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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1936 1
1949 1
1960 2
1961 1
1967 1
1972 1
1973 3
1983 1
1986 2
1993 1
1994 1
1995 3
1996 1
1997 2
1998 1
1999 1
2000 1
2001 2
2002 1
2003 1
2004 3
2005 1
2007 3
2009 6
2010 5
2012 3
2013 1
2014 1
2015 3
2016 2
2017 1
2018 4
2019 1
2020 1
2022 1
2023 1
2024 0

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63 results

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Page 1
Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and pharmacological and psychosocial management.
Bushby K, Finkel R, Birnkrant DJ, Case LE, Clemens PR, Cripe L, Kaul A, Kinnett K, McDonald C, Pandya S, Poysky J, Shapiro F, Tomezsko J, Constantin C; DMD Care Considerations Working Group. Bushby K, et al. Lancet Neurol. 2010 Jan;9(1):77-93. doi: 10.1016/S1474-4422(09)70271-6. Epub 2009 Nov 27. Lancet Neurol. 2010. PMID: 19945913 Review.
Cystic fibrosis pulmonary guidelines: treatment of pulmonary exacerbations.
Flume PA, Mogayzel PJ Jr, Robinson KA, Goss CH, Rosenblatt RL, Kuhn RJ, Marshall BC; Clinical Practice Guidelines for Pulmonary Therapies Committee. Flume PA, et al. Am J Respir Crit Care Med. 2009 Nov 1;180(9):802-8. doi: 10.1164/rccm.200812-1845PP. Epub 2009 Sep 3. Am J Respir Crit Care Med. 2009. PMID: 19729669 Review.
Pulmonary Endpoints in Duchenne Muscular Dystrophy. A Workshop Summary.
Finder J, Mayer OH, Sheehan D, Sawnani H, Abresch RT, Benditt J, Birnkrant DJ, Duong T, Henricson E, Kinnett K, McDonald CM, Connolly AM. Finder J, et al. Am J Respir Crit Care Med. 2017 Aug 15;196(4):512-519. doi: 10.1164/rccm.201703-0507WS. Am J Respir Crit Care Med. 2017. PMID: 28636407 Review.
Quality improvement in neurology: muscular dystrophy quality measures.
Narayanaswami P, Dubinsky R, Wang D, Gjorvad G, David W, Finder J, Smith B, Cheng J, Shapiro F, Mellion M, Spurney C, Wolff J, England J. Narayanaswami P, et al. Among authors: finder j. Neurology. 2015 Sep 8;85(10):905-9. doi: 10.1212/WNL.0000000000001910. Neurology. 2015. PMID: 26333798 Free PMC article. Review. No abstract available.
Cardiac Management of the Patient With Duchenne Muscular Dystrophy.
Buddhe S, Cripe L, Friedland-Little J, Kertesz N, Eghtesady P, Finder J, Hor K, Judge DP, Kinnett K, McNally EM, Raman S, Thompson WR, Wagner KR, Olson AK. Buddhe S, et al. Among authors: finder j. Pediatrics. 2018 Oct;142(Suppl 2):S72-S81. doi: 10.1542/peds.2018-0333I. Pediatrics. 2018. PMID: 30275251 Free PMC article. Review.
Management of pulmonary complications in neuromuscular disease.
Wolfe LF, Joyce NC, McDonald CM, Benditt JO, Finder J. Wolfe LF, et al. Among authors: finder j. Phys Med Rehabil Clin N Am. 2012 Nov;23(4):829-53. doi: 10.1016/j.pmr.2012.08.010. Phys Med Rehabil Clin N Am. 2012. PMID: 23137740 Review.
Congenital pulmonary lymphangiectasia.
Finder J, Steinfeld J. Finder J, et al. N Engl J Med. 2004 Feb 26;350(9):948; author reply 948. doi: 10.1056/NEJM200402263500921. N Engl J Med. 2004. PMID: 14985498 No abstract available.
Respiratory care of the patient with Duchenne muscular dystrophy: ATS consensus statement.
Finder JD, Birnkrant D, Carl J, Farber HJ, Gozal D, Iannaccone ST, Kovesi T, Kravitz RM, Panitch H, Schramm C, Schroth M, Sharma G, Sievers L, Silvestri JM, Sterni L; American Thoracic Society. Finder JD, et al. Am J Respir Crit Care Med. 2004 Aug 15;170(4):456-65. doi: 10.1164/rccm.200307-885ST. Am J Respir Crit Care Med. 2004. PMID: 15302625 Review. No abstract available.
63 results