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

Year Number of Results
1955 1
1956 2
1957 3
1958 2
1959 7
1960 8
1961 10
1962 1
1963 2
1964 6
1965 7
1966 3
1967 4
1968 7
1969 4
1970 10
1971 5
1972 3
1973 2
1974 2
1975 3
1976 1
1977 5
1978 2
1979 2
1980 6
1981 4
1982 3
1983 6
1984 1
1985 5
1986 13
1987 11
1988 11
1989 12
1990 10
1991 15
1992 15
1993 8
1994 4
1995 10
1996 6
1997 7
1998 9
1999 11
2000 7
2001 6
2002 3
2003 7
2004 10
2005 11
2006 11
2007 8
2008 9
2009 7
2010 7
2011 6
2012 10
2013 7
2014 1
2015 3
2016 9
2017 11
2018 10
2019 10
2020 6
2021 12
2022 0
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Article attribute
Article type
Publication date

Search Results

418 results
Results by year
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Page 1
Coronavirus disease 2019 in patients with inborn errors of immunity: An international study.
Meyts I, Bucciol G, Quinti I, Neven B, Fischer A, Seoane E, Lopez-Granados E, Gianelli C, Robles-Marhuenda A, Jeandel PY, Paillard C, Sankaran VG, Demirdag YY, Lougaris V, Aiuti A, Plebani A, Milito C, Dalm VA, Guevara-Hoyer K, Sánchez-Ramón S, Bezrodnik L, Barzaghi F, Gonzalez-Granado LI, Hayman GR, Uzel G, Mendonça LO, Agostini C, Spadaro G, Badolato R, Soresina A, Vermeulen F, Bosteels C, Lambrecht BN, Keller M, Mustillo PJ, Abraham RS, Gupta S, Ozen A, Karakoc-Aydiner E, Baris S, Freeman AF, Yamazaki-Nakashimada M, Scheffler-Mendoza S, Espinosa-Padilla S, Gennery AR, Jolles S, Espinosa Y, Poli MC, Fieschi C, Hauck F, Cunningham-Rundles C, Mahlaoui N; IUIS Committee of Inborn Errors of Immunity, Warnatz K, Sullivan KE, Tangye SG. Meyts I, et al. Among authors: fieschi c. J Allergy Clin Immunol. 2021 Feb;147(2):520-531. doi: 10.1016/j.jaci.2020.09.010. Epub 2020 Sep 24. J Allergy Clin Immunol. 2021. PMID: 32980424 Free PMC article.
Dominant-negative mutations in human IL6ST underlie hyper-IgE syndrome.
Béziat V, Tavernier SJ, Chen YH, Ma CS, Materna M, Laurence A, Staal J, Aschenbrenner D, Roels L, Worley L, Claes K, Gartner L, Kohn LA, De Bruyne M, Schmitz-Abe K, Charbonnier LM, Keles S, Nammour J, Vladikine N, Maglorius Renkilaraj MRL, Seeleuthner Y, Migaud M, Rosain J, Jeljeli M, Boisson B, Van Braeckel E, Rosenfeld JA, Dai H, Burrage LC, Murdock DR, Lambrecht BN, Avettand-Fenoel V, Vogel TP; Undiagnosed Diseases Network, Esther CR, Haskologlu S, Dogu F, Ciznar P, Boutboul D, Ouachée-Chardin M, Amourette J, Lebras MN, Gauvain C, Tcherakian C, Ikinciogullari A, Beyaert R, Abel L, Milner JD, Grimbacher B, Couderc LJ, Butte MJ, Freeman AF, Catherinot É, Fieschi C, Chatila TA, Tangye SG, Uhlig HH, Haerynck F, Casanova JL, Puel A. Béziat V, et al. Among authors: fieschi c. J Exp Med. 2020 Jun 1;217(6):e20191804. doi: 10.1084/jem.20191804. J Exp Med. 2020. PMID: 32207811 Free PMC article.
The full spectrum of Castleman disease: 273 patients studied over 20 years.
Oksenhendler E, Boutboul D, Fajgenbaum D, Mirouse A, Fieschi C, Malphettes M, Vercellino L, Meignin V, Gérard L, Galicier L. Oksenhendler E, et al. Among authors: fieschi c. Br J Haematol. 2018 Jan;180(2):206-216. doi: 10.1111/bjh.15019. Epub 2017 Nov 16. Br J Haematol. 2018. PMID: 29143319
Mutations in the SRP54 gene cause severe congenital neutropenia as well as Shwachman-Diamond-like syndrome.
Bellanné-Chantelot C, Schmaltz-Panneau B, Marty C, Fenneteau O, Callebaut I, Clauin S, Docet A, Damaj GL, Leblanc T, Pellier I, Stoven C, Souquere S, Antony-Debré I, Beaupain B, Aladjidi N, Barlogis V, Bauduer F, Bensaid P, Boespflug-Tanguy O, Berger C, Bertrand Y, Carausu L, Fieschi C, Galambrun C, Schmidt A, Journel H, Mazingue F, Nelken B, Quah TC, Oksenhendler E, Ouachée M, Pasquet M, Saada V, Suarez F, Pierron G, Vainchenker W, Plo I, Donadieu J. Bellanné-Chantelot C, et al. Among authors: fieschi c. Blood. 2018 Sep 20;132(12):1318-1331. doi: 10.1182/blood-2017-12-820308. Epub 2018 Jun 18. Blood. 2018. PMID: 29914977 Free PMC article.
Association of outcome with early stroke treatment: pooled analysis of ATLANTIS, ECASS, and NINDS rt-PA stroke trials.
Hacke W, Donnan G, Fieschi C, Kaste M, von Kummer R, Broderick JP, Brott T, Frankel M, Grotta JC, Haley EC Jr, Kwiatkowski T, Levine SR, Lewandowski C, Lu M, Lyden P, Marler JR, Patel S, Tilley BC, Albers G, Bluhmki E, Wilhelm M, Hamilton S; ATLANTIS Trials Investigators; ECASS Trials Investigators; NINDS rt-PA Study Group Investigators. Hacke W, et al. Among authors: fieschi c. Lancet. 2004 Mar 6;363(9411):768-74. doi: 10.1016/S0140-6736(04)15692-4. Lancet. 2004. PMID: 15016487
[Rosai-Dorfman disease].
Galicier L, Fieschi C, Meignin V, Clauvel JP, Oksenhendler E. Galicier L, et al. Among authors: fieschi c. Presse Med. 2007 Nov;36(11 Pt 2):1669-75. doi: 10.1016/j.lpm.2007.06.008. Epub 2007 Jul 3. Presse Med. 2007. PMID: 17611070 Review. French.
Revisiting human primary immunodeficiencies.
Casanova JL, Fieschi C, Zhang SY, Abel L. Casanova JL, et al. Among authors: fieschi c. J Intern Med. 2008 Aug;264(2):115-27. doi: 10.1111/j.1365-2796.2008.01971.x. Epub 2008 Jun 9. J Intern Med. 2008. PMID: 18544117 Free article. Review.
Randomised double-blind placebo-controlled trial of thrombolytic therapy with intravenous alteplase in acute ischaemic stroke (ECASS II). Second European-Australasian Acute Stroke Study Investigators.
Hacke W, Kaste M, Fieschi C, von Kummer R, Davalos A, Meier D, Larrue V, Bluhmki E, Davis S, Donnan G, Schneider D, Diez-Tejedor E, Trouillas P. Hacke W, et al. Among authors: fieschi c. Lancet. 1998 Oct 17;352(9136):1245-51. doi: 10.1016/s0140-6736(98)08020-9. Lancet. 1998. PMID: 9788453 Clinical Trial.
[Adult-onset primary hypogammaglobulinemia].
Fieschi C, Malphettes M, Galicier L, Oksenhendler E. Fieschi C, et al. Presse Med. 2006 May;35(5 Pt 2):887-94. doi: 10.1016/s0755-4982(06)74708-x. Presse Med. 2006. PMID: 16710162 Review. French.
418 results