D. Tolomeo

发表

Movement Disorders in Children with a Mitochondrial Disease: A Cross-Sectional Survey from the Nationwide Italian Collaborative Network of Mitochondrial Diseases

M. Mancuso, C. La Morgia, G. Siciliano, 2021, Journal of clinical medicine.

Active Surveillance Systems for Early Detection and Improved Recall Decision Making

D. Tolomeo, 2009 .

Evaluation of Chromosome Microarray Analysis in a Large Cohort of Females with Autism Spectrum Disorders: A Single Center Italian Study

R. Tancredi, F. Muratori, S. Calderoni, 2020, Journal of personalized medicine.

Complex multisystem phenotype associated with the mitochondrial DNA m.5522G>A mutation

F. Santorelli, A. Rubegni, J. Baldacci, 2019, Neurological Sciences.

Next-generation sequencing approach to hyperCKemia

E. Mercuri, A. Federico, G. Siciliano, 2019, Neurology: Genetics.

Clinical and neuroimaging features of the m.10197G>A mtDNA mutation: New case reports and expansion of the phenotype variability

C. Bruno, F. Santorelli, M. Severino, 2019, Journal of the Neurological Sciences.

The Diagnostic Approach to Mitochondrial Disorders in Children in the Era of Next-Generation Sequencing: A 4-Year Cohort Study

C. Bruno, F. Santorelli, R. Battini, 2021, Journal of clinical medicine.

The features of the m.10197G>A mtDNA mutation

F. Santorelli, M. Severino, A. Rubegni, 2019, Journal of Neurological Sciences.

Learning from massive testing of mitochondrial disorders: UPD explaining unorthodox transmission

A. Tessa, F. Santorelli, R. Battini, 2021, Journal of Medical Genetics.