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Exploring relationships between joint hypermobility and neurodevelopment in children (4-13 years) with hereditary connective tissue disorders and developmental coordination disorder.
Am J Med Genet B Neuropsychiatr Genet. 2018 Sep;177(6):546-556. doi: 10.1002/ajmg.b.32646. Epub 2018 Aug 2.
Am J Med Genet B Neuropsychiatr Genet. 2018.
PMID: 30070022
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.
Morlino S, Dordoni C, Sperduti I, Clark CJ, Piedimonte C, Fontana A, Colombi M, Grammatico P, Copetti M, Castori M.
Morlino S, et al. Among authors: piedimonte c.
Am J Med Genet B Neuropsychiatr Genet. 2019 Jan;180(1):25-34. doi: 10.1002/ajmg.b.32698. Epub 2018 Nov 23.
Am J Med Genet B Neuropsychiatr Genet. 2019.
PMID: 30471081
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Clinical and molecular characterization of a boy with intellectual disability, facial dysmorphism, minor digital anomalies and a complex IL1RAPL1 intragenic rearrangement.
Laino L, Bottillo I, Piedimonte C, Bernardini L, Torres B, Grammatico B, Bargiacchi S, Mulargia C, Calvani M, Cardona F, Castori M, Grammatico P.
Laino L, et al. Among authors: piedimonte c.
Eur J Paediatr Neurol. 2016 Nov;20(6):971-976. doi: 10.1016/j.ejpn.2016.07.003. Epub 2016 Jul 11.
Eur J Paediatr Neurol. 2016.
PMID: 27470653
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