Cargando…
Neurocutaneous syndromes in children /
| Clasificación: | Libro Electrónico |
|---|---|
| Otros Autores: | , |
| Formato: | Electrónico eBook |
| Idioma: | Inglés |
| Publicado: |
Montrouge :
John Libbey Eurotext,
[2006]
|
| Colección: | Mariani Foundation paediatric neurology series ;
15. |
| Temas: | |
| Acceso en línea: | Texto completo |
Tabla de Contenidos:
- NEUROCUTANEOUS SYNDROMES IN CHILDREN
- Contents
- Chapter 1
- Embryological basis of the neurocutaneous syndromes
- Chapter 2
- Neurocutaneous diseases in children and adolescents: general clinical pattern
- Chapter 3
- Hypomelanosis of Ito
- Chapter 4
- Vascular malformations and neurocutaneous disorders
- Chapter 5
- Neurocutaneous syndromes and hemimegalencephaly
- Chapter 6
- Two rare neurocutaneous syndromes: Wyburn-Mason and Proteus
- Chapter 7
- Diagnostic criteria and evaluation of patients with tuberous sclerosis complex
- Chapter 8
- Epileptic manifestations in tuberous sclerosisChapter 9
- Tuberous sclerosis complex: phenotype-genotype correlations
- Chapter 10
- Subependymal giant cell astrocytomas and tuberous sclerosis
- Chapter 11
- Neurosurgical strategies in the management of subependymal giant cell tumoursin tuberous sclerosis complex
- Chapter 12
- The neurofibromatoses: clinical manifestations, natural history and management
- Chapter 13
- Neurofibromatosis type 1: the dermatological option
- Chapter 14
- Clinical molecular genetics of the neurofibromatoses
- Chapter 15
- Cognitive-behavioural phenotype and neurobiological basis of neurofibromatosis type 1Chapter 16
- Brain tumours in neurofibromatosis type 1
- Chapter 17
- Novel therapeutic approaches for plexiform neurofibromas in neurofibromatosis type 1
- Chapter 18
- Adjuvant therapy for low-grade glioma in neurofibromatosis type 1
- Chapter 19
- Diagnostic and follow-up protocols for neurofibromatosis types 1 and 2