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David Atherton

Research Profile

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Publications

TOP 3
V A Kinsler; J Birley; David J Atherton
Great Ormond Street Hospital for Children Registry for Congenital Melanocytic Naevi: prospective study 1988-2007. Part 2--Evaluation of treatments.
V A Kinsler; J Birley; David J Atherton
Great Ormond Street Hospital for Children Registry for congenital melanocytic naevi: prospective study 1988-2007. Part 1-epidemiology, phenotype and outcomes.
E Mary Wain; Jemima E Mellerio; Alistair Robson; David J Atherton
Congenital anetoderma in a preterm infant.

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All Publications

2009: V A Kinsler; J Birley; David J Atherton
Great Ormond Street Hospital for Children Registry for Congenital Melanocytic Naevi: prospective study 1988-2007. Part 2--Evaluation of treatments.
The British journal of dermatology 2009;160(2):387-92.
2009: V A Kinsler; J Birley; David J Atherton
Great Ormond Street Hospital for Children Registry for congenital melanocytic naevi: prospective study 1988-2007. Part 1-epidemiology, phenotype and outcomes.
The British journal of dermatology 2009;160(1):143-50.
2008: E Mary Wain; Jemima E Mellerio; Alistair Robson; David J Atherton
Congenital anetoderma in a preterm infant.
Pediatric dermatology 2008;25(6):626-9.
2008: V A Kinsler; W K Chong; sarah aylett; David J Atherton
Complications of congenital melanocytic naevi in children: analysis of 16 years' experience and clinical practice.
The British journal of dermatology 2008;159(4):907-14.
2007: Juliette Mazereeuw-Hautier; Louise C Wilson; S Mohammed; Dawn T Smallwood; Sue Shackleton; David J Atherton; John I Harper
Hutchinson-Gilford progeria syndrome: clinical findings in three patients carrying the G608G mutation in LMNA and review of the literature.
The British journal of dermatology 2007;156(6):1308-14.
2007: Juliette Mazereeuw-Hautier; Emmanuelle Bitoun; J Chevrant-Breton; S Y K Man; Christine Bodemer; C Prins; C Antille; J-H Saurat; David J Atherton; John I Harper; D P Kelsell; Alain Hovnanian
Keratitis-ichthyosis-deafness syndrome: disease expression and spectrum of connexin 26 (GJB2) mutations in 14 patients.
The British journal of dermatology 2007;156(5):1015-9.
2007: S M H Chan; Michael J Dillon; Patrick G Duffy; David J Atherton
Nephro-urological complications of epidermolysis bullosa in paediatric patients.
The British journal of dermatology 2007;156(1):143-7.
2006: David J Atherton
Infantile haemangiomas.
Early human development 2006;82(12):789-95.
2006: Hiva Fassihi; Liu Lu; Vesarat Wessagowit; Linda C Ozoemena; Catherine A Jones; Patricia Dopping-Hepenstal; Lesley Foster; David J Atherton; Jemima E Mellerio; John A McGrath
Complete maternal isodisomy of chromosome 3 in a child with recessive dystrophic epidermolysis bullosa but no other phenotypic abnormalities.
The Journal of investigative dermatology 2006;126(9):2039-43.
2006: Mary S Fewtrell; J Allgrove; I Gordon; Caroline E Brain; David J Atherton; J Harper; Jemima E Mellerio; A E Martinez
Bone mineralization in children with epidermolysis bullosa.
The British journal of dermatology 2006;154(5):959-62.
2006: P Seamus Phillips; Kwame Amonoo-Kuofi; Ian D B Hore; David J Atherton; David M Albert
Successful treatment of laryngeal stenosis in laryngo-onycho-cutaneous syndrome with topical mitomycin C.
Pediatric dermatology 2006;23(1):75-7.
2005: David J Atherton
Maintaining healthy skin in infancy using prevention of irritant napkin dermatitis as a model.
Community practitioner : the journal of the Community Practitioners' & Health Visitors' Association 2005;78(7):255-7.
2005: S Ozanic Bulic; Hiva Fassihi; Jemima E Mellerio; John A McGrath; David J Atherton
Thalidomide in the management of epidermolysis bullosa pruriginosa.
The British journal of dermatology 2005;152(6):1332-4.
2005: Zahra Tejani; Puneet Batra; Carol Mason; David J Atherton
Focal dermal hypoplasia: oral and dental findings.
The Journal of clinical pediatric dentistry 2005;30(1):67-72.
2005: V A Kinsler; J L M Hawk; David J Atherton
Diffuse cutaneous mastocytosis treated with psoralen photochemotherapy: case report and review of the literature.
The British journal of dermatology 2005;152(1):179-80.
2004: Göran Darius Hildebrand; Christine Timms; Dorothy A Thompson; David J Atherton; Marian Malone; Gill A Levitt; D A H Laidlaw; Isabelle Russell-Eggitt; David S I Taylor
Juvenile xanthogranuloma with presumed involvement of the optic disc and retina.
Archives of ophthalmology 2004;122(10):1551-5.
2004: David J Atherton; Kathryn Mills
What can be done to keep babies' skin healthy?
RCM midwives : the official journal of the Royal College of Midwives 2004;7(7):288-90.
2004: Ana Terron-Kwiatkowski; Alessandro Terrinoni; Biagio Didona; Gerry Melino; David J Atherton; Alan D Irvine; W H Irwin McLean
Atypical epidermolytic palmoplantar keratoderma presentation associated with a mutation in the keratin 1 gene.
The British journal of dermatology 2004;150(6):1096-103.
2004: David J Atherton
A review of the pathophysiology, prevention and treatment of irritant diaper dermatitis.
Current medical research and opinion 2004;20(5):645-9.
2004: G H S Ashton; W H Irwin McLean; Andrew P South; Noritaka Oyama; Frances J D Smith; Raouf Al-Suwaid; Abla Al-Ismaily; David J Atherton; Catherine A Harwood; Irene M Leigh; Celia Moss; Biagio Didona; Giovanna Zambruno; Annalisa Patrizi; Robin A J Eady; John A McGrath
Recurrent mutations in kindlin-1, a novel keratinocyte focal contact protein, in the autosomal recessive skin fragility and photosensitivity disorder, Kindler syndrome.
The Journal of investigative dermatology 2004;122(1):78-83.
2003: Lesley-Ann Murphy; David J Atherton
Azathioprine as a treatment for severe atopic eczema in children with a partial thiopurine methyl transferase (TPMT) deficiency.
Pediatric dermatology 2003;20(6):531-4.
2003: W H Irwin McLean; Alan D Irvine; Kevin J Hamill; Neil Whittock; Carrie M Coleman-Campbell; Jemima E Mellerio; Gabrielle S Ashton; Patricia Dopping-Hepenstal; Robin A J Eady; Tanvir Jamil; Roderic J Phillips; S Ghulam Shabbir; Tahir Saeed Haroon; Khawar Khurshid; Jonathan E Moore; Brian Page; Jonathan Darling; David J Atherton; Maurice A M van Steensel; Colin S Munro; Frances J D Smith; John A McGrath; Rodney J Phillips
An unusual N-terminal deletion of the laminin alpha3a isoform leads to the chronic granulation tissue disorder laryngo-onycho-cutaneous syndrome.
Human molecular genetics 2003;12(18):2395-409.
2003: A T Fox; F Alderdice; David J Atherton
Are children with recessive dystrophic epidermolysis bullosa of low birthweight?
Pediatric dermatology 2003;20(4):303-6.
2002: Ana Terron-Kwiatkowski; Amy S Paller; John G Compton; David J Atherton; W H Irwin McLean; Alan D Irvine
Two cases of primarily palmoplantar keratoderma associated with novel mutations in keratin 1.
The Journal of investigative dermatology 2002;119(4):966-71.
2002: M K H Chan; A T Tucker; S Madden; C E M Golding; David J Atherton; Michael J Dillon
Erythromelalgia: an endothelial disorder responsive to sodium nitroprusside.
Archives of disease in childhood 2002;87(3):229-30.
2002: L-A Murphy; David J Atherton
A retrospective evaluation of azathioprine in severe childhood atopic eczema, using thiopurine methyltransferase levels to exclude patients at high risk of myelosuppression.
The British journal of dermatology 2002;147(2):308-15.
2001: David J Atherton
The aetiology and management of irritant diaper dermatitis.
Journal of the European Academy of Dermatology and Venereology : JEADV 2001;15 Suppl 1():1-4.
2001: Oliver Bleck; G H S Ashton; Rajeev Mallipeddi; Andrew P South; Neil Whittock; W H Irwin McLean; David J Atherton; John A McGrath
Genomic localization, organization and amplification of the human zinc transporter protein gene, ZNT4, and exclusion as a candidate gene in different clinical variants of acrodermatitis enteropathica.
Archives of dermatological research 2001;293(8):392-6.
2001: John A McGrath; Pascal Duijf; V Doetsch; Alan D Irvine; R de Waal ; Kaate R J Vanmolkot; Vesarat Wessagowit; A Kelly; David J Atherton; W Andrew Griffiths; S J Orlow; A van Haeringen; M G Ausems; A Yang; Frank McKeon; Michael Bamshad; Han G Brunner; Ben C J Hamel; Hans van Bokhoven
Hay-Wells syndrome is caused by heterozygous missense mutations in the SAM domain of p63.
Human molecular genetics 2001;10(3):221-9.
2001: V A Kinsler; sarah aylett; S C Coley; W K Chong; David J Atherton
Central nervous system imaging and congenital melanocytic naevi.
Archives of disease in childhood 2001;84(2):152-5.
2000: R U Sidwell; Robert Yates; David J Atherton
Dilated cardiomyopathy in dystrophic epidermolysis bullosa.
Archives of disease in childhood 2000;83(1):59-63.
2000: Y Hilhorst-Hofstee; Neil Shah; David J Atherton; John I Harper; Peter J Milla; Robin M Winter
Radial aplasia, poikiloderma and auto-immune enterocolitis--new syndrome or severe form of Rothmund-Thomson syndrome?
Clinical dysmorphology 2000;9(2):79-85.
2000: A E Martinez; David J Atherton
High-dose systemic corticosteroids can arrest recurrences of severe mucocutaneous erythema multiforme.
Pediatric dermatology 2000;17(2):87-90.
2000: Carrie S Shemanko; Helen M Horn; S G Keohane; N Hepburn; A I Kerr; David J Atherton; Michael J Tidman; E Birgitte Lane
Laryngeal involvement in the Dowling-Meara variant of epidermolysis bullosa simplex with keratin mutations of severely disruptive potential.
The British journal of dermatology 2000;142(2):315-20.
1999: Jemima E Mellerio; G H S Ashton; R Mohammedi; calum lyon; B Kirby; K E Harman; Julio C Salas-Alanis; David J Atherton; PV Harrison; W Andrew Griffiths; M M Black; Robin A J Eady; John A McGrath
Allelic heterogeneity of dominant and recessive COL7A1 mutations underlying epidermolysis bullosa pruriginosa.
The Journal of investigative dermatology 1999;112(6):984-7.
1999: SF Slaney; Christine M Hall; David J Atherton; Robin M Winter
A new syndrome of spondyloepimetaphyseal dysplasia, eczema and hypogammaglobulinaemia.
Clinical dysmorphology 1999;8(2):79-85.
1999: Louis Tong; Peter R Hodgkins; J Denyer; D Brosnahan; J Harper; Isabelle Russell-Eggitt; David S I Taylor; David J Atherton
The eye in epidermolysis bullosa.
The British journal of ophthalmology 1999;83(3):323-6.
1998: Jemima E Mellerio; Robin A J Eady; David J Atherton; BD Lake; John A McGrath
E210K mutation in the gene encoding the beta3 chain of laminin-5 (LAMB3) is predictive of a phenotype of generalized atrophic benign epidermolysis bullosa.
The British journal of dermatology 1998;139(2):325-31.
1998: Jemima E Mellerio; Jacqueline E Denyer; David J Atherton; Robin A J Eady; John A McGrath
Prognostic implications of determining 180 kDa bullous pemphigoid antigen (BPAG2) gene/protein pathology in neonatal junctional epidermolysis bullosa.
The British journal of dermatology 1998;138(4):661-6.
1997: L Haynes; David J Atherton; G Clayden
Constipation in epidermolysis bullosa: successful treatment with a liquid fiber-containing formula.
Pediatric dermatology 1997;14(5):393-6.