Genetic Basis for Respiratory Control Disorders

- Respiratory control disorders: from genes to patients and back

- Hereditary aspects of respiratory control in health and disease in humans

- Congenital central hypoventilation syndrome: from patients to gene discovery

- Phox2b and the homeostatic brain

- Congenital central hypoventilation syndrome: from patients to gene discovery

- Structural and functional brain abnormalities in congenital central hypoventilation syndrome

- In vitro studies of Phox2b gene mutations in congenital central hypoventilation syndrome

- Sudden infant death syndrome: study of genes pertinent to cardiorespiratory and autonomic regulation

- Genetic basis for obstructive sleep apnea syndrome: what role for variation in respiratory control?- Apnea and irregular breathing in animal models: a physiogenomic approach

- Genetic determinants of respiratory phenotype in mice

- Genes and development of respiratory rhythm generation

- Transcription factor control of central respiratory neuron development

- Lessons from mutant newborn mice with respiratory control deficits

- Tentative mouse model for the congenital central hypoventilation syndrome: heterozygous Phox2b mutant newborn mice

- Respiratory control abnormalities in necdin-deficient mice: implications for the pathogenesis of Prader-Willi syndrome

- Possible role of bioaminergic systems in respiratory disorders of Rett syndrome

- Respiratory plasticity following intermittent hypoxia: a guide for novel therapeutic approaches to ventilatory control disorders