Partnership : Academics = 
, Industrials = 
, Financial investitors = 
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- Epidemiology and molecular characterization of inherited metabolic disorders in the Cypriot population
- The Cyprus Institute of Neurology and Genetics
- Laboratory of biochemical genetics
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- FRANCE
- ILE DE FRANCE
- LE KREMLIN BICÊTRE
- Pain impact in children affected by lysosomal diseases
- CHU de Bicêtre
- Unité douleur et Soins Palliatifs
- More details
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- FRANCE
- ILE DE FRANCE
- PARIS
- Evaluation of diagnosis and treatment protocols and long-term follow-up of errors of metabolism
- CHU de Paris - Hôpital Robert Debré
- Service de neurologie pédiatrique et des maladies métaboliques
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- FRANCE
- ILE DE FRANCE
- PARIS
- Evaluation of diagnosis and treatment protocols and long-term follow-up of errors of metabolism
- Hopital Necker - Enfants Malades
- Unité fonctionnelle métabolisme
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- FRANCE
- ILE DE FRANCE
- PARIS
- Management of metabolic hereditary diseases in adults
- Hopital Necker - Enfants Malades
- Service de néphrologie adulte
- More details
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- HUNGARY
- Észak-Magyarország
- BUDAPEST
- Molecular prognostic factors in pediatric dieases
- Semmelweis University
- SOTE Pediatric clinic II
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- 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 (Molecular Genetics)
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- AAV-mediated gene transfer in animal models of mucopolysaccharidosis VI
- Telethon Institute of Genetics and Medicine (TIGEM)
- Laboratorio di Ricerca
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- Prognosis and prevention in a few inherited diseases existing in the Portuguese population
- CGMJM - Centro de Genética Médica Jacinto Magalhães
- Unidade de Investigação & Desenvolvimento; Departamento de Genética
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- Molecular studies in diseases of lisosomal origin. Characterization of mutations and new therapeutic approaches for glycolipidosis, mucopolysaccharidosis and Niemann-Pick type C disease.
- Corporació Sanitària Clínic
- Institut de Bioquímica Clínica: Sección de Errores Congénitos del Metabolismo
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- Expression of mutant alleles, approaches for gene therapy, origin of mutations and haplotype studies, and genotype/phenotype correlation in gangliosidosis GM1, Gaucher disease, and mucopolysaccharidosis type 3, 4, and 6
- Universitat de Barcelona. Facultat de Biologia.
- Departamento de Genética
- More details
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- Molecular studies in diseases with lysosomal origin. Mutations characterisation and new therapeutic approaches on sphingolipidosis, mucopolysaccharidosis and Niemann-Pick disease
- Universitat de Barcelona. Facultat de Biologia.
- Departamento de Genética
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- UNITED KINGDOM
- Greater London
- LONDON
- Systemic diseases and the lung
- UCL Institute of Child Health
- Respiratory Medicine Group
- More details
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- UNITED KINGDOM
- Greater London
- LONDON
- Development of diagnostic methods for lysosomal storage diseases
- University College London
- Biochemistry Research Group
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- UNITED KINGDOM
- Greater Manchester
- MANCHESTER
- Applied stem cell biology of MPS and related inherited metabolic disease
- St Mary's University Hospital
- Willink Biochemical Genetics Unit, Genetic Medicine 6th floor Pod1
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- UNITED KINGDOM
- Greater Manchester
- MANCHESTER
- Behavioural aspects of Mucopolysaccaridosis - an exploratory study
- St Mary's University Hospital
- Willink Biochemical Genetics Unit, Genetic Medicine 6th floor Pod1
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