Ultrastructural Identification of Basic Abnormalities as Clues to Genetic Disorders of the Epidermis.
- 1 November 1994
- journal article
- review article
- Published by Elsevier in Journal of Investigative Dermatology
- Vol. 103 (s5) , 6S-12S
- https://doi.org/10.1111/1523-1747.ep12398887
Abstract
No abstract availableKeywords
This publication has 61 references indexed in Scilit:
- Keratin and keratinizationJournal of the American Academy of Dermatology, 1994
- Is filaggrin really a filament-aggregating protein in vivo?Archives of Dermatological Research, 1993
- The dermal-epidermal junction of human skin contains a novel laminin variant.The Journal of cell biology, 1992
- Kalinin is abnormally expressed in epithelial basement membranes of Herlitz's junctional epidermolysis bullosa patientsExperimental Dermatology, 1992
- Genetic linkage of type VII collagen (COL7A1) to dominant dystrophic epidermolysis bullosa in families with abnormal anchoring fibrils.Journal of Clinical Investigation, 1992
- Epidermolysis bullosa: Evidence for linkage to genetic markers on chromosome 1 in a family with the autosomal dominant simplex formGenomics, 1990
- Ichthyosis bullosa of Siemens: A unique type of epidermolytic hyperkeratosisPublished by Elsevier ,1986
- Ichthyosis Vulgaris: Identification of a Defect in Synthesis of Filaggrin Correlated with an Absence of Keratohyaline GranulesJournal of Investigative Dermatology, 1985
- Electron Microscopy in the Early Diagnosis of Genetic Disorders of the SkinDermatology, 1978
- Dichtung und Wahrheit über die „Ichthyosis bullosa“, mit Bemerkungen zur Systematik der EpidermolysenArchives of Dermatological Research, 1937