If you made any changes in Pure these will be visible here soon.

Fingerprint Dive into the research topics where Emilia Bellone is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 1 Similar Profiles
Amyotrophic Lateral Sclerosis Medicine & Life Sciences
Charcot-Marie-Tooth Disease Medicine & Life Sciences
Mutation Medicine & Life Sciences
Motor Neuron Disease Medicine & Life Sciences
Prealbumin Medicine & Life Sciences
Genes Medicine & Life Sciences
Diagnostic Errors Medicine & Life Sciences
Familial Amyloid Neuropathies Medicine & Life Sciences

Network Recent external collaboration on country level. Dive into details by clicking on the dots.

Research Output 2018 2019

  • 2 Citations
  • 1 h-Index
  • 4 Article

Expanding the spectrum of genes responsible for hereditary motor neuropathies

Previtali, S. C., Zhao, E., Lazarevic, D., Pipitone, G. B., Fabrizi, G. M., Manganelli, F., Mazzeo, A., Pareyson, D., Schenone, A., Taroni, F., Vita, G., Bellone, E., Ferrarini, M., Garibaldi, M., Magri, S., Padua, L., Pennisi, E., Pisciotta, C., Riva, N., Scaioli, V. & 11 others, Scarlato, M., Tozza, S., Geroldi, A., Jordanova, A., Ferrari, M., Molineris, I., Reilly, M. M., Comi, G., Carrera, P., Devoto, M. & Bolino, A., Jan 1 2019, In : Journal of Neurology, Neurosurgery and Psychiatry.

Research output: Contribution to journalArticle

Charcot-Marie-Tooth Disease
Genes
Exome
Phenotype
Neuromuscular Diseases
1 Citation (Scopus)

Role of MAPT in Pure Motor Neuron Disease: Report of a Recurrent Mutation in Italian Patients

Origone, P., Geroldi, A., Lamp, M., Sanguineri, F., Caponnetto, C., Cabona, C., Gotta, F., Trevisan, L., Bellone, E., Manganelli, F., Devigili, G. & Mandich, P., Mar 20 2019, In : Neurodegenerative Diseases.

Research output: Contribution to journalArticle

Motor Neuron Disease
Amyotrophic Lateral Sclerosis
Mutation
Genes
Motor Neurons

Autosomal-dominant transthyretin (TTR)-related amyloidosis is not a frequent CMT2 neuropathy "in disguise"

Grandis, M., Geroldi, A., Gulli, R., Manganelli, F., Gotta, F., Lamp, M., Origone, P., Trevisan, L., Gemelli, C., Fabbri, S., Schenone, A., Tozza, S., Santoro, L., Bellone, E. & Mandich, P., Oct 4 2018, In : Orphanet Journal of Rare Diseases. 13, 1, 177.

Research output: Contribution to journalArticle

Prealbumin
Diagnostic Errors
Familial Amyloid Neuropathies
Nervous System Diseases
Early Diagnosis
1 Citation (Scopus)

Twenty years of molecular analyses in amyotrophic lateral sclerosis: Genetic landscape of Italian patients

Lamp, M., Origone, P., Geroldi, A., Verdiani, S., Gotta, F., Caponnetto, C., Devigili, G., Verriello, L., Scialò, C., Cabona, C., Canosa, A., Vanni, I., Bellone, E., Eleopra, R. & Mandich, P., Jan 1 2018, (Accepted/In press) In : Neurobiology of Aging.

Research output: Contribution to journalArticle

Amyotrophic Lateral Sclerosis
Mutation
Genes
Neurodegenerative Diseases
Counseling