas Ah Mew, Sarah Viall, Brian Kirmse, et al.
Molecular Genetics and Metabolism|May 29, 2020
A pandemic will not stop metabolic innovationErin MacLeod, Danielle Starin, Nicholas Ah Mew, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 21, 2009
A new capillary zone electrophoresis method for the screening of congenital disorders of glycosylation (CDG)Fabienne Parente, Nicholas Ah Mew, Jaak Jaeken, et al.
Molecular Genetics and Metabolism|May 30, 2026
Resources and care structures for management of urea cycle disorders in Japan and the United States: A system-level comparisonYoko Nakajima, Erin MacLeod, Konomi Hirano, et al.
Molecular Genetics and Metabolism|November 6, 2017
"Mild" hyperphenylalaninemia? A case series of seven treated patients following newborn screeningSarah Viall, Omar Ayyub, Matthew Rasberry, et al.
The Journal of Pediatrics|August 21, 2012
Clinical outcomes of neonatal onset proximal versus distal urea cycle disorders do not differNicholas Ah Mew, Lauren Krivitzky, Robert McCarter, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 9, 2017
Time-dependent negative bias in plasma ammonia samples in a clinical settingOmar B Ayyub, Sean Hofherr, Kristina Cusmano-Ozog, et al.
Molecular Genetics and Metabolism|November 13, 2025
Propionic acidemia and methylmalonic aciduria: A portrait of the first 3 years-Admissions and complicationsKimberly A Chapman, Nicholas Ah Mew, Nina Mickle, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 26, 2017
Do the data really support ordering fragile X testing as a first-tier test without clinical features?Veronique Weinstein, Pranoot Tanpaiboon, Kimberly A Chapman, et al.
Molecular Genetics and Metabolism|June 28, 2021
Prospective diagnosis of MT-ATP6-related mitochondrial disease by newborn screeningRyan H Peretz, Nicholas Ah Mew, Hilary J Vernon, et al.
Pageof 6