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Archives of Dermatology
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August 1, 1985
Dystrophic epidermolysis bullosa. A new variant characterized by progressive symmetrical centripetal involvement with scarring
J D Fine, L S Osment, S Gay
Pediatric Dentistry
|
November 1, 1994
Dental caries risk in hereditary epidermolysis bullosa
J 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 bullosa
J D Fine, Y Horiguchi, J R Couchman
Archives of Dermatology
|
June 1, 1987
Childhood epidermolysis bullosa acquisita. Detection in a 5-year-old girl
R 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 bullosa
J 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 leukocytes
J 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 diseases
S Gay, J D Fine, J S Storer
Pediatric Dentistry
|
July 1, 1993
Hereditary epidermolysis bullosa: oral manifestations and dental management
J 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 cohorts
J 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 gene
A M Christiano, J D Fine, J Uitto
Page
of 14
Search research articles
Search
Showing results (41-50 of 133) with videos related to
Sort By:
Page
of 14
Archives of Dermatology
|
August 1, 1985
Dystrophic epidermolysis bullosa. A new variant characterized by progressive symmetrical centripetal involvement with scarring
J D Fine, L S Osment, S Gay
Pediatric Dentistry
|
November 1, 1994
Dental caries risk in hereditary epidermolysis bullosa
J 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 bullosa
J D Fine, Y Horiguchi, J R Couchman
Archives of Dermatology
|
June 1, 1987
Childhood epidermolysis bullosa acquisita. Detection in a 5-year-old girl
R 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 bullosa
J 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 leukocytes
J 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 diseases
S Gay, J D Fine, J S Storer
Pediatric Dentistry
|
July 1, 1993
Hereditary epidermolysis bullosa: oral manifestations and dental management
J 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 cohorts
J 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 gene
A M Christiano, J D Fine, J Uitto
Page
of 14