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

Year Number of Results
1994 1
1996 1
1997 1
1999 2
2000 2
2001 1
2002 1
2003 3
2004 1
2005 2
2006 3
2007 5
2008 2
2009 2
2010 6
2011 9
2012 7
2013 5
2014 8
2015 7
2016 7
2017 5
2018 6
2019 1
2020 6
2021 3
2022 2
2023 3
2024 1

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89 results

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Page 1
High risk of progression for chronic major organ complications of sickle cell disease in adolescents and young adults: A long-term neonatal cohort study.
Borgey M, Genty I, Habibi A, Arlet JB, Dhedin N, Lionnet F, Bernit E, Julan ME, Loko G, Arnaud C, Kamdem A, Pissard S, Guémas E, Noizat C, Pondarré C. Borgey M, et al. Among authors: pissard s. Am J Hematol. 2024 Apr 30. doi: 10.1002/ajh.27346. Online ahead of print. Am J Hematol. 2024. PMID: 38686944 No abstract available.
Clinical events in a long-term prospective neonatal cohort of children with sickle cell disease: Evidence for a high disease burden without systematic preventive intensification with hydroxyurea.
Soulié A, Kamdem A, Neumann F, Hau I, Madhi F, Delestrain C, Shum M, Carlier-Gonod A, Malterre A, Lezeau H, Khazem B, Belozertseva E, Guémas E, Epaud R, Pissard S, Arnaud C, Pondarré C. Soulié A, et al. Among authors: pissard s. Am J Hematol. 2023 Dec;98(12):E395-E398. doi: 10.1002/ajh.27142. Epub 2023 Oct 26. Am J Hematol. 2023. PMID: 37883505 No abstract available.
Homozygosity for the hyperunstable hemoglobin variant Hb Agrinio (HBA2:c.89T>C) leads to severe antenatal anemia: Eight new cases in three families.
Szepetowski S, Berger C, Joly P, Baron-Joly S, Huguenin Y, Cantais A, Brun S, Ged C, Badens C, Thuret I, Giansily-Blaizot M, Pissard S, Aguilar-Martinez P. Szepetowski S, et al. Among authors: pissard s. Am J Hematol. 2022 Nov;97(11):E393-E395. doi: 10.1002/ajh.26687. Epub 2022 Sep 2. Am J Hematol. 2022. PMID: 36052950 Free article. No abstract available.
Appropriate thresholds for accurate screening for β-thalassemias in the newborn period: results from a French center for newborn screening.
Allaf B, Pondarre C, Allali S, De Montalembert M, Arnaud C, Barrey C, Benkerrou M, Benhaim P, Bensaid P, Brousse V, Dollfus C, Eyssette-Guerreau S, Galacteros F, Gajdos V, Garrec N, Guillaumat C, Guitton C, Monfort-Gouraud M, Gouraud F, Holvoet L, Ithier G, Kamdem A, Koehl B, Malric A, Missud F, Monier B, Odièvre MH, Joly P, Renoux C, Patin F, Pissard S, Couque N. Allaf B, et al. Among authors: pissard s. Clin Chem Lab Med. 2020 Aug 19;59(1):209-216. doi: 10.1515/cclm-2020-0803. Clin Chem Lab Med. 2020. PMID: 32813673
Exome sequencing for diagnosis of congenital hemolytic anemia.
Mansour-Hendili L, Aissat A, Badaoui B, Sakka M, Gameiro C, Ortonne V, Wagner-Ballon O, Pissard S, Picard V, Ghazal K, Bahuau M, Guitton C, Mansour Z, Duplan M, Petit A, Costedoat-Chalumeau N, Michel M, Bartolucci P, Moutereau S, Funalot B, Galactéros F. Mansour-Hendili L, et al. Among authors: pissard s. Orphanet J Rare Dis. 2020 Jul 8;15(1):180. doi: 10.1186/s13023-020-01425-5. Orphanet J Rare Dis. 2020. PMID: 32641076 Free PMC article.
89 results