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Publications by Hencher HC Lee
Hyperornithinaemia-Hyperammonaemia-Homocitrullinuria Syndrome: A Treatable Genetic Liver Disease Warranting Urgent Diagnosis
Hong Kong Medical Journal
Medicine
Sudden Arrhythmia Death Syndrome in Young Victims: A Five-Year Retrospective Review and Two-Year Prospective Molecular Autopsy Study by Next-Generation Sequencing and Clinical Evaluation of Their First-Degree Relatives
Hong Kong Medical Journal
Medicine
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ANCA Vasculitis in a Patient With Alport Syndrome: A Difficult Diagnosis but a Treatable Disease!
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Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome
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Scholars International Journal of Biochemistry
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Genetic Defect of the Sodium‐dependent Multivitamin Transporter: A Treatable Disease, Mimicking Biotinidase Deficiency
JIMD Reports
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Molecular Biology
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1 Antitrypsin Deficiency and Liver Disease in Childhood: Genetic, Immunochemical, Histological, and Ultrastructural Diagnosis
Journal of Clinical Pathology
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Posterior Reversible Encephalopathy Syndrome: A Truly Treatable Neurologic Illness
Peritoneal Dialysis International
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Liver Disease in Twins With Felty's Syndrome.
Annals of the Rheumatic Diseases
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Whipple´s Disease, a Rare Malabsorption Syndrome of Late Diagnosis
Galicia Clínica
