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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
SWEDEN
Region Uppsala
UPPSALA
Studies on the etiology and therapy of monogenetic dermatoses affecting the skin barrier
Akademiska Sjukhuset
Department of Medical Sciences, Dermatology and Venereology
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
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"
GERMANY
Baden-Württemberg
FREIBURG
Propekal5 : Tracing the untackled facets of Peeling Skin Disease-Targeting epidermal proteolysis for treatment - DE (partner no 1)
Albert-Ludwigs-Universität Freiburg
Institut für Molekulare Medizin und Zellforschung
GERMANY
Nordrhein-Westfalen
BONN
Propekal5 : Tracing the untackled facets of Peeling Skin Disease-Targeting epidermal proteolysis for treatment - DE (partner no 1)
Projektträger im Deutschen Zentrum für Luft- und Raumfahrt
ERA-Net for research programs on rare diseases - Germany
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
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 Génétique Moléculaire
- Hôpital Necker-Enfants Malades
- Service de dermatologie
- 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
Réseau sur le syndrome de Netherton et les ichtyoses lamellaires
FRANCE
ILE-DE-FRANCE
PARIS
KLKIN : Netherton Syndrome: From mechanisms to therapeutics
GREECE
GREECE
PATRAS