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Complications of congenital melanocytic naevi in children: analysis of 16 years' experience and clinical practice

British journal of dermatology (1951), 2008-10, Vol.159 (4), p.907-914

2008

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Great Ormond Street Hospital for Children Registry for Congenital Melanocytic Naevi: prospective study 1988-2007. Part 1-epidemiology, phenotype and outcomes

British journal of dermatology (1951), 2009-01, Vol.160 (1), p.143-150

2009

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Great Ormond Street Hospital for Children Registry for Congenital Melanocytic Naevi: prospective study 1988-2007. Part 2-evaluation of treatments

British journal of dermatology (1951), 2009-02, Vol.160 (2), p.387-392

2009

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Hutchinson-Gilford progeria syndrome: clinical findings in three patients carrying the G608G mutation in LMNA and review of the literature

British journal of dermatology (1951), 2007-06, Vol.156 (6), p.1308-1314

2007

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Thalidomide in the management of epidermolysis bullosa pruriginosa

British journal of dermatology (1951), 2005-06, Vol.152 (6), p.1332-1334

2005

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The aetiology and management of irritant diaper dermatitis

Journal of the European Academy of Dermatology and Venereology, 2001-09, Vol.15 (s1), p.1-4

Atherton, D J

2001

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Nephro‐urological complications of epidermolysis bullosa in paediatric patients

British journal of dermatology (1951), 2007-01, Vol.156 (1), p.143-147

2007

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Atypical epidermolytic palmoplantar keratoderma presentation associated with a mutation in the keratin 1 gene

British journal of dermatology (1951), 2004-06, Vol.150 (6), p.1096-1103

2004

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A controlled trial of traditional Chinese medicinal plants in widespread non-exudative atopic eczema

British journal of dermatology (1951), 1992-02, Vol.126 (2), p.179-184

1992

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One-year follow up of children treated with Chinese medicinal herbs for atopic eczema

British journal of dermatology (1951), 1994-04, Vol.130 (4), p.488-493

1994

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Efficacy of traditional Chinese herbal therapy in adult atopic dermatitis

The Lancet (British edition), 1992-07, Vol.340 (8810), p.13-17

1992

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An appraisal of acitretin therapy in children with inherited disorders of keratinization

British journal of dermatology (1951), 1996-06, Vol.134 (6), p.1023-1029

1996

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Central nervous system imaging and congenital melanocytic naevi

Archives of disease in childhood, 2001-02, Vol.84 (2), p.152-155

2001

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A double-blind controlled trial of hyposensitization to Dermatophagoides pteronyssinus in children with atopic eczema

Clinical and experimental allergy, 1992-04, Vol.22 (4), p.440-446

1992

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A Gene Affecting Wallerian Nerve Degeneration Maps Distally on Mouse Chromosome 4

Proceedings of the National Academy of Sciences - PNAS, 1993-10, Vol.90 (20), p.9717-9720

1993

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Diffuse cutaneous mastocytosis treated with psoralen photochemotherapy: case report and review of the literature

British journal of dermatology (1951), 2005-01, Vol.152 (1), p.179-180

2005

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Allelic Heterogeneity of Dominant and Recessive COL7A1 Mutations Underlying Epidermolysis Bullosa Pruriginosa

Journal of investigative dermatology, 1999-06, Vol.112 (6), p.984-987

1999

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Erythromelalgia: an endothelial disorder responsive to sodium nitroprusside

Archives of disease in childhood, 2002-09, Vol.87 (3), p.229-230

2002

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Gastrointestinal symptoms in patients with asthma

Archives of disease in childhood, 2000-02, Vol.82 (2), p.131-135

2000

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Mutations in the Gene Encoding Capillary Morphogenesis Protein 2 Cause Juvenile Hyaline Fibromatosis and Infantile Systemic Hyalinosis

American journal of human genetics, 2003-10, Vol.73 (4), p.791-800

2003

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Recalcitrant ulcers in necrobiosis lipoidica diabeticorum healed by topical granulocyte-macrophage colony-stimulating factor

British journal of dermatology (1951), 2002-11, Vol.147 (5), p.1023-1025

2002

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Measurement of nitric oxide and 8-isoprostane in exhaled breath of children with atopic eczema

Clinical and experimental dermatology, 2009-07, Vol.34 (5), p.607-612

2009

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Hay-Wells syndrome is caused by heterozygous missense mutations in the SAM domain of p63

Human molecular genetics, 2001-02, Vol.10 (3), p.221-229

2001

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A prospective study of congenital melanocytic naevi: progress report and evaluation after 6 years

British journal of dermatology (1951), 1996-04, Vol.134 (4), p.617-623

1996

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Are Children with Recessive Dystrophic Epidermolysis Bullosa of Low Birthweight?

Pediatric dermatology, 2003-07, Vol.20 (4), p.303-306

2003

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Complications of congenital melanocytic naevi in children: analysis of 16 years' experience and clinical practice

Great Ormond Street Hospital for Children Registry for Congenital Melanocytic Naevi: prospective study 1988-2007. Part 1-epidemiology, phenotype and outcomes

Great Ormond Street Hospital for Children Registry for Congenital Melanocytic Naevi: prospective study 1988-2007. Part 2-evaluation of treatments

Hutchinson-Gilford progeria syndrome: clinical findings in three patients carrying the G608G mutation in LMNA and review of the literature

Thalidomide in the management of epidermolysis bullosa pruriginosa

The aetiology and management of irritant diaper dermatitis

Nephro‐urological complications of epidermolysis bullosa in paediatric patients

Atypical epidermolytic palmoplantar keratoderma presentation associated with a mutation in the keratin 1 gene

A controlled trial of traditional Chinese medicinal plants in widespread non-exudative atopic eczema

One-year follow up of children treated with Chinese medicinal herbs for atopic eczema

Efficacy of traditional Chinese herbal therapy in adult atopic dermatitis

An appraisal of acitretin therapy in children with inherited disorders of keratinization

Central nervous system imaging and congenital melanocytic naevi

A double-blind controlled trial of hyposensitization to Dermatophagoides pteronyssinus in children with atopic eczema

A Gene Affecting Wallerian Nerve Degeneration Maps Distally on Mouse Chromosome 4

Diffuse cutaneous mastocytosis treated with psoralen photochemotherapy: case report and review of the literature

Allelic Heterogeneity of Dominant and Recessive COL7A1 Mutations Underlying Epidermolysis Bullosa Pruriginosa

Erythromelalgia: an endothelial disorder responsive to sodium nitroprusside

Gastrointestinal symptoms in patients with asthma

Mutations in the Gene Encoding Capillary Morphogenesis Protein 2 Cause Juvenile Hyaline Fibromatosis and Infantile Systemic Hyalinosis

Recalcitrant ulcers in necrobiosis lipoidica diabeticorum healed by topical granulocyte-macrophage colony-stimulating factor

Measurement of nitric oxide and 8-isoprostane in exhaled breath of children with atopic eczema

Hay-Wells syndrome is caused by heterozygous missense mutations in the SAM domain of p63

A prospective study of congenital melanocytic naevi: progress report and evaluation after 6 years

Are Children with Recessive Dystrophic Epidermolysis Bullosa of Low Birthweight?

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