• 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

Accesso utente

  • Crea nuovo profilo
  • Richiedi una nuova password

Publications

  • Elenco
  • Filtra
Found 2 results

  • Autore
  • Titolo
  • Tipo
  • Anno (Desc)
Filtri: Autore è Srivastava, A K  [Clear All Filters]
1998
Human doublecortin (DCX) and the homologous gene in mouse encode a putative Ca2+-dependent signaling protein which is mutated in human X-linked neuronal migration defects., Sossey-Alaoui, K., Hartung A. J., Guerrini R., Manchester D. K., Posar A., Puche-Mira A., Andermann E., Dobyns W. B., and Srivastava A. K. , Human molecular genetics, 1998 Aug, Volume 7, Issue 8, p.1327-32, (1998) Abstract

http://www.ncbi.nlm.nih.gov/pubmed/9668176?dopt=Abstract

1997
Linkage and physical mapping of X-linked lissencephaly/SBH (XLIS): a gene causing neuronal migration defects in human brain., Ross, M. E., Allen K. M., Srivastava A. K., Featherstone T., Gleeson J. G., Hirsch B., Harding B. N., Andermann E., Abdullah R., Berg M., et al. , Human molecular genetics, 1997 Apr, Volume 6, Issue 4, p.555-62, (1997) Abstract

http://www.ncbi.nlm.nih.gov/pubmed/9097958?dopt=Abstract

 

Renzo Guerrini - Pediatric Neurology