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- Therapeutic challenge in leukodystrophies
- Medizinische Universität Wien
- Pathobiology of the Nervous System
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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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- MYELINET: myeline repairing: role of steroids and sex
- Université Louis Pasteur
- Laboratoire d'Imagerie et de Neurosciences Cognitives
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- MYELINET: myeline repairing: cellular and gene therapies strategies
- Université Louis Pasteur
- Laboratoire d'Imagerie et de Neurosciences Cognitives
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- MYELINET: myeline repairing: animal models creation of myelin diseases
- Université Louis Pasteur
- Laboratoire d'Imagerie et de Neurosciences Cognitives
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- MYELINET: myeline repairing: noninvasive white matter imaging
- Université Louis Pasteur
- Laboratoire d'Imagerie et de Neurosciences Cognitives
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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
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- FRANCE
- ILE DE FRANCE
- LE KREMLIN-BICÊTRE
- MYELINET: myeline repairing: role of steroids and sex
- Université Paris 11 - Kremlin-Bicêtre
- Stéroïdes, neuroprotection et neurorégénération
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- FRANCE
- ILE DE FRANCE
- PARIS
- Genotype-phénotype correlation in leucodystrophies and neurolipidosis
- CHU Hôpital Pitié-Salpêtrière
- Biologie des interactions neurones / glie
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- FRANCE
- ILE DE FRANCE
- PARIS
- Diagnostic strategy in adult neurolipidoses and leucodystrophies
- CHU Hôpital Pitié-Salpêtrière
- Biologie des interactions neurones / glie
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- FRANCE
- ILE DE FRANCE
- PARIS
- Psycho-cognitive forms of adult metachromatic leucodystrophies: phenotype-genotype relationships and international network development
- CHU Hôpital Pitié-Salpêtrière
- Biologie des interactions neurones / glie
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- FRANCE
- ILE DE FRANCE
- PARIS
- Molecules of guidance and remyelinisation in the central nervous system
- CHU Hôpital Pitié-Salpêtrière
- Biologie des interactions neurones / glie
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- FRANCE
- ILE DE FRANCE
- PARIS
- Fundamental aspects and therapeutic models of remyelinisation
- CHU Hôpital Pitié-Salpêtrière
- Génétique et mécanismes des maladies de l'excitabilité membranaire et de la Sclérose en plaques
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- FRANCE
- ILE DE FRANCE
- PARIS
- Study of myelination in normal and pathological conditions
- CHU Hôpital Pitié-Salpêtrière
- Génétique et mécanismes des maladies de l'excitabilité membranaire et de la Sclérose en plaques
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- FRANCE
- ILE DE FRANCE
- PARIS
- Role of Sox17 in the development and regeneration of oligodendrocytes from mouse and humain brain
- CHU Hôpital Pitié-Salpêtrière
- Génétique et mécanismes des maladies de l'excitabilité membranaire et de la Sclérose en plaques
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- FRANCE
- ILE DE FRANCE
- PARIS
- Therapeutic approach of CNS remyelinisation: preclinical model development of demyelinisation
- CHU Hôpital Pitié-Salpêtrière
- Génétique et mécanismes des maladies de l'excitabilité membranaire et de la Sclérose en plaques
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- FRANCE
- ILE DE FRANCE
- PARIS
- Function of repulsive proteins Slit and their receptors in proliferation, migration and differenciation of SVZ derivated neuronal precursors in normal and demyelinisated CNS
- CHU Hôpital Pitié-Salpêtrière
- Génétique et mécanismes des maladies de l'excitabilité membranaire et de la Sclérose en plaques
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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
- Function of repulsive proteins Slit and their receptors in proliferation, migration and differenciation of SVZ derivated neuronal precursors in normal and demyelinisated CNS
- Centre de Recherche Institut de la Vision
- Département Biologie du Développement
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- FRANCE
- ILE DE FRANCE
- PARIS
- New mouse model to study the potential regeneration of glia, repairing of myeline and the interaction between oligodendrocytes / Schwann cells
- ENS - Ecole Normale Supérieure de Paris
- INSERM U784
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- FRANCE
- ILE DE FRANCE
- PARIS
- Gene therapy for metachromatic leukodystrophy
- GHU Cochin - Saint-Vincent de Paul / Site Saint-Vincent de Paul
- Génétique et biothérapie des maladies dégénératives et prolifératives du système nerveux
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- FRANCE
- ILE DE FRANCE
- PARIS
- AAV-mediated intracerebral gene transfer for metachromatic leukodystrophy , for adrenoleukodystrophy using transplantation of autologous CD34+ cells modified with lentiviral vector
- GHU Cochin - Saint-Vincent de Paul / Site Saint-Vincent de Paul
- Génétique et biothérapie des maladies dégénératives et prolifératives du système nerveux
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- FRANCE
- ILE DE FRANCE
- PARIS
- Vectors production for gene therapy of MLD
- GHU Cochin - Saint-Vincent de Paul / Site Saint-Vincent de Paul
- Génétique et biothérapie des maladies dégénératives et prolifératives du système nerveux
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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
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- FRANCE
- MIDI-PYRENEES
- TOULOUSE
- Cellular physiopathology of hereditary lipidosis
- Institut de Médecine Moléculaire de Rangueil
- Sphingolipides, mort cellulaire et maladies chroniques
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- FRANCE
- NORD-PAS DE CALAIS
- LILLE
- European information project on rare forms of dementia
- Centre de Recherches Jean-Pierre Aubert (CRJPA)
- Maladies neurodégénératives et mort neuronale
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- Physiopathology of human and animal lysosomal lipidoses
- Faculté de médecine - RTH Laënnec
- Métabolomique et maladies métaboliques
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- GERMANY
- Baden-Württemberg
- TÜBINGEN
- LEUKONET : Adult-onset leukodystrophies - clinical, neurophysiological and neuroradiological characterization
- Hertie-Institut für klinische Hirnforschung
- Abteilung für Neurologie mit Schwerpunkt Neurodegeneration
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- GERMANY
- Baden-Württemberg
- TÜBINGEN
- LEUKONET: Description of the various courses of leukodystrophies in children with known genetic anomalies
- Universitätsklinik für Kinderheilkunde und Jugendmedizin
- Abteilung für Neuropädiatrie, Entwicklungsneurologie, Sozialpädiatrie
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- GERMANY
- Mecklenburg-Vorpommern
- ROSTOCK
- LEUKONET : Adult-onset leukodystrophies - clinical, neurophysiological and neuroradiological characterization
- Universitätsklinikum Rostock
- Albrecht-Kossel-Institut für Neurodegeneration
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- GERMANY
- Niedersachsen
- GÖTTINGEN
- Role of the mitochondrial respiratory process in myelinisation and the interaction axons/glial cells
- Max-Planck-Institut für experimentelle Medizin
- Abteilung Neurogenetik
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- GERMANY
- Nordrhein-Westfalen
- BONN
- LEUKONET: Metachromatic leukodystrophy and Krabbe disease: Inhibition of substrate synthesis as a novel therapeutic concept, mutation analysis and development of a rapid genotyping method
- Universität Bonn
- Institut für Biochemie und Molekularbiologie
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- GERMANY
- Nordrhein-Westfalen
- BONN
- Genetics, pathobiochemistry and development of new therapies for lysosomal storage diseases with emphasis on metachromatic leukodystrophy
- Universität Bonn
- Institut für Biochemie und Molekularbiologie
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- GERMANY
- Nordrhein-Westfalen
- BONN
- Molecular mechanism of the MLD pathogenesis
- Universität Bonn
- Institut für Biochemie und Molekularbiologie
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- GERMANY
- Nordrhein-Westfalen
- BONN
- Enzyme substitution therapy in a mouse model of metachromatic leukodystrophy
- Universität Bonn
- Institut für Biochemie und Molekularbiologie
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- GERMANY
- Nordrhein-Westfalen
- BONN
- Metachromatic leukodystrophy: Strategies for substrate reduction therapy and investigations on neuronal and myelin pathology in new mouse models
- Universität Bonn
- Institut für Biochemie und Molekularbiologie
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- GERMANY
- Nordrhein-Westfalen
- BONN
- LEUKONET: Metachromatic Leukodystrophy: Structures, functions, and biophysical properties of the different MLD-causing forms of the sphingolipid activator protein B (Sap-B)
- Universität Bonn
- Kekule' Institut für Organische Chemie und Biochemie
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- GERMANY
- Rheinland-Pfalz
- MAINZ
- Production of new vectors AAV for gene therapy of leukodystrophy
- Johannes Gutenberg-Universität Mainz
- Institut für Physiologische Chemie und Pathobiochemie
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- GERMANY
- Rheinland-Pfalz
- MAINZ
- Role of the secretion of oligodendroglial exosomes in glial cells for the signaling and the protection of neurons
- Universität Mainz
- Abteilung Molekulare Zellbiologie
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- GERMANY
- Rheinland-Pfalz
- MAINZ
- Production of new vectors AAV for gene therapy of leukodystrophy
- Universität Mainz
- Abteilung Molekulare Zellbiologie
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- GERMANY
- Sachsen
- WERMSDORF
- LEUKONET : Adult-onset leukodystrophies - clinical, neurophysiological and neuroradiological characterization
- Fachkrankenhaus Hubertusburg gGmbH
- Klinik für Neurologie und neurologische Intensivmedizin
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- Role of the adhesion molecule TAG-1 in the function of glial cells
- Institute of Molecular Biology and Biotechnology (IMBB)
- Department of biology
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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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- Pathophysiological mechanism linked to elF2B of glial cells using a knock-in mouse model
- University of Tel-Aviv
- Department of cell research and immunology
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- Genetically determined leukodystrophies: new clinico-genetic protocols and identification of novel genetic determinants
- IRCCS Ospedale Pediatrico Bambino Gesù
- U.O. di Medicina Molecolare
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- PPAR-Gamma agonists as potential therapic agents to protect oligodendrocytes and to promote remyelinisation
- Istituto Superiore di Sanità
- Dipartimento di Biologia Cellulare e Neuroscienze
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- Molecular studies in leucodystrophies
- Istituto G. Gaslini - Ospedale Pediatrico IRCCS
- Laboratorio di Diagnosi Pre-Postnatale Malattie Metaboliche
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- Gene/cell therapy approach for metachromatic and globoid leukodystrophies
- Telethon Institute of Gene Therapy - Ospedale San Raffaele
- Istituto San Raffaele Telethon per la Terapia Genica
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- Combined gene/neural stem cell based approaches for globoid cell and metachromatic leukodystrophies (GLD and MLD)
- Telethon Institute of Gene Therapy - Ospedale San Raffaele
- Istituto San Raffaele Telethon per la Terapia Genica
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- Improving safety of gene transfer
- Telethon Institute of Gene Therapy - Ospedale San Raffaele
- Istituto San Raffaele Telethon per la Terapia Genica
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- Improving efficacy of gene transfer into hematopoietic stem cells
- Telethon Institute of Gene Therapy - Ospedale San Raffaele
- Istituto San Raffaele Telethon per la Terapia Genica
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- Hsc-based ex vivo gene therapy of metachromatic and globoid leukodystrophy
- Telethon Institute of Gene Therapy - Ospedale San Raffaele
- Unità di Ricerca Clinica Pediatrica
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- Overexpression of ArylsulfataseA in human hematopietic cells in the gene therapy of MLD: preclinical and clinical study
- Telethon Institute of Gene Therapy - Ospedale San Raffaele
- Unità di Ricerca Clinica Pediatrica
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- Clinical research of gene therapy in metachromatic leukodystrophy
- Telethon Institute of Gene Therapy - Ospedale San Raffaele
- Unità di Ricerca per la Clinica Pediatrica (PCRU)
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- ITALY
- PUGLIA
- SAN GIOVANNI ROTONDO
- Molecular genetics of cerebral cavernous malformations
- IRCCS Ospedale Casa Sollievo della Sofferenza
- Servizio di Genetica Medica
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- ITALY
- VENETO
- COSTOZZA DI LONGARE
- Mutations identification and genotype-phenotype correlation in Metachromatic leukodystrophy
- B.I.R.D. Foundation
- Unità di Genetica Medica
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- LEBANON
- Beyrouth
- BEYROUTH
- Localisation and identification of the responsible gene of leukodystrophy and oligodonty in a large family
- Université Saint-Joseph
- Unité de génétique médicale
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- NETHERLANDS
- Noord-Holland
- AMSTERDAM
- Biochemical and genetical analyses of the MLC1 interactome
- VUmc - VU medisch centrum
- Sectie Genoomdiagnostiek - Laboratorium voor DNA diagnostiek
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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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- Role of plasmalogenes in the structure, stability and prevention of oxidative damages of the myeline
- Instituto de Biologia Molecular e Celular
- Nerve Regeneration Group
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- Studies on frequent mutations, genotype-phenotype correlation as well as with the biochemical parameters used for diagnosis of Gaucher disease, metachromatic leukodystrophy and Fabry disease (Finished)
- Corporació Sanitària Clínic
- Institut de Bioquímica Clínica: Sección de Errores Congénitos del Metabolismo
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- SPAIN
- Cataluña
- L'HOSPITALET DE LLOBREGAT
- Biochemical and genetical analyses of the MLC1 interactome
- Instituto de Investigación Biomédica de Bellvitge (IDIBELL)
- Departamento de Ciencias Fisiológicas II
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- SPAIN
- Comunidad Valenciana
- SANT JOAN D'ALACANT
- Study of the myelinisation capacities of bone marrow stem cells and from umbilical cord in different kind of leukodystrophia
- Instituto de Neurociencias de Alicante (CSIC-UMH)
- Unidad de Neurobiología del Desarrollo
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- Understanding glutamate and ATP signalling pathways involved in oligodendrocyte death
- Universidad del País Vasco
- Laboratorio de Neurobiología
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- UNITED KINGDOM
- Cambridgeshire
- CAMBRIDGE
- Promoting the remyelinisation in aged central nervous system
- University of Cambridge, Department of Veterinary Medicine
- Department of veterinary medicine
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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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