Sökning: "Childhood CNS tumours"
Visar resultat 1 - 5 av 8 avhandlingar innehållade orden Childhood CNS tumours.
1. Glioneuronal tumours in childhood : Clinical picture, long-term outcome and possible new treatments
Sammanfattning : Background: Glioneuronal tumours are a subgroup of low-grade tumours of the central nervous system (CNS), often causing epilepsy. Overall survival is excellent, but data regarding long-term seizure outcome and late effects are scarce. LÄS MER
2. Medical, cognitive and motor outcome after treatment of pilocytic astrocytoma in the posterior fossa in childhood
Sammanfattning : Introduction: Pilocytic astrocytoma is the most common brain tumour in childhood. The aim of the studies was to investigate late medical, cognitive and motor complications in patients treated in childhood for pilocytic astrocytoma in the posterior fossa. LÄS MER
3. CNS tumours of childhood/adolescence : outcomes related to disability and identity in adult survivors
Sammanfattning : Central nervous system (CNS) tumour survivors are at increased risk for adverse health and functional late effects. Results from previous studies from the Swedish LIFE project, of which this licentiate thesis is a part, indicate needs of expanded clinical surveillance, and long-term follow-up in order to reduce late effects and protect quality of survival. LÄS MER
4. Childhood brain tumours : health and function in adult survivors and parental fears
Sammanfattning : The general aim of the present research was to investigate health and functional ability of patients treated for childhood brain tumour and systematically examine parental fears after a child s brain tumour. The aims were realised through two part-studies. LÄS MER
5. Childhood CNS tumours : health and functional outcomes in adult survivors, and follow-up needs of patients and parents
Sammanfattning : Childhood central nervous system (CNS) tumour patients represent a high-risk population regarding tumour- and treatment-related late effects. The overall purpose of the present thesis was to gain increased knowledge about the long-term consequences for survivors and their parents after a CNS tumour diagnosis in childhood. LÄS MER