Kaustuv Bhattacharya

Congenital disorder of glycosylation type Ia: Heterogeneity in the clinical presentation from multivisceral failure to hyperinsulinaemic hypoglycaemia as leading symptoms in three infants with phosphomannomutase deficiency

J. Christodoulou, P. Clayton, M. Silink, 2009, Journal of Inherited Metabolic Disease.

Newborn screening may fail to identify intermediate forms of maple syrup urine disease

K. Bhattacharya, B. Wilcken, V. Wiley, 2006, Journal of Inherited Metabolic Disease.