Showing results 4 to 10 of 10
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Title | Author(s) | Issue Date | Views | |
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Mutation analysis of the GLUT2 Gene in a Chinese Patient with Fanconi-Bickel Syndrome Proceeding/Conference:Hong Kong Journal of Paediatrics (New Series) | 2004 | 137 | ||
Mutation analysis of the GLUT2 Gene in a Chinese patient with Fanconi-Bickel Syndrome Proceeding/Conference:Biennial Scientific Meeting of the Asia Pacific Paediatric Endocrine Society, APPES 2006 | 2006 | 89 | ||
Prenatal diagnosis and prospective management of argininosuccinic aciduria in the prevention of neonatal hyperammonaemic coma Proceeding/Conference:Hong Kong Journal of Paediatrics | 2004 | 150 | ||
A rare cause of hepatosplenomegaly - transaldolase deficiency Proceeding/Conference:Annual Symposium of Society for the Study of Inborn Errors of Metabolism, SSIEM 2007 | 2007 | 120 | ||
A rare cause of hepatosplenomegaly - transaldolase deficiency Proceeding/Conference:Journal of Inherited Metabolic Disease | 2007 | 137 | ||
A rare cause of hepatosplenomegaly transaldolase deficiency Proceeding/Conference:Joint Annual Scientific Meeting for Paediatricians & Paediatric Nurses | 2007 | 107 | ||
Reversible Myocardial Damage in a Premature Infant with Carnitine-Acylcarnitine Translocase Deficiency Proceeding/Conference:Hong Kong Journal of Paediatrics | 2004 | 79 |