Grazia Annesi

Cosenza, 87050, Italy

Last Updated: 09/26/2026

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Found 72 publications

Reduced Mitochondrial DNA Copy Number and Telomere Length in Essential Tremor Patients: Evidence from an Age- and Sex-Adjusted Cross-Sectional Case-Control Study.

Reduced Mitochondrial DNA Copy Number and Telomere Length in Essential Tremor Patients: Evidence from an Age- and Sex-Adjusted Cross-Sectional Case-Control Study.

Journal: International journal of molecular sciences

Published: May 06, 2026

Genetic variation in antidiabetic drug targets: associations with Parkinson's disease risk and age at onset.

Genetic variation in antidiabetic drug targets: associations with Parkinson's disease risk and age at onset.

Journal: NPJ Parkinson's disease

Published: January 20, 2026

No evidence for the LRRK2 p.L1795F variant in a Southern Italian cohort with Parkinson's disease.

No evidence for the LRRK2 p.L1795F variant in a Southern Italian cohort with Parkinson's disease.

Journal: Gene

Published: October 27, 2025

Early-onset parkinsonism with intellectual disability in an Italian family associated with a PTRHD1 variant.

Early-onset parkinsonism with intellectual disability in an Italian family associated with a PTRHD1 variant.

Journal: Parkinsonism & related disorders

Published: October 14, 2025

Assessment of Mitochondrial DNA Copy Number in Progressive Supranuclear Palsy Patients: Evidence From a Pilot Study.

Assessment of Mitochondrial DNA Copy Number in Progressive Supranuclear Palsy Patients: Evidence From a Pilot Study.

Journal: European journal of neurology

Published: September 15, 2025

Genome-wide association study of copy number variations in Parkinson's disease.

Genome-wide association study of copy number variations in Parkinson's disease.

Journal: NPJ Parkinson's disease

Published: August 24, 2025

Genetic analysis of GBA1 gene in a cohort of patients with Parkinson's disease.

Genetic analysis of GBA1 gene in a cohort of patients with Parkinson's disease.

Journal: Parkinsonism & related disorders

Published: June 24, 2025

MAPT Subhaplotypes in Different Progressive Supranuclear Palsy Phenotypes.

MAPT Subhaplotypes in Different Progressive Supranuclear Palsy Phenotypes.

Journal: Biomedicines

Published: May 08, 2025

Novel KCNQ2 Variants Related to a Variable Phenotypic Spectrum Ranging from Epilepsy with Auditory Features to Severe Developmental and Epileptic Encephalopathies.

Novel KCNQ2 Variants Related to a Variable Phenotypic Spectrum Ranging from Epilepsy with Auditory Features to Severe Developmental and Epileptic Encephalopathies.

Journal: International journal of molecular sciences

Published: December 05, 2024

Identification of Ser71Arg mutation in RAB32 gene in familial Parkinson's disease from Southern Italy.

Identification of Ser71Arg mutation in RAB32 gene in familial Parkinson's disease from Southern Italy.

Journal: NPJ Parkinson's disease

Published: September 27, 2024

Genome-wide association study of copy number variations in Parkinson's disease.

Genome-wide association study of copy number variations in Parkinson's disease.

Journal: medRxiv : the preprint server for health sciences

Published: September 04, 2024

Two Novel Variants in the CHRNA2 and SCN2A Genes in Italian Patients with Febrile Seizures.

Two Novel Variants in the CHRNA2 and SCN2A Genes in Italian Patients with Febrile Seizures.

Journal: Genes

Published: August 29, 2024

Showing 1-12 of 72

Last Updated: 09/26/2026