Published in Pediatrics on July 01, 2006
MeCP2, a key contributor to neurological disease, activates and represses transcription. Science (2008) 10.11
Deletion of Mecp2 in Sim1-expressing neurons reveals a critical role for MeCP2 in feeding behavior, aggression, and the response to stress. Neuron (2008) 2.36
Understanding the rhythm of breathing: so near, yet so far. Annu Rev Physiol (2012) 2.01
Dads make a difference: an exploratory study of paternal support for breastfeeding in Perth, Western Australia. Int Breastfeed J (2009) 1.05
Risk of aspiration during anesthesia in patients with congenital insensitivity to pain with anhidrosis: case reports and review of the literature. J Anesth (2010) 0.96
Evidence of small-fiber polyneuropathy in unexplained, juvenile-onset, widespread pain syndromes. Pediatrics (2013) 0.85
A short in-frame deletion in NTRK1 tyrosine kinase domain caused by a novel splice site mutation in a patient with congenital insensitivity to pain with anhidrosis. BMC Med Genet (2011) 0.84
Relationship among nausea, anxiety, and orthostatic symptoms in pediatric patients with chronic unexplained nausea. Exp Brain Res (2014) 0.83
Mitochondrial disease in childhood: nuclear encoded. Neurotherapeutics (2013) 0.82
Linkage in the chain of care: a grounded theory of professional cooperation between antenatal care, postpartum care and child health care. Int J Integr Care (2008) 0.81
A narrative review on the similarities and dissimilarities between myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) and sickness behavior. BMC Med (2013) 0.79
Heart Rate Variability in Children with Attention-Deficit/Hyperactivity Disorder: A Pilot Study. Ann Neurosci (2016) 0.77
Neural and physiological responses to a cold pressor challenge in healthy adolescents. J Neurosci Res (2013) 0.76
Dysautonomia in autism spectrum disorder: case reports of a family with review of the literature. Autism Res Treat (2011) 0.76
Baroreflex dysfunction in sick newborns makes heart rate an unreliable surrogate for blood pressure changes. Pediatr Res (2016) 0.75
Sleep-disordered breathing symptoms are associated with poorer cognitive function in 5-year-old children. J Pediatr (2004) 2.71
An official ATS clinical policy statement: Congenital central hypoventilation syndrome: genetic basis, diagnosis, and management. Am J Respir Crit Care Med (2010) 2.07
Congenital central hypoventilation syndrome: PHOX2B genotype determines risk for sudden death. Pediatr Pulmonol (2008) 1.75
North American Society for Pediatric Gastroenterology, Hepatology, and Nutrition consensus statement on the diagnosis and management of cyclic vomiting syndrome. J Pediatr Gastroenterol Nutr (2008) 1.72
Congenital central hypoventilation syndrome: PHOX2B mutations and phenotype. Am J Respir Crit Care Med (2006) 1.66
Rapid-onset obesity with hypothalamic dysfunction, hypoventilation, and autonomic dysregulation presenting in childhood. Pediatrics (2007) 1.60
Developmental alterations of the respiratory human retrotrapezoid nucleus in sudden unexplained fetal and infant death. Auton Neurosci (2012) 1.48
Symptoms of sleep-disordered breathing in 5-year-old children are associated with sleepiness and problem behaviors. Pediatrics (2003) 1.32
Rapid-onset obesity with hypothalamic dysfunction, hypoventilation, and autonomic dysregulation: analysis of hypothalamic and autonomic candidate genes. Pediatr Res (2011) 1.28
Cardiorespiratory events detected by home memory monitoring and one-year neurodevelopmental outcome. J Pediatr (2004) 1.21
Carbon dioxide chemoreception and hypoventilation syndromes with autonomic dysregulation. J Appl Physiol (1985) (2010) 1.15
Autonomic abnormalities in cyclic vomiting syndrome. J Pediatr Gastroenterol Nutr (2007) 0.99
PHOX2B mutation-confirmed congenital central hypoventilation syndrome: presentation in adulthood. Am J Respir Crit Care Med (2006) 0.98
Comparison of PHOX2B testing methods in the diagnosis of congenital central hypoventilation syndrome and mosaic carriers. Diagn Mol Pathol (2010) 0.98
Sleep architecture in term and preterm infants beyond the neonatal period: the influence of gestational age, steroids, and ventilatory support. Sleep (2005) 0.96
Adult identified with congenital central hypoventilation syndrome--mutation in PHOX2b gene and late-onset CHS. Am J Respir Crit Care Med (2005) 0.95
Longitudinal assessment of hemoglobin oxygen saturation in preterm and term infants in the first six months of life. J Pediatr (2011) 0.89
Idiopathic congenital central hypoventilation syndrome: the next generation. Am J Med Genet (2002) 0.89
Sudden infant death syndrome and sudden intrauterine unexplained death: correlation between hypoplasia of raphé nuclei and serotonin transporter gene promoter polymorphism. Pediatr Res (2009) 0.88
Endoscopic retrograde cholangiopancreatography in children and adolescents. J Pediatr Gastroenterol Nutr (2002) 0.88
Monozygotic twins discordant for ROHHAD phenotype. Pediatrics (2011) 0.88
Later-onset congenital central hypoventilation syndrome due to a heterozygous 24-polyalanine repeat expansion mutation in the PHOX2B gene. Acta Paediatr (2008) 0.88
Sudden infant death syndrome: rare mutation in the serotonin system FEV gene. Pediatr Res (2007) 0.87
Infant polysomnography: reliability and validity of infant arousal assessment. J Clin Neurophysiol (2002) 0.87
Effect of a sudden infant death syndrome risk reduction education program on risk factor compliance and information sources in primarily black urban communities. Pediatrics (2003) 0.87
Variable human phenotype associated with novel deletions of the PHOX2B gene. Pediatr Pulmonol (2011) 0.86
Facial phenotype in children and young adults with PHOX2B-determined congenital central hypoventilation syndrome: quantitative pattern of dysmorphology. Pediatr Res (2005) 0.85
Medullary serotonin defects and respiratory dysfunction in sudden infant death syndrome. Respir Physiol Neurobiol (2009) 0.85
Congenital central hypoventilation syndrome and the PHOX2B gene: a model of respiratory and autonomic dysregulation. Respir Physiol Neurobiol (2010) 0.85
Sudden infant death syndrome: another year of new hope but no cure. Curr Opin Pulm Med (2007) 0.84
Dysregulation of locus coeruleus development in congenital central hypoventilation syndrome. Acta Neuropathol (2015) 0.83
Precursors of cardiorespiratory events in infants detected by home memory monitor. Pediatr Pulmonol (2008) 0.83
Pupillometry in congenital central hypoventilation syndrome (CCHS): quantitative evidence of autonomic nervous system dysregulation. Pediatr Res (2012) 0.81
Congenital central hypoventilation syndrome: neurocognitive functioning in school age children. Pediatr Pulmonol (2010) 0.80
Nicotine metabolizing genes GSTT1 and CYP1A1 in sudden infant death syndrome. Am J Med Genet A (2006) 0.80
Sudden infant death syndrome (SIDS) in African Americans: polymorphisms in the gene encoding the stress peptide pituitary adenylate cyclase-activating polypeptide (PACAP). Acta Paediatr (2008) 0.80
Genetic variation in the HTR1A gene and sudden infant death syndrome. Am J Med Genet A (2008) 0.79
3' UTR polymorphism of the serotonin transporter gene and sudden infant death syndrome: haplotype analysis. Am J Med Genet A (2006) 0.79
Home monitoring during infancy: what is normal? Paediatr Respir Rev (2002) 0.78
Residual chemosensitivity to ventilatory challenges in genotyped congenital central hypoventilation syndrome. J Appl Physiol (1985) (2013) 0.77
A triple threat: Down syndrome, congenital central hypoventilation syndrome, and Hirschsprung disease. Pediatrics (2012) 0.77
HTR2A variation and sudden infant death syndrome: a case-control analysis. Acta Paediatr (2008) 0.77
Analysis of PAC1 receptor gene variants in Caucasian and African American infants dying of sudden infant death syndrome. Acta Paediatr (2013) 0.76
Germline mosaicism of PHOX2B mutation accounts for familial recurrence of congenital central hypoventilation syndrome (CCHS). Am J Med Genet A (2012) 0.76
Ontogeny of arousal. J Clin Neurophysiol (2004) 0.76
Sudden infant death syndrome: Case-control frequency differences in paired like homeobox (PHOX) 2B gene. Am J Med Genet A (2006) 0.76
Respiratory and cardiovascular indicators of autonomic nervous system dysregulation in familial dysautonomia. Pediatr Pulmonol (2011) 0.76
Factors that influence use of a home cardiorespiratory monitor for infants: the collaborative home infant monitoring evaluation. Arch Pediatr Adolesc Med (2005) 0.76
Vagal and sympathetic heart rate and blood pressure control in adult onset PHOX2B mutation-confirmed congenital central hypoventilation syndrome. Clin Auton Res (2007) 0.76
Congenital central hypoventilation syndrome and sudden infant death syndrome: disorders of autonomic regulation. Semin Pediatr Neurol (2013) 0.75
A commentary on the importance of knowing from whence your PHOX2B mutation comes. J Hum Genet (2012) 0.75
Characterization of dermatoglyphics in PHOX2B-confirmed congenital central hypoventilation syndrome. Pediatrics (2006) 0.75
Nighttime child care: inadequate sudden infant death syndrome risk factor knowledge, practice, and policies. Pediatrics (2003) 0.75
Hyperthyroidism hidden by congenital central hypoventilation syndrome. J Pediatr Endocrinol Metab (2015) 0.75
An 8-month old infant discovered to be blue and not breathing during sleep. Paediatr Respir Rev (2002) 0.75