Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Nassima Bouzidi"'
Autor:
Juliette Varin, Nassima Bouzidi, Gregory Gauvain, Corentin Joffrois, Melissa Desrosiers, Camille Robert, Miguel Miranda De Sousa Dias, Marion Neuillé, Christelle Michiels, Marco Nassisi, José-Alain Sahel, Serge Picaud, Isabelle Audo, Deniz Dalkara, Christina Zeitz
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 22, Iss , Pp 15-25 (2021)
Complete congenital stationary night blindness (cCSNB) due to mutations in TRPM1, GRM6, GPR179, NYX, or leucine-rich repeat immunoglobulin-like transmembrane domain 3 (LRIT3) is an incurable inherited retinal disorder characterized by an ON-bipolar c
Externí odkaz:
https://doaj.org/article/1f04f05b98504f5194e6bd3d6cde288d
Autor:
Juliette Varin, Margaret M Reynolds, Nassima Bouzidi, Sarah Tick, Juliette Wohlschlegel, Ondine Becquart, Christelle Michiels, Olivier Dereure, Robert M Duvoisin, Catherine W Morgans, José-Alain Sahel, Quentin Samaran, Bernard Guillot, José S Pulido, Isabelle Audo, Christina Zeitz
Publikováno v:
PLoS ONE, Vol 15, Iss 4, p e0231750 (2020)
Melanoma-associated retinopathy (MAR) is a rare paraneoplastic retinal disorder usually occurring in the context of metastatic melanoma. Patients present with night blindness, photopsias and a constriction of the visual field. MAR is an auto-immune d
Externí odkaz:
https://doaj.org/article/7aa5b93b3b9e44f19da22f7f7d64c257
Autor:
Christina Zeitz, Jerome E. Roger, Christelle Michiels, Nuria Sánchez‐Farías, Juliette Varin, Helen Frederiksen, Baptiste Wilmet, Marie‐Laure Gimenez, Nassima Bouzidi, Frederic Blond, Xavier Guilllonneau, Thierry Léveillard, José‐Alain Sahel, Serge Picaud, Isabelle Audo
Publikováno v:
Acta Ophthalmologica. 100
Autor:
Miguel Miranda de Sousa Dias, José-Alain Sahel, Serge Picaud, Christelle Michiels, Melissa Desrosiers, Isabelle Audo, Marco Nassisi, Camille Robert, Deniz Dalkara, Christina Zeitz, Marion Neuillé, Nassima Bouzidi, Corentin Joffrois, Juliette Varin, Gregory Gauvain
Publikováno v:
Molecular Therapy-Methods and Clinical Development
Molecular Therapy-Methods and Clinical Development, 2021, 22, pp.15-25. ⟨10.1016/j.omtm.2021.05.008⟩
Molecular Therapy-Methods and Clinical Development, Nature Publishing Group, 2021, 22, pp.15-25. ⟨10.1016/j.omtm.2021.05.008⟩
Molecular Therapy: Methods & Clinical Development, Vol 22, Iss, Pp 15-25 (2021)
Molecular Therapy. Methods & Clinical Development
Molecular Therapy-Methods and Clinical Development, 2021, 22, pp.15-25. ⟨10.1016/j.omtm.2021.05.008⟩
Molecular Therapy-Methods and Clinical Development, Nature Publishing Group, 2021, 22, pp.15-25. ⟨10.1016/j.omtm.2021.05.008⟩
Molecular Therapy: Methods & Clinical Development, Vol 22, Iss, Pp 15-25 (2021)
Molecular Therapy. Methods & Clinical Development
Complete congenital stationary night blindness (cCSNB) due to mutations in TRPM1, GRM6, GPR179, NYX, or leucine-rich repeat immunoglobulin-like transmembrane domain 3 (LRIT3) is an incurable inherited retinal disorder characterized by an ON-bipolar c
Autor:
Christina Zeitz, Jérome E. Roger, Isabelle Audo, Christelle Michiels, Nuria Sánchez-Farías, Juliette Varin, Helen Frederiksen, Baptiste Wilmet, Jacques Callebert, Marie-Laure Gimenez, Nassima Bouzidi, Frederic Blond, Xavier Guilllonneau, Stéphane Fouquet, Thierry Léveillard, Vasily Smirnov, Ajoy Vincent, Elise Héon, José-Alain Sahel, Barbara Kloeckener-Gruissem, Florian Sennlaub, Catherine W. Morgans, Robert M. Duvoisin, Andrei V. Tkatchenko, Serge Picaud
Publikováno v:
Progress in Retinal and Eye Research. 93:101155
Autor:
Juliette, Varin, Nassima, Bouzidi, Miguel Miranda De Sousa, Dias, Thomas, Pugliese, Christelle, Michiels, Camille, Robert, Melissa, Desrosiers, José-Alain, Sahel, Isabelle, Audo, Deniz, Dalkara, Christina, Zeitz
Publikováno v:
Investigative Ophthalmology & Visual Science
Purpose Complete congenital stationary night blindness (cCSNB) is an incurable inherited retinal disorder characterized by an ON-bipolar cell (ON-BC) defect. GRM6 mutations are the third most prevalent cause of cCSNB. The Grm6−/− mouse model mimi
Autor:
Juliette Wohlschlegel, Juliette Varin, Margaret M. Reynolds, S. Tick, Nassima Bouzidi, O. Becquart
Publikováno v:
PLoS ONE, Vol 15, Iss 5, p e0233424 (2020)
[This corrects the article DOI: 10.1371/journal.pone.0231750.].
Autor:
Amina Tiali, Nassima Bouzidi-bekada, Bouchenak Malika, Ouarda Taleb-Belkadi, A. Kaddous, Khedidja Mekki, Hadja Fatima Tbahriti
Publikováno v:
British Journal of Medicine and Medical Research. 4:4169-4177
Aims: The purpose of this study was to evaluate the effect of vitamin E supplementation on oxidant-antioxidant balance in chronic renal failure patients treated by hemodialysis. Study Design: The study utilized a randomized experimental design. The e
Autor:
Seana O'Regan, Tiziana Mongini, Céline Buon, Anne Marie Beaufrere, Yoshiteru Azuma, Bertrand Fontaine, Hanns Lochmüller, S. Bauche, Ana Töpf, Chiara Fiorillo, Jean-François Deleuze, E. Lacène, Julien Thevenon, Gisèle Bonne, Damien Sternberg, C. Burloiu, Yannis Duffourd, Isabelle Desguerre, Isabelle Nelson, Guy Brochier, Anne Boland, Benoit Bœuf, Michèle Mayer, Laure Strochlic, Jocelyn Laporte, Laurence Faivre, Sophie Nicole, Ganaelle Remerand, Céline Pebrel-Richard, Laurent Servais, Federica Ricci, Guja Astrea, Doris Lechner, Salima El Chehadeh-Djebbar, Nassima Bouzidi, Fanny Laffargue, Bruno Eymard, Marie Christine Nougues, Norma B. Romero, Grace McMacken, Carmen Sandu, Niculina Butoianu
Publikováno v:
American Journal of Human Genetics
American Journal of Human Genetics, 2016, 99 (3), pp.753-761. ⟨10.1016/j.ajhg.2016.06.033⟩
American Journal of Human Genetics, Elsevier (Cell Press), 2016, 99 (3), pp.753-761. ⟨10.1016/j.ajhg.2016.06.033⟩
American Journal of Human Genetics, 2016, 99 (3), pp.753-761. ⟨10.1016/j.ajhg.2016.06.033⟩
American Journal of Human Genetics, Elsevier (Cell Press), 2016, 99 (3), pp.753-761. ⟨10.1016/j.ajhg.2016.06.033⟩
International audience; The neuromuscular junction (NMJ) is one of the best-studied cholinergic synapses. Inherited defects of peripheral neurotransmission result in congenital myasthenic syndromes (CMS5), a clinically and genetically heterogeneous g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b7aaebb223eac493cf088535a38db5c
https://hal.science/hal-03993840
https://hal.science/hal-03993840
Publikováno v:
Annales de Cardiologie et d'Angéiologie. 64:S47
Objectifs L'objectif de cette etude et d'evaluer l'effet de l'âge et de la menopause sur le profil lipidique et lipoproteique chez des femmes de l'ouest algerien. Methodes L'etude est realisee sur 49 femmes divisees en 3 groupes (15 femmes non menop