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Monica Gagliardi

Showing results (1-10 of 53) with videos related to

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Neurobiology of Aging|May 24, 2014
Frequency of the ASP620ASN mutation in VPS35 and Arg1205His mutation in EIF4G1 in familial Parkinson's disease from South ItalyMonica Gagliardi, Grazia Annesi, Patrizia Tarantino, et al.
Neurobiology of Aging|November 15, 2016
Analysis of CHCHD2 gene in familial Parkinson's disease from CalabriaMonica Gagliardi, Grazia Iannello, Carmela Colica, 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.
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.
Frontiers in Neurology|July 14, 2020
A Family With a Complex Phenotype Caused by Two Different Rare Metabolic Disorders: GLUT1 and Very-Long-Chain Fatty Acid Dehydrogenase (VLCAD) DeficienciesOlimpia Musumeci, Edoardo Ferlazzo, Carmelo Rodolico, 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.
Pageof 6

Showing results (1-10 of 53) with videos related to

Sort By:
Pageof 6
Neurobiology of Aging|May 24, 2014
Frequency of the ASP620ASN mutation in VPS35 and Arg1205His mutation in EIF4G1 in familial Parkinson's disease from South ItalyMonica Gagliardi, Grazia Annesi, Patrizia Tarantino, et al.
Neurobiology of Aging|November 15, 2016
Analysis of CHCHD2 gene in familial Parkinson's disease from CalabriaMonica Gagliardi, Grazia Iannello, Carmela Colica, 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.
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.
Frontiers in Neurology|July 14, 2020
A Family With a Complex Phenotype Caused by Two Different Rare Metabolic Disorders: GLUT1 and Very-Long-Chain Fatty Acid Dehydrogenase (VLCAD) DeficienciesOlimpia Musumeci, Edoardo Ferlazzo, Carmelo Rodolico, 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.
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