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Research projects
SPAIN
Cataluña
BARCELONA
Genetic dementias (genetic Alzheimer's disease, frontotemporal dementia and prion diseases): longitudinal changes and expression and epigenetic differences with sporadic cases
Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS)
Institut d'Investigacions Biomèdiques August Pi i Sunyer
CANADA
Ontario
LONDON
Physiological functions of the cellular prion protein
University of Western Ontario
Schulich School of Medicine & Dentistry
FRANCE
ILE-DE-FRANCE
PARIS
Development of therapeutic strategies for human degenerative diseases
Centre Paul Broca
Biologie et pathologie du neurone
FRANCE
OCCITANIE
MONTPELLIER
Normal and pathological function of the prion protein
Institut de Recherches en Biothérapie (IRB)
Laboratoire de Biochimie - Plate-forme Régionale de Protéomique Clinique
ITALY
CAMPANIA
NAPOLI
Role of intracellular trafficking in the pathogenesis of inherited prion diseases
Azienda Ospedaliera Universitaria "Federico II"
Dipartimento di Biologia e Patologia cellulare
PORTUGAL
SUL
FARO
Single-Molecule Detection of the Prion Protein: Characterization of Conformational Change Involved on Prion Diseases.
Universidade do Algarve
Centro de Biomedicina Molecular e Estrutural
SWEDEN
Region Uppsala
UPPSALA
Prions and trypanosomes in the nervous system: targeting, immune control and neurodegeneration
Uppsala University
Department of Neuroscience
SPAIN
Cataluña
BARCELONA
Advanced genomics and lipidomics for identifying novel causes of inherited movement disorders
Instituto de Química Avanzada de Cataluña
Unidad de Investigación en Moléculas Bioactivas
SPAIN
País Vasco
SAN SEBASTIÁN
Advanced genomics and lipidomics for identifying novel causes of inherited movement disorders
Instituto de Investigación Sanitaria Biodonostia
Área de Neurociencias
FINLAND
Finland
OULU
FINCA mouse as a tool to study mechanisms behind severe fibrosis and neurodegeneration
University of Oulu
Biocenter Oulu
SPAIN
Cataluña
BARCELONA
Igenco: In-Depth genomics and cross-omics analysis for undiagnosed rare diseases on a user-friendly collaborative platform
ISGlobal - Instituto de Salud Global de Barcelona
Programa de investigación en Enfermedades no transmisibles y medio ambiente
SPAIN
Madrid
MADRID
RAREGenomics: Network of Genomic, Functional, Clinical and Therapeutic Resources for the Study of Rare Neurological Diseases
Hospital Universitario Fundación Jiménez Díaz
Servicio de Genética Clínica
CANADA
Colombie-Britannique
VICTORIA
Silent Genomes: Reducing health care disparities and improving diagnostic success for children with genetic diseases from Indigenous populations
University of Victoria
Community Genetics Research Program/Island Medical Program
CANADA
Ontario
TORONTO
Beyond the Genome: Transcriptome Based Diagnostics for Rare Diseases and Cancer
Hospital for Sick Children, Research Institute
FRANCE
ILE-DE-FRANCE
PARIS
Neuroglobin gene overexpression: a promising tool for treating a large spectrum of neurological disorders thanks to its ability to safely and sustainably preserve mitochondrial integrity
Institut National de la Santé et de la Recherche Médicale
ITALY
LAZIO
ROMA
Diverse rare diseases caused by functional dysregulation of Rho GTPase-related proteins
ISS - Istituto Superiore di Sanità
Centro Nazionale Malattie Rare
SPAIN
Cataluña
SABADELL
Rare variant burden contribution to psychiatric disorders in a child-adolescent population with borderline/mild intellectual disability
Corporación Sanitaria Parc Taulí
Laboratorio de Genética de la UDIAT-CD
SPAIN
Madrid
MADRID
Identification of new genes causing rare diseases in pediatric patients, searching of genetic pharmacological targets, and drugs discovery, the steps for a personalized medicine
Instituto de Investigación Hospital 12 de Octubre
Grupo de investigación en enfermedades raras, mitocondriales y neuromusculares
UNITED STATES
Washington
ADDRESS: NOT PROVIDED - US
A powerful web-based discovery platform for rare disease genetics
Institution: Information not provided - US
Multicentric Research projects
- CiMUS - Centro de Investigación en Medicina Molecular y Enfermedades Crónicas
- Brain Protein Malfunction
- UniversitätsSpital Zürich
- Institut für Neuropathologie
- Institut Albert Bonniot
- INSERM U 823 - Institut d'oncologie
- CEA - Commissariat à l'Energie Atomique
- Service d'étude des prions et des infections atypiques
- Het Nederlands Kanker Instituut - Antoni van Leeuwenhoek Ziekenhuis
- Groep Tumorbiologie
- Linköping University
- Department of Physics, Chemistry and Biology (IFM)
- Azienda Ospedaliera di Padova
- Clinica Pediatrica
- Alzheimer Europe Office
- Max-Planck-Institut für experimentelle Medizin
- Abteilung Molekulare Neurobiologie
- Haukeland University Hospital
SPAIN
Galicia
SANTIAGO DE COMPOSTELA
CHAPRION: Pharmacological chaperones for genetic prion diseases
SWITZERLAND
Suisse Alémanique
ZÜRICH
PrionImmunity: Immunotherapy of familial prion diseases
FRANCE
AUVERGNE-RHONE-ALPES
LA TRONCHE
IMMUNOPRION: strains, species and immunology in prion diseases (FINISHED)
FRANCE
ILE-DE-FRANCE
FONTENAY-AUX-ROSES
NEUROPRION: European network dedicated to research on prion diseases
NETHERLANDS
Noord-Holland
AMSTERDAM
ANTEPRION: development of a pre-clinical blood test for prion diseases (COMPLETED)
SWEDEN
Region Östergötland
LINKÖPING
LUPAS: luminescent polymers for in vivo imaging of amyloid signatures
ITALY
VENETO
PADOVA
Brains for brain: research group of the European task force on brain and neurodegenerative lysosomal storage diseases
LUXEMBOURG
LUXEMBOURG
LUXEMBOURG
Alzheimer Europe: base de données européenne sur les formes rares de démence
GERMANY
Niedersachsen
GÖTTINGEN
EUROSPIN: European consortium on synaptic protein networks in Neurological and Psychiatric diseases
NORWAY
Vestlandet
BERGEN