Rezultati - Soňa Nevšímalová
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Spectral analysis of heart rate variability in sleep. od Petr Bušek, J Vaňková, J Opavský, Johanna Salinger, Soňa Nevšímalová
Izdano 2005Artigo -
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Narcolepsy in Children od Marie-Josèphe Challamel, M.E. Mazzola, Soňa Nevšímalová, Christine Cannard, J. Louis, M Révol
Izdano 1994Artigo -
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Relapsing encephalopathy with cerebellar ataxia are caused by variants involving p.Arg756 in ATP1A3 od Pascal Sabouraud, Audrey Riquet, Marie‐Aude Spitz, Kumaran Deiva, Soňa Nevšímalová, Cyril Mignot, Gaëtan Lesca, Nathalie Bednarek, Diane Doummar, Christine Piétrement, Vincent Laugel
Izdano 2019Artigo -
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The MSLT is Repeatable in Narcolepsy Type 1 But Not Narcolepsy Type 2: A Retrospective Patient Study od Chad Ruoff, Fabio Pizza, Lynn Marie Trotti, Karel Šonka, Stefano Vandi, Joseph Cheung, Swaroop Pinto, Mali Einen, Narong Simakajornboon, Fang Han, Paul E. Peppard, Soňa Nevšímalová, Giuseppe Plazzi, David B. Rye, Emmanuel Mignot
Izdano 2018Artigo -
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Evidence of a non-progressive course of alternating hemiplegia of childhood: study of a large cohort of children and adults od Eleni Panagiotakaki, Giuseppe Gobbi, Brian Neville, Friedrich Ebinger, Jaume Campistol, Soňa Nevšímalová, Laura Laan, Paul Casaer, Georg Spiel, Melania Giannotta, Carmen Fons, Miriam Ninan, Guenter Sange, Tsveta Schyns, Rosaria Vavassori, Dominique Poncelin, Alexis Arzimanoglou
Izdano 2010Artigo -
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Predictors of Hypocretin (Orexin) Deficiency in Narcolepsy Without Cataplexy od Olivier Andlauer, Hyatt Moore, Seung Chul Hong, Yves Dauvilliers, Takashi Kanbayashi, Seiji Nishino, Fang Han, Michael H. Silber, Tom Rico, Mali Einen, Birgitte Rahbek Kornum, Poul Jennum, Stine Knudsen, Soňa Nevšímalová, Francesca Poli, Giuseppe Plazzi, Emmanuel Mignot
Izdano 2012Artigo -
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HLA DQB1*06:02 Negative Narcolepsy with Hypocretin/Orexin Deficiency od Fang Han, Ling Lin, Barbara Schormair, Fabio Pizza, Giuseppe Plazzi, Hanna M. Ollila, Soňa Nevšímalová, Poul Jennum, Stine Knudsen, Juliane Winkelmann, Cristin Coquillard, Farbod Babrzadeh, Tim M. Strom, Chunlin Wang, Michael Mindrinos, Marcelo Fernández-Viña, Emmanuel Mignot
Izdano 2014Artigo -
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Suggestive evidence for linkage for restless legs syndrome on chromosome 19p13 od David Kemlink, Giuseppe Plazzi, Roberto Vetrugno, Federica Provini, Olli Polo, Karin Stiasny‐Kolster, Wolfgang H. Oertel, Soňa Nevšímalová, Karel Šonka, Birgit Högl, Birgit Frauscher, Georgios M. Hadjigeorgiou, Peter P. Pramstaller, Peter Lichtner, Thomas Meitinger, Bertram Müller-Myshok, Juliane Winkelmann, Pasquale Montagna
Izdano 2008Artigo -
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Replication of restless legs syndrome loci in three European populations od David Kemlink, Olli Polo, Birgit Frauscher, Viola Gschliesser, Birgit Högl, Werner Poewe, Pavel Vodička, Jana Vávrová, Karel Šonka, Soňa Nevšímalová, Barbara Schormair, Peter Lichtner, Kaisa Silander, L. Peltonen, Christian Gieger, H.‐Erich Wichmann, Alexander Zimprich, Darina Roeske, Bertram Müller‐Myhsok, Thomas Meitinger, Juliane Winkelmann
Izdano 2009Artigo -
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Narcolepsy and pregnancy: a retrospective <scp>E</scp>uropean evaluation of 249 pregnancies od Eszter Maurovich‐Horvat, David Kemlink, Birgit Högl, Birgit Frauscher, Laura Ehrmann, Peter Geisler, Katharina Ettenhuber, Geert Mayer, Rosa Peraita‐Adrados, Elena Calvo, Gert Jan Lammers, Astrid van der Heide, Luigi Ferini‐Strambi, Giuseppe Plazzi, Francesca Poli, Yves Dauvilliers, Poul Jennum, Helle Leonthin, Johannes Mathis, Aleksandra Wierzbicka, Francisco Javier Puertas, P. Beitinger, Isabelle Arnulf, Renata L. Riha, Mária Tormašiová, Jana Slonková, Soňa Nevšímalová, Karel Šonka
Izdano 2013Artigo -
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Clinical profile of patients with ATP1A3 mutations in Alternating Hemiplegia of Childhood—a study of 155 patients od Eleni Panagiotakaki, Elisa De Grandis, Michela Stagnaro, Erin L. Heinzen, Carmen Fons, Sanjay M. Sisodiya, Boukje de Vries, Christophe Goubau, Sarah Weckhuysen, David Kemlink, Ingrid E. Scheffer, Gaëtan Lesca, Muriel Rabilloud, Amna Klich, Alia Ramírez-Camacho, Adriana Ulate-Campos, Jaume Campistol, Melania Giannotta, Marie‐Laure Moutard, Diane Doummar, Cecile Hubsch-Bonneaud, Fatima Jaffer, J. Helen Cross, Fiorella Gurrieri, Francesco Danilo Tiziano, Soňa Nevšímalová, Sophie Nicole, Brian Neville, Arn M. J. M. van den Maagdenberg, Mohamad A. Mikati, David B. Goldstein, Rosaria Vavassori, Alexis Arzimanoglou
Izdano 2015Artigo -
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Kleine Levin syndrome is associated with birth difficulties and genetic variants in the TRANK1 gene loci od Aditya Ambati, Ryan P. Hillary, Smaranda Leu‐Semenescu, Hanna M. Ollila, Ling Lin, Emmanuel During, Neal Farber, T. Rico, Juliette Faraco, Eileen Leary, Andrea Goldstein‐Piekarski, Yu‐Shu Huang, Fang Han, Yakov Sivan, Michel Lecendreux, Pauline Dodet, Makoto Honda, Natan Gadoth, Soňa Nevšímalová, Fabio Pizza, Takashi Kanbayashi, Rosa Peraita‐Adrados, Guy Leschziner, Rosa Hasan, Francesca Cañellas, Kazuhiko Kume, Makrina Daniilidou, Patrice Bourgin, David B. Rye, José L. Vicário, Birgit Högl, Seung Chul Hong, Giuseppe Plazzi, Geert Mayer, Anne Marie Landtblom, Yves Dauvilliers, Isabelle Arnulf, Emmanuel Mignot
Izdano 2021Pré-impressão
Iskalna orodja:
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Medicine
Psychiatry
Internal medicine
Narcolepsy
Neurology
Biology
Genetics
Cataplexy
Psychology
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Gene
Pediatrics
Disease
Genotype
Immunology
Single-nucleotide polymorphism
Sleep disorder
Computer science
Insomnia
Modafinil
Antigen
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Cognition
Dystonia
Endocrinology
Excessive daytime sleepiness
Genome-wide association study
Human leukocyte antigen
Locus (genetics)
Neuropeptide