-
1
-
-
33749444308
-
Incidence and prevalence of idiopathic pulmonary fibrosis
-
DOI 10.1164/rccm.200602-163OC
-
Raghu G, Weycker D, Edelsberg J, Bradford WZ, Oster G. Incidence and prevalence of idiopathic pulmonary fibrosis. Am J Respir Crit Care Med. 2006;174(7):810-816. (Pubitemid 44511663)
-
(2006)
American Journal of Respiratory and Critical Care Medicine
, vol.174
, Issue.7
, pp. 810-816
-
-
Raghu, G.1
Weycker, D.2
Edelsberg, J.3
Bradford, W.Z.4
Oster, G.5
-
2
-
-
0037080547
-
American Thoracic Society/European Respiratory Society International Multidisciplinary Consensus Classification of the Idiopathic Interstitial Pneumonias. This joint statement of the American Thoracic Society (ATS), and the European Respiratory Society (ERS) was adopted by the ATS board of directors, June 2001 and by the ERS Executive Committee, June 2001
-
American Thoracic Society; European Respiratory Society
-
American Thoracic Society; European Respiratory Society. American Thoracic Society/European Respiratory Society International Multidisciplinary Consensus Classification of the Idiopathic Interstitial Pneumonias. This joint statement of the American Thoracic Society (ATS), and the European Respiratory Society (ERS) was adopted by the ATS board of directors, June 2001 and by the ERS Executive Committee, June 2001. Am J Respir Crit Care Med. 2002;165(2):277-304.
-
(2002)
Am J Respir Crit Care Med.
, vol.165
, Issue.2
, pp. 277-304
-
-
-
3
-
-
0034018105
-
Adult familial cryptogenic fibrosing alveolitis in the United Kingdom
-
DOI 10.1136/thorax.55.2.143
-
Marshall RP, Puddicombe A, Cookson WO, Laurent GJ. Adult familial cryptogenic fibrosing alveolitis in the United Kingdom. Thorax. 2000;55(2):143-146. (Pubitemid 30245956)
-
(2000)
Thorax
, vol.55
, Issue.2
, pp. 143-146
-
-
Marshall, R.P.1
Puddicombe, A.2
Cookson, W.O.C.3
Laurent, G.J.4
-
4
-
-
34250614359
-
Adult-onset pulmonary fibrosis caused by mutations in telomerase
-
DOI 10.1073/pnas.0701009104
-
Tsakiri KD, Cronkhite JT, Kuan PJ, et al. Adult-onset pulmonary fibrosis caused by mutations in telomerase. Proc Natl Acad Sci U S A. 2007;104(18):7552-7557. (Pubitemid 47185944)
-
(2007)
Proceedings of the National Academy of Sciences of the United States of America
, vol.104
, Issue.18
, pp. 7552-7557
-
-
Tsakiri, K.D.1
Cronkhite, J.T.2
Kuan, P.J.3
Xing, C.4
Raghu, G.5
Weissler, J.C.6
Rosenblatt, R.L.7
Shay, J.W.8
Garcia, C.K.9
-
5
-
-
52749083873
-
Telomere shortening in familial and sporadic pulmonary fibrosis
-
Cronkhite JT, Xing C, Raghu G, et al. Telomere shortening in familial and sporadic pulmonary fibrosis. Am J Respir Crit Care Med. 2008;178(7):729-737.
-
(2008)
Am J Respir Crit Care Med.
, vol.178
, Issue.7
, pp. 729-737
-
-
Cronkhite, J.T.1
Xing, C.2
Raghu, G.3
-
6
-
-
51349113450
-
Short telomeres are a risk factor for idiopathic pulmonary fibrosis
-
Alder JK, Chen JJ, Lancaster L, et al. Short telomeres are a risk factor for idiopathic pulmonary fibrosis. Proc Natl Acad Sci U S A. 2008;105(35):13051-13056.
-
(2008)
Proc Natl Acad Sci U S A.
, vol.105
, Issue.35
, pp. 13051-13056
-
-
Alder, J.K.1
Chen, J.J.2
Lancaster, L.3
-
7
-
-
77956289135
-
Telomere lengths, pulmonary fibrosis and telomerase (TERT) mutations
-
Diaz de Leon A, Cronkhite JT, Katzenstein AL, et al. Telomere lengths, pulmonary fibrosis and telomerase (TERT) mutations. PLoS ONE. 2010;5(5):e10680.
-
(2010)
PLoS ONE.
, vol.5
, Issue.5
-
-
Diaz De Leon, A.1
Cronkhite, J.T.2
Katzenstein, A.L.3
-
8
-
-
58149159548
-
Genetic defects in surfactant protein A2 are associated with pulmonary fibrosis and lung cancer
-
Wang Y, Kuan PJ, Xing C, et al. Genetic defects in surfactant protein A2 are associated with pulmonary fibrosis and lung cancer. Am J Hum Genet. 2009;84(1):52-59.
-
(2009)
Am J Hum Genet.
, vol.84
, Issue.1
, pp. 52-59
-
-
Wang, Y.1
Kuan, P.J.2
Xing, C.3
-
9
-
-
0036570052
-
Heterozygosity for a surfactant protein C gene mutation associated with usual interstitial pneumonitis and cellular nonspecific interstitial pneumonitis in one kindred
-
DOI 10.1164/rccm.200112-123OC
-
Thomas AQ, Lane K, Phillips J III, et al. Heterozygosity for a surfactant protein C gene mutation associated with usual interstitial pneumonitis and cellular nonspecific interstitial pneumonitis in one kindred. Am J Respir Crit Care Med. 2002;165(9):1322-1328. (Pubitemid 34461748)
-
(2002)
American Journal of Respiratory and Critical Care Medicine
, vol.165
, Issue.9
, pp. 1322-1328
-
-
Thomas, A.Q.1
Lane, K.2
Phillips III, J.3
Prince, M.4
Markin, C.5
Speer, M.6
Schwartz, D.A.7
Gaddipati, R.8
Marney, A.9
Johnson, J.10
Roberts, R.11
Haines, J.12
Stahlman, M.13
Loyd, J.E.14
-
10
-
-
8544245673
-
Genetic mutations in surfactant protein C are a rare cause of sporadic cases of IPF
-
DOI 10.1136/thx.2004.026336
-
Lawson WE, Grant SW, Ambrosini V, et al. Genetic mutations in surfactant protein C are a rare cause of sporadic cases of IPF. Thorax. 2004;59(11):977-980. (Pubitemid 39490784)
-
(2004)
Thorax
, vol.59
, Issue.11
, pp. 977-980
-
-
Lawson, W.E.1
Grant, S.W.2
Ambrosini, V.3
Womble, K.E.4
Dawson, E.P.5
Lane, K.B.6
Markin, C.7
Renzoni, E.8
Lympany, P.9
Thomas, A.Q.10
Roldan, J.11
Scott, T.A.12
Blackwell, T.S.13
Phillips III, J.A.14
Loyd, J.E.15
Du, B.R.M.16
-
11
-
-
0022593011
-
Familial idiopathic pulmonary fibrosis. Evidence of lung inflammation in unaffected family members
-
Bitterman PB, Rennard SI, Keogh BA, Wewers MD, Adelberg S, Crystal RG. Familial idiopathic pulmonary fibrosis. Evidence of lung inflammation in unaffected family members. N Engl J Med. 1986;314(21):1343-1347. (Pubitemid 16122467)
-
(1986)
New England Journal of Medicine
, vol.314
, Issue.21
, pp. 1343-1347
-
-
Bitterman, P.B.1
Rennard, S.I.2
Keogh, B.A.3
-
12
-
-
30344471883
-
Clinical and pathologic features of familial interstitial pneumonia
-
DOI 10.1164/rccm.200408-1104OC
-
Steele MP, Speer MC, Loyd JE, et al. Clinical and pathologic features of familial interstitial pneumonia. Am J Respir Crit Care Med. 2005;172(9):1146- 1152. (Pubitemid 43066651)
-
(2005)
American Journal of Respiratory and Critical Care Medicine
, vol.172
, Issue.9
, pp. 1146-1152
-
-
Steele, M.P.1
Speer, M.C.2
Loyd, J.E.3
Brown, K.K.4
Herron, A.5
Slifer, S.H.6
Burch, L.H.7
Wahidi, M.M.8
Phillips III, J.A.9
Sporn, T.A.10
McAdams, H.P.11
Schwarz, M.I.12
Schwartz, D.A.13
-
13
-
-
34848922100
-
Early interstitial lung disease in familial pulmonary fibrosis
-
DOI 10.1164/rccm.200702-254OC
-
Rosas IO, Ren P, Avila NA, et al. Early interstitial lung disease in familial pulmonary fibrosis. Am J Respir Crit Care Med. 2007;176(7):698-705. (Pubitemid 47503078)
-
(2007)
American Journal of Respiratory and Critical Care Medicine
, vol.176
, Issue.7
, pp. 698-705
-
-
Rosas, I.O.1
Ren, P.2
Avila, N.A.3
Chow, C.K.4
Franks, T.J.5
Travis, W.D.6
McCoy Jr., J.P.7
May, R.M.8
Wu, H.-P.9
Nguyen, D.M.10
Arcos-Burgos, M.11
MacDonald, S.D.12
Gochuico, B.R.13
-
14
-
-
77950815362
-
Identification of early interstitial lung disease in an individual with genetic variations in ABCA3 and SFTPC
-
Crossno PF, Polosukhin VV, Blackwell TS, et al. Identification of early interstitial lung disease in an individual with genetic variations in ABCA3 and SFTPC. Chest. 2010;137(4):969-973.
-
(2010)
Chest.
, vol.137
, Issue.4
, pp. 969-973
-
-
Crossno, P.F.1
Polosukhin, V.V.2
Blackwell, T.S.3
-
15
-
-
0020585150
-
Changes in the normal maximal expiratory flow-volume curve with growth and aging
-
Knudson RJ, Lebowitz MD, Holberg CJ, Burrows B. Changes in the normal maximal expiratory flow-volume curve with growth and aging. Am Rev Respir Dis. 1983;127(6):725-734. (Pubitemid 13101554)
-
(1983)
American Review of Respiratory Disease
, vol.127
, Issue.6
, pp. 725-734
-
-
Knudson, R.J.1
Lebowitz, M.D.2
Holberg, C.J.3
Burrows, B.4
-
16
-
-
73049128066
-
Clinical usefulness of the single-breath pulmonucy diffusing capacity test
-
Burrows B, Kasik JE, Niden AH, Barclay WR. Clinical usefulness of the single-breath pulmonucy diffusing capacity test. Am Rev Respir Dis. 1961;84:789-806.
-
(1961)
Am Rev Respir Dis.
, vol.84
, pp. 789-806
-
-
Burrows, B.1
Kasik, J.E.2
Niden, A.H.3
Barclay, W.R.4
-
17
-
-
0029146090
-
Reference values of pulmonary diffusing capacity during exercise by a rebreathing technique
-
Hsia CC, McBrayer DG, Ramanathan M. Reference values of pulmonary diffusing capacity during exercise by a rebreathing technique. Am J Respir Crit Care Med. 1995;152(2):658-665.
-
(1995)
Am J Respir Crit Care Med.
, vol.152
, Issue.2
, pp. 658-665
-
-
Hsia, C.C.1
McBrayer, D.G.2
Ramanathan, M.3
-
18
-
-
2142695189
-
Nitric oxide diffusing capacity and alveolar microvascular recruitment in sarcoidosis
-
Phansalkar AR, Hanson CM, Shakir AR, Johnson RL Jr, Hsia CC. Nitric oxide diffusing capacity and alveolar microvascular recruitment in sarcoidosis. Am J Respir Crit Care Med. 2004;169(9):1034-1040. (Pubitemid 38543643)
-
(2004)
American Journal of Respiratory and Critical Care Medicine
, vol.169
, Issue.9
, pp. 1034-1040
-
-
Phansalkar, A.R.1
Hanson, C.M.2
Shakir, A.R.3
Johnson Jr., R.L.4
Hsia, C.C.W.5
-
19
-
-
49649113482
-
Diminished alveolar microvascular reserves in type 2 diabetes reflect systemic microangiopathy
-
Chance WW, Rhee C, Yilmaz C, et al. Diminished alveolar microvascular reserves in type 2 diabetes reflect systemic microangiopathy. Diabetes Care. 2008;31(8):1596-1601.
-
(2008)
Diabetes Care.
, vol.31
, Issue.8
, pp. 1596-1601
-
-
Chance, W.W.1
Rhee, C.2
Yilmaz, C.3
-
20
-
-
72749094457
-
Noninvasive quantification of heterogeneous lung growth following extensive lung resection by high-resolution computed tomography
-
Yilmaz C, Ravikumar P, Dane DM, Bellotto DJ, Johnson RL Jr, Hsia CC. Noninvasive quantification of heterogeneous lung growth following extensive lung resection by high-resolution computed tomography. J Appl Physiol. 2009;107(5):1569-1578.
-
(2009)
J Appl Physiol.
, vol.107
, Issue.5
, pp. 1569-1578
-
-
Yilmaz, C.1
Ravikumar, P.2
Dane, D.M.3
Bellotto, D.J.4
Johnson Jr., R.L.5
Hsia, C.C.6
-
21
-
-
0001287271
-
Regression shrinkage and selection via the lasso
-
Tibshirani R. Regression shrinkage and selection via the lasso. J R Stat Soc, B. 1996;58(1):267-288.
-
(1996)
J R Stat Soc, B.
, vol.58
, Issue.1
, pp. 267-288
-
-
Tibshirani, R.1
-
22
-
-
70149113077
-
-
R Development Core Team. Vienna, Austria: R Foundation for Statistical Computing
-
R Development Core Team. R: A Language and Environment for Statistical Computing. Vienna, Austria: R Foundation for Statistical Computing;2009.
-
(2009)
R: A Language and Environment for Statistical Computing
-
-
-
23
-
-
70449193465
-
Relative importance of diffusion and chemical reaction rates in determining rate of exchange of gases in the human lung, with special reference to true diffusing capacity of pulmonary membrane and volume of blood in the lung capillaries
-
Roughton FJ, Forster RE. Relative importance of diffusion and chemical reaction rates in determining rate of exchange of gases in the human lung, with special reference to true diffusing capacity of pulmonary membrane and volume of blood in the lung capillaries. J Appl Physiol. 1957;11(2):290-302.
-
(1957)
J Appl Physiol.
, vol.11
, Issue.2
, pp. 290-302
-
-
Roughton, F.J.1
Forster, R.E.2
-
24
-
-
15944422499
-
Mutations in TERT, the gene for telomerase reverse transcriptase, in aplastic anemia
-
DOI 10.1056/NEJMoa042980
-
Yamaguchi H, Calado RT, Ly H, et al. Mutations in TERT, the gene for telomerase reverse transcriptase, in aplastic anemia. N Engl J Med. 2005;352(14):1413-1424. (Pubitemid 40471449)
-
(2005)
New England Journal of Medicine
, vol.352
, Issue.14
, pp. 1413-1424
-
-
Yamaguchi, H.1
Calado, R.T.2
Ly, H.3
Kajigaya, S.4
Baerlocher, G.M.5
Chanock, S.J.6
Lansdorp, P.M.7
Young, N.S.8
-
25
-
-
70350721794
-
Defining the pathogenic role of telomerase mutations in myelodysplastic syndrome and acute myeloid leukemia
-
Kirwan M, Vulliamy T, Marrone A, et al. Defining the pathogenic role of telomerase mutations in myelodysplastic syndrome and acute myeloid leukemia. Hum Mutat. 2009; 30(11):1567-1573.
-
(2009)
Hum Mutat.
, vol.30
, Issue.11
, pp. 1567-1573
-
-
Kirwan, M.1
Vulliamy, T.2
Marrone, A.3
-
26
-
-
59049087610
-
Constitutional hypomorphic telomerase mutations in patients with acute myeloid leukemia
-
Calado RT, Regal JA, Hills M, et al. Constitutional hypomorphic telomerase mutations in patients with acute myeloid leukemia. Proc Natl Acad Sci U S A. 2009;106(4):1187-1192.
-
(2009)
Proc Natl Acad Sci U S A.
, vol.106
, Issue.4
, pp. 1187-1192
-
-
Calado, R.T.1
Regal, J.A.2
Hills, M.3
-
27
-
-
0018096749
-
High mean red cell volume: its incidence and significance in routine haematology
-
Davidson RJL, Hamilton PJ. High mean red cell volume: its incidence and significance in routine haematology. J Clin Pathol. 1978;31(5):493-498. (Pubitemid 8333051)
-
(1978)
Journal of Clinical Pathology
, vol.31
, Issue.5
, pp. 493-498
-
-
Davidson, R.J.L.1
Hamilton, P.J.2
-
28
-
-
0026651205
-
A practical approach to the differential diagnosis and evaluation of the adult patient with macrocytic anemia
-
Colon-Otero G, Menke D, Hook CC. A practical approach to the differential diagnosis and evaluation of the adult patient with macrocytic anemia. Med Clin North Am. 1992;76(3):581-597.
-
(1992)
Med Clin North Am.
, vol.76
, Issue.3
, pp. 581-597
-
-
Colon-Otero, G.1
Menke, D.2
Hook, C.C.3
-
29
-
-
0033754823
-
Dyskeratosis congenita in all its forms
-
Dokal I. Dyskeratosis congenita in all its forms. Br J Haematol. 2000;110(4):768-779.
-
(2000)
Br J Haematol.
, vol.110
, Issue.4
, pp. 768-779
-
-
Dokal, I.1
-
30
-
-
27644574342
-
Haploinsufficiency of telomerase reverse transcriptase leads to anticipation in autosomal dominant dyskeratosis congenita
-
DOI 10.1073/pnas.0508124102
-
Armanios M, Chen JL, Chang YP, et al. Haploinsufficiency of telomerase reverse transcriptase leads to anticipation in autosomal dominant dyskeratosis congenita. Proc Natl Acad Sci U S A. 2005;102(44):15960-15964. (Pubitemid 41552850)
-
(2005)
Proceedings of the National Academy of Sciences of the United States of America
, vol.102
, Issue.44
, pp. 15960-15964
-
-
Armanios, M.1
Chen, J.-L.2
Chang, Y.-P.C.3
Brodsky, R.A.4
Hawkins, A.5
Griffin, C.A.6
Eshleman, J.R.7
Cohen, A.R.8
Chakravarti, A.9
Hamosh, A.10
Greider, C.W.11
-
31
-
-
0034966374
-
Very short telomeres in the peripheral blood of patients with X-linked and autosomal dyskeratosis congenita
-
DOI 10.1006/bcmd.2001.0389
-
Vulliamy TJ, Knight SW, Mason PJ, Dokal I. Very short telomeres in the peripheral blood of patients with X-linked and autosomal dyskeratosis congenita. Blood Cells Mol Dis. 2001;27(2):353-357. (Pubitemid 32547829)
-
(2001)
Blood Cells, Molecules, and Diseases
, vol.27
, Issue.2
, pp. 353-357
-
-
Vulliamy, T.J.1
Knight, S.W.2
Mason, P.J.3
Dokal, I.4
-
32
-
-
34548828783
-
Very short telomere length by flow fluorescence in situ hybridization identifies patients with dyskeratosis congenita
-
DOI 10.1182/blood-2007-02-075598
-
Alter BP, Baerlocher GM, Savage SA, et al. Very short telomere length by flow fluorescence in situ hybridization identifies patients with dyskeratosis congenita. Blood. 2007;110(5):1439-1447. (Pubitemid 47443958)
-
(2007)
Blood
, vol.110
, Issue.5
, pp. 1439-1447
-
-
Alter, B.P.1
Baerlocher, G.M.2
Savage, S.A.3
Chanock, S.J.4
Weksler, B.B.5
Willner, J.P.6
Peters, J.A.7
Giri, N.8
Lansdorp, P.M.9
-
33
-
-
28944455294
-
Short telomeres, even in the presence of telomerase, limit tissue renewal capacity
-
DOI 10.1016/j.cell.2005.11.020, PII S0092867405012304
-
Hao LY, Armanios M, Strong MA, et al. Short telomeres, even in the presence of telomerase, limit tissue renewal capacity. Cell. 2005;123(6):1121-1131. (Pubitemid 41785425)
-
(2005)
Cell
, vol.123
, Issue.6
, pp. 1121-1131
-
-
Hao, L.-Y.1
Armanios, M.2
Strong, M.A.3
Karim, B.4
Feldser, D.M.5
Huso, D.6
Greider, C.W.7
-
34
-
-
77953462060
-
Telomere length is inherited with resetting of the telomere set-point
-
Chiang YJ, Calado RT, Hathcock KS, Lansdorp PM, Young NS, Hodes RJ. Telomere length is inherited with resetting of the telomere set-point. Proc Natl Acad Sci U S A. 2010;107(22):10148-10153.
-
(2010)
Proc Natl Acad Sci U S A.
, vol.107
, Issue.22
, pp. 10148-10153
-
-
Chiang, Y.J.1
Calado, R.T.2
Hathcock, K.S.3
Lansdorp, P.M.4
Young, N.S.5
Hodes, R.J.6
-
35
-
-
71149086939
-
Short telomeres are sufficient to cause the degenerative defects associated with aging
-
Armanios M, Alder JK, Parry EM, Karim B, Strong MA, Greider CW. Short telomeres are sufficient to cause the degenerative defects associated with aging. Am J Hum Genet. 2009;85(6):823-832.
-
(2009)
Am J Hum Genet.
, vol.85
, Issue.6
, pp. 823-832
-
-
Armanios, M.1
Alder, J.K.2
Parry, E.M.3
Karim, B.4
Strong, M.A.5
Greider, C.W.6
-
36
-
-
2442617343
-
Disease anticipation is associated with progressive telomere shortening in families with dyskeratosis congenita due to mutations in TERC
-
DOI 10.1038/ng1346
-
Vulliamy T, Marrone A, Szydlo R, Walne A, Mason PJ, Dokal I. Disease anticipation is associated with progressive telomere shortening in families with dyskeratosis congenita due to mutations in TERC. Nat Genet. 2004;36(5):447-449. (Pubitemid 38620026)
-
(2004)
Nature Genetics
, vol.36
, Issue.5
, pp. 447-449
-
-
Vulliamy, T.1
Marrone, A.2
Szydlo, R.3
Walne, A.4
Mason, P.J.5
Dokal, I.6
|