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

Year Number of Results
1975 1
1976 2
1977 1
1979 2
1984 2
1986 1
1988 1
1989 2
1990 1
1991 3
1992 6
1993 6
1994 6
1996 7
1997 2
1998 1
1999 3
2000 2
2001 1
2003 2
2005 2
2006 1
2007 2
2008 1
2009 1
2010 1
2011 3
2012 2
2013 2
2014 2
2015 5
2016 5
2017 4
2018 5
2019 4
2020 1
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Similar Articles for PMID: 29610182

88 results
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Page 1
Unusual Presentations of Dystrophinopathies in Childhood.
Allen NM, Ewer A, Nakou V, Konstantoulaki E, Wraige E, Gowda V, Jungbluth H. Allen NM, et al. Pediatrics. 2018 Apr;141(Suppl 5):S510-S514. doi: 10.1542/peds.2017-2391. Pediatrics. 2018. PMID: 29610182 Free article.
HyperCKemic, proximal muscular dystrophies and the dystrophin membrane cytoskeleton, including dystrophinopathies, sarcoglycanopathies, and merosinopathies.
Hoffman EP, Clemens PR. Hoffman EP, et al. Curr Opin Rheumatol. 1996 Nov;8(6):528-38. doi: 10.1097/00002281-199611000-00006. Curr Opin Rheumatol. 1996. PMID: 9018456 Review.
The differential diagnosis of the human dystrophinopathies and related disorders.
Kakulas BA. Kakulas BA. Curr Opin Neurol. 1996 Oct;9(5):380-8. doi: 10.1097/00019052-199610000-00012. Curr Opin Neurol. 1996. PMID: 8894415 Review.
Improved diagnosis of Becker muscular dystrophy by dystrophin testing.
Hoffman EP, Kunkel LM, Angelini C, Clarke A, Johnson M, Harris JB. Hoffman EP, et al. Neurology. 1989 Aug;39(8):1011-7. doi: 10.1212/wnl.39.8.1011. Neurology. 1989. PMID: 2668783
[Post exercise myalgias as presentation form of dystrophinopathy].
Kleinsteuber K, Rocco P, Herrera L, Vainzof M, Birke ME, Yáñez M, Flandes A, Zatz M, de Carvallo P, Avaria MA. Kleinsteuber K, et al. Rev Med Chil. 2000 Jul;128(7):772-7. Rev Med Chil. 2000. PMID: 11050839 Spanish.
Three years' experience with neonatal screening for Duchenne/Becker muscular dystrophy: gene analysis, gene expression, and phenotype prediction.
Greenberg CR, Jacobs HK, Halliday W, Wrogemann K. Greenberg CR, et al. Am J Med Genet. 1991 Apr 1;39(1):68-75. doi: 10.1002/ajmg.1320390115. Am J Med Genet. 1991. PMID: 1867267
Detection of new paternal dystrophin gene mutations in isolated cases of dystrophinopathy in females.
Pegoraro E, Schimke RN, Arahata K, Hayashi Y, Stern H, Marks H, Glasberg MR, Carroll JE, Taber JW, Wessel HB, et al. Pegoraro E, et al. Am J Hum Genet. 1994 Jun;54(6):989-1003. Am J Hum Genet. 1994. PMID: 8198142 Free PMC article.
Dystrophinopathies.
Brandsema JF, Darras BT. Brandsema JF, et al. Semin Neurol. 2015 Aug;35(4):369-84. doi: 10.1055/s-0035-1558982. Epub 2015 Oct 6. Semin Neurol. 2015. PMID: 26502761 Review.
Molecular diagnosis of dystrophinopathies using a multi-technique analysis algorithm.
Luce LN, Ottaviani D, Ferrer M, Szijan I, Cotignola J, Giliberto F. Luce LN, et al. Muscle Nerve. 2014 Feb;49(2):249-56. doi: 10.1002/mus.23906. Muscle Nerve. 2014. PMID: 23695957
Clinical features of patients with dystrophinopathy sharing the 45-55 exon deletion of DMD gene.
Taglia A, Petillo R, D'Ambrosio P, Picillo E, Torella A, Orsini C, Ergoli M, Scutifero M, Passamano L, Palladino A, Nigro G, Politano L. Taglia A, et al. Acta Myol. 2015 May;34(1):9-13. Acta Myol. 2015. PMID: 26155064 Free PMC article.
88 results
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