| Protein is an important but undervalued macronutrient in the nutritional care of patients with cystic fibrosis MPKJ Engelen, G Com, NEP Deutz Current Opinion in Clinical Nutrition & Metabolic Care 17 (6), 515-520, 2014 | 83 | 2014 |
| Use of body mass index percentile to identify fat-free mass depletion in children with cystic fibrosis MPKJ Engelen, R Schroder, K Van der Hoorn, NEP Deutz, G Com Clinical nutrition 31 (6), 927-933, 2012 | 82 | 2012 |
| Impact of degree of obesity on sleep, quality of life, and depression in youth BN Whitaker, PL Fisher, S Jambhekar, G Com, S Razzaq, JE Thompson, ... Journal of Pediatric Health Care 32 (2), e37-e44, 2018 | 69 | 2018 |
| New stable isotope method to measure protein digestibility and response to pancreatic enzyme intake in cystic fibrosis M Engelen, G Com, PJ Anderson, NEP Deutz Clinical nutrition 33 (6), 1024-1032, 2014 | 51 | 2014 |
| Outcomes of children treated with tracheostomy and positive-pressure ventilation at home G Com, DZ Kuo, ML Bauer, CV Lenker, MM Melguizo-Castro, TG Nick, ... Clinical Pediatrics 52 (1), 54-61, 2013 | 43 | 2013 |
| Characteristics and surgical and clinical outcomes of severely obese children with obstructive sleep apnea G Com, JL Carroll, X Tang, MS Melguizo, C Bower, S Jambhekar Journal of Clinical Sleep Medicine 11 (4), 467-474, 2015 | 39 | 2015 |
| Clinical characteristics and epidemiology of methicillin-resistant Staphylococcus aureus (MRSA) in children with cystic fibrosis from a center with a high MRSA prevalence NS Harik, G Com, X Tang, MM Castro, ME Stemper, JL Carroll American journal of infection control 44 (4), 409-415, 2016 | 38 | 2016 |
| Predictors and outcome of low initial forced expiratory volume in 1 second measurement in children with cystic fibrosis G Com, JL Carroll, MM Castro, X Tang, S Jambhekar, A Berlinski The Journal of pediatrics 164 (4), 832-838, 2014 | 38 | 2014 |
| Assessment and treatment of obstructive sleep-disordered breathing KA Bodenner, SK Jambhekar, G Com, WL Ward Clinical Pediatrics 53 (6), 544-548, 2014 | 36 | 2014 |
| Role of a respiratory therapist in improving adherence to positive airway pressure treatment in a pediatric sleep apnea clinic SK Jambhekar, G Com, X Tang, KK Pruss, R Jackson, C Bower, JL Carroll, ... Respiratory Care 58 (12), 2038-2044, 2013 | 36 | 2013 |
| Dietary essential amino acids are highly anabolic in pediatric patients with cystic fibrosis MPKJ Engelen, G Com, RR Wolfe, NEP Deutz Journal of Cystic Fibrosis 12 (5), 445-453, 2013 | 33 | 2013 |
| Periodic limb movements during sleep in children with narcolepsy SK Jambhekar, G Com, E Jones, R Jackson, MM Castro, F Knight, ... Journal of Clinical Sleep Medicine 7 (6), 597-601, 2011 | 31 | 2011 |
| Stimulated nitric oxide production and arginine deficiency in children with cystic fibrosis with nutritional failure MPKJ Engelen, G Com, YC Luiking, NEP Deutz The Journal of pediatrics 163 (2), 369-375. e1, 2013 | 27 | 2013 |
| Transition of respiratory technology dependent patients from pediatric to adult pulmonology care A Agarwal, D Willis, X Tang, M Bauer, A Berlinski, G Com, WL Ward, ... Pediatric Pulmonology 50 (12), 1294-1300, 2015 | 26 | 2015 |
| Redesigning care to meet national recommendation of four or more yearly clinic visits in patients with cystic fibrosis A Berlinski, MJ Chambers, L Willis, K Homa, G Com BMJ quality & safety 23 (Suppl 1), i42-i49, 2014 | 26 | 2014 |
| Adenosine receptors, cystic fibrosis, and airway hydration G Com, JP Clancy Adenosine Receptors in Health and Disease, 363-381, 2009 | 25 | 2009 |
| Antibiotic hypersensitivity in CF: drug-induced life-threatening hemolytic anemia in a pediatric patient A Chavez, A Mian, AM Scurlock, D Blackall, G Com Journal of Cystic Fibrosis 9 (6), 433-438, 2010 | 24 | 2010 |
| Behaviorally based adherence program for pediatric patients treated with positive airway pressure KL Harford, S Jambhekar, G Com, K Pruss, M Kabour, K Jones, WL Ward Clinical Child Psychology and Psychiatry 18 (1), 151-163, 2013 | 22 | 2013 |
| Complicated Clostridium difficile colitis in children with cystic fibrosis: Association with gastric acid suppression? G Com, N Cetin, CE O'Brien Journal of Cystic Fibrosis 13 (1), 37-42, 2014 | 16 | 2014 |
| Increased whole body hydroxyproline production as assessed by a new stable isotope technique is associated with hip and spine bone mineral loss in cystic fibrosis M Engelen, G Com, NEP Deutz Clinical nutrition 33 (6), 1117-1121, 2014 | 13 | 2014 |
