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Radha Procopio

Showing results (1-10 of 33) with videos related to

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Journal of the Neurological Sciences|July 20, 2019
Analysis of the TMEM230 gene in familial Parkinson's disease from south ItalyRadha Procopio, Monica Gagliardi, Giuseppe Nicoletti, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|September 30, 2020
Analysis of the LRP10 gene in patients with Parkinson's disease and dementia with Lewy bodies from Southern ItalyMonica Gagliardi, Radha Procopio, Giuseppe Nicoletti, et al.
Journal of Neurogenetics|May 18, 2026
Genetic architecture of hereditary spastic paraplegia: from monogenic to oligogenic modelsGiuseppe Pedullà, Maurizio Morelli, Monica Gagliardi, et al.
NPJ Parkinson'S Disease|March 22, 2025
Identification of Ser71Arg mutation in RAB32 gene in familial Parkinson's disease from Southern ItalyMonica Gagliardi, Radha Procopio, Grazia Annesi, et al.
Parkinsonism & Related Disorders|December 18, 2017
A new CHCHD2 mutation identified in a southern italy patient with multiple system atrophyGiuseppe Nicoletti, Monica Gagliardi, Radha Procopio, et al.
Neurobiology of Aging|January 10, 2022
Multiple system atrophy and C9orf72 hexanucleotide repeat expansions in a cohort of Italian patientsGiuseppe Bonapace, Monica Gagliardi, Radha Procopio, et al.
Biomedicines|June 26, 2025
<i>MAPT</i> Subhaplotypes in Different Progressive Supranuclear Palsy PhenotypesMonica Gagliardi, Radha Procopio, Alessia Felicetti, et al.
Gene|August 10, 2019
Genetic mutation analysis of the COQ2 gene in Italian patients with multiple system atrophyRadha Procopio, Monica Gagliardi, Laura Brighina, et al.
European Journal of Neurology|April 17, 2026
Assessment of Mitochondrial DNA Copy Number in Progressive Supranuclear Palsy Patients: Evidence From a Pilot StudyLuigi Citrigno, Annamaria Cerantonio, Monica Gagliardi, et al.
Journal of the Neurological Sciences|May 27, 2018
Mutational analysis of TARDBP gene in patients affected by Parkinson's disease from CalabriaMonica Gagliardi, Gennarina Arabia, Rita Nisticò, et al.
Pageof 4

Showing results (1-10 of 33) with videos related to

Sort By:
Pageof 4
Journal of the Neurological Sciences|July 20, 2019
Analysis of the TMEM230 gene in familial Parkinson's disease from south ItalyRadha Procopio, Monica Gagliardi, Giuseppe Nicoletti, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|September 30, 2020
Analysis of the LRP10 gene in patients with Parkinson's disease and dementia with Lewy bodies from Southern ItalyMonica Gagliardi, Radha Procopio, Giuseppe Nicoletti, et al.
Journal of Neurogenetics|May 18, 2026
Genetic architecture of hereditary spastic paraplegia: from monogenic to oligogenic modelsGiuseppe Pedullà, Maurizio Morelli, Monica Gagliardi, et al.
NPJ Parkinson'S Disease|March 22, 2025
Identification of Ser71Arg mutation in RAB32 gene in familial Parkinson's disease from Southern ItalyMonica Gagliardi, Radha Procopio, Grazia Annesi, et al.
Parkinsonism & Related Disorders|December 18, 2017
A new CHCHD2 mutation identified in a southern italy patient with multiple system atrophyGiuseppe Nicoletti, Monica Gagliardi, Radha Procopio, et al.
Neurobiology of Aging|January 10, 2022
Multiple system atrophy and C9orf72 hexanucleotide repeat expansions in a cohort of Italian patientsGiuseppe Bonapace, Monica Gagliardi, Radha Procopio, et al.
Biomedicines|June 26, 2025
<i>MAPT</i> Subhaplotypes in Different Progressive Supranuclear Palsy PhenotypesMonica Gagliardi, Radha Procopio, Alessia Felicetti, et al.
Gene|August 10, 2019
Genetic mutation analysis of the COQ2 gene in Italian patients with multiple system atrophyRadha Procopio, Monica Gagliardi, Laura Brighina, et al.
European Journal of Neurology|April 17, 2026
Assessment of Mitochondrial DNA Copy Number in Progressive Supranuclear Palsy Patients: Evidence From a Pilot StudyLuigi Citrigno, Annamaria Cerantonio, Monica Gagliardi, et al.
Journal of the Neurological Sciences|May 27, 2018
Mutational analysis of TARDBP gene in patients affected by Parkinson's disease from CalabriaMonica Gagliardi, Gennarina Arabia, Rita Nisticò, et al.
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