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

Year Number of Results
1993 1
1995 1
1996 1
2000 2
2001 3
2002 2
2003 1
2004 3
2005 4
2007 2
2008 4
2009 6
2010 2
2011 7
2012 3
2013 3
2014 7
2015 7
2016 8
2017 8
2018 3
2019 3
2020 6
2021 1
2022 1
2023 3
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86 results
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Page 1
A second cohort of CHD3 patients expands the molecular mechanisms known to cause Snijders Blok-Campeau syndrome.
Drivas TG, Li D, Nair D, Alaimo JT, Alders M, Altmüller J, Barakat TS, Bebin EM, Bertsch NL, Blackburn PR, Blesson A, Bouman AM, Brockmann K, Brunelle P, Burmeister M, Cooper GM, Denecke J, Dieux-Coëslier A, Dubbs H, Ferrer A, Gal D, Bartik LE, Gunderson LB, Hasadsri L, Jain M, Karimov C, Keena B, Klee EW, Kloth K, Lace B, Macchiaiolo M, Marcadier JL, Milunsky JM, Napier MP, Ortiz-Gonzalez XR, Pichurin PN, Pinner J, Powis Z, Prasad C, Radio FC, Rasmussen KJ, Renaud DL, Rush ET, Saunders C, Selcen D, Seman AR, Shinde DN, Smith ED, Smol T, Snijders Blok L, Stoler JM, Tang S, Tartaglia M, Thompson ML, van de Kamp JM, Wang J, Weise D, Weiss K, Woitschach R, Wollnik B, Yan H, Zackai EH, Zampino G, Campeau P, Bhoj E. Drivas TG, et al. Among authors: selcen d. Eur J Hum Genet. 2020 Oct;28(10):1422-1431. doi: 10.1038/s41431-020-0654-4. Epub 2020 Jun 1. Eur J Hum Genet. 2020. PMID: 32483341 Free PMC article.
Myofibrillar myopathies.
Selcen D. Selcen D. Curr Opin Neurol. 2010 Oct;23(5):477-81. doi: 10.1097/WCO.0b013e32833d38b0. Curr Opin Neurol. 2010. PMID: 20664348 Review.
Myofibrillar myopathies.
Selcen D. Selcen D. Neuromuscul Disord. 2011 Mar;21(3):161-71. doi: 10.1016/j.nmd.2010.12.007. Epub 2011 Jan 20. Neuromuscul Disord. 2011. PMID: 21256014 Free PMC article. Review.
Myofibrillar myopathies.
Selcen D, Engel AG. Selcen D, et al. Handb Clin Neurol. 2011;101:143-54. doi: 10.1016/B978-0-08-045031-5.00011-6. Handb Clin Neurol. 2011. PMID: 21496631 Review.
Myofibrillar myopathies.
Selcen D. Selcen D. Curr Opin Neurol. 2008 Oct;21(5):585-9. doi: 10.1097/WCO.0b013e32830a752b. Curr Opin Neurol. 2008. PMID: 18769253 Free PMC article. Review.
The Z-disk diseases.
Selcen D, Carpén O. Selcen D, et al. Adv Exp Med Biol. 2008;642:116-30. doi: 10.1007/978-0-387-84847-1_10. Adv Exp Med Biol. 2008. PMID: 19181098 Review.
The unfolding landscape of the congenital myasthenic syndromes.
Engel AG, Shen XM, Selcen D. Engel AG, et al. Among authors: selcen d. Ann N Y Acad Sci. 2018 Feb;1413(1):25-34. doi: 10.1111/nyas.13539. Epub 2018 Jan 21. Ann N Y Acad Sci. 2018. PMID: 29355968 Free PMC article. Review.
Proteomic profiling of sporadic late-onset nemaline myopathy.
Naddaf E, Dasari S, Selcen D, Charlesworth MC, Johnson KL, Mauermann ML, Kourelis T. Naddaf E, et al. Among authors: selcen d. Ann Clin Transl Neurol. 2022 Mar;9(3):391-402. doi: 10.1002/acn3.51527. Epub 2022 Feb 20. Ann Clin Transl Neurol. 2022. PMID: 35187860 Free PMC article.
New horizons for congenital myasthenic syndromes.
Engel AG, Shen XM, Selcen D, Sine S. Engel AG, et al. Among authors: selcen d. Ann N Y Acad Sci. 2012 Dec;1275(1):54-62. doi: 10.1111/j.1749-6632.2012.06803.x. Ann N Y Acad Sci. 2012. PMID: 23278578 Free PMC article. Review.
86 results