Disease: Hirschsprung disease ganglioneuroblastoma
- Congenital Central Hypoventilation Syndrome
- Congenital central hypoventilation syndrome associated with Hirschsprung's disease and neuroblastoma: case of multiple neurocristopathies
- Congenital central hypoventilation syndrome: diagnosis, management, and long-term outcome in thirty-two children
- Developmental disorders affecting the respiratory system: CCHS and ROHHAD
- Multifocal ganglioneuroblastoma coexistent with total colonic aganglionosis
- Neural crest disorders and Hirschsprung's disease
- Neurocristopathy in mother (ganglioneuroblastoma) and daughter (aganglionosis): incidental or causal?
- Neurocristopathy. The association of Hirschsprung's disease-ganglioneuroma with autonomic nervous system dysfunction in 2 children
- Oncologic Phenotype of Peripheral Neuroblastic Tumors Associated With PHOX2B Non-Polyalanine Repeat Expansion Mutations
- Ondine's curse associated with Hirschsprung disease and ganglioneuroblastoma
- PHOX2B mutations and genetic predisposition to neuroblastoma
- The contribution of associated congenital anomalies in understanding Hirschsprung's disease
- Variable human phenotype associated with novel deletions of the PHOX2B gene