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Propranolol for complicated infantile haemangiomas: a case series of 30 infants

British journal of dermatology (1951), 2010-02, Vol.162 (2), p.466-468

2010

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Evaluation of methotrexate and corticosteroids for the treatment of localized scleroderma (morphoea) in children

British journal of dermatology (1951), 2006-11, Vol.155 (5), p.1013-1020

2006

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A study of matrix metalloproteinase expression and activity in atopic dermatitis using a novel skin wash sampling assay for functional biomarker analysis

British journal of dermatology (1951), 2010-02, Vol.162 (2), p.397-403

2010

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Keratitis-ichthyosis-deafness syndrome: disease expression and spectrum of connexin 26 (GJB2) mutations in 14 patients

British journal of dermatology (1951), 2007-05, Vol.156 (5), p.1015-1019

2007

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Cyclosporin for severe childhood atopic dermatitis: short course versus continuous therapy

British journal of dermatology (1951), 2000-01, Vol.142 (1), p.52-58

2000

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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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LEKTI demonstrable by immunohistochemistry of the skin: a potential diagnostic skin test for Netherton syndrome

British journal of dermatology (1951), 2004-12, Vol.151 (6), p.1253-1257

2004

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Misdiagnosis and delay in referral of children with localized scleroderma

British journal of dermatology (1951), 2011-12, Vol.165 (6), p.1308-1313

2011

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A clinical and immunological study of Netherton's syndrome

British journal of dermatology (1951), 1994-11, Vol.131 (5), p.615-621

1994

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Linear morphoea follows Blaschko's lines

British journal of dermatology (1951), 2008-07, Vol.159 (1), p.175-181

2008

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Prospective evaluation of treatment response and disease reversibility of paediatric localized scleroderma (morphoea) to steroids and methotrexate using multi‐modal imaging

Journal of the European Academy of Dermatology and Venereology, 2020-07, Vol.34 (7), p.1609-1616

2020

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Genetic studies of atopy and atopic dermatitis

British journal of dermatology (1951), 1997-01, Vol.136 (1), p.1-5

1997

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Chromosome 11 q13 and atopy underlying atopic eczema

The Lancet (British edition), 1993-05, Vol.341 (8853), p.1121-1122

1993

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Genetic studies of atopy and atopic dermatitis

British journal of dermatology (1951), 1997-01, Vol.136 (1), p.1-5

1997

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Misdiagnosis and delay in referral of children with localized scleroderma: Delayed diagnosis of localized scleroderma in children

British journal of dermatology (1951), 2011-12, Vol.165 (6), p.1308-1313

2011

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Quantification of stratum corneum ceramides and lipid envelope ceramides in the hereditary ichthyoses

British journal of dermatology (1951), 1994-07, Vol.131 (1), p.23-27

1994

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A novel microdeletion in LOR causing autosomal dominant loricrin keratoderma

British journal of dermatology (1951), 2015-01, Vol.172 (1), p.262-264

2015

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Squamous cell carcinoma in a child with Clericuzio-type poikiloderma with neutropenia

British journal of dermatology (1951), 2013-03, Vol.168 (3), p.665-667

2013

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Squamous cell carcinoma in a child with Clericuzio-type poikiloderma with neutropenia: Correspondence

British journal of dermatology (1951), 2013-03, Vol.168 (3), p.665-667

2013

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Extensive venous/lymphatic malformations causing life-threatening haematological complications

British journal of dermatology (1951), 2007-09, Vol.157 (3), p.558-563

2007

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A heterozygous null mutation combined with the G1258A polymorphism of SPINK5 causes impaired LEKTI function and abnormal expression of skin barrier proteins

British journal of dermatology (1951), 2009-08, Vol.161 (2), p.404-412

2009

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Sternal malformation/vascular dysplasia syndrome with linear hypopigmentation: PHACES syndrome with linear hypopigmentation

British journal of dermatology (1951), 2006-07, Vol.155 (1), p.192-194

2006

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A study of matrix metalloproteinase expression and activity in atopic dermatitis using a novel skin wash sampling assay for functional biomarker analysis: Matrix metalloproteinases in atopic dermatitis

British journal of dermatology (1951), 2010-02, Vol.162 (2), p.397-403

2010

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Propranolol for complicated infantile haemangiomas: a case series of 30 infants: Correspondence

British journal of dermatology (1951), 2010-02, Vol.162 (2), p.466-468

2010

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‘Wet wrap’ dressings for eczema: an effective treatment but not to be misused: CORRESPONDENCE

British journal of dermatology (1951), 2002-01, Vol.146 (1), p.159-158

2002

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Propranolol for complicated infantile haemangiomas: a case series of 30 infants

Evaluation of methotrexate and corticosteroids for the treatment of localized scleroderma (morphoea) in children

A study of matrix metalloproteinase expression and activity in atopic dermatitis using a novel skin wash sampling assay for functional biomarker analysis

Keratitis-ichthyosis-deafness syndrome: disease expression and spectrum of connexin 26 (GJB2) mutations in 14 patients

Cyclosporin for severe childhood atopic dermatitis: short course versus continuous therapy

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

LEKTI demonstrable by immunohistochemistry of the skin: a potential diagnostic skin test for Netherton syndrome

Misdiagnosis and delay in referral of children with localized scleroderma

A clinical and immunological study of Netherton's syndrome

Linear morphoea follows Blaschko's lines

Prospective evaluation of treatment response and disease reversibility of paediatric localized scleroderma (morphoea) to steroids and methotrexate using multi‐modal imaging

Genetic studies of atopy and atopic dermatitis

Chromosome 11 q13 and atopy underlying atopic eczema

Genetic studies of atopy and atopic dermatitis

Misdiagnosis and delay in referral of children with localized scleroderma: Delayed diagnosis of localized scleroderma in children

Quantification of stratum corneum ceramides and lipid envelope ceramides in the hereditary ichthyoses

A novel microdeletion in LOR causing autosomal dominant loricrin keratoderma

Squamous cell carcinoma in a child with Clericuzio-type poikiloderma with neutropenia

Squamous cell carcinoma in a child with Clericuzio-type poikiloderma with neutropenia: Correspondence

Extensive venous/lymphatic malformations causing life-threatening haematological complications

A heterozygous null mutation combined with the G1258A polymorphism of SPINK5 causes impaired LEKTI function and abnormal expression of skin barrier proteins

Sternal malformation/vascular dysplasia syndrome with linear hypopigmentation: PHACES syndrome with linear hypopigmentation

A study of matrix metalloproteinase expression and activity in atopic dermatitis using a novel skin wash sampling assay for functional biomarker analysis: Matrix metalloproteinases in atopic dermatitis

Propranolol for complicated infantile haemangiomas: a case series of 30 infants: Correspondence

‘Wet wrap’ dressings for eczema: an effective treatment but not to be misused: CORRESPONDENCE

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