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Mattin8: parliamo di LGS

Mattin8: parliamo di LGS

Mattin8: parliamo di LGS Intervista alla presidente Associazione Famiglie LGS Italia Katia Santoro, che cos'è la LGS riconosciuta come malattia rara. Intervista

Anomalie

Anomalie

Anoᴟalie https://youtu.be/8fnsoGTYPRo Servizio della rubrica "Salute" sulla sesta Giornata Mondiale della LGS in occasione della quale si

Diagnosi precoci e cure efficaci per la sindrome di Lennox-Gastaut

Diagnosi precoci e cure efficaci per la sindrome di Lennox-Gastaut

Diagnosi precoci e cure efficaci per la sindrome di Lennox-Gastaut Da Nola l'appello dell’Associazione Famiglie LGS Italia che ha promosso l’evento “Anomalie”

Presentazione di Anomalie su Mattin8

Presentazione di Anomalie su Mattin8

Presentazione di Anoᴟalie su Mattin8 https://youtu.be/sRYO_ghRP60 Katia Santoro e Mario Cesarano presentano "Anoᴟalie" a Mattin8 in occasione della sesta

Batti… il pregiudizio! 2020

Batti… il pregiudizio! 2020

Home > Batti… il pregiudizio! > Batti il pregiudizio! 2020 Batti... il pregiudizio! 2020 Evento rimandato in base alle direttive nazionali sul

Associazione Famiglie LGS Italia: un supporto concreto per chi è colpito dalla sindrome di Lennox Gastaut

Associazione Famiglie LGS Italia: un supporto concreto per chi è colpito dalla sindrome di Lennox Gastaut

Associazione Famiglie LGS Italia: un supporto concreto per chi è colpito dalla sindrome di Lennox Gastaut La famiglia che viene colpita dalla

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