Search Results - "Oertel, Wolfang"

Fine‐Mapping of SNCA in Rapid Eye Movement Sleep Behavior Disorder and Overt Synucleinopathies by Krohn, Lynne, Wu, Richard Y. J., Heilbron, Karl, Ruskey, Jennifer A., Laurent, Sandra B., Blauwendraat, Cornelis, Alam, Armaghan, Arnulf, Isabelle, Hu, Michele T. M., Dauvilliers, Yves, Högl, Birgit, Toft, Mathias, Bjørnarå, Kari Anne, Stefani, Ambra, Holzknecht, Evi, Monaca, Christelle Charley, Abril, Beatriz, Plazzi, Giuseppe, Antelmi, Elena, Ferini‐Strambi, Luigi, Young, Peter, Heidbreder, Anna, Cochen De Cock, Valérie, Mollenhauer, Brit, Sixel‐Döring, Friederike, Trenkwalder, Claudia, Sonka, Karel, Kemlink, David, Figorilli, Michela, Puligheddu, Monica, Dijkstra, Femke, Viaene, Mineke, Oertel, Wolfang, Toffoli, Marco, Gigli, Gian Luigi, Valente, Mariarosaria, Gagnon, Jean‐François, Nalls, Mike A., Singleton, Andrew B., Desautels, Alex, Montplaisir, Jacques Y., Cannon, Paul, Ross, Owen A., Boeve, Bradley F., Dupré, Nicolas, Fon, Edward A., Postuma, Ronald B., Pihlstrøm, Lasse, Rouleau, Guy A., Gan‐Or, Ziv

“…Objective Rapid eye movement sleep behavior disorder (RBD) is a prodromal synucleinopathy, as >80% will eventually convert to overt synucleinopathy. We…”
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Neurological symptoms in patients with biopsy proven celiac disease by Bürk, Katrin, Farecki, Marie-Louise, Lamprecht, Georg, Roth, Guenter, Decker, Patrice, Weller, Michael, Rammensee, Hans-Georg, Oertel, Wolfang

“…In celiac disease (CD), the gut is the typical manifestation site but atypical neurological presentations are thought to occur in 6 to 10% with cerebellar…”
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SMPD1 variants do not have a major role in rapid eye movement sleep behavior disorder by Rudakou, Uladzislau, Futhey, Naomi C., Krohn, Lynne, Ruskey, Jennifer A., Heilbron, Karl, Cannon, Paul, Alam, Armaghan, Arnulf, Isabelle, Hu, Michele T.M., Montplaisir, Jacques Y., Gagnon, Jean-François, Desautels, Alex, Dauvilliers, Yves, Toffoli, Marco, Gigli, Gian Luigi, Valente, Mariarosaria, Högl, Birgit, Stefani, Ambra, Holzknecht, Evi, Sonka, Karel, Kemlink, David, Oertel, Wolfang, Janzen, Annette, Plazzi, Giuseppe, Antelmi, Elena, Figorilli, Michela, Puligheddu, Monica, Mollenhauer, Brit, Trenkwalder, Claudia, Sixel-Döring, Friederike, De Cock, Valérie Cochen, Monaca, Christelle Charley, Heidbreder, Anna, Ferini-Strambi, Luigi, Dijkstra, Femke, Viaene, Mineke, Abril, Beatriz, Boeve, Bradley F., Postuma, Ronald B., Rouleau, Guy A., Gan-Or, Ziv

“…Mutations in the sphingomyelin phosphodiesterase 1 (SMPD1) gene were reported to be associated with Parkinson’s disease and dementia with Lewy bodies. In the…”
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Fine-mapping of SNCA in REM sleep behavior disorder and overt synucleinopathies by Krohn, Lynne, Wu, Richard YJ, Heilbron, Karl, Ruskey, Jennifer A., Laurent, Sandra B., Blauwendraat, Cornelis, Alam, Armaghan, Arnulf, Isabelle, Hu, Michele T.M., Dauvilliers, Yves, Högl, Birgit, Toft, Mathias, Bjørnarå, Kari Anne, Stefani, Ambra, Holzknecht, Evi, Monaca, Christelle Charley, Beatriz, Abril, Plazzi, Giuseppe, Antelmi, Elena, Ferini-Strambi, Luigi, Young, Peter, Heidbreder, Anna, Cochen De Cock, Valérie, Mollenhauer, Brit, Sixel-Döring, Friederike, Trenkwalder, Claudia, Sonka, Karel, Kemlink, David, Figorilli, Michela, Puligheddu, Monica, Dijkstra, Femke, Viaene, Mineke, Oertel, Wolfang, Toffoli, Marco, Gigli, Gian Luigi, Valente, Mariarosaria, Gagnon, Jean-François, Nalls, Mike A., Singleton, Andrew B., Desautels, Alex, Montplaisir, Jacques Y., Cannon, Paul, Ross, Owen A., Boeve, Bradley F., Dupré, Nicolas, Fon, Edward A., Postuma, Ronald B., Pihlstrøm, Lasse, Rouleau, Guy A., Gan-Or, Ziv

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