Longitudinal polysomnographic findings in infantile Pompe disease.

Kansagra, Sujay; Austin, Stephanie; DeArmey, Stephanie; Kazi, Zoheb; Kravitz, Richard M; Kishnani, Priya S

Kansagra, Sujay; Austin, Stephanie; DeArmey, Stephanie; Kazi, Zoheb; Kravitz, Richard M; Kishnani, Priya S.

Affiliation

Kansagra S; Division of Pediatric Neurology, Department of Pediatrics, Duke University Medical Center, Durham, North Carolina.

Am J Med Genet A ; 167A(4): 858-61, 2015 Apr.

Article in En | MEDLINE | ID: mdl-25706820

Subject(s)

Glycogen Storage Disease Type II/physiopathology; Enzyme Replacement Therapy; Female; Glucan 1,4-alpha-Glucosidase/therapeutic use; Glycogen Storage Disease Type II/drug therapy; Humans; Infant; Male; Polysomnography; Retrospective Studies; Sleep Apnea Syndromes/drug therapy; Treatment Outcome

Key words

infantile Pompe disease; nocturnal hypoventilation; obstructive sleep apnea; sleep-disordered breathing

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Full text: 1 Database: MEDLINE Main subject: Glycogen Storage Disease Type II Type of study: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Female / Humans / Infant / Male Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2015 Type: Article

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