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

Year Number of Results
2004 1
2005 6
2006 6
2007 4
2009 4
2010 2
2011 4
2012 3
2013 6
2014 1
2015 1
2016 4
2017 2
2019 3
2020 4
2021 3
2022 3
2023 1
2024 1

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52 results

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Page 1
Erythrocytosis associated with IgA nephropathy.
Cohen C, Coulon S, Bhukhai K, Neuraz A, Dussiot M, Fouquet G, Stang ML, Flamant M, Vrtovsnik F, Hummel A, Knebelmann B, Mesnard L, Rondeau E, Maciel TT, Favale F, Casadevall N, Nguyen-Khoa T, Moutereau S, Legendre C, Benhamou M, Monteiro RC, Hermine O, El Karoui K, Moura IC. Cohen C, et al. Among authors: moutereau s. EBioMedicine. 2022 Jan;75:103785. doi: 10.1016/j.ebiom.2021.103785. Epub 2021 Dec 24. EBioMedicine. 2022. PMID: 34959131 Free PMC article.
[Effect of hemoglobin N Baltimore on HbA1c measurement in six methods].
Ratnam C, Yen Tran Houangkeo TH, Moutereau S, Plantamura J, Sollier M, Garcia C, Delacour H. Ratnam C, et al. Among authors: moutereau s. Ann Biol Clin (Paris). 2019 Apr 1;77(2):155-159. doi: 10.1684/abc.2019.1427. Ann Biol Clin (Paris). 2019. PMID: 30998195 Free article. Review. French.
Prevalence and determinants of iron deficiency in cardiac amyloidosis.
Jobbé-Duval A, Bézard M, Moutereau S, Kharoubi M, Oghina S, Zaroui A, Galat A, Chalard C, Hugon-Vallet E, Lemonnier F, Eyharts D, Poulot E, Fanen P, Funalot B, Molinier-Frenkel V, Audard V, Hittinger L, Delbarre MA, Teiger E, Damy T. Jobbé-Duval A, et al. Among authors: moutereau s. ESC Heart Fail. 2022 Apr;9(2):1314-1327. doi: 10.1002/ehf2.13818. Epub 2022 Feb 6. ESC Heart Fail. 2022. PMID: 35128833 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: moutereau 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 belated diagnosis of G6PD deficiency in an 81-year-old woman.
Tran Quang V, Tarfi S, Loustau V, Moutereau S, Michel M, Wagner-Ballon O. Tran Quang V, et al. Among authors: moutereau s. Ann Hematol. 2021 Jul;100(7):1901-1902. doi: 10.1007/s00277-021-04437-8. Epub 2021 Jan 27. Ann Hematol. 2021. PMID: 33506274 No abstract available.
Neuroendocrine disturbances in Huntington's disease.
Saleh N, Moutereau S, Durr A, Krystkowiak P, Azulay JP, Tranchant C, Broussolle E, Morin F, Bachoud-Lévi AC, Maison P. Saleh N, et al. Among authors: moutereau s. PLoS One. 2009;4(3):e4962. doi: 10.1371/journal.pone.0004962. Epub 2009 Mar 25. PLoS One. 2009. PMID: 19319184 Free PMC article.
Progensa™ PCA3 test for prostate cancer.
Durand X, Moutereau S, Xylinas E, de la Taille A. Durand X, et al. Among authors: moutereau s. Expert Rev Mol Diagn. 2011 Mar;11(2):137-44. doi: 10.1586/erm.10.122. Expert Rev Mol Diagn. 2011. PMID: 21405964
COMMD1 modulates noxious inflammation in cystic fibrosis.
de Becdelièvre A, Rocca J, Aissat A, Drévillon L, Moutereau S, Le Gouvello S, Hinzpeter A, Tarze A, Fanen P. de Becdelièvre A, et al. Among authors: moutereau s. Int J Biochem Cell Biol. 2013 Nov;45(11):2402-9. doi: 10.1016/j.biocel.2013.07.012. Epub 2013 Jul 24. Int J Biochem Cell Biol. 2013. PMID: 23892095
52 results