Results 81 to 90 of about 9,316 (182)

Validity of first-time diagnoses of congenital epidermolysis bullosa in the Danish National Patient Registry and the Danish Pathology Registry

open access: yes, 2019
Mattias Hedegaard Kristensen,1 Sigrún Alba Jóhannesdóttir Schmidt,2 Line Kibsgaard,1 Mette Mogensen,3 Mette Sommerlund,1 Uffe Koppelhus1 1Department of Dermatology, Aarhus University Hospital, Aarhus, Denmark; 2Department of Clinical
Mogensen M   +5 more
core  

Orofacial Anomalies in Kindler Epidermolysis Bullosa

open access: yes
ImportanceKindler epidermolysis bullosa is a genetic skin-blistering disease associated with recessive inherited pathogenic variants in FERMT1, which encodes kindlin-1.
Klausegger, Alfred   +13 more
core   +1 more source

Acquired epidermolysis bullosa

open access: yes, 2015
Epidermolysis bullosa is a group of diseases or skin disorders genetically transmitted and it is characterized by the appearance of bullae, ulcers and skin wounds. It usually appears at birth or in the first months of life.
Yanier Serrano García   +2 more
core  

Prevalence of Genodermatoses in Finland from 1995 to 2022: A Nationwide Registry Study. [PDF]

open access: yesActa Derm Venereol
Kunnari S   +3 more
europepmc   +1 more source

Expanding the Potential of Monoclonal Antibodies against IL-4 and IL-13 in Genodermatoses: Efficacy and Safety of Dupilumab in Epidermolysis Bullosa and Ichthyosis

open access: yes
reserved.Background: Epidermolysis bullosa and ichthyosis are rare genetic skin disorders. Epidermolysis bullosa is characterized by extreme skin fragility, leading to blistering and erosions from minor trauma.
LASERRA, MARIA SOFIA
core  

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