نتائج البحث - "Holm Graessner"

1

se-atlas.de – Versorgungsatlas für Menschen mit Seltenen Erkrankungen

المؤلفون: Manuela Till, Christine Mundlos, Michaela Neff, Niels Tegtbauer, Holger Storf, Thomas O. F. Wagner, Johanna Schäfer, Holm Graeßner, Jannik Schaaf

المصدر: Der Internist

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2e09590c96d6dda0dd35c04727316b9Test
https://doi.org/10.1007/s00108-021-01085-yTest

2

Management of rare movement disorders in Europe

المؤلفون: C. Painous, Holm Graessner, N.J.H. van Os, Marina A. J. Tijssen, Wassilios G. Meissner, B.P.C. van de Warrenburg, Anna Delamarre, I. Michailoviene, María-José Martí, Carola Reinhard, Algirdas Utkus

المساهمون: Movement Disorder (MD)

المصدر: European Journal of Neurology, 27(8), 1493-1500. Wiley
European journal of neurology, Hoboken : Wiley, 2020, first published online, p. [1-8]
European Journal of Neurology, 27, 8, pp. 1493-1500
European Journal of Neurology, 27, 1493-1500
European journal of neurology, Hoboken : Wiley, 2020, vol. 27, iss. 8, p. 1493-1500
European Journal of Neurology

مصطلحات موضوعية: medicine.medical_specialty, Movement disorders, Neurodegeneration with brain iron accumulation, Disease, 03 medical and health sciences, 0302 clinical medicine, Central Nervous System Diseases, Surveys and Questionnaires, Humans, Medicine, media_common.cataloged_instance, survey, European Union, 030212 general & internal medicine, Disease management (health), European union, Genetic testing, media_common, Dystonia, disease management, Europe, movement disorders, rare diseases, medicine.diagnostic_test, business.industry, Paroxysmal dyskinesia, Disorders of movement Donders Center for Medical Neuroscience [Radboudumc 3], medicine.disease, Europe, Cross-Sectional Studies, Neurology, Dystonic Disorders, Family medicine, movement disorders, Original Article, Neurology (clinical), medicine.symptom, business, 030217 neurology & neurosurgery

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a7183394d29aa78a710987fe66dcc9aTest
https://doi.org/10.1111/ene.14302Test

3

Dual Guidance Structure for Evaluation of Patients with Unclear Diagnosis in Centers for Rare Diseases (ZSE-DUO): Study Protocol for a Controlled Multi-center Cohort Study

المساهمون: Rampp, Carina, Richter, Antonia, Rieß, Olaf, Schmidt, Annika, Schneider, Simone, Schoels, Ludger, Schwalba, Martina, Selig, Udo, Spangenberger, Astrid, Sroka, Alexandra, Steinbüchel, Toni, Stösser, Sebastian, Suchant, Steffi, Vogel, Matthias, Volk, Daniela, Vollmuth, Christoph, Volnov, Solange, Walter, Sabrina, Warrings, Bodo, Weiler, Christine, Witt, Stefanie, Zajt, Kamil Kajetan, Zeltner, Lena, Zenker, Karola, Zhang, Kailun David, Zipfel, Stephan, Akkaya, Federica, Babka, Christine, Bârlescu, Lavinia, Bärsch-Michelmann, Anja, Bergbreiter, Astrid, Blömeke, Janika, Böhm, Leonie, Böttger, Benita, Braun, Birgit, Brinkmann, Folke, Britz, Vanessa, Cario, Holger, Celiker, Melisa, de Greck, Moritz, Debatin, Klaus-Michael, Dillmann-Jehn, Katrin, Ertl, Max, Ettinger, Monika, Eymann, Jutta, Frommer, Jörg, Gabrian, Martina, Glode, Anja, Gödecke, Vega, Grasemann, Corinna, Grauer, Eva, Greger, Helmut, Haas, Astrid, Haase, Martina, Haisch, Lea, Heinrich, Isabel, Held, Melissa, Hennermann, Julia, Herrmann-Werner, Anne, Hett, Julian, Hilbig, Bettina, Holthöfer, Laura, Imhof, Christiane, Jacob, Titus, Junne, Florian, Karl, Stefanie, Kassubek, Jan, Kick, Lisa, Koschitzki, Kevin-Thomas, Krassort, Heike, Kratz, Christian, Kristensen, Kaja, Kropff, Birgit, Kuhn, Julia, Latzko, Philipp, Loew, Thomas, Lorenz, Delia, Ludolph, Albert C., Dos Santos, Isabell Meyer, Meyer, Torsten, Mohnike, Klaus, Monninger, Martina, Musacchio, Thomas, Nanciu, Amalia Nicole, Nießen, Margret, Nöhre, Mariell, Papagianni, Aikaterini, Pfeifer-Duck, Christina, Piduhn, Lea-Sophie

المصدر: Orphanet journal of rare diseases : OJRD 17(1), 47 (2022). doi:10.1186/s13023-022-02176-1

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba62672e4580218d7990ff2cc43937a5Test
https://doi.org/10.21203/rs.3.rs-936612/v1Test

4

EAN guidance for developing and reporting clinical practice guidelines on rare neurological diseases

مصطلحات موضوعية: Clinical Practice, medicine.medical_specialty, Neurology, business.industry, Medicine, Neurology (clinical), business, Intensive care medicine

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::baabab69bc6214e337c53c587b4253ebTest
https://avesis.erciyes.edu.tr/publication/details/57242475-0f20-4a25-99be-47c6bd07c1a2/oaiTest

5

Dystonia management: what to expect from the future? The perspectives of patients and clinicians within DystoniaNet Europe

المؤلفون: Marenka Smit, Alberto Albanese, Monika Benson, Mark J. Edwards, Holm Graessner, Michael Hutchinson, Robert Jech, Joachim K. Krauss, Francesca Morgante, Belen Pérez Dueñas, Richard B. Reilly, Michele Tinazzi, Maria Fiorella Contarino, Marina A. J. Tijssen, The Collaborative Working Group

المساهمون: Institut Català de la Salut, [Smit M] Expertise Centre Movement Disorders Groningen, Department of Neurology, University Medical Centre Groningen, Groningen, Netherlands. [Albanese A] Department of Neurology, Istituto di Ricovero e Cura a Carattere Scientifico Humanitas Research Hospital, Milan, Italy. [Benson M] Dystonia Europe, Brussels, Belgium. [Edwards MJ] Neuroscience Research Centre, Institute of Molecular and Clinical Sciences, St George's University of London, London, United Kingdom. [Graessner H] Institute of Medical Genetics and Applied Genomics and Centre for Rare Diseases, University of Tübingen, Tübingen, Germany. [Hutchinson M] Department of Neurology, St. Vincent's University Hospital, Dublin, Ireland. [Pérez Dueñas B] Grup de Recerca en Neurologia Pediàtrica, Vall d'Hebron Hospital Universitari, Barcelona, Spain. Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain, Vall d'Hebron Barcelona Hospital Campus

المصدر: Frontiers in Neurology, 12. FRONTIERS MEDIA SA
Scientia
Frontiers in Neurology
Frontiers in Neurology, Vol 12 (2021)

مصطلحات موضوعية: GRAY-MATTER CHANGES, Deep brain stimulation, Process (engineering), medicine.medical_treatment, Otros calificadores::/diagnóstico [Otros calificadores], unmet needs, CHILDREN, collaboration, dystonia, DystoniaNet, European network, Review, CERVICAL DYSTONIA, ENDOPHENOTYPE, Quality of life (healthcare), afecciones patológicas, signos y síntomas::procesos patológicos::atributos de la enfermedad::enfermedades raras [ENFERMEDADES], Leverage (negotiation), QUALITY-OF-LIFE, medicine, Other subheadings::/diagnosis [Other subheadings], Cervical dystonia, RC346-429, Information exchange, Nervous System Diseases::Neurologic Manifestations::Dyskinesias::Dystonia [DISEASES], ambiente y salud pública::salud pública::medidas epidemiológicas::demografía::estado de salud::calidad de vida [ATENCIÓN DE SALUD], GLOBUS-PALLIDUS INTERNUS, Dystonia, Scope (project management), business.industry, Pathological Conditions, Signs and Symptoms::Pathologic Processes::Disease Attributes::Rare Diseases [DISEASES], Distonia - Diagnòstic, Public relations, enfermedades del sistema nervioso::manifestaciones neurológicas::discinesias::distonía [ENFERMEDADES], medicine.disease, Environment and Public Health::Public Health::Epidemiologic Measurements::Demography::Health Status::Quality of Life [HEALTH CARE], Neurology, TEMPORAL DISCRIMINATION, Neurology. Diseases of the nervous system, Neurology (clinical), Malalties rares, MOTOR, Psychology, business, MOVEMENT-DISORDERS, DEEP BRAIN-STIMULATION, Qualitat de vida - Avaluació

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6da16c0776584c74ad5fc6c3bc38234fTest
https://www.frontiersin.org/articles/10.3389/fneur.2021.646841/pdfTest

6

Model für personalisierte Diagnostik und Therapie in der Neurologie – Deutsche Akademie für Seltene Neurologische Erkrankungen

المؤلفون: Christine Klein, Alexander Münchau, Holm Graessner, Ludger Schöls

المصدر: Der Nervenarzt. 90:796-803

مصطلحات موضوعية: Gynecology, medicine.medical_specialty, business.industry, General Medicine, Case conference, language.human_language, 030227 psychiatry, German, 03 medical and health sciences, Psychiatry and Mental health, 0302 clinical medicine, Neurology, language, medicine, Neurology (clinical), business, 030217 neurology & neurosurgery

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::240e8c5e3d226723449b549d399ed127Test
https://doi.org/10.1007/s00115-019-0750-2Test

7

Solving the unsolved rare diseases in Europe

المؤلفون: Birte Zurek, Alexander Hoischen, Holm Graessner, Sergi Beltran

المصدر: European Journal of Human Genetics, 29, 1319-1320
European journal of human genetics, 29(9):13191320
European Journal of Human Genetics
European Journal of Human Genetics, 29, 9, pp. 1319-1320