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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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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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The Genetic Basis of Epidermolysis Bullosa Simplex with Mottled Pigmentation

Proceedings of the National Academy of Sciences - PNAS, 1996-08, Vol.93 (17), p.9079-9084

1996

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The Genetic Basis of Weber-Cockayne Epidermolysis Bullosa Simplex

Proceedings of the National Academy of Sciences - PNAS, 1993-08, Vol.90 (15), p.7414-7418

1993

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Three new cases of transient bullous dermolysis of the newborn

Journal of the American Academy of Dermatology, 1999-03, Vol.40 (3), p.471-476

1999

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Immunofluorescence and Immunoelectron Microscopic Studies in Cicatricial Pemphigoid

Journal of investigative dermatology, 1984-01, Vol.82 (1), p.39-43

1984

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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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The Presence of Intra-lamina Lucida Blister Formation in Epidermolysis Bullosa Acquisita: Possible Role of Leukocytes

Journal of investigative dermatology, 1989-01, Vol.92 (1), p.27-32

1989

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Intracytoplasmic Retention of Type VII Collagen and Dominant Dystrophic Epidermolysis Bullosa: Reversal of Defect Following Cessation of or Marked Improvement in Disease Activity

Journal of investigative dermatology, 1993-08, Vol.101 (2), p.232-236

1993

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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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Increased Frequency of HLA-DR2 in Patients with Autoantibodies to Epidermolysis Bullosa Acquisita Antigen: Evidence that the Expression of Autoimmunity to Type VII Collagen Is HLA Class II Allele Associated

Journal of investigative dermatology, 1988-09, Vol.91 (3), p.228-232

1988

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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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Patients with severe forms of inherited epidermolysis bullosa exhibit decreased lymphokine and monokine production

Journal of clinical immunology, 1990-11, Vol.10 (6), p.321-329

1990

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Alpha-fetoprotein and acetylcholinesterase are not predictive of fetal junctional epidermolysis bullosa, Herlitz variant

Prenatal diagnosis, 1991-11, Vol.11 (11), p.813-818

1991

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LDA-1: A Ubiquitous Noncollagenous Lamina Densa Component of Basement Membrane Detected by Monoclonal Antibody Technique

Journal of investigative dermatology, 1986-03, Vol.86 (3), p.286-289

1986

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Epidermolysis bullosa simplex: identification of a kindred with autosomal recessive transmission of the Weber-Cockayne variety

Pediatric dermatology, 1989-03, Vol.6 (1), p.1-5

1989

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The TORCH syndrome: A clinical review

Journal of the American Academy of Dermatology, 1985-04, Vol.12 (4), p.697-706

1985

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Gastrointestinal Complications of Inherited Epidermolysis Bullosa: Cumulative Experience of the National Epidermolysis Bullosa Registry

Journal of pediatric gastroenterology and nutrition, 2008-02, Vol.46 (2), p.147-158

2008

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Extensive variant of cutaneous amyloidosis: report of a case with electron-microscopic and immunohistochemical studies of the basement membrane zone at sites of amyloid production

Dermatology (Basel), 1992-01, Vol.185 (3), p.181-189

1992

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Oral involvement of recessive dystrophic epidermolysis bullosa inversa

American journal of medical genetics, 1993-12, Vol.47 (8), p.1184-1188

1993

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Prenatal exclusion of pyloric atresia-junctional epidermolysis bullosa syndrome

Journal of the American Academy of Dermatology, 1994-09, Vol.31 (3), p.429-433

1994

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Salivary function of persons with hereditary epidermolysis bullosa

Oral surgery, oral medicine, oral pathology, 1991-05, Vol.71 (5), p.553-559

1991

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Impact of Social Determinants of Health on Medical Conditions Among Transgender Veterans

American journal of preventive medicine, 2017-04, Vol.52 (4), p.491-498

2017

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Kindler Syndrome: Report of Two Cases and Review of the Literature

Pediatric dermatology, 1989-06, Vol.6 (2), p.91-101

1989

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The risk of cardiomyopathy in inherited epidermolysis bullosa

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

The Genetic Basis of Epidermolysis Bullosa Simplex with Mottled Pigmentation

The Genetic Basis of Weber-Cockayne Epidermolysis Bullosa Simplex

Three new cases of transient bullous dermolysis of the newborn

Immunofluorescence and Immunoelectron Microscopic Studies in Cicatricial Pemphigoid

Idiopathic Localized Unilateral Hyperhidrosis in a Child

The Presence of Intra-lamina Lucida Blister Formation in Epidermolysis Bullosa Acquisita: Possible Role of Leukocytes

Intracytoplasmic Retention of Type VII Collagen and Dominant Dystrophic Epidermolysis Bullosa: Reversal of Defect Following Cessation of or Marked Improvement in Disease Activity

Oral soft tissues in hereditary epidermolysis bullosa

Autosomal dominant erythromelalgia

Increased Frequency of HLA-DR2 in Patients with Autoantibodies to Epidermolysis Bullosa Acquisita Antigen: Evidence that the Expression of Autoimmunity to Type VII Collagen Is HLA Class II Allele Associated

Gingival telangiectases: an underappreciated physical sign of juvenile dermatomyositis

Patients with severe forms of inherited epidermolysis bullosa exhibit decreased lymphokine and monokine production

Alpha-fetoprotein and acetylcholinesterase are not predictive of fetal junctional epidermolysis bullosa, Herlitz variant

LDA-1: A Ubiquitous Noncollagenous Lamina Densa Component of Basement Membrane Detected by Monoclonal Antibody Technique

Epidermolysis bullosa simplex: identification of a kindred with autosomal recessive transmission of the Weber-Cockayne variety

The TORCH syndrome: A clinical review

Gastrointestinal Complications of Inherited Epidermolysis Bullosa: Cumulative Experience of the National Epidermolysis Bullosa Registry

Extensive variant of cutaneous amyloidosis: report of a case with electron-microscopic and immunohistochemical studies of the basement membrane zone at sites of amyloid production

Oral involvement of recessive dystrophic epidermolysis bullosa inversa

Prenatal exclusion of pyloric atresia-junctional epidermolysis bullosa syndrome

Salivary function of persons with hereditary epidermolysis bullosa

Impact of Social Determinants of Health on Medical Conditions Among Transgender Veterans

Kindler Syndrome: Report of Two Cases and Review of the Literature

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