No gender differences in growth patterns in a cohort of children with cystic fibrosis born between 1986 and 1995
Tài liệu tham khảo
Elborn, 2016, Cystic fibrosis, Lancet, 388, 2519, 10.1016/S0140-6736(16)00576-6
Buzzetti, 2009, An overview of international literature from cystic fibrosis registries: 1. Mortality and survival studies in cystic fibrosis, J Cyst Fibros, 8, 229, 10.1016/j.jcf.2009.04.001
Harness-Brumley, 2014, Gender differences in outcomes of patients with cystic fibrosis, J Womens Health (Larchmt), 23, 1012, 10.1089/jwh.2014.4985
Viviani, 2011, Absence of a gender gap in survival. An analysis of the Italian registry for cystic fibrosis in the paediatric age, J Cyst Fibros, 10, 313, 10.1016/j.jcf.2011.03.007
Stern, 2008, From registry to quality management: the German cystic fibrosis quality assessment project 1995–2006, Eur Respir J, 31, 29, 10.1183/09031936.00056507
Verma, 2005, Is there still a gender gap in cystic fibrosis?, Chest, 128, 2824, 10.1016/S0012-3692(15)52709-8
McIntyre, 2013, Gender and survival in cystic fibrosis, Curr Opin Pulm Med, 19, 692, 10.1097/MCP.0b013e328365af49
Alicandro, 2015, Cystic fibrosis mortality trend in Italy from 1970 to 2011, J Cyst Fibros, 14, 267, 10.1016/j.jcf.2014.07.010
Kulich, 2003, Improved survival among young patients with cystic fibrosis, J Pediatr, 142, 631, 10.1067/mpd.2003.197
Abid, 2017, 17β-Estradiol dysregulates innate immune responses to Pseudomonas aeruginosa respiratory infection and is modulated by estrogen receptor antagonism, Infect Immun, 85, 10.1128/IAI.00422-17
Marson, 2016, Classification of CFTR mutation classes, Lancet Respir Med, 4, e37, 10.1016/S2213-2600(16)30188-6
Wang, 1993, Pulmonary function between 6 and 18 years of age, Pediatr Pulmonol, 15, 75, 10.1002/ppul.1950150204
Cacciari, 2006, Italian cross-sectional growth charts for height, weight and BMI (2 to 20 yr), J Endocrinol Invest, 29, 581, 10.1007/BF03344156
Zeger, 1986, Longitudinal data analysis for discrete and continuous outcomes, Biometrics, 42, 121, 10.2307/2531248
Pan, 2001, Akaike's information criterion in generalized estimating equations, Biometrics, 57, 120, 10.1111/j.0006-341X.2001.00120.x
Morison, 1997, Height and weight in cystic fibrosis: a cross sectional study. UK Cystic Fibrosis Survey Management Committee, Arch Dis Child, 77, 497, 10.1136/adc.77.6.497
Nir, 1996, Long-term survival and nutritional data in patients with cystic fibrosis treated in a Danish centre, Thorax, 51, 1023, 10.1136/thx.51.10.1023
Karlberg, 1991, Linear growth in children with cystic fibrosis. I. Birth to 8 years of age, Acta Paediatr Scand, 80, 508, 10.1111/j.1651-2227.1991.tb11894.x
Lucidi, 2009, Growth assessment of paediatric patients with CF comparing different auxologic indicators: a multicentre Italian study, J Pediatr Gastroenterol Nutr, 49, 335, 10.1097/MPG.0b013e31818f0a39
Zhang, 2016, Pubertal height growth and adult height in cystic fibrosis after newborn screening, Pediatrics, 10.1542/peds.2015-2907
Corey, 1997, Longitudinal analysis of pulmonary function decline in patients with cystic fibrosis, J Pediatr, 131, 809, 10.1016/S0022-3476(97)70025-8
Konstan, 2007, Risk factors for rate of decline in forced expiratory volume in one second in children and adolescents with cystic fibrosis, J Pediatr, 151, 134, 10.1016/j.jpeds.2007.03.006
Sutton, 2014, Effects of puberty on cystic fibrosis related pulmonary exacerbations in women versus men, Pediatr Pulmonol, 49, 28, 10.1002/ppul.22767
Schaedel, 2002, Predictors of deterioration of lung function in cystic fibrosis, Pediatr Pulmonol, 33, 483, 10.1002/ppul.10100
Welsh, 2014, Increased rate of lung function decline in Australian adolescents with cystic fibrosis, Pediatr Pulmonol, 49, 873, 10.1002/ppul.22946
Vandevanter, 2014, Improvements in lung function and height among cohorts of 6-year-olds with cystic fibrosis from 1994 to 2012, J Pediatr, 165, 1091, 10.1016/j.jpeds.2014.06.061
Que, 2006, Improving rate of decline of FEV1 in young adults with cystic fibrosis, Thorax, 61, 155, 10.1136/thx.2005.043372
Zhang, 2013, Pubertal height velocity and associations with prepubertal and adult heights in cystic fibrosis, J Pediatr, 163, 376, 10.1016/j.jpeds.2013.02.026
Ramsey, 2007, Use of lung imaging studies as outcome measures for development of new therapies in cystic fibrosis, Proc Am Thorac Soc, 4, 359, 10.1513/pats.200611-183HT
Stanojevic, 2017, Progression of lung disease in preschool patients with cystic fibrosis, Am J Respir Crit Care Med, 195, 1216, 10.1164/rccm.201610-2158OC
Smith, 2014, European cystic fibrosis society standards of care: best practice guidelines, J Cyst Fibros, 13, S23, 10.1016/j.jcf.2014.03.010