Heterogeneity of Severe Dystrophic Epidermolysis Bullosa: Overexpression of Collagen VII by Cutaneous Cells from a Patient with Mutilating Disease
- 1 February 1994
- journal article
- case report
- Published by Elsevier in Journal of Investigative Dermatology
- Vol. 102 (2) , 155-159
- https://doi.org/10.1111/1523-1747.ep12371754
Abstract
No abstract availableKeywords
This publication has 30 references indexed in Scilit:
- Genetic linkage of recessive dystrophic epidermolysis bullosa to the type VII collagen gene.Journal of Clinical Investigation, 1992
- Genetic linkage of type VII collagen (COL7A1) to dominant dystrophic epidermolysis bullosa in families with abnormal anchoring fibrils.Journal of Clinical Investigation, 1992
- Evidence for a Structural Abnormality of Collagen VII in a Patient with Dystrophic Epidermolysis Bullosa InversaJournal of Investigative Dermatology, 1992
- Revised clinical and laboratory criteria for subtypes of inherited epidermolysis bullosaJournal of the American Academy of Dermatology, 1991
- Anchoring Fibrils and Type VII collagen are Absent From Skin in Severe Recessive Dystrophic Epidermolysis BullosaJournal of Investigative Dermatology, 1989
- Lack of Type VII Collagen in Unaffected Skin of Patients with Severe Recessive Dystrophic Epidermolysis bullosaDermatology, 1988
- Identification of an epidermal basement membrane defect in recessive forms of dystrophic epidermolysis bullosa by LH 7:2 monoclonal antibody: use in diagnosisBritish Journal of Dermatology, 1986
- Evaluation of Anchoring Fibrils and Other Components of the Dermal-Epidermal Junction in Dystrophic Epidermolysis Bullosa by a Quantitative Ultrastructural TechniqueJournal of Investigative Dermatology, 1985
- Ultrastructural studies in epidermolysis bullosa hereditariaArchives of Dermatological Research, 1976
- Epidermolysis Bullosa Dystrophica-Recessive: A Possible Role Of Anchoring Fibrils In The PathogenesisJournal of Investigative Dermatology, 1975