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Items: 1 to 20 of 126

1.

Surfactant protein C mutations in sporadic forms of idiopathic interstitial pneumonias.

Markart P, Ruppert C, Wygrecka M, Schmidt R, Korfei M, Harbach H, Theruvath I, Pison U, Seeger W, Guenther A, Witt H.

Eur Respir J. 2007 Jan;29(1):134-7. Epub 2006 Sep 27.

2.

Surfactant protein C mutations are the basis of a significant portion of adult familial pulmonary fibrosis in a dutch cohort.

van Moorsel CH, van Oosterhout MF, Barlo NP, de Jong PA, van der Vis JJ, Ruven HJ, van Es HW, van den Bosch JM, Grutters JC.

Am J Respir Crit Care Med. 2010 Dec 1;182(11):1419-25. doi: 10.1164/rccm.200906-0953OC. Epub 2010 Jul 23.

PMID:
20656946
3.

Mutation of SFTPC in infantile pulmonary alveolar proteinosis with or without fibrosing lung disease.

Tredano M, Griese M, Brasch F, Schumacher S, de Blic J, Marque S, Houdayer C, Elion J, Couderc R, Bahuau M.

Am J Med Genet A. 2004 Apr 1;126A(1):18-26.

PMID:
15039969
4.

Nonspecific interstitial pneumonia and usual interstitial pneumonia with mutation in surfactant protein C in familial pulmonary fibrosis.

Chibbar R, Shih F, Baga M, Torlakovic E, Ramlall K, Skomro R, Cockcroft DW, Lemire EG.

Mod Pathol. 2004 Aug;17(8):973-80.

5.

Familial forms of nonspecific interstitial pneumonia/idiopathic pulmonary fibrosis: clinical course and genetic background.

Borie R, Kannengiesser C, Crestani B.

Curr Opin Pulm Med. 2012 Sep;18(5):455-61. doi: 10.1097/MCP.0b013e328356b15c. Review.

PMID:
22781209
6.

Genetic mutations in surfactant protein C are a rare cause of sporadic cases of IPF.

Lawson WE, Grant SW, Ambrosini V, Womble KE, Dawson EP, Lane KB, Markin C, Renzoni E, Lympany P, Thomas AQ, Roldan J, Scott TA, Blackwell TS, Phillips JA 3rd, Loyd JE, du Bois RM.

Thorax. 2004 Nov;59(11):977-80.

7.

Clinical features and genetic analysis of surfactant protein C in adult-onset familial interstitial pneumonia.

Setoguchi Y, Ikeda T, Fukuchi Y.

Respirology. 2006 Jan;11 Suppl:S41-5.

PMID:
16423270
8.

[Pulmonary surfactant protein gene mutation associated with pediatric interstitial lung disease: a case study and the review of related literature].

Zhu CM, Cao L, Huang RY, Wang YJ, Zou JZ, Yuan XY, Song F, Chen HZ.

Zhonghua Er Ke Za Zhi. 2013 Feb;51(2):84-9. Review. Chinese.

PMID:
23527967
10.

New surfactant protein C gene mutations associated with diffuse lung disease.

Guillot L, Epaud R, Thouvenin G, Jonard L, Mohsni A, Couderc R, Counil F, de Blic J, Taam RA, Le Bourgeois M, Reix P, Flamein F, Clement A, Feldmann D.

J Med Genet. 2009 Jul;46(7):490-4. doi: 10.1136/jmg.2009.066829. Epub 2009 May 13. Erratum in: J Med Genet. 2010 Jul;47(7):485.

11.

Familial interstitial pneumonia in an adolescent boy with surfactant protein C gene (Y104H) mutation.

Kuse N, Abe S, Hayashi H, Kamio K, Saito Y, Azuma A, Kudoh S, Kunugi S, Fukuda Y, Setoguchi Y, Gemma A.

Sarcoidosis Vasc Diffuse Lung Dis. 2013 Mar;30(1):73-7.

PMID:
24003539
12.

Two novel mutations in surfactant protein-C, lung function and obstructive lung disease.

Baekvad-Hansen M, Nordestgaard BG, Tybjaerg-Hansen A, Dahl M.

Respir Med. 2010 Mar;104(3):418-25. doi: 10.1016/j.rmed.2009.10.012. Epub 2009 Nov 11.

13.

Recombination as a mechanism for sporadic mutation in the surfactant protein-C gene.

McBee AD, Wegner DJ, Carlson CS, Wambach JA, Yang P, Heins HB, Saugstad OD, Trusgnich MA, Watkins-Torry J, Nogee LM, Henderson H, Cole FS, Hamvas A.

Pediatr Pulmonol. 2008 May;43(5):443-50. doi: 10.1002/ppul.20782.

14.

[Genetic basis in chronic interstitial familial pneumopathy. Familial study of SFTPC].

Somaschini M, Cavazza A, Riva S, Sassi I, Carrera P.

Pediatr Med Chir. 2005 May-Aug;27(3-4):103-7. Italian.

PMID:
16910460
15.

Heterozygosity for a surfactant protein C gene mutation associated with usual interstitial pneumonitis and cellular nonspecific interstitial pneumonitis in one kindred.

Thomas AQ, Lane K, Phillips J 3rd, Prince M, Markin C, Speer M, Schwartz DA, Gaddipati R, Marney A, Johnson J, Roberts R, Haines J, Stahlman M, Loyd JE.

Am J Respir Crit Care Med. 2002 May 1;165(9):1322-8.

PMID:
11991887
16.

Natural history of five children with surfactant protein C mutations and interstitial lung disease.

Avital A, Hevroni A, Godfrey S, Cohen S, Maayan C, Nusair S, Nogee LM, Springer C.

Pediatr Pulmonol. 2014 Nov;49(11):1097-105. doi: 10.1002/ppul.22971. Epub 2013 Dec 17.

PMID:
24347114
17.

Genetic characterization of a Chinese family with familial idiopathic pulmonary fibrosis.

Zhang X, Jiang J, Chen WJ, Su LX, Xie LX.

Chin Med J (Engl). 2012 Jun;125(11):1945-51.

PMID:
22884059
18.

Nonspecific interstitial pneumonia, alveolar proteinosis, and abnormal proprotein trafficking resulting from a spontaneous mutation in the surfactant protein C gene.

Stevens PA, Pettenazzo A, Brasch F, Mulugeta S, Baritussio A, Ochs M, Morrison L, Russo SJ, Beers MF.

Pediatr Res. 2005 Jan;57(1):89-98. Epub 2004 Nov 19.

PMID:
15557112
19.

Identification of early interstitial lung disease in an individual with genetic variations in ABCA3 and SFTPC.

Crossno PF, Polosukhin VV, Blackwell TS, Johnson JE, Markin C, Moore PE, Worrell JA, Stahlman MT, Phillips JA 3rd, Loyd JE, Cogan JD, Lawson WE.

Chest. 2010 Apr;137(4):969-73. doi: 10.1378/chest.09-0790.

20.

A common MUC5B promoter polymorphism and pulmonary fibrosis.

Seibold MA, Wise AL, Speer MC, Steele MP, Brown KK, Loyd JE, Fingerlin TE, Zhang W, Gudmundsson G, Groshong SD, Evans CM, Garantziotis S, Adler KB, Dickey BF, du Bois RM, Yang IV, Herron A, Kervitsky D, Talbert JL, Markin C, Park J, Crews AL, Slifer SH, Auerbach S, Roy MG, Lin J, Hennessy CE, Schwarz MI, Schwartz DA.

N Engl J Med. 2011 Apr 21;364(16):1503-12. doi: 10.1056/NEJMoa1013660.

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