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Funded by an IRDiRC member =

    • CANADA
    • Ontario
    • OTTAWA
    • Funded by an IRDiRC member
    • Emerging team in rare diseases: achieving the "triple aim" for inborn errors of metabolism
    • Children's Hospital of Eastern Ontario
    • Newborn Screening Ontario
    • More details
    • CANADA
    • Ontario
    • OTTAWA, ONTARIO
    • Funded by an IRDiRC member
    • Emerging team in rare diseases: achieving the "triple aim" for inborn errors of metabolism
    • University of Ottawa
    • Department of Epidemiology and Community Medicine
    • More details
    • FRANCE
    • ILE-DE-FRANCE
    • LE KREMLIN-BICÊTRE
    • Pain impact in children affected by lysosomal diseases
    • GHU Paris-Sud - Hôpital de Bicêtre
    • Unité douleur et Soins Palliatifs
    • More details
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Evaluation of diagnosis and treatment protocols and long-term follow-up of errors of metabolism
    • CHU Paris - Hôpital Necker-Enfants Malades
    • Unité fonctionnelle métabolisme
    • More details
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Evaluation of diagnosis and treatment protocols and long-term follow-up of errors of metabolism
    • CHU Paris - Hôpital Robert Debré
    • Service de neurologie pédiatrique et des maladies métaboliques
    • More details
    • FRANCE
    • MIDI-PYRENEES
    • TOULOUSE
    • Sialidase Neu4: new therapy for lysosomal diseases
    • CHU de Toulouse - Hôpital Purpan
    • Laboratoire de biochimie
    • More details
    • HUNGARY
    • Észak-Magyarország
    • BUDAPEST
    • Molecular prognostic factors in pediatric diseases
    • Semmelweis University
    • SOTE Pediatric clinic II
    • More details
    • IRELAND
    • County Dublin
    • DUBLIN
    • A prospective study on the numbers of Irish Travellers attending the metabolic clinic in Dublin
    • Our Lady's Children's Hospital
    • National Centre for Medical Genetics
    • More details
    • ITALY
    • CAMPANIA
    • NAPOLI
    • Funded by an IRDiRC member
    • Modulation of Cellular Clearance in Lysosomal Storage Disorders
    • TIGEM - Telethon Institute of Genetics and Medicine
    • Laboratorio di Ricerca
    • More details
    • ITALY
    • LAZIO
    • ROMA
    • GENESKIN: European network on rare genetic skin diseases (coordination)
    • Istituto Dermopatico dell'Immacolata - IRCCS
    • Laboratorio di Biologia Molecolare e Cellulare
    • More details
    • PORTUGAL
    • NORTE
    • PORTO
    • Splicing therapeutics for patients affected by lisosomal storage disorders.
    • Instituto Nacional de Saúde Dr. Ricardo Jorge - Porto
    • Unidade de Investigação & Desenvolvimento; Departamento de Genética
    • More details
    • PORTUGAL
    • NORTE
    • PORTO
    • The crosstalk between lipid antigen presentation and the pathogenic mechanisms of Lysosomal Storage Diseases
    • Instituto de Biologia Molecular e Celular
    • Unidade de Biologia do Lisossoma e do Peroxissoma
    • More details
    • UNITED KINGDOM
    • Cambridgeshire
    • CAMBRIDGE
    • EUCLYD: substrate reduction therapy for glycospingolipidoses and mucopolysaccharidoses (WP4)
    • Addenbrooke's Hospital
    • Lysosomal Disorders Unit
    • More details
    • UNITED KINGDOM
    • Cambridgeshire
    • CAMBRIDGE
    • Funded by an IRDiRC member
    • NIHR BioResource - Rare Disease: SPEED - Specialist Pathology: Evaluating Exomes in Diagnostics
    • Wellcome Trust/MRC Building
    • Cambridge Institute for Medical Research
    • More details
    • UNITED KINGDOM
    • Greater London
    • LONDON
    • Development of diagnostic methods for lysosomal storage diseases
    • UCL Institute of Child Health, University College London
    • Biochemistry Research Group
    • More details
    • UNITED KINGDOM
    • Lothian
    • EDINBURGH
    • Genetic disorders of human brain development
    • Western General Hospital
    • MRC Human Genetics Unit
    • More details
    • UNITED KINGDOM
    • West Midlands
    • BIRMINGHAM
    • NIPSIGEN - Clinical translation of non-invasive prenatal diagnosis (NIPD) for single gene disorders (Health Innovation Challenge Fund)
    • Birmingham Women's NHS Foundation Trust
    • Regional Genetics Unit
    • More details