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

  • 13 Similar Profiles
Mutation Medicine & Life Sciences
Hereditary Spastic Paraplegia Medicine & Life Sciences
Genes Medicine & Life Sciences
Spastic Paraparesis Medicine & Life Sciences
Phenotype Medicine & Life Sciences
Tubulin Medicine & Life Sciences
Proteins Medicine & Life Sciences
Paraplegia Medicine & Life Sciences

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Research Output 1993 2019

  • 7103 Citations
  • 40 h-Index
  • 161 Article
  • 1 Chapter
  • 1 Editorial
  • 1 Letter

A novel CAPN1 mutation causes a pure hereditary spastic paraplegia in an Italian family

Cotti Piccinelli, S., Bassi, M. T., Citterio, A., Manganelli, F., Tozza, S., Santorelli, F. M., Cassarino, S. G., Caria, F., Baldelli, E., Galvagni, A., Santoro, L., Padovani, A. & Filosto, M., Jan 1 2019, In : Frontiers in Neurology. 10, 580.

Research output: Contribution to journalArticle

Open Access
Hereditary Spastic Paraplegia
Calpain
Cerebellar Ataxia
Mutation
Spinocerebellar Ataxias
3 Citations (Scopus)

Autophagy controls neonatal myogenesis by regulating the GH-IGF1 system through a NFE2L2- and DDIT3-mediated mechanism

Zecchini, S., Giovarelli, M., Perrotta, C., Morisi, F., Touvier, T., Di Renzo, I., Moscheni, C., Bassi, M. T., Cervia, D., Sandri, M., Clementi, E. & De Palma, C., 2019, In : Autophagy.

Research output: Contribution to journalArticle

Muscle Development
Autophagy
Activating Transcription Factor 4
Eukaryotic Initiation Factors
Adult Stem Cells

Broadening the spectrum of adulthood X-linked adrenoleukodystrophy: A report of two atypical cases

Foschi, M., Vacchiano, V., Avoni, P., Incensi, A., Battaglia, S., Donadio, V., Panzeri, E., Bassi, M. T., Liguori, R. & Rizzo, G., Jan 1 2019, In : Frontiers in Neurology. 10, FEB, 70.

Research output: Contribution to journalArticle

Open Access
Adrenoleukodystrophy
Spastic Paraparesis
Spinal Cord Diseases
Phenotype
Addison Disease

Charcot-Marie-Tooth disease with pyramidal features due to a new mutation of EGR2 gene

Fusco, C., Spagnoli, C., Salerno, G. G., Pavlidis, E., Frattini, D., Pisani, F. & Bassi, M. T., Jan 24 2019, In : Acta bio-medica : Atenei Parmensis. 90, 1, p. 104-107 4 p.

Research output: Contribution to journalArticle

Charcot-Marie-Tooth Disease
Tooth
Mutation
Genes
Peripheral Nervous System Diseases
Hereditary Spastic Paraplegia
Mutation
Brain
Magnetic Resonance Imaging
Phenotype