-
1
-
-
0032913809
-
Physiological basis of cystic fibrosis: A historical perspective
-
Quinton PM. Physiological basis of cystic fibrosis: a historical perspective. Physiol Rev 1999; 79(1 Suppl):3-22.
-
(1999)
Physiol Rev
, vol.79
, Issue.1 SUPPL.
, pp. 3-22
-
-
Quinton, P.M.1
-
2
-
-
33645130994
-
Cystic fibrosis since 1938
-
Davis PB. Cystic fibrosis since 1938. Am J Respir Crit Care Med 2006; 173:475-82.
-
(2006)
Am J Respir Crit Care Med
, vol.173
, pp. 475-482
-
-
Davis, P.B.1
-
3
-
-
84920211040
-
Abnormal electrolyte composition of sweat in cystic fibrosis of the pancreas; clinical significance and relationship to the disease
-
Di Sant'agnese PA, Darling RC, Perera GA, Shea E. Abnormal electrolyte composition of sweat in cystic fibrosis of the pancreas; clinical significance and relationship to the disease. Pediatrics 1953; 12:549-63.
-
(1953)
Pediatrics
, vol.12
, pp. 549-563
-
-
Di Sant'agnese, P.A.1
Darling, R.C.2
Perera, G.A.3
Shea, E.4
-
4
-
-
9244225677
-
A test for concentration of electrolytes in sweat in cystic fibrosis of the pancreas utilizing pilocarpine by iontophoresis
-
Gibson LE, Cooke RE. A test for concentration of electrolytes in sweat in cystic fibrosis of the pancreas utilizing pilocarpine by iontophoresis. Pediatrics 1959; 23:545-9.
-
(1959)
Pediatrics
, vol.23
, pp. 545-549
-
-
Gibson, L.E.1
Cooke, R.E.2
-
5
-
-
0018769118
-
Dried-blood spot screening for cystic fibrosis in the newborn
-
Crossley JR, Elliott RB, Smith PA. Dried-blood spot screening for cystic fibrosis in the newborn. Lancet 1979; 1:472-4.
-
(1979)
Lancet
, vol.1
, pp. 472-474
-
-
Crossley, J.R.1
Elliott, R.B.2
Smith, P.A.3
-
6
-
-
0019955460
-
Suggestion of abnormal anion exchange mechanism in sweat glands of cystic fibrosis patients
-
Quinton PM. Suggestion of abnormal anion exchange mechanism in sweat glands of cystic fibrosis patients. Pediatr Res 1982; 16:533-7.
-
(1982)
Pediatr Res
, vol.16
, pp. 533-537
-
-
Quinton, P.M.1
-
7
-
-
0024424270
-
Identification of the cystic fibrosis gene: Cloning and characterization of complementary DNA
-
Riordan JR, Rommens JM, Kerem B, Alon N, Rozmahel R, 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, R.5
Grzelczak, Z.6
-
8
-
-
0024423668
-
Identification of the cystic fibrosis gene: Genetic analysis
-
Kerem B, Rommens JM, Buchanan JA, Markiewicz D, Cox TK, Chakravarti A, et al. Identification of the cystic fibrosis gene: genetic analysis. Science 1989; 245:1073-80.
-
(1989)
Science
, vol.245
, pp. 1073-1080
-
-
Kerem, B.1
Rommens, J.M.2
Buchanan, J.A.3
Markiewicz, D.4
Cox, T.K.5
Chakravarti, A.6
-
9
-
-
0024453308
-
Identification of the cystic fibrosis gene: Chromosome walking and jumping
-
Rommens JM, Iannuzzi MC, Kerem B, Drumm ML, Melmer G, Dean M, et al. Identification of the cystic fibrosis gene: chromosome walking and jumping. Science 1989; 245:1059-65.
-
(1989)
Science
, vol.245
, pp. 1059-1065
-
-
Rommens, J.M.1
Iannuzzi, M.C.2
Kerem, B.3
Drumm, M.L.4
Melmer, G.5
Dean, M.6
-
10
-
-
0036120193
-
The cystic fibrosis transmembrane conductance regulator: An intriguing protein with pleiotropic functions
-
Vankeerberghen A, Cuppens H, Cassiman JJ. The cystic fibrosis transmembrane conductance regulator: an intriguing protein with pleiotropic functions. J Cyst Fibros 2002; 1:13-29.
-
(2002)
J Cyst Fibros
, vol.1
, pp. 13-29
-
-
Vankeerberghen, A.1
Cuppens, H.2
Cassiman, J.J.3
-
11
-
-
28344435948
-
Programa de triagem neonatal para fibrose cística no estado do Paraná: Avaliação após 30 meses de sua implantação.
-
Santos G P, Domingos MT, Witting EO, Riedi CA, Rosario NA. Programa de triagem neonatal para fibrose cística no estado do Paraná: avaliação após 30 meses de sua implantação. J Pediatr (Rio J) 2005; 81:240-4.
-
(2005)
J Pediatr (Rio J)
, vol.81
, pp. 240-244
-
-
Santos, G.P.1
Domingos, M.T.2
Witting, E.O.3
Riedi, C.A.4
Rosario, N.A.5
-
12
-
-
52949124602
-
Avaliação da triagem neonatal para fibrose cística no Estado de Santa Catarina.
-
Honorio LFO, Ludwig Neto N, Barbosa E, Perin N, Gastaldi LA, Ferreira JE, et al. Avaliação da triagem neonatal para fibrose cística no Estado de Santa Catarina. J Bras Pneumol 2006; 32(1 Suppl):1-16.
-
(2006)
J Bras Pneumol
, vol.32
, Issue.1 SUPPL.
, pp. 1-16
-
-
Honorio, L.F.O.1
Ludwig Neto, N.2
Barbosa, E.3
Perin, N.4
Gastaldi, L.A.5
Ferreira, J.E.6
-
13
-
-
85069419020
-
-
Reis F, Melo SO, Vergara AA. Programa de triagem neonatal para fibrose cística de Minas Gerais (PETN-FIBROSE CÍSTICA): aspectos clínicos e laboratoriais. J Bras Pneumol 2006; 32(1 Suppl):1-16.
-
Reis F, Melo SO, Vergara AA. Programa de triagem neonatal para fibrose cística de Minas Gerais (PETN-FIBROSE CÍSTICA): aspectos clínicos e laboratoriais. J Bras Pneumol 2006; 32(1 Suppl):1-16.
-
-
-
-
15
-
-
0025994882
-
Molecular genetics of cystic fibrosis
-
Tsui LC, Rommens J, Kerem B, Rozmahel R, Ziolenski J, Kennedy D, et al. Molecular genetics of cystic fibrosis. Adv Exp Med Biol 1991; 290:9-17.
-
(1991)
Adv Exp Med Biol
, vol.290
, pp. 9-17
-
-
Tsui, L.C.1
Rommens, J.2
Kerem, B.3
Rozmahel, R.4
Ziolenski, J.5
Kennedy, D.6
-
17
-
-
0036209027
-
Improvements of lung function in cystic fibrosis
-
Tauber E, Eichler I, Gartner C, Halmerbauer G, Gotz M, Rath R, et al. Improvements of lung function in cystic fibrosis. Pediatr Pulmonol 2002; 33:263-8.
-
(2002)
Pediatr Pulmonol
, vol.33
, pp. 263-268
-
-
Tauber, E.1
Eichler, I.2
Gartner, C.3
Halmerbauer, G.4
Gotz, M.5
Rath, R.6
-
18
-
-
0035122157
-
European Epidemiologic Registry of Cystic Fibrosis (ERCF): Comparison of major disease manifestations between patients with different classes of mutations
-
Koch C, Cuppens H, Rainisio M, Madessani U, Harms H, Hodson M, et al. European Epidemiologic Registry of Cystic Fibrosis (ERCF): comparison of major disease manifestations between patients with different classes of mutations. Pediatr Pulmonol 2001; 31:1-12.
-
(2001)
Pediatr Pulmonol
, vol.31
, pp. 1-12
-
-
Koch, C.1
Cuppens, H.2
Rainisio, M.3
Madessani, U.4
Harms, H.5
Hodson, M.6
-
19
-
-
0035460651
-
Liver disease in cystic fibrosis
-
Tombazzi CR, Riely CA. Liver disease in cystic fibrosis. Rev Med Chil 2001; 129:1071-8.
-
(2001)
Rev Med Chil
, vol.129
, pp. 1071-1078
-
-
Tombazzi, C.R.1
Riely, C.A.2
-
20
-
-
0028229223
-
The origin of the major cystic fibrosis mutation (delta F508) in European populations
-
Morral N, Bertranpetit J, Estivill X, Nunes V, Casals T, Gimenez J, et al. The origin of the major cystic fibrosis mutation (delta F508) in European populations. Nat Genet 1994; 7:169-75.
-
(1994)
Nat Genet
, vol.7
, pp. 169-175
-
-
Morral, N.1
Bertranpetit, J.2
Estivill, X.3
Nunes, V.4
Casals, T.5
Gimenez, J.6
-
21
-
-
0027303876
-
DNA analysis of cystic fibrosis in Brazil by direct PCR amplification from Guthrie cards
-
Raskin S, Phillips 3rd JA, Krishnamani MR, Vnencak-Jones C, Parker RA, Rozov T, et al. DNA analysis of cystic fibrosis in Brazil by direct PCR amplification from Guthrie cards. Am J Med Genet 1993; 46:665-9.
-
(1993)
Am J Med Genet
, vol.46
, pp. 665-669
-
-
Raskin, S.1
Phillips 3rd, J.A.2
Krishnamani, M.R.3
Vnencak-Jones, C.4
Parker, R.A.5
Rozov, T.6
-
22
-
-
38049007046
-
Incidence of cystic fibrosis in five different states of Brazil as determined by screening of p.F508del, mutation at the CFTR gene in newborns and patients
-
Raskin S, Pereira-Ferrari L, Caldeira-Reis F, Abreu F, Marostica P, Rozov T, et al. Incidence of cystic fibrosis in five different states of Brazil as determined by screening of p.F508del, mutation at the CFTR gene in newborns and patients. J Cyst Fibros 2008; 7:15-22.
-
(2008)
J Cyst Fibros
, vol.7
, pp. 15-22
-
-
Raskin, S.1
Pereira-Ferrari, L.2
Caldeira-Reis, F.3
Abreu, F.4
Marostica, P.5
Rozov, T.6
-
23
-
-
0027674061
-
Frequency of the cystic fibrosis DF508 mutation in a population from São Paulo State, Brazil
-
Martins CSB, Ribeiro A F, Costa F F. Frequency of the cystic fibrosis DF508 mutation in a population from São Paulo State, Brazil. Braz J Med Biol Res 1993; 26:1037-40.
-
(1993)
Braz J Med Biol Res
, vol.26
, pp. 1037-1040
-
-
Martins, C.S.B.1
Ribeiro, A.F.2
Costa, F.F.3
-
24
-
-
0030805248
-
Molecular characterization of cystic fibrosis patients in the state of São Paulo (Brazil)
-
Parizotto EA, Bertuzzo CS. Molecular characterization of cystic fibrosis patients in the state of São Paulo (Brazil). J Med Genet 1997; 34:877-82.
-
(1997)
J Med Genet
, vol.34
, pp. 877-882
-
-
Parizotto, E.A.1
Bertuzzo, C.S.2
-
25
-
-
36348945237
-
Aspectos genéticos da fibrose cística
-
Carakushansky G, organizador, São Paulo: Editora Guanabara Koogan;
-
Raskin S, Faucz FR. Aspectos genéticos da fibrose cística. In: Carakushansky G, organizador. Doenças genéticas em pediatria. São Paulo: Editora Guanabara Koogan; 2001. p. 227-42.
-
(2001)
Doenças genéticas em pediatria
, pp. 227-242
-
-
Raskin, S.1
Faucz, F.R.2
-
26
-
-
14044255855
-
Prevalence of deltaF508, G551D, G542X, and R553X mutations among cystic fibrosis patients in the North of Brazil
-
Araujo FG, Novaes FC, Santos N P, Martins VC, Souza SM, Santos SE, et al. Prevalence of deltaF508, G551D, G542X, and R553X mutations among cystic fibrosis patients in the North of Brazil. Braz J Med Biol Res 2005; 38:11-5.
-
(2005)
Braz J Med Biol Res
, vol.38
, pp. 11-15
-
-
Araujo, F.G.1
Novaes, F.C.2
Santos, N.P.3
Martins, V.C.4
Souza, S.M.5
Santos, S.E.6
-
27
-
-
0033118948
-
Cystic fibrosis: Low frequency of DF508 mutation in 2 population samples from Rio de Janeiro, Brazil
-
Cabello GM, Moreira A F, Horovitz D, Correia P, Santa Rosa A, Llerena Jr. J, et al. Cystic fibrosis: low frequency of DF508 mutation in 2 population samples from Rio de Janeiro, Brazil. Hum Biol 1999; 71:189-96.
-
(1999)
Hum Biol
, vol.71
, pp. 189-196
-
-
Cabello, G.M.1
Moreira, A.F.2
Horovitz, D.3
Correia, P.4
Santa Rosa, A.5
Llerena Jr., J.6
-
28
-
-
0033083982
-
Geographic heterogeneity of 4 common worldwide cystic fibrosis non-DF508 mutations in Brazil
-
Raskin S, Phillips JA, Kaplan G, McClure M, Vnencak-Jones C, Rozov T, et al. Geographic heterogeneity of 4 common worldwide cystic fibrosis non-DF508 mutations in Brazil. Hum Biol 1999; 71: 111-21.
-
(1999)
Hum Biol
, vol.71
, pp. 111-121
-
-
Raskin, S.1
Phillips, J.A.2
Kaplan, G.3
McClure, M.4
Vnencak-Jones, C.5
Rozov, T.6
-
29
-
-
21744454837
-
Molecular analysis of 23 exons of the CFTR gene in Brazilian patients leads to the finding of rare cystic fibrosis mutations
-
Cabello GM, Cabello PH, Otsuki K, Gombarovits ME, Llerena Jr. JC, Fernandes O. Molecular analysis of 23 exons of the CFTR gene in Brazilian patients leads to the finding of rare cystic fibrosis mutations. Hum Biol 2005; 77:125-35.
-
(2005)
Hum Biol
, vol.77
, pp. 125-135
-
-
Cabello, G.M.1
Cabello, P.H.2
Otsuki, K.3
Gombarovits, M.E.4
Llerena Jr., J.C.5
Fernandes, O.6
-
30
-
-
34548133576
-
Cystic fibrosis in a southern Brazilian population: Characteristics of 90% of the alleles
-
Faucz FR, Gimenez J, Ramos MD, Pereira-Ferrari L, Estivill X, Raskin S, et al. Cystic fibrosis in a southern Brazilian population: characteristics of 90% of the alleles. Clin Genet 2007; 72:218-23.
-
(2007)
Clin Genet
, vol.72
, pp. 218-223
-
-
Faucz, F.R.1
Gimenez, J.2
Ramos, M.D.3
Pereira-Ferrari, L.4
Estivill, X.5
Raskin, S.6
-
31
-
-
0034743399
-
The 3120+1G→Asplicing mutation in CFTR is common in Brazilian cystic fibrosis patients
-
Cabello GMK, Cabello PH, Llerena Jr. J, Fernandes O, Harris A. The 3120+1G→Asplicing mutation in CFTR is common in Brazilian cystic fibrosis patients. Hum Biol 2001; 73:403-9.
-
(2001)
Hum Biol
, vol.73
, pp. 403-409
-
-
Cabello, G.M.K.1
Cabello, P.H.2
Llerena Jr., J.3
Fernandes, O.4
Harris, A.5
-
32
-
-
0036175259
-
Mechanisms and markers of airway inflammation in cystic fibrosis
-
De Rose V. Mechanisms and markers of airway inflammation in cystic fibrosis. Eur Respir J 2002; 19:333-40.
-
(2002)
Eur Respir J
, vol.19
, pp. 333-340
-
-
De Rose, V.1
-
33
-
-
0036866333
-
Controversies in cystic fibrosis-from pediatrician to specialist
-
Ribeiro JD, Ribeiro MA, Ribeiro AF. Controversies in cystic fibrosis-from pediatrician to specialist. J Pediatr (Rio J) 2002; 78(2 Suppl):171-85.
-
(2002)
J Pediatr (Rio J)
, vol.78
, Issue.2 SUPPL.
, pp. 171-185
-
-
Ribeiro, J.D.1
Ribeiro, M.A.2
Ribeiro, A.F.3
-
34
-
-
0035172675
-
The impact of meconium ileus on the clinical course of children with cystic fibrosis
-
Evans AK, Fitzgerald DA, McKay KO. The impact of meconium ileus on the clinical course of children with cystic fibrosis. Eur Respir J 2001; 18:784-9.
-
(2001)
Eur Respir J
, vol.18
, pp. 784-789
-
-
Evans, A.K.1
Fitzgerald, D.A.2
McKay, K.O.3
-
37
-
-
0344233251
-
Newborn screening for cystic fibrosis: Ensuring more good than harm
-
Farrell MH, Farrell PM. Newborn screening for cystic fibrosis: ensuring more good than harm. J Pediatr 2003; 143:707-12.
-
(2003)
J Pediatr
, vol.143
, pp. 707-712
-
-
Farrell, M.H.1
Farrell, P.M.2
-
38
-
-
0345169973
-
Newborn screening methods for cystic fibrosis
-
Wilcken B, Wiley V. Newborn screening methods for cystic fibrosis. Paediatr Respir Rev 2003; 4: 272-7.
-
(2003)
Paediatr Respir Rev
, vol.4
, pp. 272-277
-
-
Wilcken, B.1
Wiley, V.2
-
39
-
-
33845933518
-
A survey of newborn screening for cystic fibrosis in Europe
-
Southern KW, Munck A, Pollitt R, Travert G, Zanolla L, Dankert-Roelse J, et al. A survey of newborn screening for cystic fibrosis in Europe. J Cyst Fibros 2007; 6:57-65.
-
(2007)
J Cyst Fibros
, vol.6
, pp. 57-65
-
-
Southern, K.W.1
Munck, A.2
Pollitt, R.3
Travert, G.4
Zanolla, L.5
Dankert-Roelse, J.6
-
40
-
-
0025281614
-
Newborn screening for cystic fibrosis is complicated by age-related decline in immunoreactive trypsinogen levels
-
Rock MJ, Mischler EH, Farrell PM, Wei LJ, Bruns WT, Hassemer DJ, et al. Newborn screening for cystic fibrosis is complicated by age-related decline in immunoreactive trypsinogen levels. Pediatrics 1990; 85:1001-7.
-
(1990)
Pediatrics
, vol.85
, pp. 1001-1007
-
-
Rock, M.J.1
Mischler, E.H.2
Farrell, P.M.3
Wei, L.J.4
Bruns, W.T.5
Hassemer, D.J.6
-
42
-
-
0029558007
-
Neonatal screening for cystic fibrosis: A comparison of two strategies for case detection in 1.2 million babies
-
Wilcken B, Wiley V, Sherry G, Bayliss U. Neonatal screening for cystic fibrosis: a comparison of two strategies for case detection in 1.2 million babies. J Pediatr 1995; 127:965-70.
-
(1995)
J Pediatr
, vol.127
, pp. 965-970
-
-
Wilcken, B.1
Wiley, V.2
Sherry, G.3
Bayliss, U.4
-
43
-
-
25844445259
-
Newborn screening for cystic fibrosis in Wisconsin: Nine-year experience with routine trypsinogen/DNA testing
-
Rock MJ, Hoffman G, Laessig RH, Kopish GJ, Litsheim TJ, Farrell PM. Newborn screening for cystic fibrosis in Wisconsin: nine-year experience with routine trypsinogen/DNA testing. J Pediatr 2005; 147(3 Suppl):73-7.
-
(2005)
J Pediatr
, vol.147
, Issue.3 SUPPL.
, pp. 73-77
-
-
Rock, M.J.1
Hoffman, G.2
Laessig, R.H.3
Kopish, G.J.4
Litsheim, T.J.5
Farrell, P.M.6
-
44
-
-
0031402353
-
Neonatal screening for cystic fibrosis in the Trent region (UK): Two-stage immunoreactive trypsin screening compared with a three-stage protocol with DNA analysis as an intermediate step
-
Pollitt RJ, Dalton A, Evans S, Hughes HN, Curtis D. Neonatal screening for cystic fibrosis in the Trent region (UK): two-stage immunoreactive trypsin screening compared with a three-stage protocol with DNA analysis as an intermediate step. J Med Screen 1997; 4:23-8.
-
(1997)
J Med Screen
, vol.4
, pp. 23-28
-
-
Pollitt, R.J.1
Dalton, A.2
Evans, S.3
Hughes, H.N.4
Curtis, D.5
-
45
-
-
0033066151
-
Blood concentrations of pancreatitis associated protein in neonates: Relevance to neonatal screening for cystic fibrosis
-
Sarles J, Barthellemy S, Ferec C, Iovanna J, Roussey M, Farriaux JP, et al. Blood concentrations of pancreatitis associated protein in neonates: relevance to neonatal screening for cystic fibrosis. Arch Dis Child Fetal Neonatal Ed 1999; 80:F118-22.
-
(1999)
Arch Dis Child Fetal Neonatal Ed
, vol.80
-
-
Sarles, J.1
Barthellemy, S.2
Ferec, C.3
Iovanna, J.4
Roussey, M.5
Farriaux, J.P.6
-
46
-
-
0030921031
-
Newborn screening strategy for cystic fibrosis: A field study in an area with high allelic heterogeneity
-
Castellani C, Bonizzato A, Cabrini G, Mastella G. Newborn screening strategy for cystic fibrosis: a field study in an area with high allelic heterogeneity. Acta Paediatr 1997; 86:497-502.
-
(1997)
Acta Paediatr
, vol.86
, pp. 497-502
-
-
Castellani, C.1
Bonizzato, A.2
Cabrini, G.3
Mastella, G.4
-
47
-
-
0345169959
-
Newborn screening programmes for cystic fibrosis
-
Southern KW, Littlewood JM. Newborn screening programmes for cystic fibrosis. Paediatr Respir Rev 2003; 4:299-305.
-
(2003)
Paediatr Respir Rev
, vol.4
, pp. 299-305
-
-
Southern, K.W.1
Littlewood, J.M.2
-
48
-
-
0030803131
-
Nutritional benefits of neonatal screening for cystic fibrosis. Wisconsin Cystic Fibrosis Neonatal Screening Study Group
-
Farrell PM, Kosorok MR, Laxova A, Shen G, Koscik RE, Bruns W T, et al. Nutritional benefits of neonatal screening for cystic fibrosis. Wisconsin Cystic Fibrosis Neonatal Screening Study Group. N Engl J Med 1997; 337:963-9.
-
(1997)
N Engl J Med
, vol.337
, pp. 963-969
-
-
Farrell, P.M.1
Kosorok, M.R.2
Laxova, A.3
Shen, G.4
Koscik, R.E.5
Bruns, W.T.6
-
49
-
-
18044402585
-
Neonatal screening for cystic fibrosis: Long-term clinical balance
-
Mastella G, Zanolla L, Castellani C, Altieri S, Fur-nari M, Giglio L, et al. Neonatal screening for cystic fibrosis: long-term clinical balance. Pancreatology 2001; 1:531-7.
-
(2001)
Pancreatology
, vol.1
, pp. 531-537
-
-
Mastella, G.1
Zanolla, L.2
Castellani, C.3
Altieri, S.4
Fur-nari, M.5
Giglio, L.6
-
50
-
-
33846910543
-
United Kingdom cystic fibrosis diagnosed after 2 months of age leads to worse outcomes and requires more therapy
-
Sims EJ, Clark A, McCormick J, Mehta G, Connett G, Mehta A. United Kingdom cystic fibrosis diagnosed after 2 months of age leads to worse outcomes and requires more therapy. Pediatrics 2007; 119:19-28.
-
(2007)
Pediatrics
, vol.119
, pp. 19-28
-
-
Sims, E.J.1
Clark, A.2
McCormick, J.3
Mehta, G.4
Connett, G.5
Mehta, A.6
-
51
-
-
0344234470
-
Evidence for newborn screening for cystic fibrosis
-
Castellani C. Evidence for newborn screening for cystic fibrosis. Paediatr Respir Rev 2003; 4:278-84.
-
(2003)
Paediatr Respir Rev
, vol.4
, pp. 278-284
-
-
Castellani, C.1
-
52
-
-
0037667617
-
Cystic fibrosis: Current trends in respiratory care
-
Wagener JS, Headley AA. Cystic fibrosis: current trends in respiratory care. Respir Care 2003; 48:234-45.
-
(2003)
Respir Care
, vol.48
, pp. 234-245
-
-
Wagener, J.S.1
Headley, A.A.2
-
53
-
-
0033016804
-
Screening for cystic fibrosis
-
Murray J, Cuckle H, Taylor G, Littlewood J, Hewison J. Screening for cystic fibrosis. Health Technol Assess 1999; 3:i-iv, 1-104.
-
(1999)
Health Technol Assess
, vol.3
, Issue.I-IV
, pp. 1-104
-
-
Murray, J.1
Cuckle, H.2
Taylor, G.3
Littlewood, J.4
Hewison, J.5
-
54
-
-
0034887898
-
Influence of neonatal screening and centralized treatment on long-term clinical outcome and survival of CF patients
-
Merelle ME, Schouten J P, Gerritsen J, Dankert-Ro-else JE. Influence of neonatal screening and centralized treatment on long-term clinical outcome and survival of CF patients. Eur Respir J 2001; 18:306-15.
-
(2001)
Eur Respir J
, vol.18
, pp. 306-315
-
-
Merelle, M.E.1
Schouten, J.P.2
Gerritsen, J.3
Dankert-Ro-else, J.E.4
-
55
-
-
4944235029
-
Newborn screening for cystic fibrosis: Evaluation of benefits and risks and recommendations for state newborn screening programs
-
Grosse SD, Boyle CA, Botkin JR, Comeau AM, Kharrazi M, Rosenfeld M, et al. Newborn screening for cystic fibrosis: evaluation of benefits and risks and recommendations for state newborn screening programs. MMWR Recomm Rep 2004; 53(RR-13):1-36.
-
(2004)
MMWR Recomm Rep
, vol.53
, Issue.RR-13
, pp. 1-36
-
-
Grosse, S.D.1
Boyle, C.A.2
Botkin, J.R.3
Comeau, A.M.4
Kharrazi, M.5
Rosenfeld, M.6
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