Search research articles
Contact Us
Filters
Showing results (11-20 of 33) with videos related to
Page
of 4
Sort By:
Journal of the Neurological Sciences
|
July 30, 2018
Analysis of the TMEM230 gene in patients with multiple system atrophy
Radha Procopio, Monica Gagliardi, Laura Brighina, et al.
Parkinsonism & Related Disorders
|
June 23, 2026
Abrupt-onset cervico-truncal dystonia after Mycoplasma pneumoniae infection: Unmasking a possible CACNA1A-related susceptibility
Maurizio Morelli, Giuseppe Pedullà, Michele Trimboli, et al.
Parkinsonism & Related Disorders
|
June 12, 2018
DNAJC13 mutation screening in patients with Parkinson's disease from South Italy
Monica Gagliardi, Grazia Annesi, Radha Procopio, et al.
Neurobiology of Aging
|
May 14, 2020
DCTN1 mutation analysis in Italian patients with PSP, MSA, and DLB
Radha Procopio, Monica Gagliardi, Marco D'Amelio, et al.
Gene
|
January 7, 2026
No evidence for the LRRK2 p.L1795F variant in a Southern Italian cohort with Parkinson's disease
Monica Gagliardi, Radha Procopio, Alessia Felicetti, et al.
International Journal of Molecular Sciences
|
May 25, 2024
Phenotypic Variability in Novel Doublecortin Gene Variants Associated with Subcortical Band Heterotopia
Radha Procopio, Francesco Fortunato, Monica Gagliardi, et al.
Journal of the Neurological Sciences
|
October 25, 2021
Mutation analysis of the ATP13A2 gene in patients with PD and MSA from Italy
Monica Gagliardi, Radha Procopio, Giuseppe Nicoletti, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
December 9, 2022
Neurological manifestations in patients and disease carriers in an Italian family with osteosclerosis
Francesco Bono, Laura Rapisarda, Caterina Bombardieri, et al.
International Journal of Molecular Sciences
|
June 26, 2026
Reduced Mitochondrial DNA Copy Number and Telomere Length in Essential Tremor Patients: Evidence from an Age- and Sex-Adjusted Cross-Sectional Case-Control Study
Monica Gagliardi, Alessia Felicetti, Radha Procopio, et al.
European Journal of Neurology
|
May 28, 2024
Glucose transporter-1 deficiency syndrome with extreme phenotypic variability in a five-generation family carrying a novel SLC2A1 variant
Alessia Giugno, Elena Falcone, Francesco Fortunato, et al.
Page
of 4
Search research articles
Search
Showing results (11-20 of 33) with videos related to
Sort By:
Page
of 4
Journal of the Neurological Sciences
|
July 30, 2018
Analysis of the TMEM230 gene in patients with multiple system atrophy
Radha Procopio, Monica Gagliardi, Laura Brighina, et al.
Parkinsonism & Related Disorders
|
June 23, 2026
Abrupt-onset cervico-truncal dystonia after Mycoplasma pneumoniae infection: Unmasking a possible CACNA1A-related susceptibility
Maurizio Morelli, Giuseppe Pedullà, Michele Trimboli, et al.
Parkinsonism & Related Disorders
|
June 12, 2018
DNAJC13 mutation screening in patients with Parkinson's disease from South Italy
Monica Gagliardi, Grazia Annesi, Radha Procopio, et al.
Neurobiology of Aging
|
May 14, 2020
DCTN1 mutation analysis in Italian patients with PSP, MSA, and DLB
Radha Procopio, Monica Gagliardi, Marco D'Amelio, et al.
Gene
|
January 7, 2026
No evidence for the LRRK2 p.L1795F variant in a Southern Italian cohort with Parkinson's disease
Monica Gagliardi, Radha Procopio, Alessia Felicetti, et al.
International Journal of Molecular Sciences
|
May 25, 2024
Phenotypic Variability in Novel Doublecortin Gene Variants Associated with Subcortical Band Heterotopia
Radha Procopio, Francesco Fortunato, Monica Gagliardi, et al.
Journal of the Neurological Sciences
|
October 25, 2021
Mutation analysis of the ATP13A2 gene in patients with PD and MSA from Italy
Monica Gagliardi, Radha Procopio, Giuseppe Nicoletti, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
December 9, 2022
Neurological manifestations in patients and disease carriers in an Italian family with osteosclerosis
Francesco Bono, Laura Rapisarda, Caterina Bombardieri, et al.
International Journal of Molecular Sciences
|
June 26, 2026
Reduced Mitochondrial DNA Copy Number and Telomere Length in Essential Tremor Patients: Evidence from an Age- and Sex-Adjusted Cross-Sectional Case-Control Study
Monica Gagliardi, Alessia Felicetti, Radha Procopio, et al.
European Journal of Neurology
|
May 28, 2024
Glucose transporter-1 deficiency syndrome with extreme phenotypic variability in a five-generation family carrying a novel SLC2A1 variant
Alessia Giugno, Elena Falcone, Francesco Fortunato, et al.
Page
of 4