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

Year Number of Results
1991 1
1992 1
1993 1
1995 2
1996 2
1997 4
1998 1
2000 5
2001 4
2002 5
2003 2
2004 9
2005 10
2006 9
2007 17
2008 10
2009 11
2010 7
2011 14
2012 13
2013 9
2014 10
2015 9
2016 9
2017 10
2018 7
2019 4
2020 7
2021 12
2022 9
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187 results
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Page 1
Update of variants identified in the pancreatic β-cell KATP channel genes KCNJ11 and ABCC8 in individuals with congenital hyperinsulinism and diabetes.
De Franco E, Saint-Martin C, Brusgaard K, Knight Johnson AE, Aguilar-Bryan L, Bowman P, Arnoux JB, Larsen AR, Sanyoura M, Greeley SAW, Calzada-León R, Harman B, Houghton JAL, Nishimura-Meguro E, Laver TW, Ellard S, Del Gaudio D, Christesen HT, Bellanné-Chantelot C, Flanagan SE. De Franco E, et al. Among authors: bellanne chantelot c. Hum Mutat. 2020 May;41(5):884-905. doi: 10.1002/humu.23995. Epub 2020 Feb 17. Hum Mutat. 2020. PMID: 32027066 Free PMC article. Review.
Chronic neutropenia: how best to assess severity and approach management?
Donadieu J, Frenz S, Merz L, Sicre De Fontbrune F, Rotulo GA, Beaupain B, Biosse-Duplan M, Audrain M, Croisille L, Ancliff P, Klein C, Bellanné-Chantelot C. Donadieu J, et al. Among authors: bellanne chantelot c. Expert Rev Hematol. 2021 Oct;14(10):945-960. doi: 10.1080/17474086.2021.1976634. Epub 2021 Oct 8. Expert Rev Hematol. 2021. PMID: 34486458
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. 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.
Post-COVID-19 severe neutropenia.
Bouslama B, Pierret C, Khelfaoui F, Bellanné-Chantelot C, Donadieu J, Héritier S. Bouslama B, et al. Among authors: bellanne chantelot c. Pediatr Blood Cancer. 2021 May;68(5):e28866. doi: 10.1002/pbc.28866. Epub 2020 Dec 23. Pediatr Blood Cancer. 2021. PMID: 33355971 Free PMC article. No abstract available.
Heterozygous variants of CLPB are a cause of severe congenital neutropenia.
Warren JT, Cupo RR, Wattanasirakul P, Spencer DH, Locke AE, Makaryan V, Bolyard AA, Kelley ML, Kingston NL, Shorter J, Bellanné-Chantelot C, Donadieu J, Dale DC, Link DC. Warren JT, et al. Among authors: bellanne chantelot c. Blood. 2022 Feb 3;139(5):779-791. doi: 10.1182/blood.2021010762. Blood. 2022. PMID: 34115842
Epidemiology of congenital neutropenia.
Donadieu J, Beaupain B, Mahlaoui N, Bellanné-Chantelot C. Donadieu J, et al. Among authors: bellanne chantelot c. Hematol Oncol Clin North Am. 2013 Feb;27(1):1-17, vii. doi: 10.1016/j.hoc.2012.11.003. Hematol Oncol Clin North Am. 2013. PMID: 23351985 Review.
187 results