M. T. Giannini

Transdermal rotigotine in the treatment of aromatic L‐amino acid decarboxylase deficiency

M. Mastrangelo, V. Leuzzi, S. Galosi, 2013, Movement disorders : official journal of the Movement Disorder Society.

Movement disorder-childhood rating scale: reliability and validity.

G. Cioni, E. Mercuri, A. Guzzetta, 2008, Pediatric neurology.

A new case of malonic aciduria with a presymptomatic diagnosis and an early treatment

V. Leuzzi, C. Carducci, C. Carducci, 2013, Brain and Development.

Neuromotor and cognitive outcomes of early treatment in tyrosine hydroxylase deficiency type B

G. Hoffmann, M. Mastrangelo, V. Leuzzi, 2017, Neurology.

Very early pattern of movement disorders in sepiapterin reductase deficiency

A. Angeloni, V. Leuzzi, C. Carducci, 2013, Neurology.

Scale for evaluation of movement disorders in the first three years of life.

G. Cioni, E. Mercuri, A. Guzzetta, 2009, Pediatric neurology.

KCNQ2 encephalopathy manifesting with Rett-like features

R. Guerrini, M. Mastrangelo, V. Leuzzi, 2020, Neurology: Genetics.

Movement disorders - Childhood Rating Scale 4-18 revised in children with dyskinetic cerebral palsy.

G. Cioni, R. Battini, R. Di Pietro, 2020, European journal of physical and rehabilitation medicine.

Urinary neopterin and phenylalanine loading test as tools for the biochemical diagnosis of segawa disease.

F. Chiarotti, V. Leuzzi, C. Carducci, 2012, JIMD reports.

Exploring relationships between joint hypermobility and neurodevelopment in children (4–13 years) with hereditary connective tissue disorders and developmental coordination disorder

F. Cardona, M. Castori, S. Morlino, 2018, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Transdermal rotigotine in the treatment of aromatic L‐amino acid decarboxylase deficiency

M. Mastrangelo, V. Leuzzi, S. Galosi, 2013, Movement Disorders.