Foto del docente

Luca Soliani

Assegnista di ricerca

Dipartimento di Scienze Mediche e Chirurgiche

Pubblicazioni

  1. Soliani L, Salerno GG, Pisani F, Barigazzi I, Rizzi S, Spagnoli C, Frattini D, Zangrandi A, Fusco C. Neuropsychological and behavioral disorders as presentation symptoms in two brothers with early-infantile Niemann-Pick type C. Acta Biomed. 2020 Sep 7;91(3):e2020075. doi: 10.23750/abm.v91i3.9272. PMID: 32921771.
  2. Spagnoli C, Soliani L, Caraffi SG, Baga M, Rizzi S, Salerno GG, Frattini D, Garavelli L, Koskenvuo J, Pisani F, Fusco C. Paroxysmal movement disorder with response to carbamazepine in a patient with RHOBTB2 developmental and epileptic encephalopathy. Parkinsonism Relat Disord. 2020 Jun 1;76:54-55. doi: 10.1016/j.parkreldis.2020.05.031. Epub ahead of print. PMID: 32810689.
  3. Baga M, Spagnoli C, Soliani L, Salerno GG, Rizzi S, Frattini D, Pisani F, Fusco C. Early-onset Dopamine Transporter Deficiency Syndrome: Long-term Follow-up. Can J Neurol Sci. 2020 Jul 10:1-2. doi: 10.1017/cjn.2020.144. Epub ahead of print. PMID: 32646530.
  4. Soliani L, Spagnoli C, Salerno GG, Mehine M, Rizzi S, Frattini D, Koskenvuo J, Fusco C. A Novel De Novo KIF21A Variant in a Patient With Congenital Fibrosis of the Extraocular Muscles With a Syndromic CFEOM Phenotype. J Neuroophthalmol. 2020 Mar 3. doi: 10.1097/WNO.0000000000000921. Epub ahead of print. PMID: 32141982.
  5. Iodice A, Spagnoli C, Cangini M, Soliani L, Rizzi S, Salerno GG, Frattini D, Pisani F, Fusco C. Long-term follow-up in infantile-onset SCAR18: A case report. J Clin Neurosci. 2020 Jul;77:232-234. doi: 10.1016/j.jocn.2020.05.008. Epub 2020 May 6. PMID: 32387255.
  6.  Cordelli DM, Di Pisa V, Fetta A, et al. Neurological Phenotype of Mowat-Wilson Syndrome. Genes (Basel). 2021;12(7):982. Published 2021 Jun 27. doi:10.3390/genes12070982

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