Search

Search Constraints

You searched for: Author/Creator Conti, Valerio

Search Results

1. Analysis of 17 genes detects mutations in 81% of 811 patients with lissencephaly. (November 2018)

2. Angiocentric glioma-associated seizures: The possible role of EATT2, pyruvate carboxylase and glutamine synthetase. (March 2021)

3. Atypical Ocular Coloboma in Tuberous Sclerosis-2: Report of Two Novel Cases. Issue 3 (September 2021)

4. Characterisation of mutations of the phosphoinositide-3-kinase regulatory subunit, PIK3R2, in perisylvian polymicrogyria: a next-generation sequencing study. Issue 12 (December 2015)

5. Corrigendum to 'Angiocentric glioma-associated seizures: The possible role of EATT2, pyruvate carboxylase and glutamine synthetase [Seizure: European Journal of Epilepsy 86 (2021) 152-154]. (October 2021)

6. Genomic DNA methylation distinguishes subtypes of human focal cortical dysplasia. (10th May 2019)

7. Germline and somatic mutations in the MTOR gene in focal cortical dysplasia and epilepsy. (December 2016)

10. Multimodal fiber‐probe spectroscopy allows detecting epileptogenic focal cortical dysplasia in children. Issue 6 (9th January 2017)