Understanding irritant napkin dermatitis von Atherton, David J.

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Mutations in the Gene Encoding Capillary Morphogenesis Protein 2 Cause Juvenile Hyaline Fibromatosis and Infantile Systemic Hyalinosis von Hanks, Sandra, Adams, Sarah, Douglas, Jenny, Arbour, Laura, Atherton, David J., Balci, Sevim, Bode, Harald, Campbell, Mary E., Feingold, Murray, Keser, Gökhan, Kleijer, Wim, Mancini, Grazia, McGrath, John A., Muntoni, Francesco, Nanda, Arti, Teare, M. Dawn, Warman, Matthew, Pope, F. Michael, Superti-Furga, Andrea, Futreal, P. Andrew, Rahman, Nazneen

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Mosaic Activating Mutations in GNA11 and GNAQ Are Associated with Phakomatosis Pigmentovascularis and Extensive Dermal Melanocytosis von Thomas, Anna C., Zeng, Zhiqiang, Rivière, Jean-Baptiste, O’Shaughnessy, Ryan, Al-Olabi, Lara, St.-Onge, Judith, Atherton, David J., Aubert, Hélène, Bagazgoitia, Lorea, Barbarot, Sébastien, Bourrat, Emmanuelle, Chiaverini, Christine, Chong, W. Kling, Duffourd, Yannis, Glover, Mary, Groesser, Leopold, Hadj-Rabia, Smail, Hamm, Henning, Happle, Rudolf, Mushtaq, Imran, Lacour, Jean-Philippe, Waelchli, Regula, Wobser, Marion, Vabres, Pierre, Patton, E. Elizabeth, Kinsler, Veronica A.

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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 von Kinsler, Veronica A., Abu-Amero, Sayeda, Budd, Peter, Jackson, Ian J., Ring, Susan M., Northstone, Kate, Atherton, David J., Bulstrode, Neil W., Stanier, Philip, Hennekam, Raoul C., Sebire, Neil J., Moore, Gudrun E., Healy, Eugene

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A review of the pathophysiology, prevention and treatment of irritant diaper dermatitis von Atherton, David J.

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Topical corticosteroids in atopic dermatitis von Atherton, David J

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Mycosis fungoides with a CD56 + immunophenotype von Wain, E. Mary, Orchard, Guy E., Mayou, Susan, Atherton, David J., Misch, Klaus J., Russell-Jones, Robin

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Acrodermatitis Enteropathica Variant With Borderline Plasma Zinc Concentrations von Paul, Siba Prosad, Vamvakiti, Ekaterini, Atherton, David J, Candy, David CA

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Complete Maternal Isodisomy of Chromosome 3 in a Child with Recessive Dystrophic Epidermolysis Bullosa but No Other Phenotypic Abnormalities von Fassihi, Hiva, Lu, Liu, Wessagowit, Vesarat, Ozoemena, Linda C., Jones, Catherine A., Dopping-Hepenstal, Patricia J.C., Foster, Lesley, Atherton, David J., Mellerio, Jemima E., McGrath, John A.

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Hay-Wells syndrome is caused by heterozygous missense mutations in the SAM domain of p63 von MCGRATH, John A, DUIJF, Pascal H. G, ORLOW, Seth J, VAN HAERINGEN, Arie, AUSEMS, Margreet G. E. M, YANG, Annle, MCKEON, Frank, BAMSHAD, Michael A, BRUNNER, Han G, HAMEL, Ben C. J, VAN BOKHOVEN, Hans, DOETSCH, Volker, IRVINE, Alan D, DE WAAL, Rob, VANMOLKOT, Kaate R. J, WESSAGOWIT, Vesarat, KELLY, Alexander, ATHERTON, David J, GRIFFITHS, W. Andrew D

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Allelic Heterogeneity of Dominant and Recessive COL7A1 Mutations Underlying Epidermolysis Bullosa Pruriginosa von Mellerio, Jemima E., Ashton, Gabrielle H.S., Mohammedi, Rafik, Eady, Robin A.J., McGrath, John A., Lyon, Calum C., Kirby, Brian, Harman, Karen E., Salas-Alanis, Julio C., Atherton, David J., Harrison, Phillip V., Griffiths, W. Andrew D., Black, Martin M.

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Two Cases of Primarily Palmoplantar Keratoderma Associated with Novel Mutations in Keratin 1 von Terron-Kwiatkowski, Ana, Atherton, David J., Irwin McLean, W.H., Irvine, Alan D., Paller, Amy S., Compton, John

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Clinical Resolution of a Neonatally Eroded Giant Congenital Melanocytic Nevus von Gass, Julia K., Grant, John W., Hall, Per N., Atherton, David J., Burrows, Nigel P.

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Gastrointestinal symptoms in atopic eczema von Caffarelli, Carlo, Cavagni, Giovanni, Deriu, Franca M, Zanotti, Paola, Atherton, David J

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Successful Treatment of Laryngeal Stenosis in Laryngo-Onycho-Cutaneous Syndrome with Topical Mitomycin C von Phillips, P. Seamus, Amonoo-Kuofi, Kwame, Hore, Ian D. B., Atherton, David J., Albert, David M.

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Hay-Wells syndrome is caused by heterozygous missense mutations in the SAM domain of p63 von McGrath, J A, Duijf, P H, Doetsch, V, Irvine, A D, de Waal, R, Vanmolkot, K R, Wessagowit, V, Kelly, A, Atherton, D J, Griffiths, W A, Orlow, S J, van Haeringen, A, Ausems, M G, Yang, A, McKeon, F, Bamshad, M A, Brunner, H G, Hamel, B C, van Bokhoven, H

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Genomic localization, organization and amplification of the human zinc transporter protein gene, ZNT4, and exclusion as a candidate gene in different clinical variants of acroderma... von BLECK, Oliver, ASHTON, Gabrielle H. S, MALLIPEDDI, Rajeev, SOUTH, Andrew P, WHITTOCK, Neil V, IRWIN MCLEAN, W. H, ATHERTON, David J, MCGRATH, John A

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An unusual N-terminal deletion of the laminin α3a isoform leads to the chronic granulation tissue disorder laryngo-onycho-cutaneous syndrome von McLean, W. H. Irwin, Irvine, Alan D., Hamill, Kevin J., Whittock, Neil V., Coleman-Campbell, Carrie M., Mellerio, Jemima E., Ashton, Gabrielle S., Dopping-Hepenstal, Patricia J. H., Eady, Robin A. J., Jamil, Tanvir, Phillips, Rodney J., Shabbir, S. Ghulam, Haroon, Tahir S., Khurshid, Khawar, Moore, Jonathan E., Page, Brian, Darling, Jonathan, Atherton, David J., van Steensel, Maurice A. M., Munro, Colin S., Smith, Frances J. D., McGrath, John A.

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Bronchial hyperresponsiveness in children with atopic dermatitis von SALOB, S. P, LAVERTY, A, ATHERTON, D. J

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Germline Melanocortin-1-Receptor Genotype Is Associated with Severity of Cutaneous Phenotype in Congenital Melanocytic Nevi: A Role for MC1 R in Human Fetal Development von KINSLER, Veronica A, ABU-AMERO, Sayeda, SEBIRE, Neil J, MOORE, Gudrun E, HEALY, Eugene, BUDD, Peter, JACKSON, Ian J, RING, Susan M, NORTHSTONE, Kate, ATHERTON, David J, BULSTRODE, Neil W, STANIER, Philip, HENNEKAM, Raoul C

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