Piernanda Vigliano

Summary

Country: Italy

Publications

  1. ncbi request reprint Transmantle dysplasia in tuberous sclerosis: clinical features and surgical outcome in four children
    Piernanda Vigliano
    Department of Child Neuropsychiatry, University of Turin, Turin, Italy
    J Child Neurol 17:752-8. 2002
  2. doi request reprint Cognitive evolution of a girl submitted to right hemispherotomy when five years old
    Piernanda Vigliano
    Division of Child Neuropsychiatry, Martini Hospital, Turin, Italy
    Brain Dev 32:579-82. 2010
  3. doi request reprint LAMA2 stop-codon mutation: merosin-deficient congenital muscular dystrophy with occipital polymicrogyria, epilepsy and psychomotor regression
    Piernanda Vigliano
    Division of Child Neuropsychiatry, ASL2 Martini Hospital, Turin, Italy
    Eur J Paediatr Neurol 13:72-6. 2009

Collaborators

Detail Information

Publications3

  1. ncbi request reprint Transmantle dysplasia in tuberous sclerosis: clinical features and surgical outcome in four children
    Piernanda Vigliano
    Department of Child Neuropsychiatry, University of Turin, Turin, Italy
    J Child Neurol 17:752-8. 2002
    ..All things considered, our choice was to give these children at least temporary relief from severe epilepsy and possibly support for developmental progression...
  2. doi request reprint Cognitive evolution of a girl submitted to right hemispherotomy when five years old
    Piernanda Vigliano
    Division of Child Neuropsychiatry, Martini Hospital, Turin, Italy
    Brain Dev 32:579-82. 2010
    ..The rapidity of processing complex tasks is particularly lacking. This seems to be the expression of the defective development of the Central Executive System...
  3. doi request reprint LAMA2 stop-codon mutation: merosin-deficient congenital muscular dystrophy with occipital polymicrogyria, epilepsy and psychomotor regression
    Piernanda Vigliano
    Division of Child Neuropsychiatry, ASL2 Martini Hospital, Turin, Italy
    Eur J Paediatr Neurol 13:72-6. 2009
    ..Soon afterwards she lost ambulation and developed cognitive deterioration. Our case confirms that the clinical spectrum of MDC1A is more heterogeneous than previously thought...