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A Case of Congenital Central Hypoventilation Syndrome with a Novel Mutation of the PHOX2B Gene Presenting as Central Sleep Apnea

A Case of Congenital Central Hypoventilation Syndrome with a Novel Mutation of the PHOX2B Gene Presenting as Central Sleep Apnea
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Upper Airway Anatomical Balance Contributes to Optimal Continuous Positive Airway Pressure for Japanese Patients with Obstructive Sleep Apnea Syndrome
A Dozen Years of American Academy of Sleep Medicine (AASM) International Mini-Fellowship: Program Evaluation and Future Directions

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