3 studies found for:    PHOX2B
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PHOX2B (3 records)
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Rank Status Study
1 Recruiting 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 Completed Trial on Treatment of Patients With Primary Hyperoxaluria Type I With Pyridoxal-phosphate
Condition: Primary Hyperoxaluria Type I
Intervention: Drug: Vitamin B 6

Indicates status has not been verified in more than two years