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3 studies found for:    PHOX2B
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PHOX2B (3 records)
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Rank Status Study
1 Unknown  PHOX2B Mutation-Confirmed Congenital Central Hypoventilation Syndrome in A Chinese Family: Presentations From Newborn to Adulthood
Condition: Central Alveolar Hypoventilation Syndrome
Intervention: Device: CPAP
2 Completed Late-onset Congenital Central Hypoventilation Syndrome and the Mutation of Phox2B Gene
Condition: Congenital Central Hypoventilation Syndrome
Intervention: Device: positive airway pressure, Non-invasive mechanic ventilation
3 Recruiting International Congenital Central Hypoventilation Syndrome (CCHS) Registry
Condition: Congenital Central Hypoventilation Syndrome
Intervention:

Study has passed its completion date and status has not been verified in more than two years.