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Did you mean amino berraho (7 results)?
[Post-traumatic scleromalacia].
Elyadari M, Berraho A. Elyadari M, et al. Among authors: berraho a. Pan Afr Med J. 2017 Oct 6;28:116. doi: 10.11604/pamj.2017.28.116.12267. eCollection 2017. Pan Afr Med J. 2017. PMID: 29515734 Free PMC article. French.
[Senile scleral plaques].
Elyadari M, Berraho A. Elyadari M, et al. Among authors: berraho a. Pan Afr Med J. 2017 Sep 14;28:31. doi: 10.11604/pamj.2017.28.31.11941. eCollection 2017. Pan Afr Med J. 2017. PMID: 29138667 Free PMC article. French. No abstract available.
Elimination of trachoma from Morocco: a historical review.
Hammou J, Obtel M, Razine R, Berraho A, Belmekki M. Hammou J, et al. Among authors: berraho a. East Mediterr Health J. 2020 Jun 24;26(6):713-719. doi: 10.26719/emhj.19.014. East Mediterr Health J. 2020. PMID: 32621507 Free article. Review.
Global initiative for congenital toxoplasmosis: an observational and international comparative clinical analysis.
El Bissati K, Levigne P, Lykins J, Adlaoui EB, Barkat A, Berraho A, Laboudi M, El Mansouri B, Ibrahimi A, Rhajaoui M, Quinn F, Murugesan M, Seghrouchni F, Gómez-Marín JE, Peyron F, McLeod R. El Bissati K, et al. Among authors: berraho a. Emerg Microbes Infect. 2018 Sep 27;7(1):165. doi: 10.1038/s41426-018-0164-4. Emerg Microbes Infect. 2018. PMID: 30262847 Free PMC article. Review.
[Congenital glaucoma and neurofibromatosis type 1].
Tzili N, El Orch H, Bencherifa F, Chefchaouni MC, Abdallah el H, Berraho A. Tzili N, et al. Among authors: berraho a. Pan Afr Med J. 2015 May 25;21:56. doi: 10.11604/pamj.2015.21.56.6794. eCollection 2015. Pan Afr Med J. 2015. PMID: 26405492 Free PMC article. Review. French.
[Bilateral tuberculous dacryoadenitis: about a case].
Rezzoug B, Tzili N, Ali H, Elyamouni O, El Khaoua M, Elorch H, El Hlimi R, El Hassan A, Berraho A. Rezzoug B, et al. Among authors: berraho a. Pan Afr Med J. 2015 Jan 12;20:26. doi: 10.11604/pamj.2015.20.26.4663. eCollection 2015. Pan Afr Med J. 2015. PMID: 26015846 Free PMC article. French.
Homozygous frameshift mutations in FAT1 cause a syndrome characterized by colobomatous-microphthalmia, ptosis, nephropathy and syndactyly.
Lahrouchi N, George A, Ratbi I, Schneider R, Elalaoui SC, Moosa S, Bharti S, Sharma R, Abu-Asab M, Onojafe F, Adadi N, Lodder EM, Laarabi FZ, Lamsyah Y, Elorch H, Chebbar I, Postma AV, Lougaris V, Plebani A, Altmueller J, Kyrieleis H, Meiner V, McNeill H, Bharti K, Lyonnet S, Wollnik B, Henrion-Caude A, Berraho A, Hildebrandt F, Bezzina CR, Brooks BP, Sefiani A. Lahrouchi N, et al. Among authors: berraho a. Nat Commun. 2019 Mar 12;10(1):1180. doi: 10.1038/s41467-019-08547-w. Nat Commun. 2019. PMID: 30862798 Free PMC article.
21 results