Partnership : Academics = 
, Industrials = 
, Financial investitors = 
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- CANADA
- Colombie-Britannique
- VANCOUVER
- FORGE - Finding of Rare Disease Genes in Canada
- University of British Columbia
- Faculty of Medicine
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- Emerging team in rare diseases: achieving the "triple aim" for inborn errors of metabolism
- Children's Hospital of Eastern Ontario
- Newborn Screening Ontario
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- CANADA
- Ontario
- OTTAWA, ONTARIO
- Emerging team in rare diseases: achieving the "triple aim" for inborn errors of metabolism
- University of Ottawa
- Department of Epidemiology and Community Medicine
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- CANADA
- Ontario
- OTTAWA, ONTARIO
- FORGE - Finding of Rare Disease Genes in Canada
- University of Ottawa
- Faculty of Medicine -
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- FORGE - Finding of Rare Disease Genes in Canada
- Centre hospitalier universitaire Sainte-Justine
- Pédiatrie
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- Molecular basis of mitochondrial disorders
- Biomedicum Helsinki 1- University of Helsinki
- Department of molecular neurology
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- Molecular studies on mitochondrial disorders linked to point mutations in tRNA genes
- IBMC - Institut de biologie moléculaire et cellulaire
- Architecture et réactivité de l'ARN
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- MINATAR: Gene therapy of human diseases associated to DNA mitochondrial mutations: development of cellular models exploiting nucleic acids homing in mitochondria
- Institut de Physiologie et Chimie Biologique
- Génétique Moléculaire, Génomique et Microbiologie
- More details
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- FRANCE
- AQUITAINE
- BORDEAUX
- MITOFOOD: energetic mitochondrial metabolism study, normal and pathological: fundamental and theorical implications
- Université Bordeaux 2 - Victor Ségalen
- Physiopathologie mitochondriale
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- FRANCE
- AQUITAINE
- BORDEAUX
- DEPLETMITO: influence of the amount of mitochondrial DNA on energy metabolism: implications for mitochondrial diseases
- Université Bordeaux 2 - Victor Ségalen
- Physiopathologie mitochondriale
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- FRANCE
- ILE-DE-FRANCE
- LE KREMLIN BICETRE
- Biochemistry and genetics of mitochondrial cytopathies
- CHU de Bicêtre
- Service de neuropédiatrie
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- FRANCE
- ILE-DE-FRANCE
- PARIS
- PGCTHERAMITO: therapeutical potential of PGC-1alpha activators for the correction of hereditary deficiencies of mitochondrial energy metabolism
- CHU Paris - Hôpital Necker - Enfants Malades
- Transporteurs mitochondriaux et métabolisme
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- FRANCE
- ILE-DE-FRANCE
- PARIS
- Genetics of mitochondrial diseases - Identification of nuclear genes in mitochondrial disorders
- CHU Paris - Hôpital Necker - Enfants Malades
- Département de génétique
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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 Paris - Hôpital Necker - Enfants Malades
- Unité fonctionnelle métabolisme
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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 Paris - Hôpital Robert Debré
- Service de neurologie pédiatrique et des maladies métaboliques
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- FRANCE
- ILE-DE-FRANCE
- PARIS
- Cellular and molecular physiology of mitochondrial diseases
- Institut Cochin - Faculté de Médecine de Paris Descartes
- Département mitochondries, bioénergétique, métabolisme et signalisation
- More details
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- FRANCE
- ILE-DE-FRANCE
- PARIS
- Heteroplasmic mutations of mitochondrial DNA: inventory, physiopathologic mechanisms and complementation possibilities
- Institut Cochin - Faculté de Médecine de Paris Descartes
- Département mitochondries, bioénergétique, métabolisme et signalisation
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- FRANCE
- PAYS DE LA LOIRE
- ANGERS
- Evaluation of high-throughput sequencing microarray technology in mtDNA diseases
- CHU d'Angers
- Unité fonctionnelle de Génétique Moléculaire
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- GERMANY
- Baden-Württemberg
- REUTLINGEN
- mitoNET: subproject mitoFIBRATE - Testing pharmacological approaches in cell culture
- Klinikum am Steinenberg
- Klinik für Kinder- und Jugendmedizin
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- GERMANY
- Baden-Württemberg
- STUTTGART
- mitoNET: subproject mitoHEART - CMR-based diagnosis of cardiac involvement in patients with mitochondrial myopathy
- Robert-Bosch-Krankenhaus
- AG Molekulare Bildgebung und Kardiomyopathien
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- GERMANY
- Baden-Württemberg
- TÜBINGEN
- mitoNET: subproject mitoMORPH - Establishing the analysis of abnormal mitochondrial fission and fusion in human cells as a new assay to follow and diagnose mitochondrial cytopathies.
- Universitätsklinikum Tübingen
- Abteilung für Neurodegeneration
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- mitoNET: german Network for mitochondrial diseases - coordination
- Deutsches MITONET e.V. c/o Dr. Bert Obermaier-Kusser
- Deutsches MITONET e.V.
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- Genotype and phenotype investigations in mitochondrial diseases
- LMU Klinikum der Universität München - Campus Großhadern
- Arbeitsgruppe Neurogenetik
- More details
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- mitoNET: german Network for mitochondrial diseases - coordination
- LMU Klinikum der Universität München - Campus Großhadern
- Arbeitsgruppe Neurogenetik
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- BNE: BrainNet Europe II: European brain tissue bank - Network for clinical neuroscience and basic research (coordination)
- Ludwig-Maximilians-Universität München
- Zentrum für Neuropathologie und Prionforschung
- More details
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- mitoNET: subproject mitoGENE - High-Throughput-Screening and development of new diagnostic protocols for testing of mitochondropathies
- Technische Universität München
- Institut für Humangenetik
- More details
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- mitoNET: subproject mitoFIBRATE - Testing pharmacological approaches in cell culture
- Technische Universität München
- Institut für Humangenetik
- More details
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- Genetic Variability of mitochondrial disorders (SFB 577)
- Charité - Universitätsmedizin Berlin (CVK)
- Klinik für Pädiatrie mit Schwerpunkt Neurologie
- More details
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- mitoNET: subproject mitoSYSTEM - Using a probabilistic Bayesian network approach towards the diagnose of mitochondrial disease will quantitatively delineate and specify subsets of disease phenotypes, thus facilitating detection of the basic genetic defects
- Charité - Universitätsmedizin Berlin (CVK)
- Klinik für Pädiatrie mit Schwerpunkt Neurologie
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- GERMANY
- Hessen
- FRANKFURT AM MAIN
- mitoNET: subproject mitoPROT - Developing a simple and highly sensitive assay to quantify the five mitochondrial oxidative phosphorylation complexes from patient samples, and screening the cohort of patients of the consortium by the novel protocol
- Klinikum der Johann Wolfgang Goethe-Universität Frankfurt
- Molekulare Bioenergetik
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- GERMANY
- Niedersachsen
- GÖTTINGEN
- Clinical and genetic presentation of juvenile mitochondriopathies
- Universitätsmedizin Göttingen
- Abteilung Pädiatrie II - Neuropädiatrie, Stoffwechsel und Endokrinologie
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- GERMANY
- Niedersachsen
- GÖTTINGEN
- Clinical, morphological and genetic characterisation of unclassified juvenile mitochondrial myopathies
- Universitätsmedizin Göttingen
- Abteilung Pädiatrie II - Neuropädiatrie, Stoffwechsel und Endokrinologie
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- GERMANY
- Nordrhein-Westfalen
- BONN
- mitoNET: subproject mitoPROP - Propagation mechanisms of mitochondrial DNA mutations in patients with mitochondrial diseases
- Universitätsklinikum Bonn
- Klinik für Epileptologie
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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
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- ITALY
- EMILIA ROMAGNA
- BOLOGNA
- Pathogenetic role and biochemical dysfunctions associated with mtDNA ATPase-6 gene mutations
- Università degli Studi di Bologna
- Laboratorio di Bioenergetica
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- ITALY
- EMILIA ROMAGNA
- FERRARA
- Involvement of mitochondrial proteins in autophagy: a possible link with mitochondrial disorders
- Università degli Studi di Ferrara
- Dipartimento di Medicina Sperimentale e Diagnostica
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- Therapeutic strategies to combat mitochondrial disorders
- Fondazione Telethon
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- Construction of a database for a nation-wide italian collaborative network of mitochondrial
- IRCCS Ospedale Pediatrico Bambino Gesù
- Unità di Malattie Neuromuscolari e Neurodegenerative, Laboratorio di Medicina Molecolare
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- Center for advanced diagnostic and research on motichondrial neurological disorders of infants
- Fondazione IRCCS Istituto Neurologico "C. Besta" - sede Bicocca
- U.O. di Neurogenetica Molecolare
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- Identification and characterization of nuclear genes responsible for human mitochondrial disorders
- Fondazione IRCCS Istituto Neurologico "C. Besta" - sede Bicocca
- U.O. di Neurogenetica Molecolare
- More details
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- MitMed: a multicenter consortium for the identification and characterization of nuclear genes responsible for human mitochondrial disorders
- Fondazione IRCCS Istituto Neurologico "C. Besta" - sede Bicocca
- U.O. di Neurogenetica Molecolare
- More details
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- Therapeutic strategies to combat mitochondrial disorders
- Fondazione IRCCS Istituto Neurologico "C. Besta" - sede Bicocca
- U.O. di Neurogenetica Molecolare
- More details
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- Disorders of the synthesis and maintenance of mitochondrial DNA: clinical, histopathological and genetic in a heterogeneous population of patients with mitochondrial disorders.
- IRCCS OASI Maria Santissima
- U.O. Neurologia per il Ritardo Mentale
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- Construction of a database for a nation-wide italian collaborative network of mitochondrial
- Azienda Ospedaliero Universitaria Pisana - Ospedale S. Chiara
- Laboratorio di Neurobiologia Clinica e Neurochimica
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- Role of mitochondrial dynamic and autophagy in the segregation of mutant mtDNA
- Azienda Ospedaliera Universitaria di Padova
- Dipartimento di Neuroscienze
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- Construction of a database for a nation-wide italian collaborative network of mitochondrial
- Azienda Ospedaliera Universitaria di Padova - Campus Biomedico Pietro d'Abano
- U.O. di Neuropatologia e Psicopatologia
- More details
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- MitMed: a multicenter consortium for the identification and characterization of nuclear genes responsible for human mitochondrial disorders
- Università degli Studi di Padova
- Dipartimento di Scienze Biomediche
- More details
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- Therapeutic strategies to combat mitochondrial disorders
- Università degli Studi di Padova
- Dipartimento di Scienze Biomediche Sperimentali
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- NETHERLANDS
- Gelderland
- NIJMEGEN
- EUMITOCOMBAT: rational treatment strategies combating mitochondrial oxidative phosphorylation (OXPHOS) disorders (coordination)
- UMC St Radboud - Universitair Medisch Centrum St Radboud
- Afdeling Metabole en Endocriene Ziekten
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- Testing the xenoexpression as a gene therapy for mitochondrial diseases
- Universidad de Zaragoza. Facultad de Ciencias
- Departamento de Bioquimica y Biologia Molecular y Celular (F. Ciencias)
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- SPAIN
- Cataluña
- ESPLUGUES DE LLOBREGAT
- Folinic acid treatment in patients with oxidative phosphorylation diseases
- Hospital Universitari Sant Joan de Déu
- Servicio de Neurología
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- Identification and charactization of new nuclear encoded-genes causing mitochondrial diseases by functional complementation of OXPHOS defects
- Hospital Universitario 12 de Octubre
- Laboratorio de enfermedades raras, mitocondriales y neuromusculares
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- Identification and validation of biomarkers for mitochondrial respiratory chain disorders
- Hospital Universitario 12 de Octubre
- Laboratorio de enfermedades raras, mitocondriales y neuromusculares
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- Using induced pluripotent stem cells (iPS) for the study and treatment of mitochondrial diseases
- Instituto de Investigaciones Biomédicas "Alberto Sols" (CSIC-UAM)
- Departamento de Modelos Experimentales de Enfermedades Humanas (Laboratorio de Rafael Garesse Alarcón)
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- UNITED KINGDOM
- Greater London
- UXBRIDGE
- Prevention of transmission of mitochondrial DNA disease
- GlaxoSmithKline
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- UNITED KINGDOM
- Tyne & Wear
- NEWCASTLE UPON TYNE
- Prevention of transmission of mitochondrial DNA disease
- Newcastle University
- Mitochondrial Research Group
- More details
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- UNITED KINGDOM
- Tyne & Wear
- NEWCASTLE UPON TYNE
- Laboratory investigation and diagnosis of patients with mitochondrial disease
- Newcastle University
- Mitochondrial Research Group
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