検索結果 - Graessner, Holm

Rare disease care pathways in the EU: from odysseys and labyrinths towards highways 著者: Tumiene, Birute, Graessner, Holm

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First German Academy for Further Medical Training on Rare Diseases (FAKSE, http://www.fakse.info) 著者: Giehl, Julia, Graessner, Holm, Riess, Olaf

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Editorial: Networks in Movement Disorders. To Move or Not to Move 著者: Graessner, Holm, Albanese, Alberto, Schöls, Ludger

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Solving the unsolved rare diseases in Europe 著者: Graessner, Holm, Zurek, Birte, Hoischen, Alexander, Beltran, Sergi

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Establishing and boosting communication in the European Reference Network for Rare Neurological Diseases (ERN-RND): the impact of offering free educational webinars 著者: Brunelle Praschberger, Alicia, Post, Annemarie E. M., Hermanns, Sanja, Graessner, Holm

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Research priorities for rare neurological diseases: a representative view of patient representatives and healthcare professionals from the European Reference Network for Rare Neuro... 著者: Post, Annemarie E. M., Klockgether, Thomas, Landwehrmeyer, G. Bernhard, Pandolfo, Massimo, Arnesen, Astri, Reinhard, Carola, Graessner, Holm

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Development of a patient journey map for people living with cervical dystonia 著者: Benson, Monika, Albanese, Alberto, Bhatia, Kailash P., Cavillon, Pascale, Cuffe, Lorraine, König, Kathrin, Reinhard, Carola, Graessner, Holm

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How to approach a neurogenetics diagnosis in different European countries: The European Academy of Neurology Neurogenetics Panel survey 著者: Mancuso, Michelangelo, Houlden, Henry, Molnar, Maria Judit, Filla, Alessandro, Breza, Marianthi, Graessner, Holm, Bassetti, Claudio L. A., Boesch, Sylvia

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se-atlas.de – Versorgungsatlas für Menschen mit Seltenen Erkrankungen 著者: Neff, Michaela, Schaaf, Jannik, Tegtbauer, Niels, Schäfer, Johanna, Till, Manuela, Wagner, Thomas O. F., Graeßner, Holm, Mundlos, Christine, Storf, Holger

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European Reference Networks: challenges and opportunities 著者: Tumiene, Birute, Graessner, Holm, Mathijssen, Irene MJ, Pereira, Alberto M, Schaefer, Franz, Scarpa, Maurizio, Blay, Jean-Yves, Dollfus, Helene, Hoogerbrugge, Nicoline

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Preparing n-of-1 Antisense Oligonucleotide Treatments for Rare Neurological Diseases in Europe: Genetic, Regulatory, and Ethical Perspectives 著者: Synofzik, Matthis, van Roon-Mom, Willeke M.C, Marckmann, Georg, van Duyvenvoorde, Hermine A., Graessner, Holm, Schüle, Rebecca, Aartsma-Rus, Annemieke

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Se-atlas-cartographic representation of experts for rare diseases 著者: Storf, Holger, Hartz, Tobias, Pfeiffer, Wulf, Rommel, Kathrin, Derks, Mareike, Nyoungui, Elisabeth, Schmidtke, Joerg, Graessner, Holm, Knoell, Mirjam, Wagner, Thomas, Ueckert, Frank

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RD-Connect, NeurOmics and EURenOmics: collaborative European initiative for rare diseases 著者: Lochmüller, Hanns, Badowska, Dorota M., Thompson, Rachel, Knoers, Nine V., Aartsma-Rus, Annemieke, Gut, Ivo, Wood, Libby, Harmuth, Tina, Durudas, Andre, Graessner, Holm, Schaefer, Franz, Riess, Olaf

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Solving unsolved rare neurological diseases—a Solve-RD viewpoint 著者: Schüle, Rebecca, Timmann, Dagmar, Erasmus, Corrie E., Reichbauer, Jennifer, Wayand, Melanie, van de Warrenburg, Bart, Schöls, Ludger, Wilke, Carlo, Bevot, Andrea, Zuchner, Stephan, Beltran, Sergi, Laurie, Steven, Matalonga, Leslie, Graessner, Holm, Synofzik, Matthis

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Correction: Solving unsolved rare neurological diseases—a Solve-RD viewpoint 著者: Schüle, Rebecca, Timmann, Dagmar, Erasmus, Corrie E., Reichbauer, Jennifer, Wayand, Melanie, van de Warrenburg, Bart, Schöls, Ludger, Wilke, Carlo, Bevot, Andrea, Zuchner, Stephan, Beltran, Sergi, Laurie, Steven, Matalonga, Leslie, Graessner, Holm, Synofzik, Matthis

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Dystonia Management: What to Expect From the Future? The Perspectives of Patients and Clinicians Within DystoniaNet Europe 著者: Smit, Marenka, Albanese, Alberto, Benson, Monika, Edwards, Mark J., Graessner, Holm, Hutchinson, Michael, Jech, Robert, Krauss, Joachim K., Morgante, Francesca, Pérez Dueñas, Belen, Reilly, Richard B., Tinazzi, Michele, Contarino, Maria Fiorella, Tijssen, Marina A. J.

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A systematic review of the characteristics and validity of monitoring technologies to assess Parkinson’s disease 著者: Godinho, Catarina, Domingos, Josefa, Cunha, Guilherme, Santos, Ana T., Fernandes, Ricardo M., Abreu, Daisy, Gonçalves, Nilza, Matthews, Helen, Isaacs, Tom, Duffen, Joy, Al-Jawad, Ahmed, Larsen, Frank, Serrano, Artur, Weber, Peter, Thoms, Andrea, Sollinger, Stefan, Graessner, Holm, Maetzler, Walter, Ferreira, Joaquim J.

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Erratum to: A systematic review of the characteristics and validity of monitoring technologies to assess Parkinson’s disease 著者: Godinho, Catarina, Domingos, Josefa, Cunha, Guilherme, Santos, Ana T., Fernandes, Ricardo M., Abreu, Daisy, Gonçalves, Nilza, Matthews, Helen, Isaacs, Tom, Duffen, Joy, Al-Jawad, Ahmed, Larsen, Frank, Serrano, Artur, Weber, Peter, Thoms, Andrea, Sollinger, Stefan, Graessner, Holm, Maetzler, Walter, Ferreira, Joaquim J.

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Correction to: Solving patients with rare diseases through programmatic reanalysis of genome-phenome data 著者: Matalonga, Leslie, Hernández-Ferrer, Carles, Piscia, Davide, Schüle, Rebecca, Synofzik, Matthis, Töpf, Ana, Vissers, Lisenka E. L. M., de Voer, Richarda, Tonda, Raul, Laurie, Steven, Fernandez-Callejo, Marcos, Picó, Daniel, Garcia-Linares, Carles, Papakonstantinou, Anastasios, Corvó, Alberto, Joshi, Ricky, Diez, Hector, Gut, Ivo, Hoischen, Alexander, Graessner, Holm, Beltran, Sergi

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Solving patients with rare diseases through programmatic reanalysis of genome-phenome data 著者: Matalonga, Leslie, Hernández-Ferrer, Carles, Piscia, Davide, Schüle, Rebecca, Synofzik, Matthis, Töpf, Ana, Vissers, Lisenka E. L. M., de Voer, Richarda, Tonda, Raul, Laurie, Steven, Fernandez-Callejo, Marcos, Picó, Daniel, Garcia-Linares, Carles, Papakonstantinou, Anastasios, Corvó, Alberto, Joshi, Ricky, Diez, Hector, Gut, Ivo, Hoischen, Alexander, Graessner, Holm, Beltran, Sergi

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