• Epilepsy
    • Benign epilepsy of childhood with occipital paroxysms
    • Benign rolandic epilepsy
    • Childhood absence epilepsy and juvenile absence epilepsy
    • Epilepsy with continuous spikes and waves during sleep
    • Febrile seizures
    • Idiopathic generalised epilepsies of adolescence
    • Ketogenic diet
    • Landau-Kleffner syndrome
    • Lennox-Gastaut syndrome
    • Myoclonic-astatic epilepsy
    • Pharmacological treatment of epilepsy
    • Photosensitive epilepsies
    • Rasmussen syndrome
    • Severe myoclonic epilepsy (Dravet syndrome)
    • Symptomatic focal epilepsies
      • Frontal lobe epilepsy
      • Mesial temporal lobe epilepsy
      • Occipital lobe epilepsy
    • Surgical treatment of epilepsy
      • Cortical dysplasia
      • Hemispheric syndromes
      • Hypothalamic hamartoma
      • Mesial Temporal Syndrome (MTS)
      • Polymicrogyria
      • Tuberous sclerosis
      • Technical information of the surgical treatment of epilepsy
        • Technical information of the surgical treatment of epilepsy
  • Malformations of Cortical Development
    • Focal Cortical Dysplasia
    • Hemimegalencephaly
    • Lissencephaly (LIS)
    • Miller-Dieker Syndrome (MDS)
    • Periventricular nodular heterotopia (PNH)
    • Polymicrogyria phenotypes
      • Bilateral Frontoparietal Polymicrogyria (BFPP)
      • Bilateral Perisylvian Polymicrogyria (BPP)
      • Bilateral parasagittal parieto-occipital polymicrogyria (BPPOP)
    • Schizencephaly
    • X-linked lissencephaly (XLAG)
  • Neurobiology
  • Neurogenetics
  • Neuropharmacology
    • Antiepileptic Drugs
  • Neuroimaging

Research Group

  • Rare neurological diseases
  • Publications
    • Peer Reviewed articles
    • Books
  • About us
    • Contacts
    • Pediatric Neurology Unit team
      • Carla Marini MD, PhD
    • Neurobiology Lab Team
      • Valentina Ariù
      • Valentina Cetica
      • Valerio Conti
    • Neurogenetics Lab team
      • Claudia Bianchini
      • Daniela Pucatti
      • Domenico Rutigliano
      • Elena Cellini
      • Elena Parrini
      • Laura Chiti
      • Davide Mei
    • Neuropharmacology
      • Anna Rosati MD, PhD
    • Neuroimaging team
  • Support our research

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Periventricular nodular heterotopia in Smith-Magenis syndrome., Capra, Valeria, Biancheri Roberta, Morana Giovanni, Striano Pasquale, Novara Francesca, Ferrero Giovanni Battista, Boeri Luca, Celle Maria Elena, Mancardi Maria Margherita, Zuffardi Orsetta, et al. , American journal of medical genetics. Part A, 2014 Dec, Volume 164A, Issue 12, p.3142-7, (2014) Abstract

http://www.ncbi.nlm.nih.gov/pubmed/25257626?dopt=Abstract

Contractions in the second polyA tract of ARX are rare, non-pathogenic polymorphisms., Conti, Valerio, Marini Carla, Mei Davide, Falchi Melania, Ferrari Anna Rita, and Guerrini Renzo , American journal of medical genetics. Part A, 2010 Dec 10, (2010) Abstract

http://www.ncbi.nlm.nih.gov/pubmed/21154857?dopt=Abstract

 

Renzo Guerrini - Pediatric Neurology