Zobrazeno 1 - 10
of 94
pro vyhledávání: '"Cécile Cauquil"'
Autor:
Sébastien Gaultier, Tania Puscas, Jean Pastre, Laure Gibault, Jean-Benoît Arlet, Cécile Cauquil, Adrien Michon
Publikováno v:
Therapeutic Advances in Respiratory Disease, Vol 17 (2023)
We present a case report of transbronchial cryobiopsy proven diffuse amyloid cystic lung disease complicating a homozygous Val122Ile (V122I) transthyretin mutated amyloidosis (ATTRm). To the best of our knowledge, this is the first case in the litera
Externí odkaz:
https://doaj.org/article/7b8d6234072a417f8c3b8933623c3265
Autor:
Clément Vialatte de Pémille, Nicolas Noël, Clovis Adam, Céline Labeyrie, Adeline Not, Guillemette Beaudonnet, Andoni Echaniz-Laguna, David Adams, Cécile Cauquil
Publikováno v:
Journal of Clinical Medicine, Vol 12, Iss 9, p 3281 (2023)
Chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) is a rare autoimmune disorder of the peripheral nervous system. Diagnosis relies on clinical and electrophysiological criteria. Various disorders requiring specific treatment regimens m
Externí odkaz:
https://doaj.org/article/f0136b52e1f04ada8e779bd00b4e7944
Autor:
Benjamin Terrier, Magali Colombat, Caroline Beugnet, Astrid Quéant, Jonathan London, Jean-Baptiste Daudin, Claire Le Jeunne, Luc Mouthon, Dominique Monnet, Cécile Cauquil, Catherine Lacroix, David Adams, Antoine Brézin, Sophie Valleix
Publikováno v:
Journal of Medical Case Reports, Vol 11, Iss 1, Pp 1-5 (2017)
Abstract Background Hereditary transthyretin amyloidosis is an autosomal dominant inherited disorder, first described in families with sensorimotor and autonomic neuropathy. Since its first description, more than 120 amyloidogenic transthyretin mutat
Externí odkaz:
https://doaj.org/article/f9b53ef458b84e4986511cd3d00801fe
Autor:
Pierre Socie, Anouar Benmalek, Cécile Cauquil, Eve Piekarski, Ilias Kounis, Ludivine Eliahou, Antoine Rousseau, François Rouzet, Andoni Echaniz-Laguna, Didier Samuel, David Adams, Michel S Slama, Vincent Algalarrondo
Publikováno v:
Amyloid. :1-10
Publikováno v:
Anesthésie & Réanimation. 8:426-430
Autor:
Céline Labeyrie, Andoni Echaniz-Laguna, David Adams, A. Laparra, Clovis Adam, Cécile Cauquil, Pascale Chrétien, S. Henriquez, Olivier Lambotte, S. Hacein-Bey-Abina, P. Catalan, N. Noel, L. Pacoureau, Cécile Goujard
Publikováno v:
La Revue de Médecine Interne. 42:844-854
Resume Les syndromes lymphoproliferatifs (myelomes, maladie de Waldenstrom, leucemie lymphoide chronique, lymphomes) peuvent s’associer a la survenue de neuropathies peripheriques. Le mecanisme est variable : il peut etre dysimmunitaire, associe ou
Autor:
Gwendal Le Masson, Tanya Stojkovic, Jean-Baptiste Chanson, Bruno Francou, Kumaran Deiva, Thierry Maisonobe, Thierry Kuntzer, Laurent Magy, Philippe Latour, Peter Van den Berghe, Guilhem Solé, Cécile Cauquil, Clotilde Nardin, François Ochsner, Shahram Attarian, Alain Créange, Emilien Delmont, Fabien Hauw, Steeve Genestet, Guillaume Fargeot, David H. Adams, Thierry Gendre, Céline Tard, Andoni Echaniz-Laguna
Publikováno v:
European Journal of Neurology. 28:2846-2854
Background and purpose Charcot-Marie-Tooth (CMT) disease, an untreatable hereditary polyneuropathy, may mimic chronic inflammatory demyelinating polyradiculoneuropathy (CIDP), a treatable neuropathy. Methods In this retrospective study, we analyzed t
Autor:
Claire Peillet, David Adams, Shahram Attarian, Françoise Bouhour, Cécile Cauquil, Julien Cassereau, Jean‐Baptiste Chanson, Pascal Cintas, Alain Creange, Emilien Delmont, Guillaume Fargeot, Steeve Genestet, Antoine Gueguen, Anne Laure Kaminsky, Thierry Kuntzer, Céline Labeyrie, Maud Michaud, Yann Pereon, Angela Puma, Karine Viala, Pascale Chretien, Clovis Adam, Andoni Echaniz‐Laguna
Publikováno v:
European journal of neurologyREFERENCES. 29(12)
In this retrospective study involving 14 university hospitals from France and Switzerland, the aim was to define the clinicopathological features of chronic neuropathies with anti-disialosyl ganglioside immunoglobulin M (IgM) antibodies (CNDA).Fifty-
Autor:
Clovis Adam, Andoni Echaniz-Laguna, Cécile Cauquil, Guillaume Fargeot, C Deback, Nicolas Noel, C Périllaud-Dubois
Publikováno v:
Revue Neurologique
Publikováno v:
Pratique Neurologique - FMC. 12:149-157
Resume Les neuropathies amyloides sont le plus souvent hereditaires a transthyretine (TTR). Leur mode de presentation est pleiomorphe pouvant mimer plusieurs types de neuropathies ; le diagnostic doit etre suspecte devant toute neuropathie evolutive