Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Paul H. Sammut"'
Autor:
Paul H. Sammut, John L. Colombo
Publikováno v:
Pediatric Pulmonology, Asthma, and Sleep Medicine: A Quick Reference Guide ISBN: 9781610021432
Pediatric Pulmonology, Asthma, and Sleep Medicine: A Quick Reference Guide
Pediatric Pulmonology, Asthma, and Sleep Medicine: A Quick Reference Guide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a13525aaa3d5d4727f1fdf3d9994b4bb
https://doi.org/10.1542/9781610021432-part06-ch73
https://doi.org/10.1542/9781610021432-part06-ch73
Publikováno v:
Global Pediatric Health, Vol 5 (2018)
Global Pediatric Health
Global Pediatric Health
The aberrant right subclavian artery (ARSA) was first described by Hunauld in 1735, with the clinical symptom of the so-called “dysphagia lusoria” or “difficulty in swallowing due to a quirk of nature,” as described by David Bayford in 1787.1
Publikováno v:
Fetal and pediatric pathology. 37(1)
Introduction: Pulmonary interstitial glycogenosis (PIG) is an idiopathic lung condition that remains clinically underrecognized despite a growing body of literature. Case report: We present a case of PIG with pulmonary hypertension without underlying
Publikováno v:
The American Journal of Surgery. 179:27-30
Background: Empyema remains a cause of morbidity and mortality. Thoracoscopy has proved its versatility in the management of pleural space disorders. The suitability of video-assisted thoracic surgery (VATS) for decortication in the management of the
Publikováno v:
Pediatric Pulmonology. 27:43-53
In a recent investigation we found that hospitalized patients with cystic fibrosis who received 0.5 cc of 0.5% albuterol nebulizer solution TID significantly increased their pulmonary function across the day, but fell back to baseline overnight. To d
Autor:
John L. Colombo, Margaret A. Brooks, Jeanne R. Smay, Nancy G. Greger, Dennis M. Bier, Paul H. Sammut, Carol A. Huseman
Publikováno v:
Pediatric Pulmonology. 22:90-95
The purpose of this study was to determine whether GH treatment of cystic fibrosis (CF) patients can result in an anabolic effect, i.e., increased weight gain, improved growth rate, nitrogen retention, and improved pulmonary function. Nine prepuberta
Autor:
David R. Mack, John L. Colombo, Monica D. Traystman, Dean L. Antonson, Stuart S. Kaufman, Alan Norman Langnas, Jon A. Vanderhoof, Byers W. Shaw, Paul H. Sammut, Rodney S. Markin
Publikováno v:
The Journal of Pediatrics. 127:881-887
Objective : To describe the clinical characteristics of patients with cystic fibrosis considered for liver transplantation and the clinical outcome after transplantation. Methods : Patient charts were reviewed. Mutation analysis was performed on bloo
Autor:
Paul H. Sammut
Publikováno v:
Chest. 149:A515
Autor:
Paul H. Sammut, John L. Colombo
Publikováno v:
Pediatric Pulmonology
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::52093589772b93a7b8085e44f51ffdc4
https://doi.org/10.1542/9781581104936-07-ch32
https://doi.org/10.1542/9781581104936-07-ch32
Autor:
Rebecca Anderson, G. Bradley Schaefer, Barbara Simanek, Paul H. Sammut, Christopher Patel, Monica D. Traystman, John L. Colombo, Warren G. Sanger, William J. Kimberling, Diane Acquazzino, Nancy A. Schulte, Pam J. Reilly
Publikováno v:
Human Mutation. 2:7-15
Cystic fibrosis (CF) is the most common autosomal recessive disorder in Caucasian populations with an approximate frequency of one in 2,500 live births and a carrier frequency of one in 25. We studied 400 individuals seen at The Nebraska Regional Cys