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J D Fine

Showing results (121-130 of 133) with videos related to

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The Journal of Investigative Dermatology|August 1, 1993
Intracytoplasmic retention of type VII collagen and dominant dystrophic epidermolysis bullosa: reversal of defect following cessation of or marked improvement in disease activityJ D Fine, L B Johnson, D Cronce, et al.
Pediatric Dermatology|June 1, 1989
Kindler syndrome: report of two cases and review of the literatureA B Forman, J S Prendiville, N B Esterly, et al.
The Journal of Investigative Dermatology|September 1, 1993
Identification and partial characterization of a novel 105-kDalton lower lamina lucida autoantigen associated with a novel immune-mediated subepidermal blistering diseaseL S Chan, J D Fine, R A Briggaman, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 20, 1996
The genetic basis of epidermolysis bullosa simplex with mottled pigmentationJ Uttam, E Hutton, P A Coulombe, et al.
Archives of Dermatological Research|January 1, 1994
Ultrastructural and immunohistochemical characterization of basal cells in three-dimensional culture models of the skinY Horiguchi, T Maruguchi, Y Maruguchi, et al.
The Journal of Investigative Dermatology|November 1, 1988
Prenatal diagnosis of dominant and recessive dystrophic epidermolysis bullosa: application and limitations in the use of KF-1 and LH 7:2 monoclonal antibodies and immunofluorescence mapping techniqueJ D Fine, R A Eady, M L Levy, et al.
Archives of Dermatology|March 1, 1984
Linear IgA bullous dermatosis v dermatitis herpetiformis. Quantitative measurements of dermoepidermal alterationsS B Smith, T J Harrist, G F Murphy, et al.
Prenatal Diagnosis|November 1, 1991
Alpha-fetoprotein and acetylcholinesterase are not predictive of fetal junctional epidermolysis bullosa, Herlitz variantL P Shulman, S Elias, R N Andersen, et al.
Journal of the American Academy of Dermatology|January 1, 1991
Revised clinical and laboratory criteria for subtypes of inherited epidermolysis bullosa. A consensus report by the Subcommittee on Diagnosis and Classification of the National Epidermolysis Bullosa RegistryJ D Fine, E A Bauer, R A Briggaman, et al.
Archives of Dermatology|September 25, 1997
Immunohistochemical, ultrastructural, and molecular features of Kindler syndrome distinguish it from dystrophic epidermolysis bullosaH Shimizu, M Sato, M Ban, et al.
Pageof 14

Showing results (121-130 of 133) with videos related to

Sort By:
Pageof 14
The Journal of Investigative Dermatology|August 1, 1993
Intracytoplasmic retention of type VII collagen and dominant dystrophic epidermolysis bullosa: reversal of defect following cessation of or marked improvement in disease activityJ D Fine, L B Johnson, D Cronce, et al.
Pediatric Dermatology|June 1, 1989
Kindler syndrome: report of two cases and review of the literatureA B Forman, J S Prendiville, N B Esterly, et al.
The Journal of Investigative Dermatology|September 1, 1993
Identification and partial characterization of a novel 105-kDalton lower lamina lucida autoantigen associated with a novel immune-mediated subepidermal blistering diseaseL S Chan, J D Fine, R A Briggaman, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 20, 1996
The genetic basis of epidermolysis bullosa simplex with mottled pigmentationJ Uttam, E Hutton, P A Coulombe, et al.
Archives of Dermatological Research|January 1, 1994
Ultrastructural and immunohistochemical characterization of basal cells in three-dimensional culture models of the skinY Horiguchi, T Maruguchi, Y Maruguchi, et al.
The Journal of Investigative Dermatology|November 1, 1988
Prenatal diagnosis of dominant and recessive dystrophic epidermolysis bullosa: application and limitations in the use of KF-1 and LH 7:2 monoclonal antibodies and immunofluorescence mapping techniqueJ D Fine, R A Eady, M L Levy, et al.
Archives of Dermatology|March 1, 1984
Linear IgA bullous dermatosis v dermatitis herpetiformis. Quantitative measurements of dermoepidermal alterationsS B Smith, T J Harrist, G F Murphy, et al.
Prenatal Diagnosis|November 1, 1991
Alpha-fetoprotein and acetylcholinesterase are not predictive of fetal junctional epidermolysis bullosa, Herlitz variantL P Shulman, S Elias, R N Andersen, et al.
Journal of the American Academy of Dermatology|January 1, 1991
Revised clinical and laboratory criteria for subtypes of inherited epidermolysis bullosa. A consensus report by the Subcommittee on Diagnosis and Classification of the National Epidermolysis Bullosa RegistryJ D Fine, E A Bauer, R A Briggaman, et al.
Archives of Dermatology|September 25, 1997
Immunohistochemical, ultrastructural, and molecular features of Kindler syndrome distinguish it from dystrophic epidermolysis bullosaH Shimizu, M Sato, M Ban, et al.
Pageof 14