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Results by year

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

Year Number of Results
1961 1
1962 1
1963 1
1979 2
1981 1
1982 1
1983 3
1985 2
1986 3
1987 4
1988 3
1989 4
1990 3
1991 4
1992 3
1993 2
1994 6
1995 1
1996 2
1997 5
1998 2
1999 2
2000 5
2001 3
2002 7
2003 7
2004 5
2005 6
2006 4
2007 12
2008 13
2009 14
2010 18
2011 16
2012 12
2013 11
2014 16
2015 15
2016 21
2017 22
2018 12
2019 15
2020 11
2021 21
2022 14
2023 9
2024 9

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310 results

Results by year

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Page 1
Transcranial magnetic stimulation of the brain: What is stimulated? - A consensus and critical position paper.
Siebner HR, Funke K, Aberra AS, Antal A, Bestmann S, Chen R, Classen J, Davare M, Di Lazzaro V, Fox PT, Hallett M, Karabanov AN, Kesselheim J, Beck MM, Koch G, Liebetanz D, Meunier S, Miniussi C, Paulus W, Peterchev AV, Popa T, Ridding MC, Thielscher A, Ziemann U, Rothwell JC, Ugawa Y. Siebner HR, et al. Among authors: meunier s. Clin Neurophysiol. 2022 Aug;140:59-97. doi: 10.1016/j.clinph.2022.04.022. Epub 2022 May 18. Clin Neurophysiol. 2022. PMID: 35738037 Free PMC article. Review.
Efanesoctocog Alfa Prophylaxis for Patients with Severe Hemophilia A.
von Drygalski A, Chowdary P, Kulkarni R, Susen S, Konkle BA, Oldenburg J, Matino D, Klamroth R, Weyand AC, Jimenez-Yuste V, Nogami K, Poloskey S, Winding B, Willemze A, Knobe K; XTEND-1 Trial Group. von Drygalski A, et al. N Engl J Med. 2023 Jan 26;388(4):310-318. doi: 10.1056/NEJMoa2209226. N Engl J Med. 2023. PMID: 36720133 Clinical Trial.
A Laboratory Phenotype/Genotype Correlation of 1167 French Patients From 670 Families With von Willebrand Disease: A New Epidemiologic Picture.
Veyradier A, Boisseau P, Fressinaud E, Caron C, Ternisien C, Giraud M, Zawadzki C, Trossaert M, Itzhar-Baïkian N, Dreyfus M, d'Oiron R, Borel-Derlon A, Susen S, Bezieau S, Denis CV, Goudemand J; French Reference Center for von Willebrand disease. Veyradier A, et al. Medicine (Baltimore). 2016 Mar;95(11):e3038. doi: 10.1097/MD.0000000000003038. Medicine (Baltimore). 2016. PMID: 26986123 Free PMC article.
Editorial: Loudness: From Neuroscience to Perception.
Meunier S, Van Eeckhoutte M, Moore BCJ. Meunier S, et al. Front Psychol. 2021 Nov 15;12:785093. doi: 10.3389/fpsyg.2021.785093. eCollection 2021. Front Psychol. 2021. PMID: 34867696 Free PMC article. No abstract available.
Individualized PK-based prophylaxis in severe haemophilia.
Dargaud Y, Delavenne X, Hart DP, Meunier S, Mismetti P. Dargaud Y, et al. Among authors: meunier s. Haemophilia. 2018 Mar;24 Suppl 2:3-17. doi: 10.1111/hae.13397. Haemophilia. 2018. PMID: 29543364 Review.
Spectrum of the mutations in Bernard-Soulier syndrome.
Savoia A, Kunishima S, De Rocco D, Zieger B, Rand ML, Pujol-Moix N, Caliskan U, Tokgoz H, Pecci A, Noris P, Srivastava A, Ward C, Morel-Kopp MC, Alessi MC, Bellucci S, Beurrier P, de Maistre E, Favier R, Hézard N, Hurtaud-Roux MF, Latger-Cannard V, Lavenu-Bombled C, Proulle V, Meunier S, Négrier C, Nurden A, Randrianaivo H, Fabris F, Platokouki H, Rosenberg N, HadjKacem B, Heller PG, Karimi M, Balduini CL, Pastore A, Lanza F. Savoia A, et al. Among authors: meunier s. Hum Mutat. 2014 Sep;35(9):1033-45. doi: 10.1002/humu.22607. Epub 2014 Jul 15. Hum Mutat. 2014. PMID: 24934643 Review.
Congenital factor XIII deficiency: comprehensive overview of the FranceCoag cohort.
Bouttefroy S, Meunier S, Milien V, Boucekine M, Chamouni P, Desprez D, Harroche A, Hochart A, Thiercelin-Legrand MF, Wibaut B, Chambost H, Rugeri L; CoDeC study group. Bouttefroy S, et al. Among authors: meunier s. Br J Haematol. 2020 Jan;188(2):317-320. doi: 10.1111/bjh.16133. Epub 2019 Aug 14. Br J Haematol. 2020. PMID: 31414482 Free article. Review.
310 results