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.