• 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

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Publications

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  • Filtra
Found 2 results

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  • Titolo
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Filtri: Autore è Scheffer, Ingrid E  [Clear All Filters]
2015
Early and effective treatment of KCNQ2 encephalopathy., Pisano, Tiziana, Numis Adam L., Heavin Sinéad B., Weckhuysen Sarah, Angriman Marco, Suls Arvid, Podesta Barbara, Thibert Ronald L., Shapiro Kevin A., Guerrini Renzo, et al. , Epilepsia, 2015 May, Volume 56, Issue 5, p.685-91, (2015) Abstract

http://www.ncbi.nlm.nih.gov/pubmed/25880994?dopt=Abstract

Mutations of protocadherin 19 in female epilepsy (PCDH19-FE) lead to allopregnanolone deficiency., Tan, Chuan, Shard Chloe, Ranieri Enzo, Hynes Kim, Pham Duyen H., Leach Damian, Buchanan Grant, Corbett Mark, Shoubridge Cheryl, Kumar Raman, et al. , Human molecular genetics, 2015 Jun 29, (2015) Abstract

http://www.ncbi.nlm.nih.gov/pubmed/26123493?dopt=Abstract

 

Renzo Guerrini - Pediatric Neurology