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Skin bioequivalents and their role in the treatment of inherited epidermolysis bullosa

Archives of dermatology (1960), 2000-10, Vol.136 (10), p.1259

Fine, J D

2000

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Tetracycline and epidermolysis bullosa simplex: a new indication for one of the oldest and most widely used drugs in dermatology?

Archives of dermatology (1960), 1999-08, Vol.135 (8), p.981

1999

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Gingival telangiectases: an underappreciated physical sign of juvenile dermatomyositis

Archives of dermatology (1960), 1999-11, Vol.135 (11), p.1370

1999

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19-DEJ-1, a monoclonal antibody to the hemidesmosome-anchoring filament complex, is the only reliable immunohistochemical probe for all major forms of junctional epidermolysis bullosa

Archives of dermatology (1960), 1990-09, Vol.126 (9), p.1187

Fine, J D

1990

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Blood vitamin and trace metal levels in epidermolysis bullosa

Archives of dermatology (1960), 1989-03, Vol.125 (3), p.374-379

Fine, J. D.

1989

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Natural killer cell activity is reduced in patients with severe forms of inherited epidermolysis bullosa

Archives of dermatology (1960), 1989-06, Vol.125 (6), p.797

1989

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19-DEJ-1, a monoclonal antibody to the hemidesmosome-anchoring filament complex, is the only reliable immunohistochemical probe for all major forms of junctional epidermolysis bullosa

Archives of dermatology (1960), 1990-09, Vol.126 (9), p.1187-1190

Fine, J. D.

1990

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Efficacy of systemic phenytoin in the treatment of junctional epidermolysis bullosa

Archives of dermatology (1960), 1988-09, Vol.124 (9), p.1402-1406

Fine, J. D.

1988

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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

Archives of dermatology (1960), 1989-04, Vol.125 (4), p.520-523

Fine, J. D.

1989

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Antigenic features and structural correlates of basement membranes. Relationship to epidermolysis bullosa

Archives of dermatology (1960), 1988-05, Vol.124 (5), p.713-717

Fine, J. D.

1988

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Epidermolysis bullosa simplex superficialis. A new variant of epidermolysis bullosa characterized by subcorneal skin cleavage mimicking peeling skin syndrome

Archives of dermatology (1960), 1989-05, Vol.125 (5), p.633-638

Fine, J. D.

1989

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Autosomal recessive epidermolysis bullosa simplex. Generalized phenotypic features suggestive of junctional or dystrophic epidermolysis bullosa, and association with neuromuscular diseases

Archives of dermatology (1960), 1989-07, Vol.125 (7), p.931-938

Fine, J. D.

1989

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Changing clinical and laboratory concepts in inherited epidermolysis bullosa

Archives of dermatology (1960), 1988-04, Vol.124 (4), p.523-526

Fine, J. D.

1988

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Immunohistochemical, ultrastructural, and molecular features of Kindler syndrome distinguish it from dystrophic epidermolysis bullosa

Archives of dermatology (1960), 1997-09, Vol.133 (9), p.1111

1997

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Efficacy of systemic phenytoin in the treatment of junctional epidermolysis bullosa

Archives of dermatology (1960), 1988-09, Vol.124 (9), p.1402

1988

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Evaluation of the efficacy of topical bufexamac in epidermolysis bullosa simplex. A double-blind placebo-controlled crossover trial

Archives of dermatology (1960), 1988-11, Vol.124 (11), p.1669

1988

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Blood vitamin and trace metal levels in epidermolysis bullosa

Archives of dermatology (1960), 1989-03, Vol.125 (3), p.374

1989

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Type VII collagen and 19-DEJ-1 antigen. Comparison of expression in inversa and generalized variants of recessive dystrophic epidermolysis bullosa

Archives of dermatology (1960), 1990-12, Vol.126 (12), p.1587

1990

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Evaluation of the efficacy of topical bufexamac in epidermolysis bullosa simplex. A double-blind placebo-controlled crossover trial

Archives of dermatology (1960), 1988-11, Vol.124 (11), p.1669-1672

Fine, J. D.

1988

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Peripheral blood mononuclear cell subsets in patients with severe inherited forms of epidermolysis bullosa

Archives of dermatology (1960), 1992-02, Vol.128 (2), p.201

1992

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Development of neuroendocrine (Merkel cell) carcinoma mixed with squamous cell carcinoma in erythema ab igne

Archives of dermatology (1960), 1988-01, Vol.124 (1), p.110

1988

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Herpes gestationis. Persistent disease activity 11 years post partum

Archives of dermatology (1960), 1985-07, Vol.121 (7), p.924

1985

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Type VII collagen and 19-DEJ-1 antigen. Comparison of expression in inversa and generalized variants of recessive dystrophic epidermolysis bullosa

Archives of dermatology (1960), 1990-12, Vol.126 (12), p.1587-1593

Fine, J. D.

1990

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Distinctive eruption characterized by linear supravenous papules and erythroderma following broxuridine (bromodeoxyuridine) therapy and radiotherapy

Archives of dermatology (1960), 1986-02, Vol.122 (2), p.199

1986

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A specific defect in glycosylation of epidermal cell membranes. Definition in skin from patients with epidermolysis bullosa simplex

Archives of dermatology (1960), 1985-10, Vol.121 (10), p.1292

1985

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Skin bioequivalents and their role in the treatment of inherited epidermolysis bullosa

Tetracycline and epidermolysis bullosa simplex: a new indication for one of the oldest and most widely used drugs in dermatology?

Gingival telangiectases: an underappreciated physical sign of juvenile dermatomyositis

19-DEJ-1, a monoclonal antibody to the hemidesmosome-anchoring filament complex, is the only reliable immunohistochemical probe for all major forms of junctional epidermolysis bullosa

Blood vitamin and trace metal levels in epidermolysis bullosa

Natural killer cell activity is reduced in patients with severe forms of inherited epidermolysis bullosa

19-DEJ-1, a monoclonal antibody to the hemidesmosome-anchoring filament complex, is the only reliable immunohistochemical probe for all major forms of junctional epidermolysis bullosa

Efficacy of systemic phenytoin in the treatment of junctional epidermolysis bullosa

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

Antigenic features and structural correlates of basement membranes. Relationship to epidermolysis bullosa

Epidermolysis bullosa simplex superficialis. A new variant of epidermolysis bullosa characterized by subcorneal skin cleavage mimicking peeling skin syndrome

Autosomal recessive epidermolysis bullosa simplex. Generalized phenotypic features suggestive of junctional or dystrophic epidermolysis bullosa, and association with neuromuscular diseases

Changing clinical and laboratory concepts in inherited epidermolysis bullosa

Immunohistochemical, ultrastructural, and molecular features of Kindler syndrome distinguish it from dystrophic epidermolysis bullosa

Efficacy of systemic phenytoin in the treatment of junctional epidermolysis bullosa

Evaluation of the efficacy of topical bufexamac in epidermolysis bullosa simplex. A double-blind placebo-controlled crossover trial

Blood vitamin and trace metal levels in epidermolysis bullosa

Type VII collagen and 19-DEJ-1 antigen. Comparison of expression in inversa and generalized variants of recessive dystrophic epidermolysis bullosa

Evaluation of the efficacy of topical bufexamac in epidermolysis bullosa simplex. A double-blind placebo-controlled crossover trial

Peripheral blood mononuclear cell subsets in patients with severe inherited forms of epidermolysis bullosa

Development of neuroendocrine (Merkel cell) carcinoma mixed with squamous cell carcinoma in erythema ab igne

Herpes gestationis. Persistent disease activity 11 years post partum

Type VII collagen and 19-DEJ-1 antigen. Comparison of expression in inversa and generalized variants of recessive dystrophic epidermolysis bullosa

Distinctive eruption characterized by linear supravenous papules and erythroderma following broxuridine (bromodeoxyuridine) therapy and radiotherapy

A specific defect in glycosylation of epidermal cell membranes. Definition in skin from patients with epidermolysis bullosa simplex

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