-
1
-
-
0001752544
-
Cystic fibrosis
-
Scriver CR, Beaudet AL, Sly WS, Valle D, editors. New York: McGrave-Hill, Inc.
-
th ed. New York: McGrave-Hill, Inc., 2001; p. 5121-88.
-
(2001)
th Ed.
, pp. 5121-5188
-
-
Welsh, M.J.1
Ramsey, B.W.2
Accurso, F.3
Cutting, G.R.4
-
2
-
-
0024424270
-
Identification of the cystic fibrosis gene: Cloning and characterization of complementary DNA
-
Riordan JR, Rommens JM, Kerem B, Alon N, Rozmahel G, Grzelczak Z, et al. Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA. Science 1989;245:1066-73.
-
(1989)
Science
, vol.245
, pp. 1066-1073
-
-
Riordan, J.R.1
Rommens, J.M.2
Kerem, B.3
Alon, N.4
Rozmahel, G.5
Grzelczak, Z.6
-
3
-
-
0037460729
-
Cystic fibrosis
-
Ratjen F, Döring G. Cystic fibrosis. Lancet 2003;361:681-9.
-
(2003)
Lancet
, vol.361
, pp. 681-689
-
-
Ratjen, F.1
Döring, G.2
-
4
-
-
0038207591
-
Standarized lung function testing
-
Quanjer PH. Standarized lung function testing. Eur Respir J 1993;6(Suppl 6):3-102.
-
(1993)
Eur Respir J
, vol.6
, Issue.SUPPL. 6
, pp. 3-102
-
-
Quanjer, P.H.1
-
5
-
-
0003561168
-
-
Madrid: Ediciones Ergón S.A.
-
Hernández M, Castellet J, Narvaíza JL, Rincón JM, Ruiz I, Sánchez E, et al. Curvas y tablas de crecimiento. Madrid: Ediciones Ergón S.A., 2002.
-
(2002)
Curvas y Tablas de Crecimiento
-
-
Hernández, M.1
Castellet, J.2
Narvaíza, J.L.3
Rincón, J.M.4
Ruiz, I.5
Sánchez, E.6
-
7
-
-
0028299622
-
Analysis of the CFTR gene confirms the high genetic heterogeneity of the Spanish population: 43 Mutations account for only 78% of CF chromosomes
-
Chillón M, Casals T, Giménez J, Ramos MD, Palacio A, Morral N, et al. Analysis of the CFTR gene confirms the high genetic heterogeneity of the Spanish population: 43 mutations account for only 78% of CF chromosomes. Hum Genet 1994;93:447-51.
-
(1994)
Hum Genet
, vol.93
, pp. 447-451
-
-
Chillón, M.1
Casals, T.2
Giménez, J.3
Ramos, M.D.4
Palacio, A.5
Morral, N.6
-
8
-
-
0026004723
-
Analysis of 14 cystic fibrosis mutations in five South European populations
-
Nunes V, Gasparini P, Novelli G, Gaona A, Bonizzato A, Sangiuolo F, et al. Analysis of 14 cystic fibrosis mutations in five South European populations. Hum Genet 1991;87:737-8.
-
(1991)
Hum Genet
, vol.87
, pp. 737-738
-
-
Nunes, V.1
Gasparini, P.2
Novelli, G.3
Gaona, A.4
Bonizzato, A.5
Sangiuolo, F.6
-
9
-
-
0028033069
-
Populations variation of common cystic fibrosis mutations
-
Cystic Fibrosis Genetic Analysis Consortium. Populations variation of common cystic fibrosis mutations. Hum Mutat 1994;4:167-77.
-
(1994)
Hum Mutat
, vol.4
, pp. 167-177
-
-
-
10
-
-
0038663174
-
Effect of genotype on phenotype and mortality in cystic fibrosis: A retrospective cohort study
-
McKone EF, Emerson SS, Edwards KL, Aitken ML. Effect of genotype on phenotype and mortality in cystic fibrosis: a retrospective cohort study. Lancet 2003;361:1671-6.
-
(2003)
Lancet
, vol.361
, pp. 1671-1676
-
-
McKone, E.F.1
Emerson, S.S.2
Edwards, K.L.3
Aitken, M.L.4
-
11
-
-
0037049062
-
Fibrosis quística del adulto: Estudio de 111 pacientes
-
De Gracia J, Álvarez A, Mata F, Guarner M, Vendrell M, Gadtner S, et al. Fibrosis quística del adulto: estudio de 111 pacientes. Med Clin (Barc) 2002;1194:605-9.
-
(2002)
Med Clin (Barc)
, vol.1194
, pp. 605-609
-
-
De Gracia, J.1
Álvarez, A.2
Mata, F.3
Guarner, M.4
Vendrell, M.5
Gadtner, S.6
-
12
-
-
0034785481
-
Acceleration of lung disease in children with cystic fibrosis after Pseudomonas aeruginosa acquisition
-
Kosorok MR, Zeng L, West SE, Rock MJ, Splaingard ML, Laxova A, et al. Acceleration of lung disease in children with cystic fibrosis after Pseudomonas aeruginosa acquisition. Pediatr Pulmonol 2001;32:277-87.
-
(2001)
Pediatr Pulmonol
, vol.32
, pp. 277-287
-
-
Kosorok, M.R.1
Zeng, L.2
West, S.E.3
Rock, M.J.4
Splaingard, M.L.5
Laxova, A.6
-
13
-
-
12244306198
-
Risk factors for initial acquisition of Pseudomonas aeruginosa in children with cystic fibrosis identified by newborn screening
-
Maselli JH, Sontang MK, Norris JM, MacKenzie T, Wagener JS, Accurso FJ. Risk factors for initial acquisition of Pseudomonas aeruginosa in children with cystic fibrosis identified by newborn screening. Pediatr Pulmonol 2003;35:257-62.
-
(2003)
Pediatr Pulmonol
, vol.35
, pp. 257-262
-
-
Maselli, J.H.1
Sontang, M.K.2
Norris, J.M.3
MacKenzie, T.4
Wagener, J.S.5
Accurso, F.J.6
-
14
-
-
0032135143
-
Overproduction of the CFTR R domain leads to increased levels of asialoGM1 and increased Pseudomonas aeruginosa binding by epithelial cells
-
Bryan R, Kube D, Pérez A, Davis P, Prince A. Overproduction of the CFTR R domain leads to increased levels of asialoGM1 and increased Pseudomonas aeruginosa binding by epithelial cells. Am J Respir Cel Mol Biol 1998;19:269-77.
-
(1998)
Am J Respir Cel Mol Biol
, vol.19
, pp. 269-277
-
-
Bryan, R.1
Kube, D.2
Pérez, A.3
Davis, P.4
Prince, A.5
-
15
-
-
0028847778
-
Binding of Pseudomonas aeruginosa to respiratory epithelial cells from patients with various mutations in the cystic fibrosis transmembrane regulator
-
Zar H, Saiman L, Quittell L, Prince A. Binding of Pseudomonas aeruginosa to respiratory epithelial cells from patients with various mutations in the cystic fibrosis transmembrane regulator. J Pediatr 1995;126:230-3.
-
(1995)
J Pediatr
, vol.126
, pp. 230-233
-
-
Zar, H.1
Saiman, L.2
Quittell, L.3
Prince, A.4
-
16
-
-
0033827478
-
Longitudinal relationship among growth, nutritional status and pulmonary function in children with cystic fibrosis: Analysis of the Cystic Fibrosis Foundation National CF Patient Registry
-
Zemel BS, Jawad AF, FitzSimmons S, Stallings VA. Longitudinal relationship among growth, nutritional status and pulmonary function in children with cystic fibrosis: analysis of the Cystic Fibrosis Foundation National CF Patient Registry. J Pediatr 2000;137:374-80.
-
(2000)
J Pediatr
, vol.137
, pp. 374-380
-
-
Zemel, B.S.1
Jawad, A.F.2
FitzSimmons, S.3
Stallings, V.A.4
-
17
-
-
0036311232
-
Relationship between nutritional status and lung function in cystic fibrosis: Cross sectional and longitudinal analysis from the German CF quality assurance (CFQA) project
-
Steinkamp G, Wiedemann B, and behalf of the German CFQA Group. Relationship between nutritional status and lung function in cystic fibrosis: cross sectional and longitudinal analysis from the German CF quality assurance (CFQA) project. Thorax 2002;57:596-601.
-
(2002)
Thorax
, vol.57
, pp. 596-601
-
-
Steinkamp, G.1
Wiedemann, B.2
-
18
-
-
0036157692
-
Association between genetically determined pancreatic status and lung disease in adult cystic fibrosis patients
-
Loubières Y, Grenet D, Simon-Bouy B, Medioni J, Landais P, Férec C, et al. Association between genetically determined pancreatic status and lung disease in adult cystic fibrosis patients. Chest 2002;121:73-8.
-
(2002)
Chest
, vol.121
, pp. 73-78
-
-
Loubières, Y.1
Grenet, D.2
Simon-Bouy, B.3
Medioni, J.4
Landais, P.5
Férec, C.6
-
19
-
-
0032775756
-
Effect of elective antibiotic therapy on resting energy expenditure and inflammation in cystic fibrosis
-
Burdet L, Hugli O, Aubert JD, Schutz Y, Roulet M, Fitting JW. Effect of elective antibiotic therapy on resting energy expenditure and inflammation in cystic fibrosis. Eur J Pediatr 1999;158:711-6.
-
(1999)
Eur J Pediatr
, vol.158
, pp. 711-716
-
-
Burdet, L.1
Hugli, O.2
Aubert, J.D.3
Schutz, Y.4
Roulet, M.5
Fitting, J.W.6
-
20
-
-
0037326312
-
Glucose intolerance in children with cystic fibrosis
-
Solomon MP, Wilson DC, Corey M, Kalnins D, Zielenski J, Tsui LC, et al. Glucose intolerance in children with cystic fibrosis. J Pediatr 2003;142:128-32.
-
(2003)
J Pediatr
, vol.142
, pp. 128-132
-
-
Solomon, M.P.1
Wilson, D.C.2
Corey, M.3
Kalnins, D.4
Zielenski, J.5
Tsui, L.C.6
-
21
-
-
0034759112
-
Presence of cystic fibrosis-related diabetes mellitus is tightly linked to poor lung function in patients with cystic fibrosis: Data from the European Epidemiologic Registry of Cystic Fibrosis
-
Koch C, Rainisio M, Madessani U, Harms HK, Hodson ME, Mastella G, et al. Presence of cystic fibrosis-related diabetes mellitus is tightly linked to poor lung function in patients with cystic fibrosis: data from the European Epidemiologic Registry of Cystic Fibrosis. Pediatr Pulmonol 2001;32:343-50.
-
(2001)
Pediatr Pulmonol
, vol.32
, pp. 343-350
-
-
Koch, C.1
Rainisio, M.2
Madessani, U.3
Harms, H.K.4
Hodson, M.E.5
Mastella, G.6
-
22
-
-
0037390820
-
Median household income and mortality rate in cystic fibrosis
-
O'Connor GT, Quinton HB, Kneeland T, Kahn R, Lever T, Maddock J, et al. Median household income and mortality rate in cystic fibrosis. Pediatrics 2003;111:e333-9.
-
(2003)
Pediatrics
, vol.111
-
-
O'Connor, G.T.1
Quinton, H.B.2
Kneeland, T.3
Kahn, R.4
Lever, T.5
Maddock, J.6
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