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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 Neonate
Nicholas Ah Mew, Sarah Viall, Brian Kirmse, et al.
Molecular Genetics and Metabolism
|
May 29, 2020
A pandemic will not stop metabolic innovation
Erin 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 comparison
Yoko 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 screening
Sarah 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 differ
Nicholas 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 setting
Omar 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 complications
Kimberly 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 screening
Ryan H Peretz, Nicholas Ah Mew, Hilary J Vernon, et al.
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of 6
Search research articles
Search
Showing results (11-20 of 56) with videos related to
Sort By:
Page
of 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 Neonate
Nicholas Ah Mew, Sarah Viall, Brian Kirmse, et al.
Molecular Genetics and Metabolism
|
May 29, 2020
A pandemic will not stop metabolic innovation
Erin 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 comparison
Yoko 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 screening
Sarah 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 differ
Nicholas 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 setting
Omar 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 complications
Kimberly 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 screening
Ryan H Peretz, Nicholas Ah Mew, Hilary J Vernon, et al.
Page
of 6