Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Céline, Bellesme"'
Autor:
Perrine Marion, Aliénor De Chalus, Laetitia Giorgi, Céline Bellesme, Pascale Crétien, Hélène Maurey, Kumaran Deiva
Publikováno v:
Neuropediatrics. 54:064-067
Anti-Hu encephalitis is a paraneoplastic syndrome in adults. In children, rare cases of anti-Hu encephalitis were reported mostly without underlying tumors and clinical outcome are usually severe. Here, we describe a 4-year-old girl who developed cer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d34a5ca29dd15964226dbe5fd172c0d5
https://doi.org/10.1055/a-1896-6687
https://doi.org/10.1055/a-1896-6687
Autor:
Manoëlle, Kossorotoff, Basile, Kerleroux, Grégoire, Boulouis, Béatrice, Husson, Kim, Tran Dong, François, Eugene, Lena, Damaj, Augustin, Ozanne, Céline, Bellesme, Anne, Rolland, Romain, Bourcier, Aude, Triquenot-Bagan, Gaultier, Marnat, Jean-Philippe, Neau, Sylvie, Joriot, Alexandra, Perez, Maud, Guillen, Maximilien, Perivier, Frederique, Audic, Jean François, Hak, Christian, Denier, Olivier, Naggara, Denis, Herbreteaux
Publikováno v:
JAMA network open. 5(9)
ImportanceThere is to date limited evidence that revascularization strategies are associated with improved functional outcome in children with acute ischemic stroke (AIS).ObjectivesTo report clinical outcomes and provide estimates of revascularizatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d16e9e4c1218495d7a82f7a54c8f4b5
https://pubmed.ncbi.nlm.nih.gov/36107427
https://pubmed.ncbi.nlm.nih.gov/36107427
Autor:
Aurélia Poujois, Rodolphe Sobesky, Wassilios G. Meissner, Anne-Sophie Brunet, Emmanuel Broussolle, Chloé Laurencin, Laurence Lion-François, Olivier Guillaud, Alain Lachaux, François Maillot, Jérémie Belin, Ephrem Salamé, Claire Vanlemmens, Bruno Heyd, Céline Bellesme, Dalila Habes, Christophe Bureau, Fabienne Ory-Magne, Pascal Chaine, Jean-Marc Trocello, Daniel Cherqui, Didier Samuel, Victor de Ledinghen, Jean-Charles Duclos-Vallée, France Woimant
Publikováno v:
Neurology
Neurology, American Academy of Neurology, 2020, 94 (21), pp.e2189--e2202. ⟨10.1212/wnl.0000000000009474⟩
Neurology, 2020, 94 (21), pp.e2189--e2202. ⟨10.1212/wnl.0000000000009474⟩
Neurology, American Academy of Neurology, 2020, 94 (21), pp.e2189--e2202. ⟨10.1212/wnl.0000000000009474⟩
Neurology, 2020, 94 (21), pp.e2189--e2202. ⟨10.1212/wnl.0000000000009474⟩
ObjectiveTo evaluate the effect of liver transplantation (LT) in patients with Wilson disease (WD) with severe neurologic worsening resistant to active chelation.MethodsFrench patients with WD who underwent LT for pure neurologic indication were retr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b9342b4a8d21ba263042c841bd0161d
https://doi.org/10.1212/wnl.0000000000009474
https://doi.org/10.1212/wnl.0000000000009474
Autor:
Ivo Gut, Sarah Grotto, Céline Bellesme, Arnold Munnich, Cyril Gitiaux, Jeanne Amiel, Chloé Quélin, Annie Laquerrière, Suonavy Khung, Hanitra Ranjatoelina-Randrianaivo, Luc Rigonnot, Christine Francannet, Loic Quevarec, Jérôme Bouligand, Fabienne Prieur, Alexandra Benachi, Valérie Cormier-Daire, Laurence Perrin, Judith Melki, Pierre-Simon Jouk, Flora Nolent, Tania Attié-Bitach, Delphine Héron, Marie-Line Jacquemont, Claire Beneteau, Fabien Guimiot, Laetitia Lambert, Sandra Mercier, Valérie Biancalana, Fanny Laffargue, Elise Boucher, Jean-Louis Bessereau, P. Landrieu, Annick Toutain, Alain Verloes, Alice Goldenberg, Philippe Latour, Dominique Martin-Coignard, Anne Guiochon-Mantel, Dan Mejlachowicz, Damien Sternberg, Haluk Topaloglu, Bruno Eymard, Géraldine Viot, Catherine Fallet-Bianco, Julien Saada, Isabelle Desguerre, Marie-Hélène Saint-Frison, Catherine Vincent-Delorme, Sophie Blesson, Radka Stoeva, Alexandre J. Vivanti, Martine Bucourt, Pascaline Letard, Jérome Maluenda, Laurence Loeuillet, Lionel Van Maldergem, Didier Lacombe, Marcel Tawk, Michèle Granier, Stanislas Lyonnet, Anne-Lise Delezoide, Andrée Delahaye-Duriez, André Mégarbané, Marie Gonzales, Florence Petit, Juliette Piard, Laurence Faivre, Helene Verhelst, Bettina Bessières, Sabine Sigaudy, Sandra Whalen, Valérie Layet, Yline Capri, Fanny Pelluard, Emanuela Abiusi, Klaus Dieterich, Marie Vincent, Marine Legendre, Dana Jaber, Romulus Grigorescu, Florent Marguet, Eric Bieth, Helge Amthor, Christine Barnerias, Estelle Colin, Laetitia Trestard, Mathilde Nizon, Jelena Martinovic, Daniel Amram, Nicoletta Resta
Publikováno v:
JOURNAL OF MEDICAL GENETICS
BackgroundArthrogryposis multiplex congenita (AMC) is characterised by congenital joint contractures in two or more body areas. AMC exhibits wide phenotypic and genetic heterogeneity. Our goals were to improve the genetic diagnosis rates of AMC, to e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e5ca5c2b4280785da88a26155872ce7
https://hdl.handle.net/1854/LU-8759575
https://hdl.handle.net/1854/LU-8759575
Autor:
Laurent Spelle, Christian Denier, Bertrand Lapergue, Fernando Pico, Mathieu Zuber, Eric Jouvent, Philippe Tuppin, Sophie Crozier, Catherine Lamy, Manoelle Kossorotoff, Yannick Béjot, Céline Bellesme, Thomas Rambaud, Nicolas Legris, Didier Smadja
Publikováno v:
Neurology. 94:e158-e169
ObjectiveAdolescence represents a transition period between childhood and adulthood, and only limited information exists about stroke characteristics in this population. Our aim was to describe the clinical and neuroradiologic features, etiologies, i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8f62de5b697776379bdd3844f0232749
https://doi.org/10.1212/wnl.0000000000008783
https://doi.org/10.1212/wnl.0000000000008783
Autor:
Salima Hacein-Bey-Abina, Pierre Bougnères, Catherine Adamsbaum, Céline Bellesme, Ivan Labik, Clémence Castaignède, Manfred G. Schmidt
Publikováno v:
Human Gene Therapy
Human Gene Therapy, Mary Ann Liebert, 2021, ⟨10.1089/hum.2021.053⟩
Human Gene Therapy, Mary Ann Liebert, 2021, ⟨10.1089/hum.2021.053⟩
International audience; In 2009, cerebral adrenoleukodystrophy (c-ALD) became the first brain disease to be treated with lentiviral (LV)-based hematopoietic stem cell gene therapy with the ABCD1 gene in four boys (P1-P4) who had demyelinating lesions
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff55c0e0840f898bac28723c35978259
https://hal-cnrs.archives-ouvertes.fr/hal-03295893
https://hal-cnrs.archives-ouvertes.fr/hal-03295893
Autor:
Manoelle Kossorotoff, David Grevent, Augustin Ozanne, Christian Denier, Céline Bellesme, Laurence Tabone, Olivier Naggara, Nicolas Mediamolle, Fabrice Lesage, Catherine Lamy, Beatrice Husson, Isabelle Desguerre
Publikováno v:
Stroke. 48:2278-2281
Background and Purpose— To evaluate hyperacute management of pediatric arterial ischemic stroke, setting up dedicated management pathways is the first recommended step to prove the feasibility and safety of such treatments. A regional pediatric str
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85b6623e04905f991169de73f0a542df
https://doi.org/10.1161/strokeaha.117.016591
https://doi.org/10.1161/strokeaha.117.016591
Autor:
Khadija Abidallah, Felipe Suarez, Emmanuelle Ginglinger, Bertrand Degos, Céline Bellesme, Jean‐Paul Carriere, Nizar Mahlaoui, Guillaume Rieunier, Dorine Bellanger, Patrick Calvas, Olivier Flabeau, Dominique Stoppa-Lyonnet, Christelle Rougeot, Diane Doummar, Noel Philippe, Nathalie Auger, Virginie Moncoutier, Michèle Mathieu-Dramard, Christine Ioos, Anna Castrioto, Marie Hully, Béatrice Parfait, François Tison, Agnès Collet, Marie-Christine Nougues, Catherine Dubois d'Enghien, Alice Masurel, Karine Dahan, Thilo Dörk, Hélène Antoine-Poirel, Cecilia Altuzarra, François Demeocq, Alice Fiévet, Pierre Bordigoni, Nathalie Aladjidi, Claire Ewenczyk, Aurélie Siri, Karine Nguyen, Mathieu Anheim, Fabienne Prieur, Marc-Henri Stern, Caroline Bourjault, Fabien Touzot, Julia Sophie, Fanny Couderc, Agathe Roubertie
Publikováno v:
Human mutation. 40(10)
Ataxia-telangiectasia (A-T) is a recessive disorder caused by biallelic pathogenic variants of ataxia-telangiectasia mutated (ATM). This disease is characterized by progressive ataxia, telangiectasia, immune deficiency, predisposition to malignancies
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::169d2867167544410434395ec2c71015
https://pubmed.ncbi.nlm.nih.gov/31050087
https://pubmed.ncbi.nlm.nih.gov/31050087
Autor:
Guillaume Saliou, Kumaran Deiva, Denis Ducreux, Béatrice Husson, Céline Bellesme, Marie Théaudin, Marc Tardieu, Frédérique Toulgoat, Hina Simonnet, Sébastien Cabasson
Publikováno v:
Neuroradiology. 57:729-738
The objective of this study is to describe clinical and imaging presentation and outcome in extracranial vertebral artery dissection.Single-centre retrospective study over a 14-year period included 20 consecutive patients under the age of 16 years wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::176c868ce8b6d52c35cf25d452e842a2
https://doi.org/10.1007/s00234-015-1520-x
https://doi.org/10.1007/s00234-015-1520-x
Autor:
Guillaume Saliou, Céline Bellesme, M. Sachet, L. Chevret, Philippe Durand, Béatrice Husson, Denis Ducreux, Francesco Puccinelli, Kumaran Deiva
Publikováno v:
European Journal of Paediatric Neurology. 18:766-773
Purpose Thrombosis of cerebral arteriovenous malformation after embolization is rare, but can involve the normal venous network with extensive venous thrombosis. We report angioarchitecture findings, our management and prevention strategy for this co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf24c0c9508f500da577deee3286d067
https://doi.org/10.1016/j.ejpn.2014.07.007
https://doi.org/10.1016/j.ejpn.2014.07.007