Coates AL - Search Results

1

Skeletal muscle metabolism in cystic fibrosis and primary ciliary dyskinesia.

Wells GD, Wilkes DL, Schneiderman JE, Rayner T, Elmi M, Selvadurai H, Dell SD, Noseworthy MD, Ratjen F, Tein I, Coates AL. Wells GD, et al. Among authors: coates al. Pediatr Res. 2011 Jan;69(1):40-5. doi: 10.1203/PDR.0b013e3181fff35f. Pediatr Res. 2011. PMID: 20938370

2

Determination of maximal voluntary ventilation in children with cystic fibrosis.

Stein R, Selvadurai H, Coates A, Wilkes DL, Schneiderman-Walker J, Corey M. Stein R, et al. Pediatr Pulmonol. 2003 Jun;35(6):467-71. doi: 10.1002/ppul.10298. Pediatr Pulmonol. 2003. PMID: 12746945

3

Reliability and validity of the habitual activity estimation scale (HAES) in patients with cystic fibrosis.

Wells GD, Wilkes DL, Schneiderman-Walker J, Elmi M, Tullis E, Lands LC, Ratjen F, Coates AL. Wells GD, et al. Among authors: coates al. Pediatr Pulmonol. 2008 Apr;43(4):345-53. doi: 10.1002/ppul.20737. Pediatr Pulmonol. 2008. PMID: 18306334 Clinical Trial.

4

Assessment of body composition in pediatric patients with cystic fibrosis.

Wells GD, Heale L, Schneiderman JE, Wilkes DL, Atenafu E, Coates AL, Ratjen F. Wells GD, et al. Among authors: coates al. Pediatr Pulmonol. 2008 Oct;43(10):1025-32. doi: 10.1002/ppul.20913. Pediatr Pulmonol. 2008. PMID: 18781652

5

Exercise and physical activity in children with cystic fibrosis.

Wilkes DL, Schneiderman JE, Nguyen T, Heale L, Moola F, Ratjen F, Coates AL, Wells GD. Wilkes DL, et al. Among authors: coates al. Paediatr Respir Rev. 2009 Sep;10(3):105-9. doi: 10.1016/j.prrv.2009.04.001. Epub 2009 Jul 21. Paediatr Respir Rev. 2009. PMID: 19651380 Review.

6

Physiological correlates of pulmonary function in children with cystic fibrosis.

Wells GD, Wilkes DL, Schneiderman JE, Thompson S, Coates AL, Ratjen F. Wells GD, et al. Among authors: coates al. Pediatr Pulmonol. 2014 Sep;49(9):878-84. doi: 10.1002/ppul.22928. Epub 2013 Oct 25. Pediatr Pulmonol. 2014. PMID: 24166871

7

Longitudinal relationship between physical activity and lung health in patients with cystic fibrosis.

Schneiderman JE, Wilkes DL, Atenafu EG, Nguyen T, Wells GD, Alarie N, Tullis E, Lands LC, Coates AL, Corey M, Ratjen F. Schneiderman JE, et al. Among authors: coates al. Eur Respir J. 2014 Mar;43(3):817-23. doi: 10.1183/09031936.00055513. Epub 2013 Oct 31. Eur Respir J. 2014. PMID: 24176992 Free article.

8

Long-term pulmonary morbidity in survivors of congenital diaphragmatic hernia.

Trachsel D, Selvadurai H, Bohn D, Langer JC, Coates AL. Trachsel D, et al. Among authors: coates al. Pediatr Pulmonol. 2005 May;39(5):433-9. doi: 10.1002/ppul.20193. Pediatr Pulmonol. 2005. PMID: 15704183

9

Resting and exercise cardiorespiratory function in survivors of congenital diaphragmatic hernia.

Trachsel D, Selvadurai H, Adatia I, Bohn D, Schneiderman-Walker J, Wilkes D, Coates AL. Trachsel D, et al. Among authors: coates al. Pediatr Pulmonol. 2006 Jun;41(6):522-9. doi: 10.1002/ppul.20359. Pediatr Pulmonol. 2006. PMID: 16617447

10

Rapid pulmonary delivery of inhaled tobramycin for Pseudomonas infection in cystic fibrosis: a pilot project.

Coates AL, Green M, Leung K, Chan J, Ribeiro N, Louca E, Ratjen F, Charron M, Tservistas M, Keller M. Coates AL, et al. Pediatr Pulmonol. 2008 Aug;43(8):753-9. doi: 10.1002/ppul.20850. Pediatr Pulmonol. 2008. PMID: 18613006 Clinical Trial.

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