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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
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84 results
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Page 1
Addressing the diagnostic gaps in pyruvate kinase deficiency: Consensus recommendations on the diagnosis of pyruvate kinase deficiency.
Bianchi P, Fermo E, Glader B, Kanno H, Agarwal A, Barcellini W, Eber S, Hoyer JD, Kuter DJ, Maia TM, Mañu-Pereira MDM, Kalfa TA, Pissard S, Segovia JC, van Beers E, Gallagher PG, Rees DC, van Wijk R; with the endorsement of EuroBloodNet, the European Reference Network in Rare Hematological Diseases. Bianchi P, et al. Among authors: pissard s. Am J Hematol. 2019 Jan;94(1):149-161. doi: 10.1002/ajh.25325. Epub 2018 Nov 28. Am J Hematol. 2019. PMID: 30358897 Free PMC article.
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.
A new gene associated with a β-thalassemia phenotype: the observation of variants in SUPT5H.
Achour A, Koopmann T, Castel R, Santen GWE, den Hollander N, Knijnenburg J, Ruivenkamp CAL, Arkesteijn SGJ, Ter Huurne J, Bisoen S, Verschuren M, Vijfhuizen L, Schaap R, Grimbergen A, Slomp J, Traeger-Synodinos J, Vrettou C, Pissard S, Galacteros F, Baas F, Harteveld CL. Achour A, et al. Among authors: pissard s. Blood. 2020 Oct 8;136(15):1789-1793. doi: 10.1182/blood.2020005934. Blood. 2020. PMID: 32589702 Free article. No abstract available.
Characterization and identification of Hb Bart's hydrops fetalis caused by a compound heterozygous mutation --SEA /--CR , a novel α0 -thalassemia deletion.
Ruengdit C, Panyasai S, Kunyanone N, Phornsiricharoenphant W, Ngamphiw C, Tongsima S, Sripichai O, Pissard S, Pornprasert S. Ruengdit C, et al. Among authors: pissard s. Int J Lab Hematol. 2020 Jun;42(3):e116-e120. doi: 10.1111/ijlh.13154. Epub 2020 Jan 13. Int J Lab Hematol. 2020. PMID: 31943793 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
Elevated soluble α-hemoglobin pool in sickle cell anemia.
Vasseur C, Domingues-Hamdi E, Pakdaman S, Barau C, Pissard S, Le Corvoisier P, Pirenne F, Galactéros F, Baudin-Creuza V. Vasseur C, et al. Among authors: pissard s. Am J Hematol. 2017 Oct;92(10):E593-E595. doi: 10.1002/ajh.24835. Epub 2017 Jul 24. Am J Hematol. 2017. PMID: 28646539 Free article. No abstract available.
Amyl nitrite inhalation, a "volatile" anemia.
Filliatre L, Broséus J, Pissard S, Mekki C, Feugier P, Perrin J. Filliatre L, et al. Among authors: pissard s. Am J Hematol. 2016 Jun;91(4):448. doi: 10.1002/ajh.24229. Am J Hematol. 2016. PMID: 26526075 Free article. No abstract available.
[SaO2 and PaO2 mismatch: Do not forget hemoglobinopathy].
Virot E, Hirschi S, Oswald M, Degot T, Canuet M, Galoisy AC, Kiger L, Pissard S, Kessler R. Virot E, et al. Among authors: pissard s. Rev Mal Respir. 2018 Mar;35(3):328-332. doi: 10.1016/j.rmr.2018.01.006. Epub 2018 Mar 24. Rev Mal Respir. 2018. PMID: 29580615 French.
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