Odou MF - Search Results

1

Contribution of genetic analysis in screening for MEN1 among patients with sporadic disease and one or more typical manifestation.

Odou MF, Cardot-Bauters C, Vantyghem MC, Carnaille B, Leteurtre E, Pigny P, Verier-Mine O, Desailloud R, Porchet N. Odou MF, et al. Ann Endocrinol (Paris). 2006 Dec;67(6):581-7. doi: 10.1016/s0003-4266(06)73010-4. Ann Endocrinol (Paris). 2006. PMID: 17194968

2

[Calcium sensing receptor: physiology and pathology].

Faivre-Defrance F, Marcelli-Tourvieille S, Odou MF, Porchet N, Wemeau JL, Vantyghem MC. Faivre-Defrance F, et al. Among authors: odou mf. Ann Endocrinol (Paris). 2006 Mar;67(1):45-53. doi: 10.1016/s0003-4266(06)72540-9. Ann Endocrinol (Paris). 2006. PMID: 16596058 Review. French.

3

Multiple Endocrine Neoplasia Type 4: Novel CDNK1B variant and immune anomalies.

Chevalier B, Odou MF, Demonchy J, Cardot-Bauters C, Vantyghem MC. Chevalier B, et al. Among authors: odou mf. Ann Endocrinol (Paris). 2020 Jun;81(2-3):124-125. doi: 10.1016/j.ando.2020.04.002. Epub 2020 Apr 10. Ann Endocrinol (Paris). 2020. PMID: 32386678 No abstract available.

4

Diagnosis of alpha-1 antitrypsin deficiency: modalities, indications and diagnosis strategy.

Balduyck M, Odou MF, Zerimech F, Porchet N, Lafitte JJ, Maitre B. Balduyck M, et al. Among authors: odou mf. Rev Mal Respir. 2014 Oct;31(8):729-45. doi: 10.1016/j.rmr.2014.06.001. Epub 2014 Jul 3. Rev Mal Respir. 2014. PMID: 25391508 Review.

5

Diseases associated with calcium-sensing receptor.

Vahe C, Benomar K, Espiard S, Coppin L, Jannin A, Odou MF, Vantyghem MC. Vahe C, et al. Among authors: odou mf. Orphanet J Rare Dis. 2017 Jan 25;12(1):19. doi: 10.1186/s13023-017-0570-z. Orphanet J Rare Dis. 2017. PMID: 28122587 Free PMC article. Review.

6

Hereditary phaeochromocytomas and paragangliomas: a study of five susceptibility genes.

Bauters C, Vantyghem MC, Leteurtre E, Odou MF, Mouton C, Porchet N, Wemeau JL, Proye C, Pigny P. Bauters C, et al. Among authors: odou mf. J Med Genet. 2003 Jun;40(6):e75. doi: 10.1136/jmg.40.6.e75. J Med Genet. 2003. PMID: 12807974 Free PMC article. No abstract available.

7

[Screening for alpha1-antitrypsin deficiency using dried blood spot: Assessment of the first 20 months].

Chapuis Cellier C, Narjoz C, Zerimech F, Odou MF, Joly P, Lombard C, Mornex JF, Balduyck M. Chapuis Cellier C, et al. Among authors: odou mf. Rev Mal Respir. 2020 Oct;37(8):633-643. doi: 10.1016/j.rmr.2020.08.001. Epub 2020 Aug 25. Rev Mal Respir. 2020. PMID: 32859429 French.

8

[Alpha-1 antitrypsin deficiency caused by Null mutation].

Perrin J, Aimone-Gastin I, Balduyck M, Mercy M, Filhine-Trésarrieu P, Odou MF, Chaouat A, Chabot F. Perrin J, et al. Among authors: odou mf. Rev Mal Respir. 2016 Sep;33(7):612-7. doi: 10.1016/j.rmr.2015.10.007. Epub 2015 Nov 18. Rev Mal Respir. 2016. PMID: 26604020 French.

9

[Erratum to "Screening for alpha1-antitrypsin deficiency using dried blood spot: Assessment of the first 20 months" [Rev. Mal. Respir. 37 (2020) 633-43]].

Chapuis Cellier C, Narjoz C, Zerimech F, Odou MF, Joly P, Lombard C, Mornex JF, Balduyck M. Chapuis Cellier C, et al. Among authors: odou mf. Rev Mal Respir. 2021 Jan;38(1):125-126. doi: 10.1016/j.rmr.2020.11.011. Epub 2020 Dec 17. Rev Mal Respir. 2021. PMID: 33342663 French. No abstract available.

10

In vitro activity against anaerobes of retapamulin, a new topical antibiotic for treatment of skin infections.

Odou MF, Muller C, Calvet L, Dubreuil L. Odou MF, et al. J Antimicrob Chemother. 2007 Apr;59(4):646-51. doi: 10.1093/jac/dkm019. Epub 2007 Mar 9. J Antimicrob Chemother. 2007. PMID: 17350985

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