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Рекомендации ESPEN-ESPGHAN-ECFS по диетотерапии при муковисцидозе у младенцев, детей и взрослых
100
Smyth AR, Bell SC, Bojcin S, Bryon M, Duff A, Flume P, et al. European cystic fibrosis Society standards of care: best practice guidelines. J Cyst Fibres 2014;13 (Suppl. l):S23-42
101
Cystic Fibrosis Trust. Standards for the clinical care of children and adults with cystic fibrosis in the UK. Bromley, UK: Cystic Fibrosis Trust; December 2011
102
Alicandro G, Bisogno A, Battezzati A, Bianchi ML, Corti F, Colombo С Recurrent pulmonary exacerbations are associated with low fat free mass and low bone mineral density in young adults with cystic fibrosis. J Cyst Fibres 2014;13:328-34
103
Alicandro G, Bisogno A, Battezzati A, Bianchi ML, Corti F, Colombo С Recurrent pulmonary exacerbations are associated with low fat free mass and low bone mineral density in young adults with cystic fibrosis. J Cyst Fibres 2014;13:328-34
104
Ionescu AA, Nixon LS, Luzio S, Lewis-Jenkins V. Evans WD, Stone MD, et al. Pulmonary function, body composition, and protein catabolism in adults with cystic fibrosis. Am J Respir Crit Care Med 2002;165:495-500
105
Sermet-Gaudelus I, Bianchi ML, Garabedian M, Aris RM, Morton A, Hardin DS, et al. European cystic fibrosis bone mineralisation guidelines. J Cyst Fibres 2011;10(Suppl. 2):S16-23
106
Aris RM, Merkel PA, Bachrach LK, Borowitz DS, Boyle MP, Elkin SL, et al. Guide to bone health and disease in cystic fibrosis. J Clin Endocrinol Metab 2005;90:1888-96
107
Sermet-Gaudelus I, Bianchi ML, Garabedian M, Aris RM, Morton A, Hardin DS, et al. European cystic fibrosis bone mineralisation guidelines. J Cyst Fibres 2011;10(Suppl. 2):S16-23
108
Sermet-Gaudelus I, Bianchi ML, Garabedian M, Aris RM, Morton A, Hardin DS, et al. European cystic fibrosis bone mineralisation guidelines. J Cyst Fibres 2011;10(Suppl. 2):S16-23
109
Borowitz D, Baker RD, Stallings V. Consensus report on nutrition for pediatric patients with cystic fibrosis. J Pediatr Gastroenterol Nutr 2002;35:246-59
110
Borowitz D, Baker RD, Stallings V. Consensus report on nutrition for pediatric patients with cystic fibrosis. J Pediatr Gastroenterol Nutr 2002;35:246-59
111
Sinaasappel M, Stern M, Littlewood J, Wolfe S, Steinkamp G, Heijerman HG, et al. Nutrition in patients with cystic fibrosis: a European Consensus. J Cyst Fibres 2002;1:51-75
112
Stallings VA, Stark LJ, Robinson KA, Feranchak AP, Quinton H. Evidence-based practice recommendations for nutrition-related management of children and adults with cystic fibrosis and pancreatic insufficiency: results of a systematic review. J Am Diet Assoc 2008;108:832-9
113
Smyth AR, Bell SC, Bojcin S, Bryon M, Duff A, Flume P, et al. European cystic fibrosis Society standards of care: best practice guidelines. J Cyst Fibres 2014;13(Suppl. l):S23-42
114
Doring G, Flume P, Heijerman H, Elborn JS, G.. Treatment of lung infection in patients with cystic fibrosis: current and future strategies. J Cyst Fibres 2012;11:461-79
115
DiMagno EP, Go VL, Summerskill WH. Relations between pancreatic enzyme ouputs and malabsorption in severe pancreatic insufficiency. N Engl J Med 1973;288:813-5
116
Stallings VA, Stark LJ, Robinson KA, Feranchak AP, Quinton H. Evidence-based practice recommendations for nutrition-related management of children and adults with cystic fibrosis and pancreatic insufficiency: results of a systematic review. J Am Diet Assoc 2008;108:832-9
117
Cystic Fibrosis Foundation, Borowitz D, Robinson KA, Rosenfeld M, Davis SD, Sabadosa KA, et al. Cystic Fibrosis Foundation evidence-based guidelines for management of infants with cystic fibrosis. J Pediatr 2009; 155:S73-93
118
Sermet-Gaudelus I, Mayell SJ, Southern KW, European Cystic Fibrosis Society NSWG Guidelines on the early management of infants diagnosed with cystic fibrosis following newborn screening. J Cyst Fibres 2010;9:323-9
119
Dodge JA, Turck D. Cystic fibrosis: nutritional consequences and management. Best Pract Res Clin Gastroenterol 2006;20:531-46
120
Cystic Fibrosis Foundation, Borowitz D, Robinson KA, Rosenfeld M, Davis SD, Sabadosa KA, et al. Cystic Fibrosis Foundation evidence-based guidelines for management of infants with cystic fibrosis. J Pediatr 2009; 155:S73-93
121
Dodge JA, Turck D. Cystic fibrosis: nutritional consequences and management. Best Pract Res Clin Gastroenterol 2006;20:531-46
122
Sinaasappel M, Stern M, Littlewood J, Wolfe S, Steinkamp G, Heijerman HG, et al. Nutrition in patients with cystic fibrosis: a European Consensus. J Cyst Fibres 2002;1:51-75
123
Cystic Fibrosis Foundation, Borowitz D, Robinson KA, Rosenfeld M, Davis SD, Sabadosa KA, et al. Cystic Fibrosis Foundation evidence-based guidelines for management of infants with cystic fibrosis. J Pediatr 2009; 155:S73-93
124
Sermet-Gaudelus I, Mayell SJ, Southern KW, European Cystic Fibrosis Society NSWG Guidelines on the early management of infants diagnosed with cystic fibrosis following newborn screening. J Cyst Fibres 2010;9:323-9
125
Ledder O, Haller W, Couper RT, Lewindon P, Oliver M. Cystic fibrosis: an update for clinicians. Part 2: Hepatobiliary and pancreatic manifestations. J Gastroenterol Hepatol 2014;29:1954-62
126
Debray D, Kelly D, Houwen R, Strandvik B, Colombo С Best practice guidance for the diagnosis and management of cystic fibrosis-associated liver disease. J Cyst Fibres 2011;10(Suppl. 2):S29-36
127
Debray D, Kelly D, Houwen R, Strandvik B, Colombo С Best practice guidance for the diagnosis and management of cystic fibrosis-associated liver disease. J Cyst Fibres 2011;10(Suppl. 2):S29-36
128
Debray D, Kelly D, Houwen R, Strandvik B, Colombo С Best practice guidance for the diagnosis and management of cystic fibrosis-associated liver disease. J Cyst Fibres 2011;10(Suppl. 2):S29-36
129
Debray D, Kelly D, Houwen R, Strandvik B, Colombo С Best practice guidance for the diagnosis and management of cystic fibrosis-associated liver disease. J Cyst Fibres 2011;10(Suppl. 2):S29-36
130
Edenborough FP, Borgo G, Knoop C, Lannefors L, Mackenzie WE, Madge S, et al. Guidelines for the management of pregnancy in women with cystic fibrosis. J Cyst Fibres 2008;7(Suppl. l):S2-32
131
McArdle JR. Pregnancy in cystic fibrosis. Clin Chest Med 2011;32.111–120,IX
132
Edenborough FP, Borgo G, Knoop C, Lannefors L, Mackenzie WE, Madge S, et al. Guidelines for the management of pregnancy in women with cystic fibrosis. J Cyst Fibres 2008;7(Suppl. l):S2-32
133
Cystic Fibrosis Foundation, Borowitz D, Robinson KA, Rosenfeld M, Davis SD, Sabadosa KA, et al. Cystic Fibrosis Foundation evidence-based guidelines for management of infants with cystic fibrosis. J Pediatr 2009; 155:S73-93
134
Sermet-Gaudelus I, Mayell SJ, Southern KW, European Cystic Fibrosis Society NSWG Guidelines on the early management of infants diagnosed with cystic fibrosis following newborn screening. J Cyst Fibres 2010;9:323-9
135
Sermet-Gaudelus I, Mayell SJ, Southern KW, European Cystic Fibrosis Society NSWG Guidelines on the early management of infants diagnosed with cystic fibrosis following newborn screening. J Cyst Fibres 2010;9:323-9
136
Smyth AR, Bell SC, Bojcin S, Bryon M, Duff A, Flume P, et al. European cystic fibrosis Society standards of care: best practice guidelines. J Cyst Fibres 2014;13(Suppl. l):S23-42
137
Maqbool A, Schall JI, Garcia-Espana JF, Zemel BS, Strandvik B, Stallings VA. Serum linoleic acid status as a clinical indicator of essential fatty acid status in children with cystic fibrosis. J Pediatr Gastroenterol Nutr 2008;47: 635-44
138
Steinkamp G, Demmelmair H, Ruhl-Bagheri I, von der Hardt H, Koletzko B. Energy supplements rich in linoleic acid improve body weight and essential fatty acid status of cystic fibrosis patients. J Pediatr Gastroenterol Nutr 2000;31:418-23
139
van Egmond AW, Kosorok MR, Koscik R, Laxova A, Farrell PM. Effect of linoleic acid intake on growth of infants with cystic fibrosis. Am J Clin Nutr 1996;63:746-52
140
Conway S, Morton A, Wolfe S. Enteral tube feeding for cystic fibrosis. Cochrane Database Syst Rev 2012;12:CD001198
141
Olsen EM, Petersen J, Skovgaard AM, Weile B, Jorgensen T, Wright CM. Failure to thrive: the prevalence and concurrence of anthropometric criteria in a general infant population. Arch Dis Child 2007;92:109-14
142
van Egmond AW, Kosorok MR, Koscik R, Laxova A, Farrell PM. Effect of linoleic acid intake on growth of infants with cystic fibrosis. Am J Clin Nutr 1996;63:746-52
143
Kindstedt-Arfwidson K, Strandvik B. Food intake in patients with cystic fibrosis on an ordinary diet. Scand J Gastroenterol Suppl 1988;143:160-2
144
Roulet M, Frascarolo P, Rappaz I, Pilet M. Essential fatty acid deficiency in well nourished young cystic fibrosis patients. Eur J Pediatr 1997;156: 952-6
145
Hammons AJ, Fiese B. Mealtime interactions in families of a child with cystic fibrosis: a meta-analysis. J Cyst Fibres 2010;9:377-84
146
Stark LJ, Jelalian E, Powers SW, Mulvihill MM, Opipari LC, Bowen A, et al. Parent and child mealtime behavior in families of children with cystic fibrosis. J Pediatr 2000;136:195-200
147
Jelalian E, Stark LJ, Reynolds L, Seifer R. Nutrition intervention for weight gain in cystic fibrosis: a meta analysis. J Pediatr 1998;132:486-92
148
Powers SW, Mitchell MJ, Patton SR, Byars КС, Jelalian E, Mulvihill MM, et al. Mealtime behaviors in families of infants and toddlers with cystic fibrosis. J Cyst Fibres 2005;4:175-82
149
Stark LJ, Quittner AL, Powers SW, Opipari-Arrigan L, Bean JA, Duggan C, et al. Randomized clinical trial of behavioral intervention and nutrition education to improve caloric intake and weight in children with cystic fibrosis. Arch Pediatr Adolesc Med 2009;163:915-21
150
Stark LJ, Opipari-Arrigan L, Quittner AL, Bean J, Powers SW. The effects of an intensive behavior and nutrition intervention compared to standard of care on weight outcomes in CF. Pediatr Pulmonol 2011;46:31-5
151
Abbott J, Morton AM, Musson H, Conway SP, Etherington C, Gee L, et al. Nutritional status, perceived body image and eating behaviours in adults with cystic fibrosis. Clin Nutr 2007;26:91-9
152
Shearer JE, Bryon M. The nature and prevalence of eating disorders and eating disturbance in adolescents with cystic fibrosis. J R Soc Med 2004;97(Suppl. 44):36-42
153
Gunnell S, Christensen NK, McDonald C, Jackson D. Attitudes toward percutaneous endoscopic gastrostomy placement in cystic fibrosis patients. J Pediatr Gastroenterol Nutr 2005;40:334-8
154
Steinkamp G, Demmelmair H, Ruhl-Bagheri I, von der Hardt H, Koletzko B. Energy supplements rich in linoleic acid improve body weight and essential fatty acid status of cystic fibrosis patients. J Pediatr Gastroenterol Nutr 2000;31:418-23
155
Rettammel AL, Marcus MS, Farrell PM, Sondel SA, Koscik RE, Mischler EH. Oral supplementation with a high-fat, high-energy product improves nutritional status and alters serum lipids in patients with cystic fibrosis. J Am Diet Assoc 1995;95:454-9
156
Shepherd RW, Holt TL, Cleghorn G, Ward LC, Isles A, Francis P. Short-term nutritional supplementation during management of pulmonary exacerbations in cystic fibrosis: a controlled study, including effects of protein turn-over. Am J Clin Nutr 1988;48:235-9
157
Steinkamp G, Demmelmair H, Ruhl-Bagheri I, von der Hardt H, Koletzko B. Energy supplements rich in linoleic acid improve body weight and essential fatty acid status of cystic fibrosis patients. J Pediatr Gastroenterol Nutr 2000;31:418-23
158
Caramia G, Cocchi M, Gagliardini R, Malavolta M, Mozzon M, Frega NG. Fatty acids composition of plasma phospholipids and triglycerides in children with cystic fibrosis. The effect of dietary supplementation with an olive and soybean oils mixture. Pediatr Med Chir 2003;25:42-9
159
Olveira G, Olveira C, Acosta E, Espildora F, Garrido-Sanchez L, Garcia- Escobar E, et al. Fatty acid supplements improve respiratory, inflammatory and nutritional parameters in adults with cystic fibrosis. Arch Bronconeumol 2010;46:70-7
160
Conway S, Morton A, Wolfe S. Enteral tube feeding for cystic fibrosis. Cochrane Database Syst Rev 2012;12:CD001198
161
Best C, Brearley A, Gaillard P, Regelmann W, Billings J, Dunitz J, et al. A prepost retrospective study of patients with cystic fibrosis and gastrostomy tubes. J Pediatr Gastroenterol Nutr 2011;53:453-8
162
Van Biervliet S, De Waele K, Van Winckel M, Robberecht E. Percutaneous endoscopic gastrostomy in cystic fibrosis: patient acceptance and effect of overnight tube feeding on nutritional status. Acta Gastroenterol Belg 2004;67:241-4
163
Conway S, Morton A, Wolfe S. Enteral tube feeding for cystic fibrosis. Cochrane Database Syst Rev 2012;12:CD001198
164
Best C, Brearley A, Gaillard P, Regelmann W, Billings J, Dunitz J, et al. A prepost retrospective study of patients with cystic fibrosis and gastrostomy tubes. J Pediatr Gastroenterol Nutr 2011;53:453-8
165
Efrati O, Mei-Zahav M, Rivlin J, Kerem E, Blau H, Barak A, et al. Long term nutritional rehabilitation by gastrostomy in Israeli patients with cystic fibrosis: clinical outcome in advanced pulmonary disease. J Pediatr Gastroenterol Nutr 2006;42:222-8
166
Steinkamp G, von der Hardt H. Improvement of nutritional status and lung function after long-term nocturnal gastrostomy feedings in cystic fibrosis. J Pediatr 1994;124:244-9
167
Walker SA, Gozal D. Pulmonary function correlates in the prediction of long-term weight gain in cystic fibrosis patients with gastrostomy tube feedings. J Pediatr Gastroenterol Nutr 1998;27:53-6
168
Houwen RH, van der Doef HP, Sermet I, Munck A, Hauser B, Walkowiak J, et al. Denning DIOS and constipation in cystic fibrosis with a multicentre study on the incidence, characteristics, and treatment of DIOS. J Pediatr Gastroenterol Nutr 2010;50:38-42
169
Colombo C, Ellemunter H, Houwen R, Munck A, Taylor C, Wilschanski M, et al. Guidelines for the diagnosis and management of distal intestinal obstruction syndrome in cystic fibrosis patients. J Cyst Fibres 2011;10(Suppl. 2):S24-8
170
Haworth CS. Impact of cystic fibrosis on bone health. Curr Opin Pulm Med 2010;16:616-22
171
Buntain HM, Schluter PJ, Bell SC, Greer RM, WongJC, Batch J, etal. Controlled [216 longitudinal study of bone mass accrual in children and adolescents with cystic fibrosis. Thorax 2006;61:146-54
172
Lucidi V, Bizzarri C, Alghisi F, Bella S, Russo B, Ubertini G, et al. Bone and body composition analyzed by Dual-energy X-ray Absorptiometry (DXA) in clin- [217 ical and nutritional evaluation ofyoung patients with Cystic Fibrosis: a crosssectional study. BMC Pediatr 2009;9:61
173
Gronowitz E, Pitkanen S, Kjellmer I, Heikinheimo M, Strandvik B. Association [218 between serum oncofetal antigens CA 19-9 and CA125 and clinical status in patients with cystic fibrosis. Acta Paediatr 2003;92:1267-71
174
Gronowitz E, Lorentzon M, Ohlsson C, Mellstrom D, Strandvik B. Docosa-hexaenoic acid is associated with endosteal circumference in long bones in [219 young males with cystic fibrosis. Br J Nutr 2008;99:160-7
175
Gronowitz E, Mellstrom D, Strandvik B. Serum phospholipid fatty acid pattern is associated with bone mineral density in children, but not adults, with cystic fibrosis. Br J Nutr 2006;95:1159-65
176
Conway SP, Oldroyd B, Brownlee KG, Wolfe SP, Truscott JG A cross-sectional study of bone mineral density in children and adolescents attending a Cystic Fibrosis Centre. J Cyst Fibres 2008;7:469-76
177
Gronowitz E, Garemo M, Lindblad A, Mellstrom D, Strandvik B. Decreased [221 bone mineral density in normal-growing patients with cystic fibrosis. Acta Paediatr 2003;92:688-93
178
Fewtrell MS, Benden C, Williams JE, Chomtho S, Ginty F, Nigdikar SV, et al. Undercarboxylated osteocalcin and bone mass in 8-12 year old children with cystic fibrosis. J Cyst Fibres 2008;7:307-12
179
Sermet-Gaudelus I, Bianchi ML, Garabedian M, Aris RM, Morton A, Hardin DS, et al. European cystic fibrosis bone mineralisation guidelines. J Cyst Fibres 2011;10(Suppl. 2):S16-23
180
Sermet-Gaudelus I, Bianchi ML, Garabedian M, Aris RM, Morton A, Hardin DS, et al. European cystic fibrosis bone mineralisation guidelines. J Cyst Fibres 2011;10(Suppl. 2):S16-23
181
Cystic Fibrosis Trust. Bone Mineralisation Working Group, Bone mineralisation in cystic fibrosis. Bromley, UK: Cystic Fibrosis Trust; 2007
182
Cystic Fibrosis Trust. Bone Mineralisation Working Group, Bone mineralisation in cystic fibrosis. Bromley, UK: Cystic Fibrosis Trust; 2007
183
Gronowitz E, Garemo M, Lindblad A, Mellstrom D, Strandvik B. Decreased [221 bone mineral density in normal-growing patients with cystic fibrosis. Acta Paediatr 2003;92:688-93
184
Moran A, Dunitz J, Nathan B, Saeed A, Holme B, Thomas W. Cystic fibrosis- related diabetes: current trends in prevalence, incidence, and mortality. [223 Diabetes Care 2009;32:1626-31
185
Moran A, Pillay K, Becker DJ, Acerini CL. Management of cystic fibrosis. [224 related diabetes in children and adolescents. Pediatr Diabetes 2014; 15 (Suppl. 20):65-76
186
Moran A, Brunzell C, Cohen RC, Katz M, Marshall ВС, Onady G, et al. Clinical care guidelines for cystic fibrosis-related diabetes: a position statement of [225 the American Diabetes Association and a clinical practice guideline of the Cystic Fibrosis Foundation, endorsed by the Pediatric Endocrine Society. Diabetes Care 2010;33:2697-708
187
Moran A, Brunzell C, Cohen RC, Katz M, Marshall ВС, Onady G, et al. Clinical care guidelines for cystic fibrosis-related diabetes: a position statement of [225 the American Diabetes Association and a clinical practice guideline of the Cystic Fibrosis Foundation, endorsed by the Pediatric Endocrine Society. Diabetes Care 2010;33:2697-708
188
Colombo C, Battezzati PM, Crosignani A, Morabito A, Costantini D, Padoan R, et al. Liver disease in cystic fibrosis: a prospective study on incidence, risk factors, and outcome. Hepatology 2002;36:1374-82
189
Van Biervliet S, Van Biervliet JP, Robberecht E, Christophe A. Fatty acid composition of serum phospholipids in cystic fibrosis (CF) patients with or without CF related liver disease. Clin Chem Lab Med 2010;48:1751-5
190
Colombo C, Costantini D, Rocchi A, Romano G, Rossi G, Bianchi ML, et al. Effects of liver transplantation on the nutritional status of patients with cystic fibrosis. Transpl Int 2005;18:246-55
191
Maqbool A, Schall JI, Garcia-Espana JF, Zemel BS, Strandvik B, Stallings VA. Serum linoleic acid status as a clinical indicator of essential fatty acid status in children with cystic fibrosis. J Pediatr Gastroenterol Nutr 2008;47: 635-44
192
Christophe A, Robberecht E. Current knowledge on fatty acids in cystic fibrosis. Prostagl Leukot Essent Fat Acids 1996;55:129-38
193
Coste TC, Armand M, Lebacq J, Lebecque P, Wallemacq P, Leal T. An overview of monitoring and supplementation of omega 3 fatty acids in cystic fibrosis. [234 Clin Biochem 2007;40:511-20
194
Lloyd-Still JD, Bibus DM, Powers CA, Johnson SB, Holman RT. Essential fatty acid deficiency and predisposition to lung disease in cystic fibrosis. ActaPaediatr 1996;85:1426-32
195
Walkowiak J, LisowskaA, Blaszczynski M, Przyslawski J, Walczak M. Poly-unsaturated fatty acids in cystic fibrosis are related to nutrition and clinical expression of the disease. J Pediatr Gastroenterol Nutr 2007;45:488-9. author reply 489
196
Jorgensen MH, Ott P, Michaelsen KF, Porsgaard T, Jensen F, Lanng S. Long- chain PUFA in granulocytes, mononuclear cells, and RBC in patients with [236 cystic fibrosis: relation to liver disease. J Pediatr Gastroenterol Nutr 2012;55:76-81
197
Freedman SD, Blanco PG, Zaman MM, Shea JC, Ollero M, Hopper IK, et al. [230 Association of cystic fibrosis with abnormalities in fatty acid metabolism. N Engl J Med 2004;350:560-9
198
Lloyd-Still JD, Bibus DM, Powers CA, Johnson SB, Holman RT. Essential fatty acid deficiency and predisposition to lung disease in cystic fibrosis. ActaPaediatr 1996;85:1426-32
199
Walkowiak J, LisowskaA, Blaszczynski M, Przyslawski J, Walczak M. Poly-unsaturated fatty acids in cystic fibrosis are related to nutrition and clinical expression of the disease. J Pediatr Gastroenterol Nutr 2007;45:488-9. author reply 489
200
Gronowitz E, Lorentzon M, Ohlsson C, Mellstrom D, Strandvik B. Docosa-hexaenoic acid is associated with endosteal circumference in long bones in [219 young males with cystic fibrosis. Br J Nutr 2008;99:160-7
201
Gronowitz E, Mellstrom D, Strandvik B. Serum phospholipid fatty acid pattern is associated with bone mineral density in children, but not adults, with cystic fibrosis. Br J Nutr 2006;95:1159-65
202
Njoroge SW, Seegmiller AC, Katrangi W, Laposata M. Increased Delta5- and [237 Delta6-desaturase, cyclooxygenase-2, and lipoxygenase-5 expression and activity are associated with fatty acid and eicosanoid changes in cystic fibrosis. Biochim Biophys Acta 2011;1811:431-40
203
Jorgensen MH, Ott P, Michaelsen KF, Porsgaard T, Jensen F, Lanng S. Long- chain PUFA in granulocytes, mononuclear cells, and RBC in patients with [236 cystic fibrosis: relation to liver disease. J Pediatr Gastroenterol Nutr 2012;55:76-81
204
Panchaud A, Sauty A, Kernen Y, Decosterd LA, Buclin T, Boulat O, et al. Biological effects of a dietary omega-3 polyunsaturated fatty acids supplementation in cystic fibrosis patients: a randomized, crossover placebo-controlled trial. Clin Nutr 2006;25:418-27
205
Strandvik B, Berg U, Kallner A, Kusoffsky E. Effect on renal function of essential fatty acid supplementation in cystic fibrosis. J Pediatr 1989;115: 242-50
206
Maqbool A, Schall JI, Garcia-Espana JF, Zemel BS, Strandvik B, Stallings VA. Serum linoleic acid status as a clinical indicator of essential fatty acid status in children with cystic fibrosis. J Pediatr Gastroenterol Nutr 2008;47: 635-44
207
Coste TC, Armand M, Lebacq J, Lebecque P, Wallemacq P, Leal T. An overview of monitoring and supplementation of omega 3 fatty acids in cystic fibrosis. [234 Clin Biochem 2007;40:511-20