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Le informazioni sui progetti di Orizzonte 2020 e ora anche le relative sintesi delle relazioni sono disponibili su CORDIS. Tutti i progetti H2020 possono essere scaricati dal Portale Open Data dell'UE .

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Results 1 - 10 of 19413
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Mid-Term Report Summary - CARDIO-IPS (Induced Pluripotent stem Cells: A Novel Strategy to Study Inherited Cardiac Disorders)
The study of several cardiac genetic disorders is hampered by the lack of suitable in vitro human models. The overarching hypothesis of the current project is that the generation of patient-specific human induced pluripotent stem cells (hiPSCs) can allow the development of...
Programme: FP7-IDEAS-ERC
Record Number: 180508
Last updated on: 2016-04-15
Induced Pluripotent stem Cells: A Novel Strategy to Study Inherited Cardiac Disorders
ID: 260830
Data di inizio: 2011-03-01, Termine: 2016-02-29
The study of several genetic disorders is hampered by the lack of suitable in vitro human models. We hypothesize that the generation of patient-specific induced pluripotent stem cells (iPSCs) will allow the development of disease-specific in vitro models; yielding new pathoph...
Programme: FP7-IDEAS-ERC
Record Number: 98107
Last updated on: 2016-12-05
Therapeutic challenge in Leukodystrophies: Translational and ethical research towards clinical trials
ID: 241622
Data di inizio: 2010-03-01, Termine: 2013-08-31
Leukodystrophies (LDs) are inherited rare neurodegenerative diseases of the white matter and its main component, the myelin, that are affecting predominantly children. Severity of the disease is related to the axonal dysfunction due to myelin deficiency or destruction. Despit...
Programme: FP7-HEALTH
Record Number: 98077
Last updated on: 2016-12-05
Un innovador tratamiento para la leucodistrofia
Las leucodistrofias son unas enfermedades genéticas raras caracterizadas por la degeneración de la materia blanca del cerebro. Unos investigadores europeos unieron esfuerzos para desarrollar novedosas terapias para el tratamiento de estas enfermedades discapacitantes.
Programme: FP7-HEALTH
Record Number: 89614
Last updated on: 2015-06-17
Available languages: DE, EN, ES, FR, IT, PL
Innovatively treating leukodystrophy
Leukodystrophies are rare genetic disorders characterised by degeneration of the white matter of the brain. European researchers joined forces to develop innovative therapies against these debilitating disorders.
Programme: FP7-HEALTH
Record Number: 89614
Last updated on: 2015-06-17
Available languages: DE, EN, ES, FR, IT, PL
Un traitement innovant pour la leucodystrophie
La leucodystrophie est un trouble générique rare caractérisé par la dégénération de la matière blanche du cerveau. Les chercheurs européens ont joint leurs forces pour développer des thérapies innovantes face à ces troubles débilitants.
Programme: FP7-HEALTH
Record Number: 89614
Last updated on: 2015-06-17
Available languages: DE, EN, ES, FR, IT, PL
Innowacyjne leczenie leukodystrofii
Leukodystrofie to rzadkie schorzenia genetyczne polegające na degeneracji istoty białej mózgu. Europejscy naukowcy połączyli siły, by opracować innowacyjne metody leczenia tych destrukcyjnych schorzeń.
Programme: FP7-HEALTH
Record Number: 89614
Last updated on: 2015-06-17
Available languages: DE, EN, ES, FR, IT, PL
Trattare in modo innovativo la leucodistrofia
Le leucodistrofie sono rari disturbi genetici, caratterizzati da degenerazione della sostanza bianca del cervello. Alcuni ricercatori europei hanno fatto confluire le loro competenze per sviluppare terapie innovative capaci di contrastare tali disturbi debilitanti.
Programme: FP7-HEALTH
Record Number: 89614
Last updated on: 2015-06-17
Available languages: DE, EN, ES, FR, IT, PL
Innovative Therapien für Leukodystrophien
Leukodystrophien sind seltene genetische Erkrankungen, die mit dem Abbau der weißen Substanz im Gehirn einhergehen. Europäische Forscher entwickelten gemeinsam innovative Therapien gegen diese schweren Erkrankungen.
Programme: FP7-HEALTH
Record Number: 89614
Last updated on: 2015-06-17
Available languages: DE, EN, ES, FR, IT, PL
Final Report Summary - LEUKOTREAT (Therapeutic challenge in Leukodystrophies: Translational and ethical research towards clinical trials)
Leukodystrophies (LDs) are inherited rare neurodegenerative diseases of the white matter and its main component, the myelin that are affecting predominantly children. Severity of the disease is related to the axonal dysfunction due to myelin deficiency or destruction. Despite ...
Programme: FP7-HEALTH
Record Number: 147641
Last updated on: 2014-09-05
12 3 4 5 6 7 8 9 10 > >| 
List retrieved on: 2016-12-07