-
1
-
-
0142074353
-
Nonclassic cystic fibrosis and CFTR-related diseases
-
Boyle M.P. Nonclassic cystic fibrosis and CFTR-related diseases. Curr Opin Pulm Med Nov 2003, 9(6):498-503.
-
(2003)
Curr Opin Pulm Med
, vol.9
, Issue.6
, pp. 498-503
-
-
Boyle, M.P.1
-
2
-
-
79958122789
-
Recommendations for the classification of diseases as CFTR-related disorders
-
Bombieri C., Claustres M., De Boeck K., Derichs N., Dodge J., Girodon E., et al. Recommendations for the classification of diseases as CFTR-related disorders. J Cyst Fibros Jun 2011, 10(Suppl. 2):S86-S102.
-
(2011)
J Cyst Fibros
, vol.10
, Issue.SUPPL. 2
-
-
Bombieri, C.1
Claustres, M.2
De Boeck, K.3
Derichs, N.4
Dodge, J.5
Girodon, E.6
-
3
-
-
33745809841
-
Cystic fibrosis: terminology and diagnostic algorithms
-
De Boeck K., Wilschanski M., Castellani C., Taylor C., Cuppens H., Dodge J., et al. Cystic fibrosis: terminology and diagnostic algorithms. Thorax Jul 2006, 61(7):627-635.
-
(2006)
Thorax
, vol.61
, Issue.7
, pp. 627-635
-
-
De Boeck, K.1
Wilschanski, M.2
Castellani, C.3
Taylor, C.4
Cuppens, H.5
Dodge, J.6
-
4
-
-
68049096166
-
Phenotypic characterisation of patients with intermediate sweat chloride values: towards validation of the European diagnostic algorithm for cystic fibrosis
-
Goubau C., Wilschanski M., Skalicka V., Lebecque P., Southern K.W., Sermet I., et al. Phenotypic characterisation of patients with intermediate sweat chloride values: towards validation of the European diagnostic algorithm for cystic fibrosis. Thorax Aug 2009, 64(8):683-691.
-
(2009)
Thorax
, vol.64
, Issue.8
, pp. 683-691
-
-
Goubau, C.1
Wilschanski, M.2
Skalicka, V.3
Lebecque, P.4
Southern, K.W.5
Sermet, I.6
-
5
-
-
47049115524
-
Guidelines for diagnosis of cystic fibrosis in newborns through older adults: Cystic Fibrosis Foundation consensus report
-
Farrell P.M., Rosenstein B.J., White T.B., Accurso F.J., Castellani C., Cutting G.R., et al. Guidelines for diagnosis of cystic fibrosis in newborns through older adults: Cystic Fibrosis Foundation consensus report. J Pediatr Aug 2008, 153(2):S4-S14.
-
(2008)
J Pediatr
, vol.153
, Issue.2
-
-
Farrell, P.M.1
Rosenstein, B.J.2
White, T.B.3
Accurso, F.J.4
Castellani, C.5
Cutting, G.R.6
-
6
-
-
84878127369
-
CFTR2: how will it help care?
-
Castellani C. CFTR2: how will it help care?. Paediatr Respir Rev May 2013, 14(Suppl. 1):2-5.
-
(2013)
Paediatr Respir Rev
, vol.14
, Issue.SUPPL. 1
, pp. 2-5
-
-
Castellani, C.1
-
7
-
-
4644361735
-
Cystic fibrosis population carrier screening: 2004 revision of American College of Medical Genetics mutation panel
-
Watson M.S., Cutting G.R., Desnick R.J., Driscoll D.A., Klinger K., Mennuti M., et al. Cystic fibrosis population carrier screening: 2004 revision of American College of Medical Genetics mutation panel. Genet Med Sep 2004, 6(5):387-391.
-
(2004)
Genet Med
, vol.6
, Issue.5
, pp. 387-391
-
-
Watson, M.S.1
Cutting, G.R.2
Desnick, R.J.3
Driscoll, D.A.4
Klinger, K.5
Mennuti, M.6
-
8
-
-
0027551290
-
Pulmonary function between 6 and 18years of age
-
Wang X., Dockery D.W., Wypij D., Fay M.E., Ferris B.G. Pulmonary function between 6 and 18years of age. Pediatr Pulmonol Feb 1993, 15(2):75-88.
-
(1993)
Pediatr Pulmonol
, vol.15
, Issue.2
, pp. 75-88
-
-
Wang, X.1
Dockery, D.W.2
Wypij, D.3
Fay, M.E.4
Ferris, B.G.5
-
9
-
-
0032926069
-
Spirometric reference values from a sample of the general U.S. population
-
Hankinson J.L., Odencrantz J.R., Fedan K.B. Spirometric reference values from a sample of the general U.S. population. Am J Respir Crit Care Med Jan 1999, 159(1):179-187.
-
(1999)
Am J Respir Crit Care Med
, vol.159
, Issue.1
, pp. 179-187
-
-
Hankinson, J.L.1
Odencrantz, J.R.2
Fedan, K.B.3
-
10
-
-
0038102859
-
Evaluation of a new definition for chronic Pseudomonas aeruginosa infection in cystic fibrosis patients
-
Lee T.W., Brownlee K.G., Conway S.P., Denton M., Littlewood J.M. Evaluation of a new definition for chronic Pseudomonas aeruginosa infection in cystic fibrosis patients. J Cyst Fibros Mar 2003, 2(1):29-34.
-
(2003)
J Cyst Fibros
, vol.2
, Issue.1
, pp. 29-34
-
-
Lee, T.W.1
Brownlee, K.G.2
Conway, S.P.3
Denton, M.4
Littlewood, J.M.5
-
11
-
-
84880044346
-
A new era in the treatment of cystic fibrosis: correction of underlying the CFTR defect
-
Boyle M.P., De Boeck K. A new era in the treatment of cystic fibrosis: correction of underlying the CFTR defect. Lancet Resp Med 2013, 1:158-163.
-
(2013)
Lancet Resp Med
, vol.1
, pp. 158-163
-
-
Boyle, M.P.1
De Boeck, K.2
-
13
-
-
84897111733
-
-
Cystic Fibrosis Australia
-
Cystic Fibrosis Australia Annual report Australian Cystic Fibrosis Data Registry 2011 http://www.cysticfibrosis.org.au/media/wysiwyg/CF-Australia/medical-documents/ACFDR_2011/ACFDR_2011_Report.pdf.
-
Annual report Australian Cystic Fibrosis Data Registry 2011
-
-
-
15
-
-
33750949242
-
Immunoreactive trypsin/DNA newborn screening for cystic fibrosis: should the R117H variant be included in CFTR mutation panels?
-
Scotet V., Audrezet M.P., Roussey M., Rault G., Dirou-Prigent A., Journel H., et al. Immunoreactive trypsin/DNA newborn screening for cystic fibrosis: should the R117H variant be included in CFTR mutation panels?. Pediatrics Nov 2006, 118(5):e1523-e1529.
-
(2006)
Pediatrics
, vol.118
, Issue.5
-
-
Scotet, V.1
Audrezet, M.P.2
Roussey, M.3
Rault, G.4
Dirou-Prigent, A.5
Journel, H.6
-
16
-
-
84870727190
-
Misdiagnosis of cystic fibrosis: experience from Germany
-
Naehrlich L., Bagheri-Behrouzi A. Misdiagnosis of cystic fibrosis: experience from Germany. J Cyst Fibros Jan 2013, 12(1):68-73.
-
(2013)
J Cyst Fibros
, vol.12
, Issue.1
, pp. 68-73
-
-
Naehrlich, L.1
Bagheri-Behrouzi, A.2
|