Výsledky vyhledávání - "Bessières, B"

Akademický článek

Foetal achondroplasia: Prenatal diagnosis, outcome and perspectives.

Autor: Vallin AL; Department of Obstetrics, Foetal Medicine and Surgery, Necker-Enfants Malades Hospital, APHP, University Paris Cité, Paris, France; URP FETUS 7328, Federation for Research into Innovative Explorations and Therapeutics in Utero, and LUMIERE Platform, University of Paris Cité, Paris, France., Grévent D; URP FETUS 7328, Federation for Research into Innovative Explorations and Therapeutics in Utero, and LUMIERE Platform, University of Paris Cité, Paris, France; Department of Paediatric Radiology, Necker-Enfants Malades Hospital, APHP, University Paris Cité, Paris, France., Bessières B; URP FETUS 7328, Federation for Research into Innovative Explorations and Therapeutics in Utero, and LUMIERE Platform, University of Paris Cité, Paris, France; Department of anatomical pathology, Necker-Enfants Malades Hospital, APHP, University Paris Cité, Paris, France., Salomon LJ; Department of Obstetrics, Foetal Medicine and Surgery, Necker-Enfants Malades Hospital, APHP, University Paris Cité, Paris, France; URP FETUS 7328, Federation for Research into Innovative Explorations and Therapeutics in Utero, and LUMIERE Platform, University of Paris Cité, Paris, France., Legeai-Mallet L; INSERM UMR 1163, Molecular and physiopathological bases of osteochondrodysplasia, Institut IMAGINE, Paris, France., Cormier-Daire V; INSERM UMR 1163, Molecular and physiopathological bases of osteochondrodysplasia, Institut IMAGINE, Paris, France; Université Paris Cité, Centre Référence des Maladies Osseuses Constitutionnelles, Hôpital Necker Enfants Malades, Paris, France., Baujat G; INSERM UMR 1163, Molecular and physiopathological bases of osteochondrodysplasia, Institut IMAGINE, Paris, France; Université Paris Cité, Centre Référence des Maladies Osseuses Constitutionnelles, Hôpital Necker Enfants Malades, Paris, France., Ville Y; Department of Obstetrics, Foetal Medicine and Surgery, Necker-Enfants Malades Hospital, APHP, University Paris Cité, Paris, France; URP FETUS 7328, Federation for Research into Innovative Explorations and Therapeutics in Utero, and LUMIERE Platform, University of Paris Cité, Paris, France., Faure-Bardon V; URP FETUS 7328, Federation for Research into Innovative Explorations and Therapeutics in Utero, and LUMIERE Platform, University of Paris Cité, Paris, France; Department of Obstetrics and Gynecology, Pitié-Salpêtrière Hospital, APHP, Sorbonne University, Paris, France. Electronic address: valentine.faure@aphp.fr.

Publikováno v: Journal of gynecology obstetrics and human reproduction [J Gynecol Obstet Hum Reprod] 2024 Dec 05; Vol. 54 (2), pp. 102891. Date of Electronic Publication: 2024 Dec 05.

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Akademický článek

An exceptional anomaly of the coronary venous drainage: anatomic description.

Autor: Hily M; Congenital and Pediatric Cardiology Unit, M3C-Necker, APHP, Hôpital Necker-Enfants malades, Paris, France.; Université Paris Cité, Paris, France., Bessières B; Fetal Pathology Unit, APHP, Hôpital Necker-Enfants malades, Paris, France., Bonnet D; Congenital and Pediatric Cardiology Unit, M3C-Necker, APHP, Hôpital Necker-Enfants malades, Paris, France.; Université Paris Cité, Paris, France., Houyel L; Congenital and Pediatric Cardiology Unit, M3C-Necker, APHP, Hôpital Necker-Enfants malades, Paris, France.; Université Paris Cité, Paris, France.

Publikováno v: Cardiology in the young [Cardiol Young] 2024 Nov 18, pp. 1-5. Date of Electronic Publication: 2024 Nov 18.

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Akademický článek

Synaptic rearrangement of NMDA receptors controls memory engram formation and malleability in the cortex.

Autor: Bessières B; Institut des Maladies Neurodégénératives, CNRS UMR 5293, Université de Bordeaux, Bordeaux 33000, France., Dupuis J; Institut Interdisciplinaire de Neurosciences, CNRS UMR 5297, Université de Bordeaux, Bordeaux 33000, France., Groc L; Institut Interdisciplinaire de Neurosciences, CNRS UMR 5297, Université de Bordeaux, Bordeaux 33000, France., Bontempi B; Institut des Maladies Neurodégénératives, CNRS UMR 5293, Université de Bordeaux, Bordeaux 33000, France.; Institut de Neurosciences Cognitives et Intégratives d'Aquitaine, CNRS UMR 5287, Université de Bordeaux, Bordeaux 33000, France., Nicole O; Institut des Maladies Neurodégénératives, CNRS UMR 5293, Université de Bordeaux, Bordeaux 33000, France.; Institut Interdisciplinaire de Neurosciences, CNRS UMR 5297, Université de Bordeaux, Bordeaux 33000, France.

Publikováno v: Science advances [Sci Adv] 2024 Aug 30; Vol. 10 (35), pp. eado1148. Date of Electronic Publication: 2024 Aug 30.

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Periodical

Matthew‐Wood syndrome: Report of two new cases supporting autosomal recessive inheritance and exclusion of FGF10 and FGFR2How to cite this article: Martinovic‐Bouriel J, Bernabé‐Dupont C, Golzio C, Grattagliano‐Bessières B, Malan V, Bonnière M, Esculpavit C, Fallet‐Bianco C, Mirlesse V, Le Bidois J, Aubry M‐C, Vekemans M, Morichon N, Etchevers H, Attié‐Bitach T, Encha‐Razavi F, Benachi A. 2007. Matthew‐Wood syndrome: Report of two new cases supporting autosomal recessive inheritance and exclusion of FGF10 and FGFR2. Am J Med Genet Part A.Jelena Martinovic‐Bouriel, Céline Bernabé‐Dupont, and Christelle Golzio have contributed equally to this work.

Autor: Martinovic‐Bouriel, Jelena, Bernabé‐Dupont, Céline, Golzio, Christelle, Grattagliano‐Bessières, Bettina, Malan, Valérie, Bonnière, Maryse, Esculpavit, Chantal, Fallet‐Bianco, Catherine, Mirlesse, Véronique, Le Bidois, Jerôme, Aubry, Marie‐Cécile, Vekemans, Michel, Morichon, Nicole, Etchevers, Heather, Attié‐Bitach, Tania, Encha‐Razavi, Féréchté, Benachi, Alexandra

Publikováno v: American Journal of Medical Genetics. Part A; February 2007, Vol. 143 Issue: 3 p219-228, 10p

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Akademický článek

Prenatally diagnosed periventricular nodular heterotopia: Further delineation of the imaging phenotype and outcome

Autor: Deloison, B., Sonigo, P., Millischer-Bellaiche, A.E., Quibel, T., Cavallin, M., Benoist, G., Quelin, C., Jouk, P.S., Lev, D., Alison, M., Baumann, C., Beldjord, C., Razavi, F., Bessières, B., Boddaert, N., Ville, Y., Salomon, L.J., Bahi-Buisson, N.

Publikováno v: In European Journal of Medical Genetics December 2018 61(12):773-782

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Akademický článek

A cell fate decision map reveals abundant direct neurogenesis bypassing intermediate progenitors in the human developing neocortex.

Autor: Coquand L; Institut Curie, PSL Research University, CNRS UMR144, Paris, France.; Sorbonne Université, Ecole Doctorale complexité du vivant, Paris, France., Brunet Avalos C; Institut Curie, PSL Research University, CNRS UMR144, Paris, France. clarisse.brunet@curie.fr., Macé AS; UMR 144-Cell and Tissue Imaging Facility (PICT-IBiSA), CNRS-Institut Curie, Paris, France., Farcy S; Institut Curie, PSL Research University, CNRS UMR144, Paris, France., Di Cicco A; Institut Curie, PSL Research University, CNRS UMR144, Paris, France., Lampic M; Institut Curie, PSL Research University, CNRS UMR144, Paris, France., Wimmer R; Institut Curie, PSL Research University, CNRS UMR144, Paris, France.; Sorbonne Université, Ecole Doctorale complexité du vivant, Paris, France., Bessières B; UF Embryofœtopathologie, Hopital Necker-enfants malades, Paris, France., Attie-Bitach T; UF Embryofœtopathologie, Hopital Necker-enfants malades, Paris, France., Fraisier V; UMR 144-Cell and Tissue Imaging Facility (PICT-IBiSA), CNRS-Institut Curie, Paris, France., Sens P; Institut Curie, PSL Research University, CNRS UMR168, Paris, France., Guimiot F; UF de Fœtopathologie - Université de Paris et Inserm UMR1141, Hôpital Robert Debré, Paris, France., Brault JB; Institut Curie, PSL Research University, CNRS UMR144, Paris, France., Baffet AD; Institut Curie, PSL Research University, CNRS UMR144, Paris, France. alexandre.baffet@curie.fr.; Institut national de la santé et de la recherche médicale, Paris, France. alexandre.baffet@curie.fr.

Publikováno v: Nature cell biology [Nat Cell Biol] 2024 May; Vol. 26 (5), pp. 698-709. Date of Electronic Publication: 2024 Mar 28.

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