Bittencourt, Lia Rita Azeredo <br/><br/>
Late-onset, insidious course and invasive treatment of congenital central hypoventilation syndrome in a case with the Phox2B mutation: case report.  [electronic resource] 

 -  Sleep & breathing = Schlaf & Atmung  Dec 2012 
 - 951-5 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1522-1709 
<br/><br/><label>Standard No.: </label>10.1007/s11325-011-0614-x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Child<br/>Child, Preschool<br/>Continuous Positive Airway Pressure<br/>DNA Mutational Analysis<br/>DNA Repeat Expansion--genetics<br/>Follow-Up Studies<br/>Homeodomain Proteins--genetics<br/>Humans<br/>Hypoventilation--congenital<br/>Infant<br/>Infant, Newborn<br/>Male<br/>Middle Aged<br/>Patient Compliance<br/>Phenotype<br/>Polysomnography<br/>Recurrence<br/>Respiratory Distress Syndrome, Newborn--diagnosis<br/>Sleep Apnea, Central--diagnosis<br/>Tracheotomy<br/>Transcription Factors--genetics