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

Year Number of Results
1999 2
2001 1
2002 2
2004 2
2005 2
2006 1
2007 1
2008 3
2009 1
2010 2
2014 1
2015 1
2018 1
2024 0

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Page 1
Genetics of laminopathies.
Ben Yaou R, Muchir A, Arimura T, Massart C, Demay L, Richard P, Bonne G. Ben Yaou R, et al. Among authors: demay l. Novartis Found Symp. 2005;264:81-90; discussion 90-97, 227-30. Novartis Found Symp. 2005. PMID: 15773749 Review.
Heart involvement in lamin A/C related diseases.
Ben Yaou R, Gueneau L, Demay L, Stora S, Chikhaoui K, Richard P, Bonne G. Ben Yaou R, et al. Among authors: demay l. Arch Mal Coeur Vaiss. 2006 Sep;99(9):848-55. Arch Mal Coeur Vaiss. 2006. PMID: 17067107 Review.
PABPN1 (GCN)11 as a Dominant Allele in Oculopharyngeal Muscular Dystrophy -Consequences in Clinical Diagnosis and Genetic Counselling.
Richard P, Trollet C, Gidaro T, Demay L, Brochier G, Malfatti E, Tom FM, Fardeau M, Lafor P, Romero N, Martin-N ML, Sol G, Ferrer-Monasterio X, Saint-Guily JL, Eymard B. Richard P, et al. Among authors: demay l. J Neuromuscul Dis. 2015 Jun 4;2(2):175-180. doi: 10.3233/JND-140060. J Neuromuscul Dis. 2015. PMID: 27858728 Free PMC article.
Heart-hand syndrome of Slovenian type: a new kind of laminopathy.
Renou L, Stora S, Yaou RB, Volk M, Sinkovec M, Demay L, Richard P, Peterlin B, Bonne G. Renou L, et al. Among authors: demay l. J Med Genet. 2008 Oct;45(10):666-71. doi: 10.1136/jmg.2008.060020. Epub 2008 Jul 8. J Med Genet. 2008. PMID: 18611980
Desmin myopathy with severe cardiomyopathy in a Uruguayan family due to a codon deletion in a new location within the desmin 1A rod domain.
Vernengo L, Chourbagi O, Panuncio A, Lilienbaum A, Batonnet-Pichon S, Bruston F, Rodrigues-Lima F, Mesa R, Pizzarossa C, Demay L, Richard P, Vicart P, Rodriguez MM. Vernengo L, et al. Among authors: demay l. Neuromuscul Disord. 2010 Mar;20(3):178-87. doi: 10.1016/j.nmd.2010.01.001. Epub 2010 Feb 4. Neuromuscul Disord. 2010. PMID: 20133133
19 results