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Mariano Oliva

Showing results (1-10 of 9) with videos related to

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Reviews in the Neurosciences|June 6, 2022
Is the pathology of posterior cortical atrophy clinically predictable?Lorenzo Cipriano, Mariano Oliva, Gianfranco Puoti, et al.
Clinical Neurology and Neurosurgery|February 1, 2020
A novel missense mutation in CAV3 gene in an Italian family with persistent hyperCKemia, myalgia and hypercholesterolemia: Double-troubleGiorgia Bruno, Gianfranco Puoti, Mariano Oliva, et al.
Molecular Neurobiology|August 2, 2020
MicroRNA Expression Signature in Mild Cognitive Impairment Due to Alzheimer's DiseaseBruna De Felice, Concetta Montanino, Mariano Oliva, et al.
BJR Case Reports|March 24, 2020
Multi-imaging study in a patient with cerebrotendinous xanthomatosis: radiology, clinic and pathology correlation of a rare conditionGiuseppina Dell'Aversano Orabona, Clemente Dato, Mariano Oliva, et al.
Journal of the Peripheral Nervous System : JPNS|May 30, 2020
Expanding the spectrum of SPTLC1-related disorders beyond hereditary sensory and autonomic neuropathies: A novel case of the distinct "S331 syndrome"Fabiana Rossi, Giorgia Bruno, Mario Fratta, et al.
Journal of Alzheimer'S Disease : JAD|February 18, 2022
Systematic Review on the Role of Lobar Cerebral Microbleeds in CognitionLorenzo Cipriano, Dario Saracino, Mariano Oliva, et al.
Neurobiology of Aging|December 16, 2019
One novel GRN null mutation, two different aphasia phenotypesCinzia Coppola, Mariano Oliva, Dario Saracino, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|October 2, 2020
Singular cases of Alzheimer's disease disclose new and old genetic "acquaintances"Cinzia Coppola, Dario Saracino, Mariano Oliva, et al.
Journal of Alzheimer'S Disease : JAD|October 5, 2020
The Rise of the GRN C157KfsX97 Mutation in Southern Italy: Going Back to the Fall of the Western Roman EmpireCinzia Coppola, Dario Saracino, Mariano Oliva, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Reviews in the Neurosciences|June 6, 2022
Is the pathology of posterior cortical atrophy clinically predictable?Lorenzo Cipriano, Mariano Oliva, Gianfranco Puoti, et al.
Clinical Neurology and Neurosurgery|February 1, 2020
A novel missense mutation in CAV3 gene in an Italian family with persistent hyperCKemia, myalgia and hypercholesterolemia: Double-troubleGiorgia Bruno, Gianfranco Puoti, Mariano Oliva, et al.
Molecular Neurobiology|August 2, 2020
MicroRNA Expression Signature in Mild Cognitive Impairment Due to Alzheimer's DiseaseBruna De Felice, Concetta Montanino, Mariano Oliva, et al.
BJR Case Reports|March 24, 2020
Multi-imaging study in a patient with cerebrotendinous xanthomatosis: radiology, clinic and pathology correlation of a rare conditionGiuseppina Dell'Aversano Orabona, Clemente Dato, Mariano Oliva, et al.
Journal of the Peripheral Nervous System : JPNS|May 30, 2020
Expanding the spectrum of SPTLC1-related disorders beyond hereditary sensory and autonomic neuropathies: A novel case of the distinct "S331 syndrome"Fabiana Rossi, Giorgia Bruno, Mario Fratta, et al.
Journal of Alzheimer'S Disease : JAD|February 18, 2022
Systematic Review on the Role of Lobar Cerebral Microbleeds in CognitionLorenzo Cipriano, Dario Saracino, Mariano Oliva, et al.
Neurobiology of Aging|December 16, 2019
One novel GRN null mutation, two different aphasia phenotypesCinzia Coppola, Mariano Oliva, Dario Saracino, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|October 2, 2020
Singular cases of Alzheimer's disease disclose new and old genetic "acquaintances"Cinzia Coppola, Dario Saracino, Mariano Oliva, et al.
Journal of Alzheimer'S Disease : JAD|October 5, 2020
The Rise of the GRN C157KfsX97 Mutation in Southern Italy: Going Back to the Fall of the Western Roman EmpireCinzia Coppola, Dario Saracino, Mariano Oliva, et al.
Pageof 1