Resultados da busca - Graessner, Holm

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

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

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

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Solving the unsolved rare diseases in Europe por 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 por 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... por 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 por 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 por 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 por 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 por 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 por 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 por 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 por 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 por 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 por 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 por 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 por 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 por 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 por 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 por 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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