Publication & Citation Trends
Publications
0 total
Rare causes of early-onset dystonia-parkinsonism with cognitive impairment: a de novo PSEN-1 mutation
Cited by 18
Semantic Scholar
Mutations in SLC39A14 disrupt manganese homeostasis and cause childhood-onset parkinsonism–dystonia OA
Cited by 261
Semantic Scholar
MECR Mutations Cause Childhood-Onset Dystonia and Optic Atrophy, a Mitochondrial Fatty Acid Synthesis Disorder. OA
Cited by 92
Semantic Scholar
Effective immuno-targeting of the IDH1 mutation R132H in a murine model of intracranial glioma OA
Cited by 122
Semantic Scholar
Alteration of the coenzyme A biosynthetic pathway in neurodegeneration with brain iron accumulation syndromes.
Cited by 28
Semantic Scholar
Exome sequence reveals mutations in CoA synthase as a cause of neurodegeneration with brain iron accumulation. OA
Cited by 198
Semantic Scholar
DNA microarray analysis identifies CKS2 and LEPR as potential markers of meningioma recurrence. OA
Cited by 31
Semantic Scholar
Research Topics
Glioma Diagnosis and Treatment
(6)
Mitochondrial Function and Pathology
(3)
Neurological diseases and metabolism
(3)
MicroRNA in disease regulation
(2)
Epigenetics and DNA Methylation
(2)
Affiliations
Wellcome Centre for Mitochondrial Research
Fondazione IRCCS Istituto Neurologico Carlo Besta