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Molecular Genetics and Metabolism
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August 22, 2018
One-step synthesis of carbon-13-labeled globotriaosylsphingosine (lyso-Gb3), an internal standard for biomarker analysis of Fabry disease
Xinying Hong, Michael H Gelb
Clinical Chemistry
|
April 3, 2023
Thymine Hyperexcretion in a Patient with Abnormal Newborn Screen for Glutaric Aciduria Type I
Parith Wongkittichote, Andrew Edmondson, Xinying Hong
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 21, 2020
A highly multiplexed biochemical assay for analytes in dried blood spots: application to newborn screening and diagnosis of lysosomal storage disorders and other inborn errors of metabolism
Xinying Hong, Martin Sadilek, Michael H Gelb
The Analyst
|
July 17, 2015
A simple approach to study the conformational switching of i-motif DNA by fluorescence anisotropy
Hongduan Huang, Xinying Hong, Feng Liu, et al.
Molecular Genetics and Metabolism Reports
|
November 17, 2022
Stratification of patients with lysosomal acid lipase deficiency by enzyme activity in dried blood spots
Xinying Hong, Yicheng Chen, Marianne Barr, et al.
Clinical Chemistry
|
July 3, 2022
A 6-Month-Old Infant with Severe Failure to Thrive during COVID-19 Pandemic
Xinying Hong, Hana Alharbi, Daniah Albokhari, et al.
The Journal of Applied Laboratory Medicine
|
February 27, 2026
Investigating Elevated Glutaric Acid in Early Infancy
Shubhnita Singh, Caitlin Menello, Xinying Hong, et al.
Molecular Genetics and Metabolism
|
April 23, 2018
Multiplex tandem mass spectrometry assay for newborn screening of X-linked adrenoleukodystrophy, biotinidase deficiency, and galactosemia with flexibility to assay other enzyme assays and biomarkers
Xinying Hong, Arun Babu Kumar, C Ronald Scott, et al.
JIMD Reports
|
March 6, 2024
Clinical, biochemical and molecular characterization of a new case with <i>FDX2</i>-related mitochondrial disorder: Potential biomarkers and treatment options
Parith Wongkittichote, Cassandra Pantano, Miao He, et al.
Molecular Genetics and Metabolism
|
October 11, 2023
Newborn screening for the full set of mucopolysaccharidoses in dried blood spots based on first-tier enzymatic assay followed by second-tier analysis of glycosaminoglycans
Zackary M Herbst, Xinying Hong, Martin Sadilek, et al.
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of 5
Search research articles
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Showing results (1-10 of 43) with videos related to
Sort By:
Page
of 5
Molecular Genetics and Metabolism
|
August 22, 2018
One-step synthesis of carbon-13-labeled globotriaosylsphingosine (lyso-Gb3), an internal standard for biomarker analysis of Fabry disease
Xinying Hong, Michael H Gelb
Clinical Chemistry
|
April 3, 2023
Thymine Hyperexcretion in a Patient with Abnormal Newborn Screen for Glutaric Aciduria Type I
Parith Wongkittichote, Andrew Edmondson, Xinying Hong
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 21, 2020
A highly multiplexed biochemical assay for analytes in dried blood spots: application to newborn screening and diagnosis of lysosomal storage disorders and other inborn errors of metabolism
Xinying Hong, Martin Sadilek, Michael H Gelb
The Analyst
|
July 17, 2015
A simple approach to study the conformational switching of i-motif DNA by fluorescence anisotropy
Hongduan Huang, Xinying Hong, Feng Liu, et al.
Molecular Genetics and Metabolism Reports
|
November 17, 2022
Stratification of patients with lysosomal acid lipase deficiency by enzyme activity in dried blood spots
Xinying Hong, Yicheng Chen, Marianne Barr, et al.
Clinical Chemistry
|
July 3, 2022
A 6-Month-Old Infant with Severe Failure to Thrive during COVID-19 Pandemic
Xinying Hong, Hana Alharbi, Daniah Albokhari, et al.
The Journal of Applied Laboratory Medicine
|
February 27, 2026
Investigating Elevated Glutaric Acid in Early Infancy
Shubhnita Singh, Caitlin Menello, Xinying Hong, et al.
Molecular Genetics and Metabolism
|
April 23, 2018
Multiplex tandem mass spectrometry assay for newborn screening of X-linked adrenoleukodystrophy, biotinidase deficiency, and galactosemia with flexibility to assay other enzyme assays and biomarkers
Xinying Hong, Arun Babu Kumar, C Ronald Scott, et al.
JIMD Reports
|
March 6, 2024
Clinical, biochemical and molecular characterization of a new case with <i>FDX2</i>-related mitochondrial disorder: Potential biomarkers and treatment options
Parith Wongkittichote, Cassandra Pantano, Miao He, et al.
Molecular Genetics and Metabolism
|
October 11, 2023
Newborn screening for the full set of mucopolysaccharidoses in dried blood spots based on first-tier enzymatic assay followed by second-tier analysis of glycosaminoglycans
Zackary M Herbst, Xinying Hong, Martin Sadilek, et al.
Page
of 5