Zobrazeno 91 - 100
of 1 168
pro vyhledávání: '"Lévy, A."'
Autor:
Pascal Cintas, Emmanuelle Campana-Salort, Alexandra Salvi, A. Maues de Paula, Jérémie Mortreux, T. Stojkovic, Céline Tard, Marc Bartoli, F. Leturcq, S. Attarian, Jean Pouget, Svetlana Gorokhova, Nathalie Bonello-Palot, Mathieu Cerino, Nicolas Lévy, Mireille Cossée, Martin Krahn, R. Juntas Morales, Dimitri Renard
Publikováno v:
Neuropathology and Applied Neurobiology
Neuropathology and Applied Neurobiology, Wiley, 2020, ⟨10.1111/nan.12624⟩
Neuropathology and Applied Neurobiology, 2020, ⟨10.1111/nan.12624⟩
Neuropathology and Applied Neurobiology, Wiley, 2020, ⟨10.1111/nan.12624⟩
Neuropathology and Applied Neurobiology, 2020, ⟨10.1111/nan.12624⟩
International audience; AimsThe most common autosomal recessive limb girdle muscular dystrophy is associated with the CAPN3 gene. The exclusively recessive inheritance of this disorder has been recently challenged by the description of the recurrent
Autor:
Maxime Palazzo, Christine Lefort, Philippe Lévy, Anne Couvelard, Bertrand Napoleon, Monique Fabre, Vincent Hautefeuille, Alain Sauvanet, Philippe Ruszniewski, Laurent Palazzo, Bertrand Pujol, Mathieu Pioche, Jérôme Cros, Fabien Fumex, Rodica Gincul, Michele Felce
Publikováno v:
Gastrointestinal Endoscopy. 87:1481-1488
Background and Aims Contrast harmonic EUS (CH-EUS) has the ability to depict tumor microvasculature. Decreased microvascular density has been identified as a factor associated with tumor aggressiveness. We aimed to study the accuracy of CH-EUS for th
Autor:
Violaine, Flory, Gwendoline, Lévy, Julien, Viotti, Renaud, Schiappa, Laura, Elkind, Céline, Ghez, Amélie, Pellegrin, Aurélie, Occelli, Magali, Dejode, Yann, Delpech, Yves, Fouché, Andrea, Figl, Jean-Christophe, Machiavello, Juliette, Haudebourg, Isabelle, Peyrottes, Claire, Chapellier, Emmanuel, Barranger
Publikováno v:
Bulletin du cancer. 107(3)
To evaluate the impact of systematic radiological review by breast specialist radiologist of malignant breast lesion imaging on the therapeutic management of patients.Data collection was performed for patients with histopathologically proved breast c
Autor:
Olivia Hentic, Louis de Mestier, Pascal Bardet, Matthieu Faron, Christine Do Cao, Philippe Ruszniewski, Anne-Laure Védie, Pascal Hammel, Vinciane Rebours, Alain Sauvanet, Philippe Lévy, Jérôme Cros
Publikováno v:
Neuroendocrinology. 110(11-12)
Introduction: The goal of this retrospective study was to investigate the potential link between diabetes mellitus (DM) and the recurrence of pancreatic neuroendocrine tumors (PanNET) following curative intent surgery. Methods: We included patients w
Autor:
Murray Krahn, J Bacquet, Karine Nguyen, R Bellance, S. Attarian, Valérie Delague, Brigitte Chabrol, V Laugel, Jérémie Mortreux, Annie Verschueren, Nathalie Bonello-Palot, Frédérique Audic, Amandine Boyer, Chantal Missirian, Mathieu Cerino, Jean-Pierre Desvignes, Christophe Béroud, E Alazard, Nicolas Lévy, A G Giguet-Valard
Publikováno v:
Journal of Human Genetics
Journal of Human Genetics, Nature Publishing Group, 2019, 65 (3), pp.313-323. ⟨10.1038/s10038-019-0710-5⟩
Journal of Human Genetics, 2019, 65 (3), pp.313-323. ⟨10.1038/s10038-019-0710-5⟩
Journal of Human Genetics, Nature Publishing Group, 2019, 65 (3), pp.313-323. ⟨10.1038/s10038-019-0710-5⟩
Journal of Human Genetics, 2019, 65 (3), pp.313-323. ⟨10.1038/s10038-019-0710-5⟩
Charcot-Marie-Tooth disease (CMT) is a hereditary sensory-motor neuropathy characterized by a strong clinical and genetic heterogeneity. Over the past few years, with the occurrence of whole-exome sequencing (WES) or whole-genome sequencing (WGS), th
Autor:
G. Casu, Alain Verloes, N. Marziliano, Brigitte Benzacken, D. Haye, Pierre Gressens, Fabien Guimiot, J. Lévy, Eva Pipiras, Anne-Claude Tabet, C. Dupont, N. Teissier
Publikováno v:
Clinical Genetics. 93:1141-1147
Ephrin B2, one of the ligand of the EphB receptors, is involved in a complex signaling pathway regulating the development of the nervous system, neuronal migration, erythropoiesis and vasculogenesis. We report a patient with a de novo variant in EFNB
Autor:
Aline Cano, Melissa Baravalle, Caroline Lacoste, Anne-Sophie Monnier, Alexandre Fabre, Marie Loosveld, Véronique Secq, Marie-Edith Coste, Catherine Badens, Patrice Bourgeois, Nicolas Lévy, Céline Roman, Violaine Bresson, André Maues De Paula, Cécile DeLeusse, Karine Bertaux, Clothilde Esteve, Clémence Delteil, Frederic Blanc
Publikováno v:
European Journal of Medical Genetics
European Journal of Medical Genetics, 2021, 64 (10), pp.104294. ⟨10.1016/j.ejmg.2021.104294⟩
European Journal of Medical Genetics, 2021, 64 (10), pp.104294. ⟨10.1016/j.ejmg.2021.104294⟩
Cytoplasmic aminoacyl-tRNA synthetases (ARSs) are emerging as a cause of numerous rare inherited diseases. Recently, biallelic variants in tyrosyl-tRNA synthetase 1 (YARS1) have been described in ten patients of three families with multi-systemic dis
Autor:
Mireille Canal-Raffin, Mathieu Molimard, Caroline Dutriaux, Stéphane Bouchet, Karine Titier, Pauline Bosco-Lévy, Marine Rousset, Léa Dousset, Sorilla Prey, Anne Pham-Ledard, Emilie Gérard
Publikováno v:
Clinica Chimica Acta. 472:26-29
Introduction Dabrafenib and trametinib bitherapy provides significant benefits in BRAFV600 mut metastatic melanoma patients; however, adverse events (AE) occur, leading to dose reduction in 33% of patients. We aimed to investigate a relation between
Autor:
Damien Bonnet, Sophie Malekzadeh-Milani, Aleksander Sizarov, Younes Boudjemline, Cristian Mirabile, Diala Khraiche, Marien Lenoir, Marilyne Lévy
Publikováno v:
Canadian Journal of Cardiology. 33:1188-1196
Background The reversed Potts shunt improves right ventricular (RV) function in patients with suprasystemic pulmonary arterial hypertension (PAH). The proximity of the left pulmonary artery (LPA) to the descending aorta (DAo) permits the creation of
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