Literature DB >> 33519696

The European Reference Network for Rare Neurological Diseases.

Carola Reinhard1,2, Anne-Catherine Bachoud-Lévi3,4,5, Tobias Bäumer6,7, Enrico Bertini8, Alicia Brunelle1,2, Annemieke I Buizer9, Antonio Federico10, Thomas Gasser11,12, Samuel Groeschel13, Sanja Hermanns1,2, Thomas Klockgether14, Ingeborg Krägeloh-Mann13, G Bernhard Landwehrmeyer15, Isabelle Leber16,17, Alfons Macaya18, Caterina Mariotti19, Wassilios G Meissner20,21, Maria Judit Molnar22, Jorik Nonnekes23, Juan Dario Ortigoza Escobar24, Belen Pérez Dueñas25, Lori Renna Linton26, Ludger Schöls27, Rebecca Schuele12,28, Marina A J Tijssen29, Rik Vandenberghe30,31, Anna Volkmer32,33, Nicole I Wolf34, Holm Graessner1,2.   

Abstract

While rare diseases (RDs) are by definition of low prevalence, the total number of patients suffering from an RD is high, and the majority of them have neurologic manifestations, involving central, peripheral nerve, and muscle. In 2017, 24 European Reference Networks (ERNs), each focusing on a specific group of rare or low-prevalence complex diseases, were formed to improve the care for patients with an RD. One major aim is to have "the knowledge travel instead of the patient," which has been put into practice by the implementation of the Clinical Patient Management System (CPMS) that enables clinicians to perform pan-European virtual consultations. The European Reference Network for Rare Neurological Diseases (ERN-RND) provides an infrastructure for knowledge sharing and care coordination for patients affected by a rare neurological disease (RND) involving the most common central nervous system pathological conditions. It covers the following disease groups: (i) Cerebellar Ataxias and Hereditary Spastic Paraplegias; (ii) Huntington's disease and Other Choreas; (iii) Frontotemporal dementia; (iv) Dystonia, (non-epileptic) paroxysmal disorders, and Neurodegeneration with Brain Iron Accumulation; (v) Leukoencephalopathies; and (vi) Atypical Parkinsonian Syndromes. At the moment, it unites 32 expert centers and 10 affiliated partners in 21 European countries, as well as patient representatives, but will soon cover nearly all countries of the European Union as a result of the ongoing expansion process. Disease expert groups developed and consented on diagnostic flowcharts and disease scales to assess the different aspects of RNDs. ERN-RND has started to discuss diagnostically unclear patients in the CPMS, is one of four ERNs that serve as foundation of Solve-RD, and has established an RND training and education program. The network will facilitate trial readiness through the establishment of an ERN-RND registry with a minimal data of all patients seen at the ERN-RND centers, thus providing a unique overview of existing genotype-based cohorts. The overall aim of the ERNs is to improve access for patients with RDs to quality diagnosis, care, and treatment. Based on this objective, ERNs are monitored by the European Commission on a regular basis to provide transparency and reassurance to the RD community and the general public.
Copyright © 2021 Reinhard, Bachoud-Lévi, Bäumer, Bertini, Brunelle, Buizer, Federico, Gasser, Groeschel, Hermanns, Klockgether, Krägeloh-Mann, Landwehrmeyer, Leber, Macaya, Mariotti, Meissner, Molnar, Nonnekes, Ortigoza Escobar, Pérez Dueñas, Renna Linton, Schöls, Schuele, Tijssen, Vandenberghe, Volkmer, Wolf and Graessner.

Entities:  

Keywords:  European reference network; rare neurological diseases; standards of care; training and education; virtual healthcare

Year:  2021        PMID: 33519696      PMCID: PMC7840612          DOI: 10.3389/fneur.2020.616569

Source DB:  PubMed          Journal:  Front Neurol        ISSN: 1664-2295            Impact factor:   4.003


  9 in total

1.  An Exploratory Survey on the Care for Ataxic Patients in the American Continents and the Caribbean.

Authors:  Laura Bannach Jardim; Ali Hasan; Sheng-Han Kuo; Jonathan Javier Magaña; Marcondes França; Wilson Marques; Claudia Camejo; Luiz Carlos Santana-da-Silva; Emília Embiruçu Leão; Gisele Espíndola; Francisca Canals; Marcelo Miranda; Igor Salvatierra; Mario Cornejo-Olivas; Juan Fernandez-Ruiz; Pedro Braga-Neto; David José Dávila-Ortiz de Montellano; Luis Leonardo Flores-Lagunes; Nicolas Dupré; Bernard Brais; Fernando Regla Vargas; Clécio Godeiro; Léo Coutinho; Helio G Teive; Marcelo Kaufmann; Paula Saffie; Gabriel Vasata Furtado; Maria Luiza Saraiva-Pereira; Orlando Barsottini; José Luiz Pedroso; Roberto Rodríguez-Labrada; Luis Velázquez-Pérez; Christopher Gomez
Journal:  Cerebellum       Date:  2022-07-07       Impact factor: 3.847

2.  Development of a patient journey map for people living with cervical dystonia.

Authors:  Monika Benson; Alberto Albanese; Kailash P Bhatia; Pascale Cavillon; Lorraine Cuffe; Kathrin König; Carola Reinhard; Holm Graessner
Journal:  Orphanet J Rare Dis       Date:  2022-03-21       Impact factor: 4.123

Review 3.  Human iPSC-Derived Astrocytes: A Powerful Tool to Study Primary Astrocyte Dysfunction in the Pathogenesis of Rare Leukodystrophies.

Authors:  Angela Lanciotti; Maria Stefania Brignone; Pompeo Macioce; Sergio Visentin; Elena Ambrosini
Journal:  Int J Mol Sci       Date:  2021-12-27       Impact factor: 5.923

Review 4.  Surgical Outcomes in Rare Movement Disorders: A Report of Seventeen Patients from India and Review of Literature.

Authors:  Debjyoti Dhar; Vikram Venkappayya Holla; Nitish Kamble; Ravi Yadav; Dwarakanath Srinivas; Pramod Kumar Pal
Journal:  Tremor Other Hyperkinet Mov (N Y)       Date:  2022-06-20

5.  Dystonia management across Europe within ERN-RND: current state and future challenges.

Authors:  Liesanne M Centen; David Pinter; Martje E van Egmond; Holm Graessner; Norbert Kovacs; Anne Koy; Belen Perez-Dueñas; Carola Reinhard; Marina A J Tijssen; Sylvia Boesch
Journal:  J Neurol       Date:  2022-10-06       Impact factor: 6.682

6.  Parental experiences of having a child with CLN3 disease (juvenile Batten disease) and how these experiences relate to family resilience.

Authors:  Mattias Krantz; Emma Malm; Niklas Darin; Kalliopi Sofou; Antri Savvidou; Colin Reilly; Petra Boström
Journal:  Child Care Health Dev       Date:  2022-03-04       Impact factor: 2.943

Review 7.  Cognitive and Behavioral Manifestations in ALS: Beyond Motor System Involvement.

Authors:  Robert Rusina; Rik Vandenberghe; Rose Bruffaerts
Journal:  Diagnostics (Basel)       Date:  2021-03-30

8.  Solving unsolved rare neurological diseases-a Solve-RD viewpoint.

Authors:  Holm Graessner; Matthis Synofzik; Rebecca Schüle; Dagmar Timmann; Corrie E Erasmus; Jennifer Reichbauer; Melanie Wayand; Bart van de Warrenburg; Ludger Schöls; Carlo Wilke; Andrea Bevot; Stephan Zuchner; Sergi Beltran; Steven Laurie; Leslie Matalonga
Journal:  Eur J Hum Genet       Date:  2021-05-10       Impact factor: 4.246

9.  The road to successful people-centric research in rare diseases: the web-based case study of the Immunology and Congenital Disorders of Glycosylation questionnaire (ImmunoCDGQ).

Authors:  Rita Francisco; Sandra Brasil; Carlota Pascoal; Jaak Jaeken; Merell Liddle; Paula A Videira; Vanessa Dos Reis Ferreira
Journal:  Orphanet J Rare Dis       Date:  2022-03-24       Impact factor: 4.123

  9 in total

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