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• • AUSTRIA
  • TIROL
  • INNSBRUCK
  • 
  • Skin barrier abnormality in disorders of cornification
  • Medizinische Universität Innsbruck
  • Dermatologie und Venerologie
  • Ulteriori dettagli
• • CANADA
  • Colombie-Britannique
  • VANCOUVER
  • FORGE - Finding of Rare Disease Genes in Canada
  • University of British Columbia
  • Faculty of Medicine
  • Ulteriori dettagli
• • CANADA
  • Ontario
  • OTTAWA, ONTARIO
  • FORGE - Finding of Rare Disease Genes in Canada
  • University of Ottawa
  • Faculty of Medicine -
  • Ulteriori dettagli
• • CANADA
  • Québec
  • MONTREAL
  • FORGE - Finding of Rare Disease Genes in Canada
  • Centre hospitalier universitaire Sainte-Justine
  • Pédiatrie
  • Ulteriori dettagli
• • FRANCIA
  • ILE-DE-FRANCE
  • PARIS
  • Clinic, histologic, ultrastructural and molecular analysis in ichtyosis and Netherton syndrome
  • CHU Paris - Hôpital Necker - Enfants Malades
  • MAGEC - Service de dermatologie
  • Ulteriori dettagli
• • FRANCIA
  • ILE-DE-FRANCE
  • PARIS
  • Netherton disease functional genetics
  • CHU Paris - Hôpital Necker - Enfants Malades
  • Département de génétique
  • Ulteriori dettagli
• • FRANCIA
  • ILE-DE-FRANCE
  • PARIS
  • Murin models development in Netherton disease
  • CHU Paris - Hôpital Necker - Enfants Malades
  • Département de génétique
  • Ulteriori dettagli
• • FRANCIA
  • ILE-DE-FRANCE
  • PARIS
  • Therapeutic targets identification in Netherton disease
  • CHU Paris - Hôpital Necker - Enfants Malades
  • Département de génétique
  • Ulteriori dettagli
• • FRANCIA
  • ILE-DE-FRANCE
  • PARIS
  • Allergic manifestations mechanisms study in Netherton disease
  • CHU Paris - Hôpital Necker - Enfants Malades
  • Département de génétique
  • Ulteriori dettagli
• • GERMANIA
  • Nordrhein-Westfalen
  • KÖLN
  • SkinDev: In vitro and in vivo models of congenital rare skin diseases for molecular characterization and drug screening (coordination)
  • Universität zu Köln
  • Abteilung Dermatogenetik
  • Ulteriori dettagli
• • ITALIA
  • LAZIO
  • ROMA
  • Studio delle genodermatosi: patogenesi molecolare, diagnosi e correlazione genotipo-fenotipo
  • IRCCS Ospedale Pediatrico Bambino Gesù
  • U.O.C. di Dermatologia
  • Ulteriori dettagli
• • ITALIA
  • LAZIO
  • ROMA
  • Sindrome di Netherton: studio funzionale del gene difettivo, SPINK5, e del suo prodotto proteico LEKTI
  • Istituto Dermopatico dell'Immacolata - IRCCS
  • Laboratorio di Biologia Molecolare e Cellulare
  • Ulteriori dettagli
• • ITALIA
  • LAZIO
  • ROMA
  • Sindrome di Netherton: dalla patogenesi allo sviluppo diagnostico e cura dei pazienti
  • Istituto Dermopatico dell'Immacolata - IRCCS
  • Laboratorio di Biologia Molecolare e Cellulare
  • Ulteriori dettagli
• • ITALIA
  • LAZIO
  • ROMA
  • GENESKIN: European network on rare genetic skin diseases (coordination)
  • Istituto Dermopatico dell'Immacolata - IRCCS
  • Laboratorio di Biologia Molecolare e Cellulare
  • Ulteriori dettagli
• • REGNO UNITO; GRAN BRETAGNA
  • Greater London
  • LONDON
  • Establishing keratinocyte cell lines from children with Netherton's syndrome, eczema (atopic dermatitis) and normal skin, and developing a novel technique of "organotypic culture"
  • UCL Institute of Child Health
  • Immunobiology
  • Ulteriori dettagli
• • REGNO UNITO; GRAN BRETAGNA
  • Greater London
  • LONDON
  • Gene therapy for Netherton's syndrome
  • UCL Institute of Child Health
  • Immunobiology
  • Ulteriori dettagli
• • SVEZIA
  • Landstinget i Uppsala län
  • UPPSALA
  • Studies on the etiology and therapy of monogenetic dermatoses affecting the skin barrier
  • Uppsala University Hospital
  • Department of Medical Sciences, Dermatology and Venereology
  • Ulteriori dettagli