MA Cleary

The presenting features of mucopolysaccharidosis type IH (Hurler syndrome)

MA Cleary, J E Wraith · Acta Paediatrica · 1995 · 108 citations

Cardiovascular changes in children with mucopolysaccharide disorders

U R Mohan, A A Hay, MA Cleary et al. · Acta Paediatrica · 2002 · 80 citations

Response of 33 UK patients with infantile‐onset Pompe disease to enzyme replacement therapy

Alexander Broomfield, Joan Fletcher, James Davison et al. · Journal of Inherited Metabolic Disease · 2015 · 70 citations

Ornithine aminotransferase deficiency: Diagnostic difficulties in neonatal presentation

MA Cleary, L. Dorland, Tom J. de Koning et al. · Journal of Inherited Metabolic Disease · 2004 · 41 citations

Absence of acidosis in the initial presentation of propionic acidaemia.

J. H. Walter, J. E. Wraith, MA Cleary · Archives of Disease in Childhood Fetal & Neonatal · 1995 · 34 citations · Full text

Electrolyte Disorder, Neonatology, Blood Ammonia +9