A.P. Burlina

Clinical and molecular spectra in galactosemic patients from neonatal screening in northeastern Italy: Structural and functional characterization of new variations in the galactose-1-phosphate uridyltransferase (GALT) gene

Emanuela Viggiano, Anna Marabotti, A.P. Burlina et al. · Gene · 2015 · 28 citations

Life Sciences, Genetics, Molecular Genetics +15

Diffusion‐weighted imaging in the assessment of neurological damage in patients with methylmalonic aciduria

A.P. Burlina, A.P. Burlina, Renzo Manara et al. · Journal of Inherited Metabolic Disease · 2003 · 22 citations

Medicine, Neurology, Neuroscience +14

The Utility of CSF for the Diagnosis of Primary and Secondary Monoamine Neurotransmitter Deficiencies.

Alberto Burlina, Andrea Celato, Giulia Polo et al. · PubMed · 2017 · 14 citations

Medicine, Neurology, Neuroscience +16

Treatment of extrapyramidal symptoms in a patient with homozygous homocystinuria

A.P. Burlina, A.P. Burlina, C. Edini et al. · Journal of Inherited Metabolic Disease · 2002 · 11 citations

Life Sciences, Neurology, Pharmacotherapy +8

Propionic acidaemia with basal ganglia stroke: Treatment of acute extrapyramidal symptoms with L‐DOPA

A.P. Burlina, A.P. Burlina, Claudio Baracchini et al. · Journal of Inherited Metabolic Disease · 2001 · 10 citations

Medicine, Neurology, Pharmacology +16