0000000000504844

AUTHOR

T. Piccoli.

showing 2 related works from this author

Frequency and clinical features of progranulin mutation carriers in a series of patients affected by frontotemporal lobar de generation: report of a …

2010

Settore MED/26 - Neurologiaprogranulin mutation frontotemporal dementia
researchProduct

A PATIENT WITH FRONTOTEMPORAL DEMENTIA (FTD) AND MOTOR NEURON DISEASE (MND) CARRYING THE INTRON10+29 SUBSTITUTION IN MAPT

2008

FTD - MNDFTD ALS intronic mutation
researchProduct