Format
Sort by

Send to

Choose Destination

Search results

Items: 5

1.

Cough.

Kasi AS, Kamerman-Kretzmer RJ.

Pediatr Rev. 2019 Apr;40(4):157-167. doi: 10.1542/pir.2018-0116. No abstract available.

PMID:
30936397
2.

Adult With PHOX2B Mutation and Late-Onset Congenital Central Hypoventilation Syndrome.

Kasi AS, Kun SS, Keens TG, Perez IA.

J Clin Sleep Med. 2018 Dec 15;14(12):2079-2081. doi: 10.5664/jcsm.7542.

3.

Refining the Application of Microbial Lipids as Tracers of Staphylococcus aureus Growth Rates in Cystic Fibrosis Sputum.

Neubauer C, Kasi AS, Grahl N, Sessions AL, Kopf SH, Kato R, Hogan DA, Newman DK.

J Bacteriol. 2018 Nov 26;200(24). pii: e00365-18. doi: 10.1128/JB.00365-18. Print 2018 Dec 15.

4.

Three-Generation Family With Congenital Central Hypoventilation Syndrome and Novel PHOX2B Gene Non-Polyalanine Repeat Mutation.

Kasi AS, Jurgensen TJ, Yen S, Kun SS, Keens TG, Perez IA.

J Clin Sleep Med. 2017 Jul 15;13(7):925-927. doi: 10.5664/jcsm.6670.

5.

Congenital central hypoventilation syndrome: diagnostic and management challenges.

Kasi AS, Perez IA, Kun SS, Keens TG.

Pediatric Health Med Ther. 2016 Aug 18;7:99-107. doi: 10.2147/PHMT.S95054. eCollection 2016. Review.

Supplemental Content

Support Center