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Publications by KM Au

Hyperornithinaemia-Hyperammonaemia-Homocitrullinuria Syndrome: A Treatable Genetic Liver Disease Warranting Urgent Diagnosis

Hong Kong Medical Journal
Medicine
2014English

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ANCA Vasculitis in a Patient With Alport Syndrome: A Difficult Diagnosis but a Treatable Disease!

BMC Nephrology
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2017English

Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome

2020English

Carpenter Syndrome—A Genetic Disease

Scholars International Journal of Biochemistry
2019English

Diagnosis of Liver Disease

Gut
Gastroenterology
1979English

Genetic Defect of the Sodium‐dependent Multivitamin Transporter: A Treatable Disease, Mimicking Biotinidase Deficiency

JIMD Reports
Internal MedicineGeneticsMolecular BiologyBiochemistryEndocrinologyMetabolismDiabetes
2019English

1 Antitrypsin Deficiency and Liver Disease in Childhood: Genetic, Immunochemical, Histological, and Ultrastructural Diagnosis

Journal of Clinical Pathology
MedicineForensic MedicinePathology
1974English

Posterior Reversible Encephalopathy Syndrome: A Truly Treatable Neurologic Illness

Peritoneal Dialysis International
MedicineNephrology
2012English

Liver Disease in Twins With Felty's Syndrome.

Annals of the Rheumatic Diseases
ImmunologyMolecular BiologyBiochemistryRheumatologyAllergyGenetics
1994English

Whipple´s Disease, a Rare Malabsorption Syndrome of Late Diagnosis

Galicia Clínica
2018English

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