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

Year Number of Results
1826 1
1836 1
1837 1
1911 1
1919 1
1923 1
1945 1
1948 2
1949 1
1953 2
1955 1
1959 1
1962 1
1964 2
1965 2
1966 2
1967 1
1968 2
1969 1
1971 2
1972 2
1973 2
1974 2
1976 1
1977 1
1979 2
1981 2
1982 6
1983 5
1984 3
1985 2
1986 2
1987 3
1988 3
1989 2
1990 1
1991 1
1993 1
1994 1
1995 1
1996 6
1997 10
1998 4
1999 5
2000 15
2001 5
2002 9
2003 8
2004 7
2005 6
2006 6
2007 9
2008 14
2009 12
2010 11
2011 17
2012 14
2013 15
2014 19
2015 29
2016 25
2017 24
2018 22
2019 33
2020 29
2021 25
2022 40
2023 5
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Article type
Publication date

Search Results

449 results
Results by year
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Page 1
A Placebo-Controlled Trial of Bezafibrate in Primary Biliary Cholangitis.
Corpechot C, Chazouillères O, Rousseau A, Le Gruyer A, Habersetzer F, Mathurin P, Goria O, Potier P, Minello A, Silvain C, Abergel A, Debette-Gratien M, Larrey D, Roux O, Bronowicki JP, Boursier J, de Ledinghen V, Heurgue-Berlot A, Nguyen-Khac E, Zoulim F, Ollivier-Hourmand I, Zarski JP, Nkontchou G, Lemoinne S, Humbert L, Rainteau D, Lefèvre G, de Chaisemartin L, Chollet-Martin S, Gaouar F, Admane FH, Simon T, Poupon R. Corpechot C, et al. Among authors: lefevre g. N Engl J Med. 2018 Jun 7;378(23):2171-2181. doi: 10.1056/NEJMoa1714519. N Engl J Med. 2018. PMID: 29874528 Free article. Clinical Trial.
Ultrarare heterozygous pathogenic variants of genes causing dominant forms of early-onset deafness underlie severe presbycusis.
Boucher S, Tai FWJ, Delmaghani S, Lelli A, Singh-Estivalet A, Dupont T, Niasme-Grare M, Michel V, Wolff N, Bahloul A, Bouyacoub Y, Bouccara D, Fraysse B, Deguine O, Collet L, Thai-Van H, Ionescu E, Kemeny JL, Giraudet F, Lavieille JP, Devèze A, Roudevitch-Pujol AL, Vincent C, Renard C, Franco-Vidal V, Thibult-Apt C, Darrouzet V, Bizaguet E, Coez A, Aschard H, Michalski N, Lefevre GM, Aubois A, Avan P, Bonnet C, Petit C. Boucher S, et al. Among authors: lefevre gm. Proc Natl Acad Sci U S A. 2020 Dec 8;117(49):31278-31289. doi: 10.1073/pnas.2010782117. Epub 2020 Nov 23. Proc Natl Acad Sci U S A. 2020. PMID: 33229591 Free PMC article.
An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patients.
Bonnet C, Riahi Z, Chantot-Bastaraud S, Smagghe L, Letexier M, Marcaillou C, Lefèvre GM, Hardelin JP, El-Amraoui A, Singh-Estivalet A, Mohand-Saïd S, Kohl S, Kurtenbach A, Sliesoraityte I, Zobor D, Gherbi S, Testa F, Simonelli F, Banfi S, Fakin A, Glavač D, Jarc-Vidmar M, Zupan A, Battelino S, Martorell Sampol L, Claveria MA, Catala Mora J, Dad S, Møller LB, Rodriguez Jorge J, Hawlina M, Auricchio A, Sahel JA, Marlin S, Zrenner E, Audo I, Petit C. Bonnet C, et al. Among authors: lefevre gm. Eur J Hum Genet. 2016 Dec;24(12):1730-1738. doi: 10.1038/ejhg.2016.99. Epub 2016 Jul 27. Eur J Hum Genet. 2016. PMID: 27460420 Free PMC article.
[Hypereosinophilic syndromes].
Groh M, Lefèvre G, Ackermann F, Étienne N, Kahn JE. Groh M, et al. Among authors: lefevre g. Rev Prat. 2019 Sep;69(7):767-773. Rev Prat. 2019. PMID: 32233322 French.
Cutaneous manifestations of lymphoid-variant hypereosinophilic syndrome.
Laurent C, Lefèvre G, Kahn JE, Staumont-Salle D, Felten R, Puget M, Moulinet T, Machelart I, Launay D, Charvet E, Bouaziz JD, Jachiet M, Espitia A, Mahr A, Le Clech C, Malphettes M, Morice C, Mourah S, Moins-Teisserenc H, Lifermann F, Soulier-Guérin K, Villate A, Baillou C, Grados A, Robbins A, Abisror N, Bagot M, Boutboul D, Panel K, Vignon-Pennamen MD, Rivet J, Battistella M, Groh M, de Masson A; CEREO network. Laurent C, et al. Among authors: lefevre g. Br J Dermatol. 2022 Dec;187(6):1011-1013. doi: 10.1111/bjd.21782. Epub 2022 Aug 12. Br J Dermatol. 2022. PMID: 35862277 No abstract available.
Iron-catalyzed coupling of three reactants.
Lefèvre G. Lefèvre G. Science. 2021 Oct 22;374(6566):396-397. doi: 10.1126/science.abl4762. Epub 2021 Oct 21. Science. 2021. PMID: 34672754
[Atypical gastritis].
Rochoy M, Lefèvre G, Fontaine A, Boualit M, Le Roy P, Neugebauer Y, Chanson N, Le Gouellec N, Launay D, Lambert M, Hachulla E, Hatron PY. Rochoy M, et al. Among authors: lefevre g. Rev Med Interne. 2013 Sep;34(9):581-2. doi: 10.1016/j.revmed.2013.02.004. Epub 2013 Mar 7. Rev Med Interne. 2013. PMID: 23478158 French. No abstract available.
[Telomeropathies: A study of 15 cases].
Antoine P, Terriou L, Lefèvre G, Kannengiesser C, Sanges S, Launay D, Sobanski V, Hachulla É, Louvet A, Willemin MC, Renaut-Marceau A, Lainey E, Sicre de Fontbrune F, Farhat MM. Antoine P, et al. Among authors: lefevre g. Rev Med Interne. 2022 Jan;43(1):3-8. doi: 10.1016/j.revmed.2021.09.003. Epub 2021 Oct 11. Rev Med Interne. 2022. PMID: 34649755 French.
Reply to Dr Khan.
Bertrand V, Groh M, Lefèvre G, Kahn JE. Bertrand V, et al. Among authors: lefevre g. Pediatr Allergy Immunol. 2020 May;31(4):432. doi: 10.1111/pai.13222. Epub 2020 Feb 27. Pediatr Allergy Immunol. 2020. PMID: 32012338 No abstract available.
449 results