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Plectin defects in epidermolysis bullosa simplex with muscular dystrophy

Muscle & nerve, 2007-01, Vol.35 (1), p.24-35

2007

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Striate palmoplantar keratoderma arising from desmoplakin and desmoglein 1 mutations is associated with contrasting perturbations of desmosomes and the keratin filament network

British journal of dermatology (1951), 2004-05, Vol.150 (5), p.878-891

2004

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EEC (Ectrodactyly, Ectodermal dysplasia, Clefting) syndrome: heterozygous mutation in the p63 gene (R279H) and DNA-based prenatal diagnosis

British journal of dermatology (1951), 2002-02, Vol.146 (2), p.216-220

2002

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Defining target antigens in linear IgA disease using skin from subjects with inherited epidermolysis bullosa as a substrate for indirect immunofluorescence microscopy

British journal of dermatology (1951), 1999-09, Vol.141 (3), p.475-480

1999

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Epidermolysis bullosa complicated by squamous cell carcinoma: report of 10 cases

Journal of cutaneous pathology, 1992-04, Vol.19 (2), p.116-123

1992

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The eye in dystrophic epidermolysis bullosa: Clinical and immunopathological findings

Eye (London), 1989-01, Vol.3 (1), p.79-83

1989

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Morphology of the keratin filament network in palm and sole skin : evidence for site-dependent features based on stereological analysis

Archives of Dermatological Research, 1996-02, Vol.288 (2), p.55-62

1996

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Specialized keratin expression pattern in human ridged skin as an adaptation to high physical stress

British journal of dermatology (1951), 1998-11, Vol.139 (5), p.767-775

1998

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Increased risk of squamous cell carcinoma in junctional epidermolysis bullosa

Journal of the European Academy of Dermatology and Venereology, 2004-09, Vol.18 (5), p.521-526

2004

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Loricrin Mutation in Vohwinkel’s Keratoderma Is Unique to the Variant with Ichthyosis

Journal of investigative dermatology, 1997-10, Vol.109 (4), p.604-610

1997

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Hemidesmosomes Show Abnormal Association with the Keratin Filament Network in Junctional Forms of Epidermolysis Bullosa

Journal of investigative dermatology, 1998-02, Vol.110 (2), p.132-137

1998

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Epidermolysis bullosa pruriginosa: dystrophic epidermolysis bullosa with distinctive clinicopathological features

British journal of dermatology (1951), 1994-05, Vol.130 (5), p.617-625

1994

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Epidermolysis Bullosa Simplex (Dowling-Meara Type) Is a Genetic Disease Characterized by an Abnormal Keratin-Filament Network Involving Keratins K5 and K14

Journal of investigative dermatology, 1991-12, Vol.97 (6), p.959-968

1991

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Structural Variations in Anchoring Fibrils in Dystrophic Epidermolysis Bullosa: Correlation with Type VII Collagen Expression

Journal of investigative dermatology, 1993-04, Vol.100 (4), p.366-372

1993

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Ichthyosis bullosa of Siemens: report of a family with evidence of a keratin 2e mutation, and a review of the literature

British journal of dermatology (1951), 1999-04, Vol.140 (4), p.689-695

1999

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Human dermal microvasculature: I. Its segmental differentiation. Light and electron microscopic study

British journal of dermatology (1951), 1981-02, Vol.104 (2), p.117-129

1981

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Immunohistochemical analysis of the skin in junctional epidermolysis bullosa using laminin 5 chain specific antibodies is of limited value in predicting the underlying gene mutation

British journal of dermatology (1951), 1997-06, Vol.136 (6), p.817-822

1997

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Oral and gastrointestinal manifestations of epidermolysis bullosa

The Lancet (British edition), 1992-12, Vol.340 (8834), p.1505-1506

1992

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Epidermolysis bullosa simplex (Dowling-Meara). A clinicopathological review

British journal of dermatology (1951), 1992-05, Vol.126 (5), p.421-430

1992

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Hemidesmosome Heterogeneity in Junctional Epidermolysis Bullosa Revealed by Morphometric Analysis

Journal of investigative dermatology, 1986-01, Vol.86 (1), p.51-56

1986

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Cultured keratinocyte allografts and wound healing in severe recessive dystrophic epidermolysis bullosa

Journal of the American Academy of Dermatology, 1993-09, Vol.29 (3), p.407-419

1993

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The prevalence of epidermolysis bullosa in Scotland

British journal of dermatology (1951), 1997-04, Vol.136 (4), p.560-564

1997

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Ultrastructural Morphometry of Normal Human Dermal-Epidermal Junction. The Influence of Age, Sex, and Body Region on Laminar and Nonlaminar Components

Journal of investigative dermatology, 1984-12, Vol.83 (6), p.448-453

1984

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Fibrillin immunoreactivity is associated with normal or fragmented elastic microfibrils at the dermal-epidermal junction in recessive dystrophic epidermolysis bullosa

British journal of dermatology (1951), 1994-10, Vol.131 (4), p.465-471

1994

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Abnormal binding of an anti-amnion antibody to epidermal basement membrane provides a novel diagnostic probe for junctional epidermolysis bullosa

British journal of dermatology (1951), 1985-12, Vol.113 (6), p.651-659

1985

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Plectin defects in epidermolysis bullosa simplex with muscular dystrophy

Striate palmoplantar keratoderma arising from desmoplakin and desmoglein 1 mutations is associated with contrasting perturbations of desmosomes and the keratin filament network

EEC (Ectrodactyly, Ectodermal dysplasia, Clefting) syndrome: heterozygous mutation in the p63 gene (R279H) and DNA-based prenatal diagnosis

Defining target antigens in linear IgA disease using skin from subjects with inherited epidermolysis bullosa as a substrate for indirect immunofluorescence microscopy

Epidermolysis bullosa complicated by squamous cell carcinoma: report of 10 cases

The eye in dystrophic epidermolysis bullosa: Clinical and immunopathological findings

Morphology of the keratin filament network in palm and sole skin : evidence for site-dependent features based on stereological analysis

Specialized keratin expression pattern in human ridged skin as an adaptation to high physical stress

Increased risk of squamous cell carcinoma in junctional epidermolysis bullosa

Loricrin Mutation in Vohwinkel’s Keratoderma Is Unique to the Variant with Ichthyosis

Hemidesmosomes Show Abnormal Association with the Keratin Filament Network in Junctional Forms of Epidermolysis Bullosa

Epidermolysis bullosa pruriginosa: dystrophic epidermolysis bullosa with distinctive clinicopathological features

Epidermolysis Bullosa Simplex (Dowling-Meara Type) Is a Genetic Disease Characterized by an Abnormal Keratin-Filament Network Involving Keratins K5 and K14

Structural Variations in Anchoring Fibrils in Dystrophic Epidermolysis Bullosa: Correlation with Type VII Collagen Expression

Ichthyosis bullosa of Siemens: report of a family with evidence of a keratin 2e mutation, and a review of the literature

Human dermal microvasculature: I. Its segmental differentiation. Light and electron microscopic study

Immunohistochemical analysis of the skin in junctional epidermolysis bullosa using laminin 5 chain specific antibodies is of limited value in predicting the underlying gene mutation

Oral and gastrointestinal manifestations of epidermolysis bullosa

Epidermolysis bullosa simplex (Dowling-Meara). A clinicopathological review

Hemidesmosome Heterogeneity in Junctional Epidermolysis Bullosa Revealed by Morphometric Analysis

Cultured keratinocyte allografts and wound healing in severe recessive dystrophic epidermolysis bullosa

The prevalence of epidermolysis bullosa in Scotland

Ultrastructural Morphometry of Normal Human Dermal-Epidermal Junction. The Influence of Age, Sex, and Body Region on Laminar and Nonlaminar Components

Fibrillin immunoreactivity is associated with normal or fragmented elastic microfibrils at the dermal-epidermal junction in recessive dystrophic epidermolysis bullosa

Abnormal binding of an anti-amnion antibody to epidermal basement membrane provides a novel diagnostic probe for junctional epidermolysis bullosa

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