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

Year Number of Results
1986 1
1987 2
1989 3
1990 2
1991 6
1992 5
1993 5
1994 7
1995 6
1996 5
1997 1
1998 4
1999 3
2000 8
2001 2
2002 7
2003 5
2004 7
2005 7
2006 12
2007 10
2008 8
2009 9
2010 6
2011 9
2012 11
2013 12
2014 16
2015 11
2016 15
2017 5
2018 6
2019 9
2020 16
2021 10
2022 6
2023 7
2024 4

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Search Results

250 results

Results by year

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Page 1
Adverse effects of immune-checkpoint inhibitors: epidemiology, management and surveillance.
Martins F, Sofiya L, Sykiotis GP, Lamine F, Maillard M, Fraga M, Shabafrouz K, Ribi C, Cairoli A, Guex-Crosier Y, Kuntzer T, Michielin O, Peters S, Coukos G, Spertini F, Thompson JA, Obeid M. Martins F, et al. Among authors: kuntzer t. Nat Rev Clin Oncol. 2019 Sep;16(9):563-580. doi: 10.1038/s41571-019-0218-0. Nat Rev Clin Oncol. 2019. PMID: 31092901 Review.
Genotype-phenotype correlations in recessive titinopathies.
Savarese M, Vihola A, Oates EC, Barresi R, Fiorillo C, Tasca G, Jokela M, Sarkozy A, Luo S, Díaz-Manera J, Ehrstedt C, Rojas-García R, Sáenz A, Muelas N, Lonardo F, Fodstad H, Qureshi T, Johari M, Välipakka S, Luque H, Petiot P, de Munain AL, Pane M, Mercuri E, Torella A, Nigro V, Astrea G, Santorelli FM, Bruno C, Kuntzer T, Illa I, Vílchez JJ, Julien C, Ferreiro A, Malandrini A, Zhao CB, Casar-Borota O, Davis M, Muntoni F, Hackman P, Udd B. Savarese M, et al. Among authors: kuntzer t. Genet Med. 2020 Dec;22(12):2029-2040. doi: 10.1038/s41436-020-0914-2. Epub 2020 Aug 11. Genet Med. 2020. PMID: 32778822 Free article.
[Neurology].
Eskioglou E, Benninger D, Di Virgilio G, Hirt L, Kuntzer T, Michel P, Novy J, Rossetti AO, Rouaud O, Ryvlin P, Theaudin M, Du Pasquier R. Eskioglou E, et al. Among authors: kuntzer t. Rev Med Suisse. 2019 Jan 9;15(N° 632-633):74-77. Rev Med Suisse. 2019. PMID: 30629375 French.
[Neurology].
Chopard I, Benninger D, Demonet JF, Du Pasquier R, Hirt L, Kuntzer T, Michel P, Nater B, Novy J, Rossetti A, Rouaud O, Ryvlin P, Schluep M, Theaudin M. Chopard I, et al. Among authors: kuntzer t. Rev Med Suisse. 2018 Jan 10;14(588-589):58-61. Rev Med Suisse. 2018. PMID: 29337452 French.
Corticosteroids for the treatment of Duchenne muscular dystrophy.
Matthews E, Brassington R, Kuntzer T, Jichi F, Manzur AY. Matthews E, et al. Among authors: kuntzer t. Cochrane Database Syst Rev. 2016 May 5;2016(5):CD003725. doi: 10.1002/14651858.CD003725.pub4. Cochrane Database Syst Rev. 2016. PMID: 27149418 Free PMC article. Review.
Implication of folate deficiency in CYP2U1 loss of function.
Pujol C, Legrand A, Parodi L, Thomas P, Mochel F, Saracino D, Coarelli G, Croon M, Popovic M, Valet M, Villain N, Elshafie S, Issa M, Zuily S, Renaud M, Marelli-Tosi C, Legendre M, Trimouille A, Kemlin I, Mathieu S, Gleeson JG, Lamari F, Galatolo D, Alkouri R, Tse C, Rodriguez D, Ewenczyk C, Fellmann F, Kuntzer T, Blond E, El Hachimi KH, Darios F, Seyer A, Gazi AD, Giavalisco P, Perin S, Boucher JL, Le Corre L, Santorelli FM, Goizet C, Zaki MS, Picaud S, Mourier A, Steculorum SM, Mignot C, Durr A, Trifunovic A, Stevanin G. Pujol C, et al. Among authors: kuntzer t. J Exp Med. 2021 Nov 1;218(11):e20210846. doi: 10.1084/jem.20210846. Epub 2021 Sep 21. J Exp Med. 2021. PMID: 34546337 Free PMC article.
[Neurology].
Maulucci F, Benninger D, Démonet JF, Du Pasquier RA, Hirt L, Hottinger A, Kuntzer T, Michel P, Nater B, Novy J, Rossetti AO, Schluep M, Vingerhoets FJG. Maulucci F, et al. Among authors: kuntzer t. Rev Med Suisse. 2017 Jan 11;13(544-545):79-83. Rev Med Suisse. 2017. PMID: 28703543 Review. French.
[Neurology].
Sokolov AA, Rossetti AO, Michel P, Benninger D, Nater B, Wider C, Hirt L, Kuntzer T, Démonet JF, Du Pasquier RA, Vingerhoets F. Sokolov AA, et al. Among authors: kuntzer t. Rev Med Suisse. 2016 Jan 13;12(500):62, 64-6. Rev Med Suisse. 2016. PMID: 26946707 French.
[Neurology 2019].
Perrenoud M, Pantazou V, Michel P, Hirt L, Ryvlin P, Theaudin M, Rouaud O, Benninger D, Novy J, Rossetti AO, Kuntzer T, Diserens K, Pasquier RD. Perrenoud M, et al. Among authors: kuntzer t. Rev Med Suisse. 2020 Jan 15;16(676-7):68-71. Rev Med Suisse. 2020. PMID: 31961088 French.
The emerging spectrum of fetal acetylcholine receptor antibody-related disorders (FARAD).
Allen NM, O'Rahelly M, Eymard B, Chouchane M, Hahn A, Kearns G, Kim DS, Byun SY, Nguyen CE, Schara-Schmidt U, Kölbel H, Marina AD, Schneider-Gold C, Roefke K, Thieme A, Van den Bergh P, Avalos G, Álvarez-Velasco R, Natera-de Benito D, Cheng MHM, Chan WK, Wan HS, Thomas MA, Borch L, Lauzon J, Kornblum C, Reimann J, Mueller A, Kuntzer T, Norwood F, Ramdas S, Jacobson LW, Jie X, Fernandez-Garcia MA, Wraige E, Lim M, Lin JP, Claeys KG, Aktas S, Oskoui M, Hacohen Y, Masud A, Leite MI, Palace J, De Vivo D, Vincent A, Jungbluth H. Allen NM, et al. Among authors: kuntzer t. Brain. 2023 Oct 3;146(10):4233-4246. doi: 10.1093/brain/awad153. Brain. 2023. PMID: 37186601 Free PMC article.
250 results