Partnership : Academics = 
, Industrials = 
, Financial investitors = 
-
- Identification of causative genes for new forms of autosomic recessive cerebellar ataxias
- Institut de génétique et de biologie moléculaire et cellulaire - IGBMC
- Département Neurobiologie et Génétique
- More details
-
- FRANCE
- ILE DE FRANCE
- GIF-SUR-YVETTE
- Biosynthesis and secretion of lipoproteins (healthy individuals and individuals affected by congenital defect in lipids absorption)
- CNRS
- Centre de génétique moléculaire Bat 26
- More details
-
- FRANCE
- ILE DE FRANCE
- PARIS
- Epigenetic factors involvement (especially DNA methylation) in lipidic metabolism regulation's key genes
- CHU Hôpital Pitié-Salpêtrière
- Unité fonctionnelle d'endocrinologie moléculaire et oncologique - Service de biochimie endocrinienne et oncologique
- More details
-
- FRANCE
- ILE DE FRANCE
- PARIS
- Genetic and clinical characterization of new forms of autosomic recessive cerebellar ataxias
- CHU Hôpital Pitié-Salpêtrière
- Institut du Cerveau et de la Moëlle épinière
- More details
-
- FRANCE
- ILE DE FRANCE
- PARIS
- Cerebellar ataxias neuropathology
- CHU Hôpital Pitié-Salpêtrière
- Laboratoire de neuropathologie Raymond Escourolle
- More details
-
- FRANCE
- ILE DE FRANCE
- PARIS
- Phenotype-genotype correlations in familial dyslipidemias; search for new phenotypes
- CHU Hôpital Saint-Antoine
- Laboratoire de biochimie
- More details
-
- FRANCE
- ILE DE FRANCE
- PARIS
- Dyslipidemia genetics: phenotype-genotype relationships; vascular consequences in children of hereditary dyslipidemia
- CHU Hôpital d'Enfants Armand-Trousseau
- Service de gastro-entérologie et nutrition pédiatriques
- More details
-
- FRANCE
- ILE DE FRANCE
- PARIS
- Genetic lipidic malabsorption: study of biosynthesis and apolipoprotein B's lipoprotein secretion
- Hopital Necker - Enfants Malades
- Génétique et épigénétique des maladies métaboliques, neurosensorielles et du développement
- More details
-
- 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
- More details
-
- ITALY
- EMILIA ROMAGNA
- MODENA
- Molecular genetics of monogenis disorders of Hypobetalipoprotein metabolism
- Università degli Studi di Modena e Reggio Emilia
- Laboratorio di Genetica Molecolare
- More details
-
- ITALY
- EMILIA ROMAGNA
- MODENA
- Molecular genetics of monogenis disorders of Abetalipoprotein metabolism
- Università degli Studi di Modena e Reggio Emilia
- Laboratorio di Genetica Molecolare
- More details
-
- DNA single strand breaks and neurodegeneration: the role of aprataxin and senataxin in dna repair
- A.O. S. Andrea
- Servizio di Genetica Medica
- More details
-
- Functional characterization of missense mutations in SCA28 patients, development of a mouse model of the disease, and screening of candidate genes for cerebellar ataxia
- Azienda Ospedaliero-Universitaria San Giovanni Battista di Torino
- Genetica Medica, Struttura Complessa a Direzione Universitaria
- More details
-
- ITALY
- PUGLIA
- SAN GIOVANNI ROTONDO
- Molecular genetics of cerebral cavernous malformations
- IRCCS Ospedale Casa Sollievo della Sofferenza
- Servizio di Genetica Medica
- More details
-
- ITALY
- TRENTINO ALTO ADIGE
- RIVA DEL GARDA
- Linkage study in a family affected by novel form of autosomal recessive hereditary ataxia
- MAGI'S LAB srl
- Ambulatorio di Genetica Medica
- More details
-
- LEBANON
- Beyrouth
- BEYROUTH
- Mapping of the gene responsible of the CAMOS syndrome
- Université Saint-Joseph
- Unité de génétique médicale
- More details
-
- PORTUGAL
- NORTE
- SANTA MARIA DA FEIRA
- SPATAX - Autosomal recessive spastic paraplegia: identification of new genes and of mechanisms of degeneration
- Hospital São Sebastião
- Serviço de Neurologia
- More details
-
- PORTUGAL
- NORTE
- SANTA MARIA DA FEIRA
- After the survey: helping (and hoping) to find new genes for hereditary ataxias and spastic paraplegias. (POCI/SAU-ESP/59114/2004)
- Hospital São Sebastião
- Serviço de Neurologia
- More details
-
- SPAIN
- Cantabria
- SANTANDER
- Epidemiological, clinical, electrophysiological and neuroimaging studies of hereditary ataxias
- Hospital Universitario Marqués de Valdecilla
- Servicio de Neurología
- More details
-
- SPAIN
- Cataluña
- ESPLUGUES DE LLOBREGAT
- Etiologic diagnosis and treatment monitorisation in ataxia patients due to different causes: Friedreich ataxia and other early onset ataxias
- Hospital Universitari Sant Joan de Déu
- Servicio de Neurología
- More details
-
- SPAIN
- Comunidad Valenciana
- BURJASSOT
- Development of new cell therapies in ataxias, studying the neurogenic potential of mouse's cerebral areas, and the integration ability of anterior periventricular (APV) cells.
- Institut Cavanilles de Biodiversitat i Biologia Evolutiva
- Grupo de Neurobiología Comparada
- More details
-
- Receptor CB2 role in the cannabinoids neuroprotective effects in ataxias, amyotrophic lateral sclerosis and Huntington disease
- Universidad Complutense de Madrid. Facultad de Medicina
- Grupo de Neuroquímica de los Cannabinoides
- More details
-
- UNITED KINGDOM
- Berkshire
- READING
- Neuroprotective potential of modulators of cannabinoid receptors in Cerebellar Ataxias
- University of Reading
- School of Pharmacy
- More details
-
- UNITED KINGDOM
- Strathclyde
- GLASGOW
- Rhythm and Intonation in Ataxic Dysarthria
- University of Strathclyde
- Speech and Language Therapy Division
- More details
