Showing results 1 to 7 of 7
| Title | Author(s) | Issue Date | |
|---|---|---|---|
6-pyruvoyl-tetrahydropterin synthase deficiency: the clinical spectrum in 3 Chinese patients Proceeding/Conference:Neuropediatrics | 2006 | ||
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 | ||
A rare cause of hepatosplenomegaly - transaldolase deficiency Proceeding/Conference:Journal of Inherited Metabolic Disease | 2007 | ||
A rare cause of hepatosplenomegaly - transaldolase deficiency Proceeding/Conference:Annual Symposium of Society for the Study of Inborn Errors of Metabolism, SSIEM 2007 | 2007 | ||
A rare cause of hepatosplenomegaly transaldolase deficiency Proceeding/Conference:Joint Annual Scientific Meeting for Paediatricians & Paediatric Nurses | 2007 | ||
Regional white matter anisotropy and general intelligence in preterm born children: a voxelwise analysis Proceeding/Conference:International Society for Magnetic Resonance in Medicine Scientific Meeting and Exhibition Proceedings | 2006 | ||
White matter volume and anisotropy in very low birth weight preterm born children: association with cognitive outcome Proceeding/Conference:International Society for Magnetic Resonance in Medicine Scientific Meeting and Exhibition Proceedings | 2006 |