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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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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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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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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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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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Oral and gastrointestinal manifestations of epidermolysis bullosa

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

1992

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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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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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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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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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Eye involvement in junctional epidermolysis bullosa

Archives of ophthalmology (1960), 1989-11, Vol.107 (11), p.1635

1989

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Plasma immunoreactive melanotrophic hormones in patients on maintenance haemodialysis

BMJ, 1975-03, Vol.1 (5959), p.656-657

1975

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Variation in gene expression profiles of peripheral blood mononuclear cells from healthy volunteers

Physiological genomics, 2005-08, Vol.22 (3), p.402-411

2005

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Weight-Based Enoxaparin Achieves Adequate Anti-Xa Levels More Often in Trauma Patients: A Prospective Study

The American surgeon, 2021-01, Vol.87 (1), p.77-82

2021

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Effect of intracoronary delivery of autologous bone marrow mononuclear cells 2 to 3 weeks following acute myocardial infarction on left ventricular function: the LateTIME randomized trial

JAMA : the journal of the American Medical Association, 2011-11, Vol.306 (19), p.2110

2011

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Differential localization of γ-aminobutyric acid type a and glycine receptor subunits and gephyrin in the human pons, medulla oblongata and uppermost cervical segment of the spinal cord: An immunohistochemical study

Journal of comparative neurology (1911), 2010-02, Vol.518 (3), p.305-328

2010

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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

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

Epidermolysis bullosa pruriginosa: dystrophic epidermolysis bullosa with distinctive clinicopathological features

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

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

Oral and gastrointestinal manifestations of epidermolysis bullosa

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

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

Filaggrin immunoreactive composite keratohyalin granules specific to acrosyringia and related tumours

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

Eye involvement in junctional epidermolysis bullosa

Plasma immunoreactive melanotrophic hormones in patients on maintenance haemodialysis

Variation in gene expression profiles of peripheral blood mononuclear cells from healthy volunteers

Weight-Based Enoxaparin Achieves Adequate Anti-Xa Levels More Often in Trauma Patients: A Prospective Study

Effect of intracoronary delivery of autologous bone marrow mononuclear cells 2 to 3 weeks following acute myocardial infarction on left ventricular function: the LateTIME randomized trial

Differential localization of γ-aminobutyric acid type a and glycine receptor subunits and gephyrin in the human pons, medulla oblongata and uppermost cervical segment of the spinal cord: An immunohistochemical study

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