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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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Genotype-phenotype correlation in skin fragility-ectodermal dysplasia syndrome resulting from mutations in plakophilin 1

Experimental dermatology, 2002-04, Vol.11 (2), p.107-114

2002

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Mutation in DSG1 causing autosomal dominant striate palmoplantar keratoderma

British journal of dermatology (1951), 2009-09, Vol.161 (3), p.692-694

2009

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Retrospective diagnosis of Kindler syndrome in a 37-year-old man

Clinical and experimental dermatology, 2006-01, Vol.31 (1), p.45-47

2006

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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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Pustular psoriasis of pregnancy treated with ciclosporin and high-dose prednisolone

Clinical and experimental dermatology, 2005-11, Vol.30 (6), p.709-710

2005

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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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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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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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Altered distribution of keratinization markers in epidermolytic hyperkeratosis

Archives of Dermatological Research, 1995, Vol.287 (8), p.705-711

1995

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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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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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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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Filaggrin expression in epidermolytic ichthyosis (epidermolytic hyperkeratosis)

British journal of dermatology (1951), 1994-12, Vol.131 (6), p.767-779

1994

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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

Volltextzugriff (PDF)

Genetic basis of lethal junctional epidermolysis bullosa in an affected fetus: Implications for prenatal diagnosis in one family

Prenatal diagnosis, 1995-07, Vol.15 (7), p.647-654

1995

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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

Volltextzugriff (PDF)

The first report of familial adult T‐cell leukaemia lymphoma in the United Kingdom

British journal of haematology, 1995-03, Vol.89 (3), p.615-619

1995

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Filaggrin immunoreactive composite keratohyalin granules specific to acrosyringia and related tumours

Acta dermato-venereologica, 1994, Vol.74 (1), p.37-42

1994

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The surgical management of Dystrophic Epidermolysis Bullosa (excluding the hand)

British journal of plastic surgery, 1992, Vol.45 (6), p.426-434

1992

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Aquagenic pruritus

British medical journal (Clinical research ed.), 1981-06, Vol.282 (6281), p.2008

1981

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Endothelial cell pathology as a marker for urticarial vasculitis: a light microscopic study

British journal of dermatology (1951), 1984-02, Vol.110 (2), p.139-149

1984

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Plectin defects in epidermolysis bullosa simplex with muscular dystrophy

Genotype-phenotype correlation in skin fragility-ectodermal dysplasia syndrome resulting from mutations in plakophilin 1

Mutation in DSG1 causing autosomal dominant striate palmoplantar keratoderma

Retrospective diagnosis of Kindler syndrome in a 37-year-old man

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

Pustular psoriasis of pregnancy treated with ciclosporin and high-dose prednisolone

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

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

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

Altered distribution of keratinization markers in epidermolytic hyperkeratosis

Increased risk of squamous cell carcinoma in junctional epidermolysis bullosa

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

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

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

Filaggrin expression in epidermolytic ichthyosis (epidermolytic hyperkeratosis)

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

Genetic basis of lethal junctional epidermolysis bullosa in an affected fetus: Implications for prenatal diagnosis in one family

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

The first report of familial adult T‐cell leukaemia lymphoma in the United Kingdom

Filaggrin immunoreactive composite keratohyalin granules specific to acrosyringia and related tumours

The surgical management of Dystrophic Epidermolysis Bullosa (excluding the hand)

Aquagenic pruritus

Endothelial cell pathology as a marker for urticarial vasculitis: a light microscopic study

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