Copin H - Search Results

1

CENTRAL RETINAL VEIN OCCLUSION IN OTHERWISE HEALTHY CHILDREN AND ADOLESCENTS: Association With Multigenetic Variants of Thrombophilia.

Bremond-Gignac D, Daruich A, Gallet M, Menoud PA, Nowomiejska K, Rejdak R, Behar-Cohen F, Benkhalifa M, Copin H. Bremond-Gignac D, et al. Among authors: copin h. Retina. 2020 Jul;40(7):1339-1343. doi: 10.1097/IAE.0000000000002563. Retina. 2020. PMID: 31095065

2

Corneal epithelial stem cells for corneal injury.

Bremond-Gignac D, Copin H, Benkhalifa M. Bremond-Gignac D, et al. Among authors: copin h. Expert Opin Biol Ther. 2018 Sep;18(9):997-1003. doi: 10.1080/14712598.2018.1508443. Epub 2018 Aug 9. Expert Opin Biol Ther. 2018. PMID: 30092649 Review.

3

Contribution of Electronic Medical Records to the Management of Rare Diseases.

Bremond-Gignac D, Lewandowski E, Copin H. Bremond-Gignac D, et al. Among authors: copin h. Biomed Res Int. 2015;2015:954283. doi: 10.1155/2015/954283. Epub 2015 Oct 11. Biomed Res Int. 2015. PMID: 26539543 Free PMC article.

4

Azoospermia and trisomy 18p syndrome: a fortuitous association? A patient report and a review of the literature.

Jedraszak G, Copin H, Demailly M, Quibel C, Leclerc T, Gallet M, Benkhalifa M, Receveur A. Jedraszak G, et al. Among authors: copin h. Mol Cytogenet. 2015 Jun 4;8:34. doi: 10.1186/s13039-015-0141-8. eCollection 2015. Mol Cytogenet. 2015. PMID: 26042156 Free PMC article.

5

Comparison of two preventive treatments for patients with recurrent miscarriages carrying a C677T methylenetetrahydrofolate reductase mutation: 5-year experience.

Merviel P, Cabry R, Lourdel E, Lanta S, Amant C, Copin H, Benkhalifa M. Merviel P, et al. Among authors: copin h. J Int Med Res. 2017 Dec;45(6):1720-1730. doi: 10.1177/0300060516675111. Epub 2017 Jan 12. J Int Med Res. 2017. PMID: 28703660 Free PMC article.

6

Does the dysregulation of matrix metalloproteinases contribute to recurrent implantation failure?

Benkhalifa M, Zayani Y, Bach V, Copin H, Feki M, Benkhalifa M, Allal-Elasmi M. Benkhalifa M, et al. Among authors: copin h. Expert Rev Proteomics. 2018 Apr;15(4):311-323. doi: 10.1080/14789450.2018.1464915. Epub 2018 Apr 20. Expert Rev Proteomics. 2018. PMID: 29648896 Review.

7

Emerging molecular methods for male infertility investigation.

Benkhalifa M, Montjean D, Belloc S, Dalleac A, Ducasse M, Boyer P, Merviel P, Copin H. Benkhalifa M, et al. Among authors: copin h. Expert Rev Mol Diagn. 2014 Jan;14(1):37-45. doi: 10.1586/14737159.2014.864558. Epub 2013 Dec 5. Expert Rev Mol Diagn. 2014. PMID: 24308377 Review.

8

[Ocular manifestations of Down syndrome and cytogenic aspects].

Copin H, Brémond-Gignac D. Copin H, et al. J Fr Ophtalmol. 2004 Oct;27(8):958-9. doi: 10.1016/s0181-5512(04)96244-4. J Fr Ophtalmol. 2004. PMID: 15547481 French. No abstract available.

9

Visual development in infants: physiological and pathological mechanisms.

Brémond-Gignac D, Copin H, Lapillonne A, Milazzo S; European Network of Study and Research in Eye Development. Brémond-Gignac D, et al. Among authors: copin h. Curr Opin Ophthalmol. 2011 Apr;22 Suppl:S1-8. doi: 10.1097/01.icu.0000397180.37316.5d. Curr Opin Ophthalmol. 2011. PMID: 21478704 Review.

10

[WAGR Syndrome].

Brémond-Gignac D, Copin H. Brémond-Gignac D, et al. Among authors: copin h. J Fr Ophtalmol. 2004 Dec;27(10):1198-9. doi: 10.1016/s0181-5512(04)96295-x. J Fr Ophtalmol. 2004. PMID: 15687936 French. No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

97 results

Search Page