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Year | Number of Results |
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2001 | 1 |
2002 | 1 |
2003 | 1 |
2004 | 1 |
2023 | 1 |
2024 | 0 |
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Hypertrophic cardiomyopathy: distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy.
Circulation. 2003 May 6;107(17):2227-32. doi: 10.1161/01.CIR.0000066323.15244.54. Epub 2003 Apr 21.
Circulation. 2003.
PMID: 12707239
Factors Associated with Survival in Anaplastic Thyroid Carcinoma: A Multicenter Study from the ENDOCAN-TUTHYREF Network.
Jannin A, Giudici F, de la Fouchardière C, Al Ghuzlan A, Wassermann J, Chougnet CN, Drui D, Godbert Y, Ilouz F, Bardet S, Zanetta S, Roudaut N, Batisse Lignier M, Groussin L, Klein M, Zerdoud S, Lamartina L, Baudin E, Decaussin-Petrucci M, Leteurtre E, Borson Chazot F, Do Cao C, Borget I, Hadoux J; ENDOCAN-TUTHYREF Network.
Jannin A, et al.
Thyroid. 2023 Oct;33(10):1190-1200. doi: 10.1089/thy.2023.0164.
Thyroid. 2023.
PMID: 37855745
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Human homozygous R403W mutant cardiac myosin presents disproportionate enhancement of mechanical and enzymatic properties.
Keller DI, Coirault C, Rau T, Cheav T, Weyand M, Amann K, Lecarpentier Y, Richard P, Eschenhagen T, Carrier L.
Keller DI, et al. Among authors: cheav t.
J Mol Cell Cardiol. 2004 Mar;36(3):355-62. doi: 10.1016/j.yjmcc.2003.12.006.
J Mol Cell Cardiol. 2004.
PMID: 15010274
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Homozygous SCN5A mutation in long-QT syndrome with functional two-to-one atrioventricular block.
Lupoglazoff JM, Cheav T, Baroudi G, Berthet M, Denjoy I, Cauchemez B, Extramiana F, Chahine M, Guicheney P.
Lupoglazoff JM, et al. Among authors: cheav t.
Circ Res. 2001 Jul 20;89(2):E16-21. doi: 10.1161/hh1401.095087.
Circ Res. 2001.
PMID: 11463728
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[Homozygotous mutation of the SCN5A gene responsible for congenital long QT syndrome with 2/1 atrioventricular block].
Lupoglazoff JM, Denjoy I, Cheav T, Berthet M, Extramiana F, Cauchemez B, Villain E, Leenhardt A, Guicheney P.
Lupoglazoff JM, et al. Among authors: cheav t.
Arch Mal Coeur Vaiss. 2002 May;95(5):440-6.
Arch Mal Coeur Vaiss. 2002.
PMID: 12085742
French.
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