Miryam Carecchio

发表

Defining the phenotypic signature of DYT11 mutations in myoclonus-dystonia patients

Mj Edwards, Kailash P. Bhatia, Miryam Carecchio, 2010 .

Predicting Cognitive Decline in Parkinson’s Disease: Can We Ask the Genes?

Miryam Carecchio, R. Cantello, F. De Marchi, 2014, Front. Neurol..

A missense mutation in KCTD17 causes autosomal dominant myoclonus-dystonia.

Deborah Hughes, Christine Klein, Thomas Foltynie, 2015, American journal of human genetics.