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Showing results (161-170 of 206) with videos related to

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Archives of Dermatological Research|January 1, 1995
Altered distribution of keratinization markers in epidermolytic hyperkeratosisA Ishida-Yamamoto, H Iizuka, M Manabe, et al.
The Journal of Investigative Dermatology|August 1, 1997
Recurrent mutations in the type VII collagen gene (COL7A1) in patients with recessive dystrophic epidermolysis bullosaJ E Mellerio, M G Dunnill, W Allison, et al.
The British Journal of Dermatology|May 1, 1990
Epidermolysis bullosa acquisita antigen and the carboxy terminus of type VII collagen have a common immunolocalization to anchoring fibrils and lamina densa of basement membraneH Shimizu, J N McDonald, D B Gunner, et al.
The British Journal of Dermatology|January 20, 1999
Specialized keratin expression pattern in human ridged skin as an adaptation to high physical stressO Swensson, L Langbein, J R McMillan, et al.
The British Journal of Dermatology|May 1, 1997
A recurrent laminin 5 mutation in British patients with lethal (Herlitz) junctional epidermolysis bullosa: evidence for a mutational hotspot rather than propagation of an ancestral alleleG H Ashton, J E Mellerio, M G Dunnill, et al.
Journal of the American Academy of Dermatology|September 1, 1993
Cultured keratinocyte allografts and wound healing in severe recessive dystrophic epidermolysis bullosaJ A McGrath, O M Schofield, A Ishida-Yamamoto, et al.
The Journal of Investigative Dermatology|October 27, 1997
Loricrin mutation in Vohwinkel's keratoderma is unique to the variant with ichthyosisB P Korge, A Ishida-Yamamoto, C Pünter, et al.
The Journal of Investigative Dermatology|December 14, 1999
Striate palmoplantar keratoderma resulting from desmoplakin haploinsufficiencyN V Whittock, G H Ashton, P J Dopping-Hepenstal, et al.
Clinical and Experimental Dermatology|June 3, 1999
Recurrent molecular abnormalities in type VII collagen in Southern Italian patients with recessive dystrophic epidermolysis bullosaG H Ashton, J E Mellerio, M G Dunnill, et al.
Journal of Medical Genetics|September 1, 1995
Use of type VII collagen gene (COL7A1) markers in prenatal diagnosis of recessive dystrophic epidermolysis bullosaM G Dunnill, C H Rodeck, A J Richards, et al.
Pageof 21

Showing results (161-170 of 206) with videos related to

Sort By:
Pageof 21
Archives of Dermatological Research|January 1, 1995
Altered distribution of keratinization markers in epidermolytic hyperkeratosisA Ishida-Yamamoto, H Iizuka, M Manabe, et al.
The Journal of Investigative Dermatology|August 1, 1997
Recurrent mutations in the type VII collagen gene (COL7A1) in patients with recessive dystrophic epidermolysis bullosaJ E Mellerio, M G Dunnill, W Allison, et al.
The British Journal of Dermatology|May 1, 1990
Epidermolysis bullosa acquisita antigen and the carboxy terminus of type VII collagen have a common immunolocalization to anchoring fibrils and lamina densa of basement membraneH Shimizu, J N McDonald, D B Gunner, et al.
The British Journal of Dermatology|January 20, 1999
Specialized keratin expression pattern in human ridged skin as an adaptation to high physical stressO Swensson, L Langbein, J R McMillan, et al.
The British Journal of Dermatology|May 1, 1997
A recurrent laminin 5 mutation in British patients with lethal (Herlitz) junctional epidermolysis bullosa: evidence for a mutational hotspot rather than propagation of an ancestral alleleG H Ashton, J E Mellerio, M G Dunnill, et al.
Journal of the American Academy of Dermatology|September 1, 1993
Cultured keratinocyte allografts and wound healing in severe recessive dystrophic epidermolysis bullosaJ A McGrath, O M Schofield, A Ishida-Yamamoto, et al.
The Journal of Investigative Dermatology|October 27, 1997
Loricrin mutation in Vohwinkel's keratoderma is unique to the variant with ichthyosisB P Korge, A Ishida-Yamamoto, C Pünter, et al.
The Journal of Investigative Dermatology|December 14, 1999
Striate palmoplantar keratoderma resulting from desmoplakin haploinsufficiencyN V Whittock, G H Ashton, P J Dopping-Hepenstal, et al.
Clinical and Experimental Dermatology|June 3, 1999
Recurrent molecular abnormalities in type VII collagen in Southern Italian patients with recessive dystrophic epidermolysis bullosaG H Ashton, J E Mellerio, M G Dunnill, et al.
Journal of Medical Genetics|September 1, 1995
Use of type VII collagen gene (COL7A1) markers in prenatal diagnosis of recessive dystrophic epidermolysis bullosaM G Dunnill, C H Rodeck, A J Richards, et al.
Pageof 21