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Archives of Dermatological Research|January 1, 1990
Bicomponent keratohyalin in normal human ridged skinI Kastl, I Anton-LamprechtArchives of Dermatological Research|January 1, 1990
Hereditary palmoplantar keratosis of the Gamborg Nielsen type. Clinical and ultrastructural characteristics of a new type of autosomal recessive palmoplantar keratosisI Kastl, I Anton-Lamprecht, P Gamborg NielsenDermatologica|January 1, 1978
Electron microscopy in the early diagnosis of genetic disorders of the skinI Anton-LamprechtThe Journal of Investigative Dermatology|November 1, 1994
Ultrastructural identification of basic abnormalities as clues to genetic disorders of the epidermisI Anton-LamprechtThe Journal of Investigative Dermatology|July 1, 1983
Genetically induced abnormalities of epidermal differentiation and ultrastructure in ichthyoses and epidermolyses: pathogenesis, heterogeneity, fetal manifestation, and prenatal diagnosisI Anton-LamprechtHuman Genetics|April 15, 1976
Epidermolysis bullosa dystrophica dominans (Pasini)-a primary structural defect of the anchoring fibrilsI Anton-Lamprecht, I HashimotoHuman Genetics|April 1, 1994
Differential ultrastructural aberrations of collagen fibrils in Ehlers-Danlos syndrome types I-IV as a means of diagnostics and classificationI Hausser, I Anton-LamprechtHuman Genetics|May 1, 1987
Electron microscopy as a means for carrier detection and genetic counselling in families at risk of tuberous sclerosisI Hausser, I Anton-LamprechtPediatric Dermatology|May 1, 1996
Severe congenital generalized exfoliative erythroderma in newborns and infants: a possible sign of Netherton syndromeI Hausser, I Anton-LamprechtPageof 10