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Archives of Dermatology
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July 1, 1989
Autosomal recessive epidermolysis bullosa simplex. Generalized phenotypic features suggestive of junctional or dystrophic epidermolysis bullosa, and association with neuromuscular diseases
J D Fine, J Stenn, L Johnson, et al.
The British Journal of Dermatology
|
May 1, 1995
Defective in vivo expression and apparently normal in vitro expression of a newly identified 105-kDa lower lamina lucida protein in dystrophic epidermolysis bullosa
L S Chan, J D Fine, C Hammerberg, et al.
Archives of Dermatology
|
February 1, 1988
Persistent subepidermal blistering in split-thickness skin graft sites. Ultrastructural and antigenic features simulating dystrophic or immunofluorescence-negative acquired epidermolysis bullosa
A Epstein, S J Hendrick, R L Sanchez, et al.
Acta Dermato-Venereologica
|
May 1, 1994
Immunoelectron microscopy of skin basement membrane zone antigens: a pre-embedding method using 1-nm immunogold with silver enhancement
J A McGrath, A Ishida-Yamamoto, H Shimizu, et al.
Biochemical Society Transactions
|
October 1, 1990
Immunological and molecular approaches to the study of basement membrane proteoglycan diversity
J R Couchman, K J McCarthy, D R Abrahamson, et al.
Archives of Internal Medicine
|
June 1, 1983
Pyoderma gangrenosum associated with primary biliary cirrhosis
M F Maturi, J D Fine, E H Schaffer, et al.
Archives of Dermatology
|
April 1, 1982
Neutrophilic eccrine hidradenitis. A distinctive type of neutrophilic dermatosis associated with myelogenous leukemia and chemotherapy
T J Harrist, J D Fine, R S Berman, et al.
Archives of Dermatology
|
November 24, 1999
Gingival telangiectases: an underappreciated physical sign of juvenile dermatomyositis
F E Ghali, L D Stein, J D Fine, et al.
American Journal of Medical Genetics
|
February 11, 1992
Autosomal dominant erythromelalgia
W H Finley, J R Lindsey, J D Fine, et al.
Oral Surgery, Oral Medicine, and Oral Pathology
|
May 1, 1991
Salivary function of persons with hereditary epidermolysis bullosa
J T Wright, N K Childers, K L Evans, et al.
Page
of 14
Search research articles
Search
Showing results (101-110 of 133) with videos related to
Sort By:
Page
of 14
Archives of Dermatology
|
July 1, 1989
Autosomal recessive epidermolysis bullosa simplex. Generalized phenotypic features suggestive of junctional or dystrophic epidermolysis bullosa, and association with neuromuscular diseases
J D Fine, J Stenn, L Johnson, et al.
The British Journal of Dermatology
|
May 1, 1995
Defective in vivo expression and apparently normal in vitro expression of a newly identified 105-kDa lower lamina lucida protein in dystrophic epidermolysis bullosa
L S Chan, J D Fine, C Hammerberg, et al.
Archives of Dermatology
|
February 1, 1988
Persistent subepidermal blistering in split-thickness skin graft sites. Ultrastructural and antigenic features simulating dystrophic or immunofluorescence-negative acquired epidermolysis bullosa
A Epstein, S J Hendrick, R L Sanchez, et al.
Acta Dermato-Venereologica
|
May 1, 1994
Immunoelectron microscopy of skin basement membrane zone antigens: a pre-embedding method using 1-nm immunogold with silver enhancement
J A McGrath, A Ishida-Yamamoto, H Shimizu, et al.
Biochemical Society Transactions
|
October 1, 1990
Immunological and molecular approaches to the study of basement membrane proteoglycan diversity
J R Couchman, K J McCarthy, D R Abrahamson, et al.
Archives of Internal Medicine
|
June 1, 1983
Pyoderma gangrenosum associated with primary biliary cirrhosis
M F Maturi, J D Fine, E H Schaffer, et al.
Archives of Dermatology
|
April 1, 1982
Neutrophilic eccrine hidradenitis. A distinctive type of neutrophilic dermatosis associated with myelogenous leukemia and chemotherapy
T J Harrist, J D Fine, R S Berman, et al.
Archives of Dermatology
|
November 24, 1999
Gingival telangiectases: an underappreciated physical sign of juvenile dermatomyositis
F E Ghali, L D Stein, J D Fine, et al.
American Journal of Medical Genetics
|
February 11, 1992
Autosomal dominant erythromelalgia
W H Finley, J R Lindsey, J D Fine, et al.
Oral Surgery, Oral Medicine, and Oral Pathology
|
May 1, 1991
Salivary function of persons with hereditary epidermolysis bullosa
J T Wright, N K Childers, K L Evans, et al.
Page
of 14