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Consensus reclassification of inherited epidermolysis bullosa and other disorders with skin fragility

British journal of dermatology (1951), 2020-10, Vol.183 (4), p.614-627

2020

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Phaeohyphomycosis caused by Rhytidhysteron rufulum

Clinical and experimental dermatology, 2020-06, Vol.45 (4), p.524-526

2020

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The risk of cardiomyopathy in inherited epidermolysis bullosa

British journal of dermatology (1951), 2008-09, Vol.159 (3), p.677-682

2008

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Assessment of mobility, activities and pain in different subtypes of epidermolysis bullosa

Clinical and experimental dermatology, 2004-03, Vol.29 (2), p.122-127

2004

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Impact of inherited epidermolysis bullosa on parental interpersonal relationships, marital status and family size

British journal of dermatology (1951), 2005-05, Vol.152 (5), p.1009-1014

2005

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Management of cutaneous squamous cell carcinoma in patients with epidermolysis bullosa: best clinical practice guidelines

British journal of dermatology (1951), 2016-01, Vol.174 (1), p.56-67

2016

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Revised classification system for inherited epidermolysis bullosa: Report of the second international consensus meeting on diagnosis and classification of epidermolysis bullosa

Journal of the American Academy of Dermatology, 2000-06, Vol.42 (6), p.1051-1066

2000

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Tetracycline and epidermolysis bullosa simplex: a double-blind, placebo-controlled, crossover randomized clinical trial

British journal of dermatology (1951), 2004-03, Vol.150 (3), p.613-614

2004

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Congenital pyloric atresia in a newborn with extensive aplasia cutis congenita and epidermolysis bullosa simplex

British journal of dermatology (1951), 2000-12, Vol.143 (6), p.1342-1343

2000

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Crateriform papule on the left knee in a 7-year-old boy

Clinical and experimental dermatology, 2014-01, Vol.39 (1), p.97-98

2014

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Gastric outlet obstruction and epidermolysis bullosa

Journal of the American Academy of Dermatology, 1997-02, Vol.36 (2), p.304-310

1997

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Developmental defects of enamel in humans with hereditary epidermolysis bullosa

Archives of oral biology, 1993-11, Vol.38 (11), p.945-955

1993

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Remission of severe epidermolysis bullosa acquisita induced by extracorporeal photochemotherapy

British journal of dermatology (1951), 1995-09, Vol.133 (3), p.467-471

1995

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Immunofluorescence on split skin for the detection and differentiation of basement membrane zone autoantibodies

Journal of the American Academy of Dermatology, 1992-07, Vol.27 (1), p.79-87

1992

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Eye involvement in inherited epidermolysis bullosa: Experience of the National Epidermolysis Bullosa Registry

American journal of ophthalmology, 2004-08, Vol.138 (2), p.254-262

2004

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Structural and Compositional Alteration of Tooth Enamel in Hereditary Epidermolysis Bullosa

Connective tissue research, 1996, Vol.34 (4), p.271-279

1996

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Defective in vivo expression and apparently normal in vitro expression of a newly identified 105-kDa lower lamina lucida protein in dystrophic epidermolysis bullosa

British journal of dermatology (1951), 1995-05, Vol.132 (5), p.725-729

1995

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Idiopathic Localized Unilateral Hyperhidrosis in a Child

Pediatric dermatology, 2000-01, Vol.17 (1), p.25-28

2000

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Oral soft tissues in hereditary epidermolysis bullosa

Oral surgery, oral medicine, oral pathology, 1991-04, Vol.71 (4), p.440-446

1991

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Autosomal dominant erythromelalgia

American journal of medical genetics, 1992-02, Vol.42 (3), p.310-315

1992

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Inherited epidermolysis bullosa comes into the new millenium: A revised classification system based on current knowledge of pathogenetic mechanisms and the clinical, laboratory, and epidemiologic findings of large, well-defined patient cohorts

Journal of the American Academy of Dermatology, 2000-07, Vol.43 (1), p.135-137

2000

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Mosaic expression of uncein, linear IgA bullous dermatosis antigen and 180-kDa bullous pemphigoid antigen in generalized atrophic benign epidermolysis bullosa

British journal of dermatology (1951), 1998-05, Vol.138 (5), p.904-904

1998

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Pseudosyndactyly and musculoskeletal contractures in inherited epidermolysis bullosa: experience of the national epidermolysis bullosa registry, 1986–2002

Journal of hand surgery, British volume, 2005-02, Vol.30 (1), p.14-22

2005

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Structure and antigenicity of the skin basement membrane zone

Journal of cutaneous pathology, 1991-12, Vol.18 (6), p.401-409

Fine, Jo-David

1991

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Epidermolysis Bullosa: Application of Epidemiologic Principles to the Study of a Group of Rare Diseases Via a Disease Registry

Dermatologic clinics, 1995-07, Vol.13 (3), p.659-670

Fine, Jo-David

1995

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Consensus reclassification of inherited epidermolysis bullosa and other disorders with skin fragility

Phaeohyphomycosis caused by Rhytidhysteron rufulum

The risk of cardiomyopathy in inherited epidermolysis bullosa

Assessment of mobility, activities and pain in different subtypes of epidermolysis bullosa

Impact of inherited epidermolysis bullosa on parental interpersonal relationships, marital status and family size

Management of cutaneous squamous cell carcinoma in patients with epidermolysis bullosa: best clinical practice guidelines

Revised classification system for inherited epidermolysis bullosa: Report of the second international consensus meeting on diagnosis and classification of epidermolysis bullosa

Tetracycline and epidermolysis bullosa simplex: a double-blind, placebo-controlled, crossover randomized clinical trial

Congenital pyloric atresia in a newborn with extensive aplasia cutis congenita and epidermolysis bullosa simplex

Crateriform papule on the left knee in a 7-year-old boy

Gastric outlet obstruction and epidermolysis bullosa

Developmental defects of enamel in humans with hereditary epidermolysis bullosa

Remission of severe epidermolysis bullosa acquisita induced by extracorporeal photochemotherapy

Immunofluorescence on split skin for the detection and differentiation of basement membrane zone autoantibodies

Eye involvement in inherited epidermolysis bullosa: Experience of the National Epidermolysis Bullosa Registry

Structural and Compositional Alteration of Tooth Enamel in Hereditary Epidermolysis Bullosa

Defective in vivo expression and apparently normal in vitro expression of a newly identified 105-kDa lower lamina lucida protein in dystrophic epidermolysis bullosa

Idiopathic Localized Unilateral Hyperhidrosis in a Child

Oral soft tissues in hereditary epidermolysis bullosa

Autosomal dominant erythromelalgia

Inherited epidermolysis bullosa comes into the new millenium: A revised classification system based on current knowledge of pathogenetic mechanisms and the clinical, laboratory, and epidemiologic findings of large, well-defined patient cohorts

Mosaic expression of uncein, linear IgA bullous dermatosis antigen and 180-kDa bullous pemphigoid antigen in generalized atrophic benign epidermolysis bullosa

Pseudosyndactyly and musculoskeletal contractures in inherited epidermolysis bullosa: experience of the national epidermolysis bullosa registry, 1986–2002

Structure and antigenicity of the skin basement membrane zone

Epidermolysis Bullosa: Application of Epidemiologic Principles to the Study of a Group of Rare Diseases Via a Disease Registry

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