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Understanding irritant napkin dermatitis

International journal of dermatology, 2016-07, Vol.55 (S1), p.7-9

Atherton, David J.

2016

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Observation of a classical Cheshire cat in an optical interferometer

Optics letters, 2015-03, Vol.40 (6), p.879-881

2015

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Mosaic Activating Mutations in GNA11 and GNAQ Are Associated with Phakomatosis Pigmentovascularis and Extensive Dermal Melanocytosis

Journal of investigative dermatology, 2016-04, Vol.136 (4), p.770-778

2016

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The Author as Protagonist: Professionalizing the Craft of the Kusazōshi Writer

Monumenta Nipponica, 2020, Vol.75 (1), p.45-89

Atherton, David C

2020

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ADSSL1 Myopathy: A Case Report (P12-13.003)

Neurology, 2022-05, Vol.98 (18_supplement)

2022

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A review of the pathophysiology, prevention and treatment of irritant diaper dermatitis

Current medical research and opinion, 2004-05, Vol.20 (5), p.645-649

Atherton, David J.

2004

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Germline Melanocortin-1-Receptor Genotype Is Associated with Severity of Cutaneous Phenotype in Congenital Melanocytic Nevi: A Role for MC1R in Human Fetal Development

Journal of investigative dermatology, 2012-08, Vol.132 (8), p.2026-2032

2012

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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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Attonewton force detection using microspheres in a dual-beam optical trap in high vacuum

Physical review. A, Atomic, molecular, and optical physics, 2015-05, Vol.91 (5), Article 051805

2015

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Topical corticosteroids in atopic dermatitis

BMJ, 2003-10, Vol.327 (7421), p.942-943

Atherton, David J

International edition, 2003

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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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Infantile haemangiomas

Early human development, 2006-12, Vol.82 (12), p.789-795

Atherton, David J.

2006

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Editorial

Proceedings of the Institution of Civil Engineers. Civil engineering, 2016-02, Vol.169 (1), p.2-2

Atherton, David

2016

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Micro-sized tunable liquid crystal optical filters

Optics letters, 2017-06, Vol.42 (11), p.2090-2093

2017

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Recurrent Mutations in Kindlin-1, a Novel Keratinocyte Focal Contact Protein, in the Autosomal Recessive Skin Fragility and Photosensitivity Disorder, Kindler Syndrome

Journal of investigative dermatology, 2004-01, Vol.122 (1), p.78-83

2004

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Acrodermatitis Enteropathica Variant With Borderline Plasma Zinc Concentrations

Journal of pediatric gastroenterology and nutrition, 2011-05, Vol.52 (5), p.630-630

2011

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Two-way development

Nursing standard, 2014-02, Vol.28 (26), p.55

Atherton, David

2014

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Two-way development: Limited resources and staffshortages mean that healthcare workers in Malawi have to be creative. Nurse David Atherton has learned a great deal from local people

Nursing standard, 2014-02, Vol.28 (26), p.55-55

Atherton, David

2014

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Mycosis fungoides with a CD56 + immunophenotype

Journal of the American Academy of Dermatology, 2005-07, Vol.53 (1), p.158-163

2005

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Complete Maternal Isodisomy of Chromosome 3 in a Child with Recessive Dystrophic Epidermolysis Bullosa but No Other Phenotypic Abnormalities

Journal of investigative dermatology, 2006-09, Vol.126 (9), p.2039-2043

2006

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Azathioprine as a Treatment for Severe Atopic Eczema in Children with a Partial Thiopurine Methyl Transferase (TPMT) Deficiency

Pediatric dermatology, 2003-11, Vol.20 (6), p.531-534

2003

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Congenital Anetoderma in a Preterm Infant

Pediatric dermatology, 2008-11, Vol.25 (6), p.626-629

2008

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Ideal Families in Crisis: Official and Fictional Archetypes at the Turn of the Nineteenth Century

What Is a Family?, 2019, p.239

1, 2019

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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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Long term follow up of topical mustine treatment for cutaneous Langerhans cell histiocytosis

Archives of disease in childhood, 2000-06, Vol.82 (6), p.483-487

2000

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Understanding irritant napkin dermatitis

Observation of a classical Cheshire cat in an optical interferometer

Mosaic Activating Mutations in GNA11 and GNAQ Are Associated with Phakomatosis Pigmentovascularis and Extensive Dermal Melanocytosis

The Author as Protagonist: Professionalizing the Craft of the Kusazōshi Writer

ADSSL1 Myopathy: A Case Report (P12-13.003)

A review of the pathophysiology, prevention and treatment of irritant diaper dermatitis

Germline Melanocortin-1-Receptor Genotype Is Associated with Severity of Cutaneous Phenotype in Congenital Melanocytic Nevi: A Role for MC1R in Human Fetal Development

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

Attonewton force detection using microspheres in a dual-beam optical trap in high vacuum

Topical corticosteroids in atopic dermatitis

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

Infantile haemangiomas

Editorial

Micro-sized tunable liquid crystal optical filters

Recurrent Mutations in Kindlin-1, a Novel Keratinocyte Focal Contact Protein, in the Autosomal Recessive Skin Fragility and Photosensitivity Disorder, Kindler Syndrome

Acrodermatitis Enteropathica Variant With Borderline Plasma Zinc Concentrations

Two-way development

Two-way development: Limited resources and staffshortages mean that healthcare workers in Malawi have to be creative. Nurse David Atherton has learned a great deal from local people

Mycosis fungoides with a CD56 + immunophenotype

Complete Maternal Isodisomy of Chromosome 3 in a Child with Recessive Dystrophic Epidermolysis Bullosa but No Other Phenotypic Abnormalities

Azathioprine as a Treatment for Severe Atopic Eczema in Children with a Partial Thiopurine Methyl Transferase (TPMT) Deficiency

Congenital Anetoderma in a Preterm Infant

Ideal Families in Crisis: Official and Fictional Archetypes at the Turn of the Nineteenth Century

Gastrointestinal symptoms in patients with asthma

Long term follow up of topical mustine treatment for cutaneous Langerhans cell histiocytosis

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