Výsledky vyhledávání - Press, Rayomand

Microangiopathy—A Potential Contributing Factor to Idiopathic Polyneuropathy: A Mini Review Autor Samuelsson, Kristin, Press, Rayomand

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Idiopathic Small Fiber Neuropathy: Phenotype, Etiologies, and the Search for Fabry Disease Autor Samuelsson, Kristin, Kostulas, Konstantinos, Vrethem, Magnus, Rolfs, Arndt, Press, Rayomand

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Nonopportunistic infection leading to rapidly progressive dementia in a patient with HIV/AIDS: A case report Autor Eimer, Johannes, Vesterbacka, Jan, Savitcheva, Irina, Press, Rayomand, Roshanisefat, Homayoun, Nowak, Piotr

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Study of Autophagy and Microangiopathy in Sural Nerves of Patients with Chronic Idiopathic Axonal Polyneuropathy Autor Samuelsson, Kristin, Osman, Ayman A. M., Angeria, Maria, Risling, Mårten, Mohseni, Simin, Press, Rayomand

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Comparison Between Rituximab Treatment for New-Onset Generalized Myasthenia Gravis and Refractory Generalized Myasthenia Gravis Autor Brauner, Susanna, Eriksson-Dufva, Ann, Hietala, Max Albert, Frisell, Thomas, Press, Rayomand, Piehl, Fredrik

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Expanding the ataxia with oculomotor apraxia type 4 phenotype Autor Paucar, Martin, Malmgren, Helena, Taylor, Malcolm, Reynolds, John J., Svenningsson, Per, Press, Rayomand, Nordgren, Ann

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The cerebellar phenotype of Charcot-Marie-Tooth neuropathy type 4C Autor Skott, Humberto, Muntean-Firanescu, Cristina, Samuelsson, Kristin, Verrecchia, Luca, Svenningsson, Per, Malmgren, Helena, Cananau, Carmen, Espay, Alberto J., Press, Rayomand, Solders, Göran, Paucar, Martin

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Novel Mutation m.10372A>G in MT-ND3 Causing Sensorimotor Axonal Polyneuropathy Autor Bruhn, Helene, Samuelsson, Kristin, Schober, Florian A., Engvall, Martin, Lesko, Nicole, Wibom, Rolf, Nennesmo, Inger, Calvo-Garrido, Javier, Press, Rayomand, Stranneheim, Henrik, Freyer, Christoph, Wedell, Anna, Wredenberg, Anna

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Homozygous SMN2 deletion is a protective factor in the Swedish ALS population Autor Corcia, Philippe, Ingre, Caroline, Blasco, Helene, Press, Rayomand, Praline, Julien, Antar, Catherine, Veyrat-Durebex, Charlotte, Guettard, Yves-Olivier, Camu, William, Andersen, Peter M, Vourc'h, Patrick, Andres, Christian R

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A novel phosphorylation site mutation in profilin 1 revealed in a large screen of US, Nordic, and German amyotrophic lateral sclerosis/frontotemporal dementia cohorts Autor Ingre, Caroline, Landers, John E., Rizik, Naji, Volk, Alexander E., Akimoto, Chizuru, Birve, Anna, Hübers, Annemarie, Keagle, Pamela J., Piotrowska, Katarzyna, Press, Rayomand, Andersen, Peter Munch, Ludolph, Albert C., Weishaupt, Jochen H.

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Increasing involvement of CAPN1 variants in spastic ataxias and phenotype-genotype correlations Autor Méreaux, Jean-Loup, Firanescu, Cristina, Coarelli, Giulia, Kvarnung, Malin, Rodrigues, Rita, Pegoraro, Elena, Tazir, Meriem, Taithe, Frédéric, Valter, Rémi, Huin, Vincent, Lidström, Kristina, Banneau, Guillaume, Morais, Sara, Parodi, Livia, Coutelier, Marie, Papin, Mélanie, Svenningsson, Per, Azulay, Jean-Philippe, Alonso, Isabel, Nilsson, Daniel, Brice, Alexis, Le Guern, Eric, Press, Rayomand, Vazza, Giovanni, Loureiro, José Leal, Goizet, Cyril, Durr, Alexandra, Paucar, Martin, Stevanin, Giovanni

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