• 40 Citations
  • 3 h-Index
20162019
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Research Output 2016 2019

  • 40 Citations
  • 3 h-Index
  • 10 Article
  • 1 Letter
2019
Open Access
Alzheimer Disease
Brain
Gyrus Cinguli
Parahippocampal Gyrus
Inositol
1 Citation (Scopus)
Normal Pressure Hydrocephalus
Cerebrospinal Fluid
Biomarkers
Alzheimer Disease
Dementia
2018
6 Citations (Scopus)
Frontotemporal Dementia
Cerebrospinal Fluid
Biomarkers
Frontotemporal Lobar Degeneration
Alzheimer Disease
2 Citations (Scopus)

Human figure drawing distinguishes Alzheimer’s patients: a cognitive screening test study

Stanzani Maserati, M., D’Onofrio, R., Matacena, C., Sambati, L., Oppi, F., Poda, R., De Matteis, M., Naldi, I., Liguori, R. & Capellari, S., May 1 2018, In : Neurological Sciences. 39, 5, p. 851-855 5 p.

Research output: Contribution to journalArticle

Human Body
Alzheimer Disease
Body Height
Healthy Volunteers
Cognitive Dysfunction

Mitochondrial dysfunction in myotonic dystrophy type 1

Gramegna, L. L., Giannoccaro, M. P., Manners, D. N., Testa, C., Zanigni, S., Evangelisti, S., Bianchini, C., Oppi, F., Poda, R., Avoni, P., Lodi, R., Liguori, R. & Tonon, C., 2018, In : Neuromuscular Disorders. 28, p. 144-9

Research output: Contribution to journalArticle

Myotonic Dystrophy
Phosphocreatine
Muscles
Brain
Exercise
1 Citation (Scopus)

Recurrent Reversible Cognitive Impairment in a Cluster Headache Patient: A Case Report

Favoni, V., Sambati, L., Oppi, F., Stanzani Maserati, M., Cevoli, S. & Pierangeli, G., Oct 1 2018, In : Headache. 58, 9, p. 1472-1474 3 p.

Research output: Contribution to journalLetter

1 Citation (Scopus)

The First Historically Reported Italian Family with FTD/ALS Teaches a Lesson on C9orf72 RE: Clinical Heterogeneity and Oligogenic Inheritance

Giannoccaro, M. P., Bartoletti-Stella, A., Piras, S., Casalena, A., Oppi, F., Ambrosetto, G., Montagna, P., Liguori, R., Parchi, P. & Capellari, S., Jan 1 2018, In : Journal of Alzheimer's Disease. 62, 2, p. 687-697 11 p.

Research output: Contribution to journalArticle

Multifactorial Inheritance
Mutation
Dementia
Genes
Phenotype
2017
10 Citations (Scopus)

Multiple variants in families with amyotrophic lateral sclerosis and frontotemporal dementia related to C9orf72 repeat expansion: further observations on their oligogenic nature

Giannoccaro, M. P., Bartoletti-Stella, A., Piras, S., Pession, A., De Massis, P., Oppi, F., Stanzani-Maserati, M., Pasini, E., Baiardi, S., Avoni, P., Parchi, P., Liguori, R. & Capellari, S., Jul 1 2017, In : Journal of Neurology. 264, 7, p. 1426-1433 8 p.

Research output: Contribution to journalArticle

Amyotrophic Lateral Sclerosis
Mutation
Pedigree
Genes
Dementia
2 Citations (Scopus)

Precuneal Thickness and Depression in Parkinson Disease

Zanigni, S., Sambati, L., Evangelisti, S., Testa, C., Calandra Buonaura, G., Manners, D. N., Terlizzi, R., Poda, R., Oppi, F., Lodi, R., Cortelli, P. & Tonon, C., 2017, In : Neurodegenerative Diseases. 17, 2-3, p. 97-102 6 p.

Research output: Contribution to journalArticle

Parkinson Disease
Parietal Lobe
Software
Equipment and Supplies
Brain
2016
17 Citations (Scopus)

Relationship of white and gray matter abnormalities to clinical and genetic features in myotonic dystrophy type 1

Zanigni, S., Evangelisti, S., Giannoccaro, M. P., Oppi, F., Poda, R., Giorgio, A., Testa, C., Manners, D. N., Avoni, P., Gramegna, L. L., De Stefano, N., Lodi, R., Tonon, C. & Liguori, R., 2016, In : NeuroImage: Clinical. 11, p. 678-685 8 p.

Research output: Contribution to journalArticle

Myotonic Dystrophy
Brain
Occipital Lobe
White Matter
Gray Matter
Siderosis
Orthostatic Hypotension
Sensorineural Hearing Loss
Hydrocephalus