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Page 1
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
Multiple thrombosis in a patient with Gardos channelopathy and a new KCNN4 mutation.
Mansour-Hendili L, Egée S, Monedero-Alonso D, Bouyer G, Godeau B, Badaoui B, Lunati A, Noizat C, Aissat A, Kiger L, Mekki C, Picard V, Moutereau S, Fanen P, Bartolucci P, Garçon L, Galactéros F, Funalot B. Mansour-Hendili L, et al. Among authors: moutereau s. Am J Hematol. 2021 Sep 1;96(9):E318-E321. doi: 10.1002/ajh.26245. Epub 2021 Jun 2. Am J Hematol. 2021. PMID: 34004026 Free article. No abstract available.
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.
'Desperate house genes': the dramatic example of hypoxia.
Caradec J, Sirab N, Keumeugni C, Moutereau S, Chimingqi M, Matar C, Revaud D, Bah M, Manivet P, Conti M, Loric S. Caradec J, et al. Among authors: moutereau s. Br J Cancer. 2010 Mar 16;102(6):1037-43. doi: 10.1038/sj.bjc.6605573. Epub 2010 Feb 23. Br J Cancer. 2010. PMID: 20179706 Free PMC article.
Insulin-Like Growth Factor-1 but Not Insulin Predicts Cognitive Decline in Huntington's Disease.
Salem L, Saleh N, Désaméricq G, Youssov K, Dolbeau G, Cleret L, Bourhis ML, Azulay JP, Krystkowiak P, Verny C, Morin F, Moutereau S; French Huntington Study Group; Bachoud-Lévi AC, Maison P. Salem L, et al. Among authors: moutereau s. PLoS One. 2016 Sep 14;11(9):e0162890. doi: 10.1371/journal.pone.0162890. eCollection 2016. PLoS One. 2016. PMID: 27627435 Free PMC article.
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.
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 diagnostic nomogram for delayed hemolytic transfusion reaction in sickle cell disease.
Mekontso Dessap A, Pirenne F, Razazi K, Moutereau S, Abid S, Brun-Buisson C, Maitre B, Michel M, Galacteros F, Bartolucci P, Habibi A. Mekontso Dessap A, et al. Among authors: moutereau s. Am J Hematol. 2016 Dec;91(12):1181-1184. doi: 10.1002/ajh.24537. Epub 2016 Sep 7. Am J Hematol. 2016. PMID: 27538126 Free article.
64 results