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11 results

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Page 1
[Subacute, rapidly evolving paraneoplastic retinopathy of unusual severity].
de Saint Sauveur G, Bacquet JL, Barreau E, Bénichou J, Chaabouni H, Gratiot C, Remichi R, Abdellaoui M, Chanson N, Lambotte O, Labetoulle M, Souied EH. de Saint Sauveur G, et al. Among authors: bacquet jl. J Fr Ophtalmol. 2021 May;44(5):e307-e311. doi: 10.1016/j.jfo.2020.08.014. Epub 2021 Jan 23. J Fr Ophtalmol. 2021. PMID: 33494973 French. No abstract available.
[A rare pigmented foveal lesion].
Bacquet JL, Uzzan J, Souied EH. Bacquet JL, et al. J Fr Ophtalmol. 2019 Oct;42(8):e379-e380. doi: 10.1016/j.jfo.2019.03.019. Epub 2019 Jun 1. J Fr Ophtalmol. 2019. PMID: 31164293 Review. French. No abstract available.
[Deep intracorneal foreign body: Anterior segment OCT].
Bacquet JL, Fel A, Belazzougui R, Bodaghi B. Bacquet JL, et al. J Fr Ophtalmol. 2015 Dec;38(10):1012-3. doi: 10.1016/j.jfo.2015.07.008. Epub 2015 Nov 25. J Fr Ophtalmol. 2015. PMID: 26612561 French. No abstract available.
Loss of Function of RIMS2 Causes a Syndromic Congenital Cone-Rod Synaptic Disease with Neurodevelopmental and Pancreatic Involvement.
Mechaussier S, Almoallem B, Zeitz C, Van Schil K, Jeddawi L, Van Dorpe J, Dueñas Rey A, Condroyer C, Pelle O, Polak M, Boddaert N, Bahi-Buisson N, Cavallin M, Bacquet JL, Mouallem-Bézière A, Zambrowski O, Sahel JA, Audo I, Kaplan J, Rozet JM, De Baere E, Perrault I. Mechaussier S, et al. Among authors: bacquet jl. Am J Hum Genet. 2020 Jun 4;106(6):859-871. doi: 10.1016/j.ajhg.2020.04.018. Epub 2020 May 28. Am J Hum Genet. 2020. PMID: 32470375 Free PMC article.
Loss of Function of RIMS2 Causes a Syndromic Congenital Cone-Rod Synaptic Disease with Neurodevelopmental and Pancreatic Involvement.
Mechaussier S, Almoallem B, Zeitz C, Van Schil K, Jeddawi L, Van Dorpe J, Rey AD, Condroyer C, Pelle O, Polak M, Boddaert N, Bahi-Buisson N, Cavallin M, Bacquet JL, Mouallem-Bézière A, Zambrowski O, Sahel JA, Audo I, Kaplan J, Rozet JM, De Baere E, Perrault I. Mechaussier S, et al. Among authors: bacquet jl. Am J Hum Genet. 2020 Sep 3;107(3):580. doi: 10.1016/j.ajhg.2020.08.004. Am J Hum Genet. 2020. PMID: 32888510 Free PMC article. No abstract available.
11 results