# Fondazione IRCCS Istituto Neurologico Carlo Besta

**Type:** Institutions  
**Canonical URL:** https://scholariq.org/institutions/fondazione-irccs-istituto-neurologico-carlo-besta/

## Facts

| Field | Value |
| --- | --- |
| Avg h-index | 58.3 |
| Citations | 1,414,818 |
| City | Milan |
| Country | IT |
| Description | Fondazione IRCCS Istituto Neurologico Carlo Besta is a research organisation in Milan, IT. OpenAlex records 13,285 works and 1,414,818 citations for it. 1,789 researchers list it as their most recent affiliation. |
| Homepage | https://www.istituto-besta.it |
| OpenAlex ID | https://openalex.org/I4210164485 |
| Researchers | 1,789 |
| ROR ID | https://ror.org/05rbx8m02 |
| Type | healthcare |
| Works | 13,285 |

## University papers

Showing 12 of 14.

- [The clinicopathologic spectrum of focal cortical dysplasias: A consensus classification proposed by an ad hoc Task Force of the ILAE Diagnostic Methods Commission1](https://scholariq.org/papers/the-clinicopathologic-spectrum-of-focal-cortical-dysplasias-a-consensus/)
- [Terminology and classification of the cortical dysplasias](https://scholariq.org/papers/terminology-and-classification-of-the-cortical-dysplasias/)
- [Histopathological Findings in Brain Tissue Obtained during Epilepsy Surgery](https://scholariq.org/papers/histopathological-findings-in-brain-tissue-obtained-during-epilepsy-surgery/)
- [Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosis](https://scholariq.org/papers/mutations-in-the-profilin-1-gene-cause-familial-amyotrophic-lateral-sclerosis/)
- [Exome-wide Rare Variant Analysis Identifies TUBA4A Mutations Associated with Familial ALS](https://scholariq.org/papers/exome-wide-rare-variant-analysis-identifies-tuba4a-mutations-associated-with/)
- [Long-term disease progression in spinocerebellar ataxia types 1, 2, 3, and 6: a longitudinal cohort study](https://scholariq.org/papers/long-term-disease-progression-in-spinocerebellar-ataxia-types-1-2-3-and-6-a/)
- [Mutations in the vesicular trafficking protein annexin A11 are associated with amyotrophic lateral sclerosis](https://scholariq.org/papers/mutations-in-the-vesicular-trafficking-protein-annexin-a11-are-associated-with/)
- [The C9ORF72 expansion mutation is a common cause of ALS+/−FTD in Europe and has a single founder](https://scholariq.org/papers/the-c9orf72-expansion-mutation-is-a-common-cause-of-als-ftd-in-europe-and-has-a/)
- [CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia](https://scholariq.org/papers/ccnf-mutations-in-amyotrophic-lateral-sclerosis-and-frontotemporal-dementia/)
- [Visualization, quantification and correlation of brain atrophy with clinical symptoms in spinocerebellar ataxia types 1, 3 and 6](https://scholariq.org/papers/visualization-quantification-and-correlation-of-brain-atrophy-with-clinical/)
- [Reliability and validity of the International Cooperative Ataxia Rating Scale: A study in 156 spinocerebellar ataxia patients](https://scholariq.org/papers/reliability-and-validity-of-the-international-cooperative-ataxia-rating-scale-a/)
- [Early symptoms in spinocerebellar ataxia type 1, 2, 3, and 6](https://scholariq.org/papers/early-symptoms-in-spinocerebellar-ataxia-type-1-2-3-and-6/)

## University researchers

- [Alberto Raggi](https://scholariq.org/researchers/alberto-raggi/)

## University top topics

Showing 8 of 25.

- [Glioma Diagnosis and Treatment](https://scholariq.org/topics/glioma-diagnosis-and-treatment/)
- [Genetic Neurodegenerative Diseases](https://scholariq.org/topics/genetic-neurodegenerative-diseases/)
- [Mitochondrial Function and Pathology](https://scholariq.org/topics/mitochondrial-function-and-pathology/)
- [Neurological disorders and treatments](https://scholariq.org/topics/neurological-disorders-and-treatments/)
- [Epilepsy research and treatment](https://scholariq.org/topics/epilepsy-research-and-treatment/)
- [Migraine and Headache Studies](https://scholariq.org/topics/migraine-and-headache-studies/)
- [Parkinson's Disease Mechanisms and Treatments](https://scholariq.org/topics/parkinson-s-disease-mechanisms-and-treatments/)
- [Metabolism and Genetic Disorders](https://scholariq.org/topics/metabolism-and-genetic-disorders/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.