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J D Fine

Showing results (41-50 of 133) with videos related to

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Archives of Dermatology|August 1, 1985
Dystrophic epidermolysis bullosa. A new variant characterized by progressive symmetrical centripetal involvement with scarringJ D Fine, L S Osment, S Gay
Pediatric Dentistry|November 1, 1994
Dental caries risk in hereditary epidermolysis bullosaJ T Wright, J D Fine, L Johnson
Archives of Dermatology|April 1, 1989
19-DEJ-1, a hemidesmosome-anchoring filament complex-associated monoclonal antibody. Definition of a new skin basement membrane antigenic defect in junctional and dystrophic epidermolysis bullosaJ D Fine, Y Horiguchi, J R Couchman
Archives of Dermatology|June 1, 1987
Childhood epidermolysis bullosa acquisita. Detection in a 5-year-old girlR Rubenstein, N B Esterly, J D Fine
Archives of Dermatology|December 1, 1990
Type VII collagen and 19-DEJ-1 antigen. Comparison of expression in inversa and generalized variants of recessive dystrophic epidermolysis bullosaJ D Fine, L B Johnson, T Wright
The Journal of Investigative Dermatology|January 1, 1989
The presence of intra-lamina lucida blister formation in epidermolysis bullosa acquisita: possible role of leukocytesJ D Fine, S Tyring, W R Gammon
Archives of Dermatological Research|January 1, 1988
Autoantibodies to extracellular collagen matrix components in epidermolysis bullosa and other bullous diseasesS Gay, J D Fine, J S Storer
Pediatric Dentistry|July 1, 1993
Hereditary epidermolysis bullosa: oral manifestations and dental managementJ T Wright, J D Fine, L Johnson
Journal of the American Academy of Dermatology|June 23, 2000
Inherited epidermolysis bullosa comes into the new millenium: a revised classification system based on current knowledge of pathogenetic mechanisms and the clinical, laboratory, and epidemiologic findings of large, well-defined patient cohortsJ D Fine, J McGrath, R A Eady
The Journal of Investigative Dermatology|December 24, 1997
Genetic basis of dominantly inherited transient bullous dermolysis of the newborn: a splice site mutation in the type VII collagen geneA M Christiano, J D Fine, J Uitto
Pageof 14

Showing results (41-50 of 133) with videos related to

Sort By:
Pageof 14
Archives of Dermatology|August 1, 1985
Dystrophic epidermolysis bullosa. A new variant characterized by progressive symmetrical centripetal involvement with scarringJ D Fine, L S Osment, S Gay
Pediatric Dentistry|November 1, 1994
Dental caries risk in hereditary epidermolysis bullosaJ T Wright, J D Fine, L Johnson
Archives of Dermatology|April 1, 1989
19-DEJ-1, a hemidesmosome-anchoring filament complex-associated monoclonal antibody. Definition of a new skin basement membrane antigenic defect in junctional and dystrophic epidermolysis bullosaJ D Fine, Y Horiguchi, J R Couchman
Archives of Dermatology|June 1, 1987
Childhood epidermolysis bullosa acquisita. Detection in a 5-year-old girlR Rubenstein, N B Esterly, J D Fine
Archives of Dermatology|December 1, 1990
Type VII collagen and 19-DEJ-1 antigen. Comparison of expression in inversa and generalized variants of recessive dystrophic epidermolysis bullosaJ D Fine, L B Johnson, T Wright
The Journal of Investigative Dermatology|January 1, 1989
The presence of intra-lamina lucida blister formation in epidermolysis bullosa acquisita: possible role of leukocytesJ D Fine, S Tyring, W R Gammon
Archives of Dermatological Research|January 1, 1988
Autoantibodies to extracellular collagen matrix components in epidermolysis bullosa and other bullous diseasesS Gay, J D Fine, J S Storer
Pediatric Dentistry|July 1, 1993
Hereditary epidermolysis bullosa: oral manifestations and dental managementJ T Wright, J D Fine, L Johnson
Journal of the American Academy of Dermatology|June 23, 2000
Inherited epidermolysis bullosa comes into the new millenium: a revised classification system based on current knowledge of pathogenetic mechanisms and the clinical, laboratory, and epidemiologic findings of large, well-defined patient cohortsJ D Fine, J McGrath, R A Eady
The Journal of Investigative Dermatology|December 24, 1997
Genetic basis of dominantly inherited transient bullous dermolysis of the newborn: a splice site mutation in the type VII collagen geneA M Christiano, J D Fine, J Uitto
Pageof 14