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Research projects
NORWAY
Østlandet
OSLO
Når barnet fødes med en sjelden huddiagnose: En eksplorerende undersøkelse om hvordan diagnosen påvirker tilknytning og omsorgsutøvelse
Oslo Universitetssykehus HF, Rikshospitalet
SSD - Senter for sjeldne diagnoser
NORWAY
Østlandet
OSLO
Oversettelse og pilotutprøving av online intervensjonsprogram for ungdom
Oslo Universitetssykehus HF, Rikshospitalet
SSD - Senter for sjeldne diagnoser
SWEDEN
Region Uppsala
UPPSALA
Studies on the etiology and therapy of monogenetic dermatoses affecting the skin barrier
Uppsala University Hospital - Akademiska Sjukhuset
Department of Medical Sciences, Dermatology and Venereology
FRANCE
ILE-DE-FRANCE
PARIS
Rho GTPases and rare skin diseases
IMAGINE - Institut des Maladies Génétiques
Institut IMAGINE - INSERM U1163
AUSTRIA
WIEN
ADDRESS: NOT PROVIDED - AT
ABHD5 and PNPLA1 Function in the Skin
Institution: Information not provided - AT
SWITZERLAND
Suisse Alémanique
BASEL
Consequences of keratin mislocalization using ichthyosis with confetti (IWC) as a model disease
Universitätsspital Basel
Departement Biomedizin
FRANCE
GRAND-EST
STRASBOURG
TC NER: Transcription stress Counteracted by Nutritional interventions of Exceptional importance for rare DNA Repair diseases - FR
CHU de Strasbourg - Hôpital de Hautepierre
Service de Neuropédiatrie
FRANCE
ILE-DE-FRANCE
PARIS
Development of a new biotherapy targeting the inflammatory mechanisms of Netherton syndrome
IMAGINE - Institut des Maladies Génétiques
Equipe "Maladies génétiques cutanées: du mécanisme de la maladie aux thérapies"
ITALY
LAZIO
ROMA
Study of inherited skin disorders: molecular pathogenesis, diagnosis and genotype-phenotype correlation
IRCCS Ospedale Pediatrico Bambino Gesù - SEDE GIANICOLO
U.O.C. di Dermatologia
ITALY
LAZIO
ROMA
Netherton syndrome: from disease pathogenesis to improved diagnosis and patient care
Istituto Dermopatico dell'Immacolata - IRCCS
Laboratorio di Biologia Molecolare e Cellulare
ITALY
LOMBARDIA
MILANO
TC NER: Transcription stress Counteracted by Nutritional interventions of Exceptional importance for rare DNA Repair diseases - IT
IFOM - Istituto FIRC di Oncologia Molecolare
Firc Institute of Molecular Oncology (IFOM)
ITALY
VENETO
PADOVA
A therapeutic approach for rare genodermatoses caused by aberrant connexin hemichannels
Venetian Institute of Molecular Medicine
Centro Interdipartimentale per lo Studio dei Segnali Cellulari
Multicentric Research projects
- Fondation René Touraine
- Institut de Recherche sur la Peau, Fondation René Touraine
- Cologne Center for Genomics (CCG) der Universität zu Köln
- Abteilung Dermatogenetik
- Hôpital Necker-Enfants Malades
- Service de dermatologie
- CECAD Research Center
- Exzellenzcluster CECAD in der Universität zu Köln
- University of Patras, School of Health Sciences
- Department of Pharmacy
FRANCE
ILE-DE-FRANCE
PAROS
TAG: TogetherAgainstGenodermatoses - amélioration des soins de santé et assistance sociale pour les patients et les familles touchées par les génodermatoses sévères
GERMANY
Nordrhein-Westfalen
KÖLN
SkinDev: In vitro and in vivo models of congenital rare skin diseases for molecular characterization and drug screening
FRANCE
ILE-DE-FRANCE
PARIS
KLKIN : Netherton Syndrome: From mechanisms to therapeutics
GERMANY
Nordrhein-Westfalen
KÖLN
TC NER: Transcription stress Counteracted by Nutritional interventions of Exceptional importance for rare DNA Repair diseases
GREECE
GREECE
PATRAS