Odou MF - Search Results

1

[Development of a laboratory test on dried blood spots for facilitating early diagnosis of alpha-1-antitrypsin deficiency].

Balduyck M, Chapuis Cellier C, Roche D, Odou MF, Joly P, Madelain V, Vergne A, Nouadje G, Lafitte JJ, Porchet N, Beaune P, Zerimech F. Balduyck M, et al. Among authors: odou mf. Ann Biol Clin (Paris). 2014 Nov-Dec;72(6):689-704. doi: 10.1684/abc.2014.1004. Ann Biol Clin (Paris). 2014. PMID: 25486665 Free article. French.

2

Efficient mutation detection in MEN1 gene using a combination of single-strand conformation polymorphism (MDGA) and heteroduplex analysis.

Crépin M, Escande F, Pigny P, Buisine MP, Calender A, Porchet N, Odou MF; Groupe d'Etude des Neoplasies Endocriniennes Multiples, Lyon. Crépin M, et al. Among authors: odou mf. Electrophoresis. 2003 Jan;24(1-2):26-33. doi: 10.1002/elps.200390023. Electrophoresis. 2003. PMID: 12652570

3

Evaluation of denaturing high performance liquid chromatography for the mutational analysis of the MEN1 gene.

Crépin M, Pigny P, Escande F, Bauters CC, Calender A, Lefevre S, Buisine MP, Porchet N, Odou MF. Crépin M, et al. Among authors: odou mf. J Mol Endocrinol. 2006 Apr;36(2):369-76. doi: 10.1677/jme.1.01903. J Mol Endocrinol. 2006. PMID: 16595707

4

Frequent large germline HRPT2 deletions in a French National cohort of patients with primary hyperparathyroidism.

Bricaire L, Odou MF, Cardot-Bauters C, Delemer B, North MO, Salenave S, Vezzosi D, Kuhn JM, Murat A, Caron P, Sadoul JL, Silve C, Chanson P, Barlier A, Clauser E, Porchet N, Groussin L; GTE Group. Bricaire L, et al. Among authors: odou mf. J Clin Endocrinol Metab. 2013 Feb;98(2):E403-8. doi: 10.1210/jc.2012-2789. Epub 2013 Jan 4. J Clin Endocrinol Metab. 2013. PMID: 23293331

5

Hyperparathyroidism complicating CYP 24A1 mutations.

Loyer C, Leroy C, Molin A, Odou MF, Huglo D, Lion G, Ernst O, Hoffmann M, Porchet N, Carnaille B, Pattou F, Kottler ML, Vantyghem MC. Loyer C, et al. Among authors: odou mf. Ann Endocrinol (Paris). 2016 Oct;77(5):615-619. doi: 10.1016/j.ando.2016.03.002. Epub 2016 Jul 1. Ann Endocrinol (Paris). 2016. PMID: 27378451

6

Alpha1 antitrypsin deficiency due to an homozygous PI* Null Q0Cairo mutation: Early onset of pulmonary manifestations and variability of clinical expression.

Jouhadi Z, Odou MF, Zerimech F, Bousfiha AA, Mikou N, Porchet N, Crepin M, Najib J, Balduyck M. Jouhadi Z, et al. Among authors: odou mf. Respir Med Case Rep. 2018 Apr 10;24:58-62. doi: 10.1016/j.rmcr.2018.04.005. eCollection 2018. Respir Med Case Rep. 2018. PMID: 29977761 Free PMC article.

7

Description of 22 new alpha-1 antitrypsin genetic variants.

Renoux C, Odou MF, Tosato G, Teoli J, Abbou N, Lombard C, Zerimech F, Porchet N, Chapuis Cellier C, Balduyck M, Joly P. Renoux C, et al. Among authors: odou mf. Orphanet J Rare Dis. 2018 Sep 17;13(1):161. doi: 10.1186/s13023-018-0897-0. Orphanet J Rare Dis. 2018. PMID: 30223862 Free PMC article.

8

Multiplex targeted high-throughput sequencing in a series of 352 patients with congenital limb malformations.

Jourdain AS, Petit F, Odou MF, Balduyck M, Brunelle P, Dufour W, Boussion S, Brischoux-Boucher E, Colson C, Dieux A, Gérard M, Ghoumid J, Giuliano F, Goldenberg A, Khau Van Kien P, Lehalle D, Morin G, Moutton S, Smol T, Vanlerberghe C, Manouvrier-Hanu S, Escande F. Jourdain AS, et al. Among authors: odou mf. Hum Mutat. 2020 Jan;41(1):222-239. doi: 10.1002/humu.23912. Epub 2019 Sep 23. Hum Mutat. 2020. PMID: 31502745

9

p.Ala541Thr variant of MEN1 gene: a non deleterious polymorphism or a pathogenic mutation?

Nozières C, Zhang CX, Buffet A, Dupasquier S, Vargas-Poussou R, Guillaud-Bataille M, Cordier-Bussat M, Ruszniewski P, Christin-Maitre S, Murat A, Groussin L, Vezzosi D, Cardot-Bauters C, Hervieu V, Joly MO, Giraud S, Odou MF, Gimenez-Roqueplo AP, Goudet P, Borson-Chazot F, Calender A; Groupe français des tumeurs endocrines (GTE). Nozières C, et al. Among authors: odou mf. Ann Endocrinol (Paris). 2014 Jul;75(3):133-40. doi: 10.1016/j.ando.2014.05.003. Epub 2014 Jul 2. Ann Endocrinol (Paris). 2014. PMID: 24997771

10

Should the GCM2 gene be tested when screening for familial primary hyperparathyroidism?

Coppin L, Dufosse M, Romanet P, Giraud S, North MO, Cardot Bauters C, Borson-Chazot F, Duchesne L, Métallo M, Lovecchio T, Barlier A, Odou MF. Coppin L, et al. Among authors: odou mf. Eur J Endocrinol. 2020 Jan;182(1):57-65. doi: 10.1530/EJE-19-0641. Eur J Endocrinol. 2020. PMID: 31671402

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