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

Year Number of Results
1993 1
1996 1
1999 1
2000 4
2001 1
2002 3
2003 1
2004 3
2005 4
2006 4
2007 2
2008 10
2009 6
2010 3
2011 6
2012 4
2013 5
2014 7
2015 5
2016 4
2017 5
2018 6
2019 1
2020 3
2021 0
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Similar articles for PMID: 24488829

81 results
Results by year
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Page 1
Muscle disease.
Tsao CY. Tsao CY. Pediatr Rev. 2014 Feb;35(2):49-61; quiz 61. doi: 10.1542/pir.35-2-49. Pediatr Rev. 2014. PMID: 24488829
Dystrophinopathies.
Darras BT, Urion DK, Ghosh PS. Darras BT, et al. 2000 Sep 5 [updated 2018 Apr 26]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Mirzaa G, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2021. GeneReviews®. 1993–2021. PMID: 20301298 Free Books & Documents. Review.
Genetic and Early Clinical Manifestations of Females Heterozygous for Duchenne/Becker Muscular Dystrophy.
Papa R, Madia F, Bartolomeo D, Trucco F, Pedemonte M, Traverso M, Broda P, Bruno C, Zara F, Minetti C, Fiorillo C. Papa R, et al. Pediatr Neurol. 2016 Feb;55:58-63. doi: 10.1016/j.pediatrneurol.2015.11.004. Epub 2015 Nov 26. Pediatr Neurol. 2016. PMID: 26718981
[From gene to disease; the dystrophin gene involved in Duchenne and Becker muscular dystrophy].
den Dunnen JT, de Visser M, Bakker E. den Dunnen JT, et al. Ned Tijdschr Geneeskd. 2002 Feb 23;146(8):364-7. Ned Tijdschr Geneeskd. 2002. PMID: 11887623 Review. Dutch.
[The heartache of muscular dystrophy].
Hoogerwaard EM, Ginjaar HB, Wilde AA, Leschot NJ, de Voogt WG, de Visser M. Hoogerwaard EM, et al. Ned Tijdschr Geneeskd. 2000 Nov 11;144(46):2181-4. Ned Tijdschr Geneeskd. 2000. PMID: 11103252 Review. Dutch.
Targeting fibrosis in Duchenne muscular dystrophy.
Zhou L, Lu H. Zhou L, et al. J Neuropathol Exp Neurol. 2010 Aug;69(8):771-6. doi: 10.1097/NEN.0b013e3181e9a34b. J Neuropathol Exp Neurol. 2010. PMID: 20613637 Free PMC article. Review.
Follow-up of three patients with a large in-frame deletion of exons 45-55 in the Duchenne muscular dystrophy (DMD) gene.
Nakamura A, Yoshida K, Fukushima K, Ueda H, Urasawa N, Koyama J, Yazaki Y, Yazaki M, Sakai T, Haruta S, Takeda S, Ikeda S. Nakamura A, et al. J Clin Neurosci. 2008 Jul;15(7):757-63. doi: 10.1016/j.jocn.2006.12.012. Epub 2008 Feb 7. J Clin Neurosci. 2008. PMID: 18261911
Congestive heart failure with rhabdomyolysis and acute renal failure in a manifesting female carrier of Duchenne muscular dystrophy with duplication of dystrophin gene.
Tunteeratum A, Witoonpanich R, Phudhichareonrat S, Eu-ahsunthornwattana J, Pingsuthiwong S, Srichan K, Sura T. Tunteeratum A, et al. J Clin Neuromuscul Dis. 2009 Sep;11(1):49-53. doi: 10.1097/CND.0b013e3181adcda7. J Clin Neuromuscul Dis. 2009. PMID: 19730022
Duchenne muscular dystrophy: a clinical, histopathological and genetic study at a neurology tertiary care center in Southern India.
Swaminathan B, Shubha GN, Shubha D, Murthy AR, Kiran Kumar HB, Shylashree S, Gayathri N, Jamuna R, Jain S, Purushottam M, Nalini A. Swaminathan B, et al. Neurol India. 2009 Nov-Dec;57(6):734-8. doi: 10.4103/0028-3886.59468. Neurol India. 2009. PMID: 20139501 Free article.
[Duchenne muscular dystrophy: rational basis, state of the art].
Palmieri B, Sblendorio V. Palmieri B, et al. Recenti Prog Med. 2006 Sep;97(9):441-7. Recenti Prog Med. 2006. PMID: 17017293 Review. Italian.
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