G. Romeo

Mental Retardation and Early Onset of Weakness in a Girl With a Dystrophinopathy and a Large Xp21-23 Deletion

A. Connolly, R. Falsaperla, T. Trigilia, 2003, Journal of child neurology.

A double‐blind, parallel, multicenter comparison of L‐acetylcarnitine with placebo on the attention deficit hyperactivity disorder in fragile X syndrome boys

L. Vallée, G. Neri, F. Ramos, 2008, American journal of medical genetics. Part A.

A Novel Homozygous ALG12 Mutation in a Patient with CDG Type Ig: New Report of a Case with a Mild Phenotype

F. Calì, S. Musumeci, A. Musumeci, 2021, Molecular Syndromology.

Long-Term Survival in a Child With Arthrogryposis Multiplex Congenita and Spinal Muscular Atrophy

A. Connolly, R. Falsaperla, P. Pavone, 2001, Journal of child neurology.

[Neonatal muscular spinal atrophy: a case report].

R. Falsaperla, P. Pavone, T. Trigilia, 2004, La Pediatria medica e chirurgica : Medical and surgical pediatrics.

Impact of daytime routine modifications on people with severe intellectual disability amid COVID‐19 pandemic

M. Elia, S. Musumeci, L. Vetri, 2021, Perspectives in psychiatric care.