Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Fanny Sauvestre"'
Autor:
Aurélien Mattuizzi, Fanny Sauvestre, Tiphaine Fargeix, Eoghann White, Claire Leibler, Marine Cargou, Nathalie Dugot-Senant, Isabelle Douchet, Dorothée Duluc, Cécile Bordes, Marie-Élise Truchetet, Christophe Richez, Édouard Forcade, Pierre Duffau, Jean-François Viallard, Loïc Sentilhes, Patrick Blanco, Estibaliz Lazaro
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-9 (2024)
Abstract Chronic histiocytic intervillositis of unknown origin (CHI) is a rare placental disorder associated with adverse pregnancy outcomes, frequent recurrence, and a lack of effective preventive strategies. Recent insights indicate a potential lin
Externí odkaz:
https://doaj.org/article/280de072b126442aae0d33eab281516f
Autor:
Florent Marguet, Mélanie Brosolo, Gaëlle Friocourt, Fanny Sauvestre, Pascale Marcorelles, Céline Lesueur, Stéphane Marret, Bruno J. Gonzalez, Annie Laquerrière
Publikováno v:
Acta Neuropathologica Communications, Vol 10, Iss 1, Pp 1-14 (2022)
Abstract Prenatal alcohol exposure is a major cause of neurobehavioral disabilities. MRI studies in humans have shown that alcohol is associated with white matter microstructural anomalies but these studies focused on myelin abnormalities only after
Externí odkaz:
https://doaj.org/article/c6fe454e7389405893008d9f46d22ed9
Autor:
Florent Marguet, Gaëlle Friocourt, Mélanie Brosolo, Fanny Sauvestre, Pascale Marcorelles, Céline Lesueur, Stéphane Marret, Bruno J. Gonzalez, Annie Laquerrière
Publikováno v:
Acta Neuropathologica Communications, Vol 8, Iss 1, Pp 1-18 (2020)
Abstract Alcohol affects multiple neurotransmitter systems, notably the GABAergic system and has been recognised for a long time as particularly damaging during critical stages of brain development. Nevertheless, data from the literature are most oft
Externí odkaz:
https://doaj.org/article/a5d8bc55a1d04ab0bee1d4b0d9ca9fcb
Autor:
Aurélien Trimouille, Florent Marguet, Fanny Sauvestre, Eulalie Lasseaux, Fanny Pelluard, Marie-Laure Martin-Négrier, Claudio Plaisant, Caroline Rooryck, Didier Lacombe, Benoît Arveiler, Odile Boespflug-Tanguy, Sophie Naudion, Annie Laquerrière
Publikováno v:
Acta Neuropathologica Communications, Vol 8, Iss 1, Pp 1-7 (2020)
Abstract Bi-allelic pathogenic variants in genes of the EIF2B family are responsible for Childhood Ataxia with Central nervous system Hypomyelination/Vanishing White Matter disease, a progressive neurodegenerative disorder of the central white matter
Externí odkaz:
https://doaj.org/article/8c691012645f42059f22d1f2c7825268
Autor:
Eva Kohaut, Flavie Ader, Caroline Rooryck, Fanny Pelluard, Maryse Bonnière, Gwenaelle André, Fanny Sauvestre, Philippe Roth, Diala Khraiche, Bettina Bessières, Tania Attié‐Bitach, Pascale Richard
Publikováno v:
Clinical Genetics.
Autor:
Cécile Courdier, John Boudjarane, Valérie Malan, Christine Muti, Brian Sperelakis‐Beedham, Sylvie Odent, Sylvie Jaillard, Chloé Quelin, Cédric Le Caignec, Olivier Patat, Charlotte Dubucs, Sophie Julia, Caroline Schluth‐Bolard, Carole Goumy, Sylvia Redon, Jean‐Baptiste Gaillard, Minh Tuan Huynh, Céline Dupont, Anne‐Claude Tabet, Guillaume Cogan, François Vialard, Rodolphe Dard, Guillaume Jedraszak, Florence Jobic, Mathilde Lefebvre, Geneviève Quenum, Saori Inai, Mélanie Rama, Fanny Sauvestre, Frédéric Coatleven, Julie Thomas, Caroline Rooryck
Publikováno v:
Prenatal Diagnosis
Prenatal Diagnosis, 2023, ⟨10.1002/pd.6340⟩
Prenatal Diagnosis, 2023, ⟨10.1002/pd.6340⟩
International audience; Objective: We aimed to gather fetal cases carrying a 7q11.23 copy number variation (CNV) and collect precise clinical data to broaden knowledge of antenatal features in these syndromes.Methods: We retrospectively recruited unr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2298cfc427024007f848f111933c8ba8
https://hal-u-picardie.archives-ouvertes.fr/hal-04032330
https://hal-u-picardie.archives-ouvertes.fr/hal-04032330
Autor:
Audrey Lamouroux, Coralie Dauge, Constance Wells, Eve Mousty, Lucile Pinson, Hélène Cavé, Yline Capri, Jean‐Michel Faure, Frédéric Grosjean, Fanny Sauvestre, Tania Attié‐Bitach, Fanny Pelluard, David Geneviève
Publikováno v:
Prenatal Diagnosis. 42:574-582
The antenatal phenotypic spectrum of Noonan Syndrome (NS) requires better characterization.This multicenter retrospective observational included 16 fetuses with molecularly confirmed NS admitted for fetopathological examination between 2009 and 2016.
Autor:
Pierre-Emmanuel Séguéla, Julie Thomas, Xavier Iriart, Beatrice Bonello, Zakaria Jalal, Fanny Sauvestre, Emmanuelle Fournier, Jean-Benoit Thambo
Publikováno v:
JACC: Cardiovascular Imaging. 13:2245-2253
Cardiac tumors are rare in children, with an incidence ranging between 0.01% and 0.32% ([1][1]). Although most cardiac tumors are benign, some of them may lead to serious complications. Early diagnosis is crucial because treatment is dependent on the
Autor:
Marion Poingt, Dominique Carles, Gwenaëlle André, Patrick Blanco, Aurélien Mattuizzi, Loïc Sentilhes, Clémence Houssin, Estibaliz Lazaro, Fanny Sauvestre, Fanny Pelluard
Publikováno v:
American Journal of Surgical Pathology. 44:1367-1373
Chronic intervillositis of unknown etiology (CIUE) is a rare placental disease characterized by intervillous infiltration of maternal macrophages and associated with poor pregnancy outcomes and a high risk of recurrence in subsequent pregnancies. Its
Autor:
Bernard Thébaud, Laurent Renesme, Robert P Jankov, Fanny Sauvestre, Yupu Deng, Duncan J. Stewart, Flore Lesage, Nadya Ben Fadel, Arul Vadivel, Shumei Zhong
Publikováno v:
American journal of respiratory cell and molecular biology. 65(3)