Caterina Piedimonte

Recognizing and treating Ehlers-Danlos syndrome(s): the need for a multidisciplinary approach

M. Castori, S. Morlino, Caterina Piedimonte, 2016 .

Clinical and molecular characterization of a boy with intellectual disability, facial dysmorphism, minor digital anomalies and a complex IL1RAPL1 intragenic rearrangement.

L. Bernardini, I. Bottillo, F. Cardona, 2016, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Italian validation of the functional difficulties questionnaire (FDQ‐9) and its correlation with major determinants of quality of life in adults with hypermobile Ehlers–Danlos syndrome/hypermobility spectrum disorder

M. Copetti, A. Fontana, C. Clark, 2018, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

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.