Výsledky vyhledávání - Mathis, Stephane
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A Rare Cause of Stroke in Young Adults: Occlusion of the Middle Cerebral Artery by a Meningioma Postpartum Autor Mathis, Stéphane, Bataille, Benoît, Boucebci, Samy, Jeantet, Marion, Ciron, Jonathan, Vandamme, Laurène, Neau, Jean-Philippe
Vydáno 2013Text -
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Paroxysmal Sneezing at the Onset of Syncopes and Transient Ischemic Attack Revealing a Papillary Cardiac Fibroelastoma Autor Mathis, Stéphane, Lamy, Matthias, Ciron, Jonathan, Iljicsov, Anna, Arjmand, Roxana, Agius, Pierre, Neau, Jean-Philippe
Vydáno 2014Text -
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Simultaneous Combined Myositis, Inflammatory Polyneuropathy, and Overlap Myasthenic Syndrome Autor Mathis, Stéphane, Magy, Laurent, Corcia, Philippe, Ghorab, Karima, Richard, Laurence, Ciron, Jonathan, Duchesne, Mathilde, Vallat, Jean-Michel
Vydáno 2016Text -
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Sensory neuropathy in progressive motor neuronopathy (pmn) mice is associated with defects in microtubule polymerization and axonal transport Autor Schäfer, Michael K., Bellouze, Sarah, Jacquier, Arnaud, Schaller, Sébastien, Richard, Laurence, Mathis, Stéphane, Vallat, Jean‐Michel, Haase, Georg
Vydáno 2016Text -
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Long-term outcome of basilar stenosis in Erdheim–Chester disease: A case report Autor Mathis, Stéphane, Godenèche, Gaëlle, Haroche, Julien, Milin, Serge, Julian, Adrien, Berthomet, Aline, Baron, Clément, Palazzo, Paola, Neau, Jean-Philippe
Vydáno 2016Text -
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Contactin-Associated Protein 1 (CNTNAP1) Mutations Induce Characteristic Lesions of the Paranodal Region Autor Vallat, Jean-Michel, Nizon, Mathilde, Magee, Alex, Isidor, Bertrand, Magy, Laurent, Péréon, Yann, Richard, Laurence, Ouvrier, Robert, Cogné, Benjamin, Devaux, Jérôme, Zuchner, Stephan, Mathis, Stéphane
Vydáno 2016Text -
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Autosomal dominant eccentric core disease caused by a heterozygous mutation in the MYH7 gene Autor Romero, Norma B, Xie, Ting, Malfatti, Edoardo, Schaeffer, Ursula, Böhm, Johann, Wu, Bin, Xu, Fengping, Boucebci, Samy, Mathis, Stéphane, Neau, Jean-Philippe, Monnier, Nicole, Fardeau, Michel, Laporte, Jocelyn
Vydáno 2014Text