Webinar EB – Join the Meeting
Marie Guillou2021-06-29T17:39:48+02:00ERN-Skin Webinar Combined cell and gene therapy for Epidermolysis Bullosa – Michele De Luca Chaired by Cristina Has (Freiburg) / Christine Bodemer (Paris) [...]
S2k guidelines (consensus statement) for diagnosis and therapy of dermatitis herpetiformis initiated by the European Academy of Dermatology and Venereology (EADV)
Marie Guillou2024-09-26T14:24:46+02:00J Eur Acad Dermatol Venereol. 2021 Jun;35(6):1251-1277 S2k guidelines (consensus statement) for diagnosis and therapy of dermatitis herpetiformis initiated by the European Academy of Dermatology [...]
Dermatitis herpetiformis guidelines – S2k guidelines (consensus statement) for diagnosis and therapy of dermatitis herpetiformis initiated by EADV
Marie Guillou2024-09-16T14:55:45+02:00Dermatitis herpetiformis guidelines – S2k guidelines (consensus statement) for diagnosis and therapy of dermatitis herpetiformis initiated by the European Academy of Dermatology and Venereology (EADV).
Hereditary palmoplantar keratoderma – phenotypes and mutations in 64 patients
Marie Guillou2024-10-16T11:06:40+02:00Publication - 2021 Apr 29. Hereditary palmoplantar keratoderma - phenotypes and mutations in 64 patients Authors L Harjama, V Karvonen, K [...]
QR-313, an Antisense Oligonucleotide, Shows Therapeutic Efficacy for Treatment of Dominant and Recessive Dystrophic Epidermolysis Bullosa: A Preclinical Study
Marie Guillou2024-10-01T10:49:47+02:00Publication - Epub 2020 Sep 16. QR-313, an Antisense Oligonucleotide, Shows Therapeutic Efficacy for Treatment of Dominant and Recessive Dystrophic Epidermolysis Bullosa: A Preclinical Study [...]
Initial validation of the epidermolysis bullosa-specific module of the Infants and Toddlers Dermatology Quality of Life questionnaire
Marie Guillou2024-10-01T10:50:35+02:00Publication - Epub 2020 Sep 7. Initial validation of the epidermolysis bullosa-specific module of the Infants and Toddlers Dermatology Quality of Life questionnaire [...]
Meta-Analysis of Mutations in ALOX12B or ALOXE3 Identified in a Large Cohort of 224 Patients
Marie Guillou2024-10-16T11:06:59+02:00Publication - 2021 Jan 9. Meta-Analysis of Mutations in ALOX12B or ALOXE3 Identified in a Large Cohort of 224 Patients Authors [...]
What causes hidradenitis suppurativa ?-15 years after
Marie Guillou2024-10-01T10:29:53+02:00Publication - 2020 Dec. What causes hidradenitis suppurativa ? - 15 years after Authors Christos C Zouboulis, Farida Benhadou, Angel S [...]
Development of an international core domain set for medium, large and giant congenital melanocytic naevi as a first step towards a core outcome set for clinical practice and research
Marie Guillou2024-10-16T11:15:33+02:00Publication - Epub 2020 Nov 25. Development of an international core domain set for medium, large and giant congenital melanocytic naevi as a first step [...]