Celeste Montecchiani
Rome, Italy
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 8 publications
SPG11-related parkinsonism: Clinical profile, molecular imaging and l-dopa response.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: March 05, 2018
SPG11 mutations cause widespread white matter and basal ganglia abnormalities, but restricted cortical damage.
Journal: NeuroImage. Clinical
Published: February 17, 2018
Phenotype variability and allelic heterogeneity in KMT2B-Associated disease.
Journal: Parkinsonism & related disorders
Published: December 05, 2017
Spastic paraplegia type 31: A novel REEP1 splice site donor variant and expansion of the phenotype variability.
Journal: Parkinsonism & related disorders
Published: April 18, 2017
Spastic paraplegia type 4: A novel SPAST splice site donor mutation and expansion of the phenotype variability.
Journal: Journal of the neurological sciences
Published: April 07, 2017
Trans-crocetin improves amyloid-β degradation in monocytes from Alzheimer's Disease patients.
Journal: Journal of the neurological sciences
Published: May 01, 2016
ALS5/SPG11/KIAA1840 mutations cause autosomal recessive axonal Charcot-Marie-Tooth disease.
Journal: Brain : a journal of neurology
Published: July 13, 2015
Long-term miR-669a therapy alleviates chronic dilated cardiomyopathy in dystrophic mice.
Journal: Journal of the American Heart Association
Published: August 22, 2013
Showing 1-8 of 8
Last Updated: 09/26/2026