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The neuropsychiatric phenotype in Darier disease

British journal of dermatology (1951), 2010-09, Vol.163 (3), p.515-522

2010

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Novel autosomal dominant mutation in loricrin presenting as prominent ichthyosis

British journal of dermatology (1951), 2015-11, Vol.173 (5), p.1291-1294

2015

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Genes, growth factors and acanthosis nigricans

British journal of dermatology (1951), 2002-12, Vol.147 (6), p.1096-1101

2002

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Localization of a Gene ( MCUL1) for Multiple Cutaneous Leiomyomata and Uterine Fibroids to Chromosome 1q42.3-q43

American journal of human genetics, 2001-05, Vol.68 (5), p.1264-1269

2001

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Genetic epidemiology of Darier's disease: a population study in the west of Scotland

British journal of dermatology (1951), 2002-01, Vol.146 (1), p.107-109

2002

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A Novel Mutation in the Keratin 13 Gene Causing Oral White Sponge Nevus

Journal of dental research, 2001-03, Vol.80 (3), p.919-923

2001

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Successful treatment with oral alitretinoin in women of childbearing potential with Darier's disease

British journal of dermatology (1951), 2013-09, Vol.169 (3), p.709-710

2013

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The phenotype of Darier's disease: penetrance and expressivity in adults and children

British journal of dermatology (1951), 1992-08, Vol.127 (2), p.126-130

MUNRO, C.S.

1992

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A mutation in the mucosal keratin K4 is associated with oral white sponge nevus

Nature genetics, 1995-12, Vol.11 (4), p.450-452

1995

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Peripheral nerve blockade for biopsy of plantar skin: Correspondence

British journal of dermatology (1951), 2010-07, Vol.163 (1), p.219-221

2010

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Haplotype analysis in western European patients with mal de Meleda: founder effect for the W15R mutation in the SLURP1 gene: Correspondence

British journal of dermatology (1951), 2013-06, Vol.168 (6), p.1372-1374

2013

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Haplotype analysis in western European patients with mal de Meleda: founder effect for the W15R mutation in the SLURP1 gene

British journal of dermatology (1951), 2013-06, Vol.168 (6), p.1372-1374

2013

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Peripheral nerve blockade for biopsy of plantar skin

British journal of dermatology (1951), 2010-07, Vol.163 (1), p.219-221

2010

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Pachyonychia congenita: mutations and clinical presentations

British journal of dermatology (1951), 2001-05, Vol.144 (5), p.929-930

Munro, C.S.

2001

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Mutation in DSG1 causing autosomal dominant striate palmoplantar keratoderma

British journal of dermatology (1951), 2009-09, Vol.161 (3), p.692-694

2009

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Linear lichen planus related to hepatitis C infection?: CORRESPONDENCE

British journal of dermatology (1951), 2000-04, Vol.142 (4), p.836-837

2000

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Pachyonychia congenita type 2: abnormal dentition extending into adulthood

British journal of dermatology (1951), 2008-08, Vol.159 (2), p.500-501

2008

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Pachyonychia congenita: mutations and clinical presentations

British journal of dermatology (1951), 2001-05, Vol.144 (5), p.929-930

Munro, C.S.

2001

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Keratin 16 and keratin 17 mutations cause pachyonychia congenita

Nature genetics, 1995-03, Vol.9 (3), p.273-278

1995

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Expression of the sarco/endoplasmic reticulum calcium ATPase type 2 and 3 isoforms in normal skin and Darier's disease

British journal of dermatology (1951), 2004-08, Vol.151 (2), p.440-445

2004

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Angiolymphoid hyperplasia with eosinophilia: successful treatment with pulsed dye laser using the double pulse technique

British journal of dermatology (1951), 2000-07, Vol.143 (1), p.214-215

2000

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Symptomatic zinc deficiency in breast-fed premature infants

British journal of dermatology (1951), 1989-12, Vol.121 (6), p.773-778

1989

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Genetic epidemiology of Darier's disease: a population study  in the west of Scotland: GENETIC EPIDEMIOLOGY OF DARIER'S DISEASE

British journal of dermatology (1951), 2002-01, Vol.146 (1), p.107-109

2002

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Cross-linked envelopes in nail plate in lamellar ichthyosis

British journal of dermatology (1951), 2003-11, Vol.149 (5), p.1050-1054

2003

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Linear lichen planus related to hepatitis C infection?

British journal of dermatology (1951), 2000-04, Vol.142 (4), p.836-837

2000

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The neuropsychiatric phenotype in Darier disease

Novel autosomal dominant mutation in loricrin presenting as prominent ichthyosis

Genes, growth factors and acanthosis nigricans

Localization of a Gene ( MCUL1) for Multiple Cutaneous Leiomyomata and Uterine Fibroids to Chromosome 1q42.3-q43

Genetic epidemiology of Darier's disease: a population study in the west of Scotland

A Novel Mutation in the Keratin 13 Gene Causing Oral White Sponge Nevus

Successful treatment with oral alitretinoin in women of childbearing potential with Darier's disease

The phenotype of Darier's disease: penetrance and expressivity in adults and children

A mutation in the mucosal keratin K4 is associated with oral white sponge nevus

Peripheral nerve blockade for biopsy of plantar skin: Correspondence

Haplotype analysis in western European patients with mal de Meleda: founder effect for the W15R mutation in the SLURP1 gene: Correspondence

Haplotype analysis in western European patients with mal de Meleda: founder effect for the W15R mutation in the SLURP1 gene

Peripheral nerve blockade for biopsy of plantar skin

Pachyonychia congenita: mutations and clinical presentations

Mutation in DSG1 causing autosomal dominant striate palmoplantar keratoderma

Linear lichen planus related to hepatitis C infection?: CORRESPONDENCE

Pachyonychia congenita type 2: abnormal dentition extending into adulthood

Pachyonychia congenita: mutations and clinical presentations

Keratin 16 and keratin 17 mutations cause pachyonychia congenita

Expression of the sarco/endoplasmic reticulum calcium ATPase type 2 and 3 isoforms in normal skin and Darier's disease

Angiolymphoid hyperplasia with eosinophilia: successful treatment with pulsed dye laser using the double pulse technique

Symptomatic zinc deficiency in breast-fed premature infants

Genetic epidemiology of Darier's disease: a population study  in the west of Scotland: GENETIC EPIDEMIOLOGY OF DARIER'S DISEASE

Cross-linked envelopes in nail plate in lamellar ichthyosis

Linear lichen planus related to hepatitis C infection?

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