Fiorenza Ulgiati

Evaluation of the basal ganglia in neurofibromatosis type 1

S. Cecchini, V. Salpietro, M. Ruggieri, 2014, Child's Nervous System.

Early Myoclonic Encephalopathy in 9q33‐q34 Deletion Encompassing STXBP1 and SPTAN1

L. Bernardini, A. Novelli, A. Spalice, 2015, Annals of human genetics.

The Retina in Patients With Triple A Syndrome: A Window Into Neurodegeneration?

I. Balikova, C. Heinrichs, C. Vilain, 2021, Frontiers in Endocrinology.

Recent Understanding on Diagnosis and Management of Central Nervous System Vasculitis in Children

A. Spalice, L. Iannetti, L. Papetti, 2012, Clinical & developmental immunology.

Novel mutations in the glycine receptor alpha subunit gene in two sisters with hyperekplexia.

A. Spalice, L. Papetti, F. Nicita, 2014, Pediatric Neurology.

Posterior fossa malformations and sex chromosomes anomalies. Report of a case with XYY syndrome and overview of known associations

A. Spalice, L. Papetti, F. Nicita, 2013, European Journal of Pediatrics.