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Publications by Wuh-Liang Hwu

In This Issue

Genetics in Medicine

Medicine

Genetics

2013

English

Primary Coenzyme Q10 Deficiency-7: Expanded Phenotypic Spectrum and a Founder Mutation in Southern Chinese

English

Introduction to the Newborn Screening, Diagnosis, and Treatment for Pompe Disease Guidance Supplement

English

The Initial Evaluation of Patients After Positive Newborn Screening: Recommended Algorithms Leading to a Confirmed Diagnosis of Pompe Disease

English

Differences in the Predominance of Lysosomal and Autophagic Pathologies Between Infants and Adults With Pompe Disease: Implications for Therapy

Molecular Genetics and Metabolism

English

Erratum To: A Mutation in Taiwanese Newborns—Superiority of DNA-Based to Enzyme-Based Newborn Screening for Common Mutations

English

Myostatin and Insulin-Like Growth Factor I: Potential Therapeutic Biomarkers for Pompe Disease

PLoS ONE

Multidisciplinary

2013

English

Children Conceived by Assisted Reproductive Technology Prone to Low Birth Weight, Preterm Birth, and Birth Defects: A Cohort Review of More Than 50,000 Live Births During 2011–2017 in Taiwan

Frontiers in Pediatrics

English

Baseline Urinary Glucose Tetrasaccharide Concentrations in Patients With Infantile- And Late-Onset Pompe Disease Identified by Newborn Screening

English

Hypertrophic Cardiomyopathy in Pompe Disease Is Not Limited to the Classic Infantile-Onset Phenotype

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Wuh-Liang Hwu

In This Issue

Primary Coenzyme Q10 Deficiency-7: Expanded Phenotypic Spectrum and a Founder Mutation in Southern Chinese

Introduction to the Newborn Screening, Diagnosis, and Treatment for Pompe Disease Guidance Supplement

The Initial Evaluation of Patients After Positive Newborn Screening: Recommended Algorithms Leading to a Confirmed Diagnosis of Pompe Disease

Differences in the Predominance of Lysosomal and Autophagic Pathologies Between Infants and Adults With Pompe Disease: Implications for Therapy

Erratum To: A Mutation in Taiwanese Newborns—Superiority of DNA-Based to Enzyme-Based Newborn Screening for Common Mutations

Myostatin and Insulin-Like Growth Factor I: Potential Therapeutic Biomarkers for Pompe Disease

Children Conceived by Assisted Reproductive Technology Prone to Low Birth Weight, Preterm Birth, and Birth Defects: A Cohort Review of More Than 50,000 Live Births During 2011–2017 in Taiwan

Baseline Urinary Glucose Tetrasaccharide Concentrations in Patients With Infantile- And Late-Onset Pompe Disease Identified by Newborn Screening

Hypertrophic Cardiomyopathy in Pompe Disease Is Not Limited to the Classic Infantile-Onset Phenotype