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Sweat production in children's feet.
Published in:
Clinical & Experimental Dermatology, 1985, v. 10, n. 3, p. 229, doi. 10.1111/j.1365-2230.1985.tb00562.x
By:
- Bromberg, Jacoline E. C.;
- Creutzberg, Carien L.;
- Atherton, David J.
Publication type:
Article
The role of foods in atopic eczema.
Published in:
Clinical & Experimental Dermatology, 1983, v. 8, n. 3, p. 227, doi. 10.1111/j.1365-2230.1983.tb01775.x
By:
- Atherton, David J.
Publication type:
Article
Razoxane.
Published in:
Clinical & Experimental Dermatology, 1981, v. 6, n. 4, p. 647, doi. 10.1111/j.1365-2230.1981.tb02371.x
By:
- Atherton, David J.
Publication type:
Article
The 1978 Annual Meeting of the American Academy of Dermatology.
Published in:
1979
By:
- Atherton, David J.
Publication type:
Proceeding
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.
Published in:
Archives of Dermatological Research, 2001, v. 293, n. 8, p. 392, doi. 10.1007/s004030100246
By:
- Bleck, Oliver;
- Ashton, Gabrielle H. S.;
- Mallipeddi, Rajeev;
- South, Andrew P.;
- Whittock, Neil V.;
- McLean, W. H. Irwin;
- Atherton, David J.;
- McGrath, J. A.
Publication type:
Article
Understanding irritant napkin dermatitis.
Published in:
International Journal of Dermatology, 2016, v. 55, p. 7, doi. 10.1111/ijd.13334
By:
- Atherton, David J.
Publication type:
Article
Congenital Anetoderma in a Preterm Infant.
Published in:
Pediatric Dermatology, 2008, v. 25, n. 6, p. 626, doi. 10.1111/j.1525-1470.2008.00785.x
By:
- Wain, E. Mary;
- Mellerio, Jemima E.;
- Robson, Alistair;
- Atherton, David J.
Publication type:
Article
Clinical Resolution of a Neonatally Eroded Giant Congenital Melanocytic Nevus.
Published in:
Pediatric Dermatology, 2006, v. 23, n. 6, p. 567, doi. 10.1111/j.1525-1470.2006.00311.x
By:
- Gass, Julia K.;
- Grant, John W.;
- Hall, Per N.;
- Atherton, David J.;
- Burrows, Nigel P.
Publication type:
Article
Successful Treatment of Laryngeal Stenosis in Laryngo-Onycho-Cutaneous Syndrome with Topical Mitomycin C.
Published in:
2006
By:
- Phillips, P. Seamus;
- Amonoo-Kuofi, Kwame;
- Hore, Ian D. B.;
- Atherton, David J.;
- Albert, David M.
Publication type:
Other
PHARMACOLOGY AND THERAPEUTICS Azathioprine as a Treatment for Severe Atopic Eczema in Children with a Partial Thiopurine Methyl Transferase (TPMT) Deficiency.
Published in:
2003
By:
- Murphy, Lesley-Ann;
- Atherton, David J.
Publication type:
Other
High-Dose Systemic Corticosteroids Can Arrest Recurrences of Severe Mucocutaneous Erythema Multiforme.
Published in:
Pediatric Dermatology, 2000, v. 17, n. 2, p. 87, doi. 10.1046/j.1525-1470.2000.01720.x
By:
- Martinez, Anna E.;
- Atherton, David J.
Publication type:
Article
Treatment of Atopic Eczema with Traditional Chinese Medicinal Plants.
Published in:
Pediatric Dermatology, 1992, v. 9, n. 4, p. 373, doi. 10.1111/j.1525-1470.1992.tb00635.x
By:
- Atherton, David J.;
- Sheehan, Mary P.;
- Rustin, Malcolm H. A.;
- Whittle, Brian;
- Guy, Geoffrey
Publication type:
Article
Nutrition in Dystrophic Epidermolysis Bullosa.
Published in:
Pediatric Dermatology, 1992, v. 9, n. 3, p. 231, doi. 10.1111/j.1525-1470.1992.tb00337.x
By:
- Allman, Susan;
- Haynes, Lesley;
- MacKinnon, Petrina;
- Atherton, David J.
Publication type:
Article
Fecal α-Antitrypsin Concentration and Gastrointestinal Permeability to Oligosaccharides in Atopic Dermatitis.
Published in:
Pediatric Dermatology, 1989, v. 6, n. 1, p. 10, doi. 10.1111/j.1525-1470.1989.tb00258.x
By:
- Pike, Michael G.;
- Riches, Pamela;
- Atherton, David J.
Publication type:
Article
ADDENDUM.
Published in:
1987
By:
- Atherton, David J.
Publication type:
Letter
Acute Laryngeal Obstruction in Junctional Epidermolysis Buliosa.
Published in:
Pediatric Dermatology, 1987, v. 4, n. 2, p. 98, doi. 10.1111/j.1525-1470.1987.tb00760.x
By:
- Davies, Hugh;
- Atherton, David J.
Publication type:
Article
Protein-Losing Enteropathy in Atopic Dermatitis.
Published in:
Pediatric Dermatology, 1986, v. 3, n. 2, p. 125, doi. 10.1111/j.1525-1470.1986.tb00502.x
By:
- Jenkins, Huw R.;
- Walkersmith, John A.;
- Atherton, David J.
Publication type:
Article
Germline Melanocortin-1-Receptor Genotype Is Associated with Severity of Cutaneous Phenotype in Congenital Melanocytic Nevi: A Role for MC1R in Human Fetal Development.
Published in:
Journal of Investigative Dermatology, 2012, v. 132, n. 8, p. 2026, doi. 10.1038/jid.2012.95
By:
- 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
Publication type:
Article
Complete Maternal Isodisomy of Chromosome 3 in a Child with Recessive Dystrophic Epidermolysis Bullosa but No Other Phenotypic Abnormalities.
Published in:
Journal of Investigative Dermatology, 2006, v. 126, n. 9, p. 2039, doi. 10.1038/sj.jid.5700348
By:
- Fassihi, Hiva;
- Liu Lu;
- Wessagowit, Vesarat;
- Ozoemena, Linda C.;
- Jones, Catherine A.;
- Dopping-Hepenstal, Patricia J. C.;
- Foster, Lesley;
- Atherton, David J.;
- Mellerio, Jemima E.;
- McGrath, John A.
Publication type:
Article
Recurrent Mutations in Kindlin-1, a Novel Keratinocyte Focal Contact Protein, in the Autosomal Recessive Skin Fragility and Photosensitivity Disorder, Kindler Syndrome.
Published in:
Journal of Investigative Dermatology, 2004, v. 122, n. 1, p. 78, doi. 10.1046/j.0022-202X.2003.22136.x
By:
- Ashton, Gabrielle H.S.;
- McLean, W.H. Irwin;
- South, Andrew P.;
- Oyama, Noritaka;
- Smith, Frances J.D.;
- Al-Suwaid, Raouf;
- Al Ismaily, Abla;
- Atherton, David J.;
- Harwood, Catherine A.;
- Leigh, Irene M.;
- Moss, Celia;
- Didona, Biagio;
- Zambruno, Giovanna;
- Patrizi, Annalisa;
- Eady, Robin A.J.;
- McGrath, John A.
Publication type:
Article
Two Cases of Primarily Palmoplantar Keratoderma Associated with Novel Mutations in Keratin 1.
Published in:
Journal of Investigative Dermatology, 2002, v. 119, n. 4, p. 966, doi. 10.1046/j.1523-1747.2002.00186.x
By:
- Terron-Kwiatkowski, Ana;
- Paller, Amy S.;
- Compton, John;
- Atherton, David J.;
- McLean, W. H. Irwin;
- Irvine, Alan D.
Publication type:
Article
Allelic Heterogeneity of Dominant and Recessive COL7A1 Mutations Underlying Epidermolysis Bullosa Pruriginosa.
Published in:
Journal of Investigative Dermatology, 1999, v. 112, n. 6, p. 984, doi. 10.1046/j.1523-1747.1999.00614.x
By:
- Mellerio, Jemima E.;
- Ashton, Gabrielle H. S.;
- Mohammedi, Rafik;
- 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.;
- Eady, Robin A. J.;
- McGrath, John A.
Publication type:
Article
Eczema Herpeticum.
Published in:
Clinical Pediatrics, 1988, v. 27, n. 5, p. 231, doi. 10.1177/000992288802700502
By:
- Novelli, Valerio M.;
- Atherton, David J.;
- Marshall, William C.
Publication type:
Article
Book reviews.
Published in:
1992
By:
- Pipe, Roderic Alan;
- Walker-Smith, J. A.;
- Fixsen, John;
- Atherton, David J.
Publication type:
Book Review
Increased Intestinal Permeability in Atopic Eczema.
Published in:
Journal of Investigative Dermatology, 1986, v. 86, n. 2, p. 101, doi. 10.1111/1523-1747.ep12284035
By:
- Pike, Michael G.;
- Heddle, Robert J.;
- Boulton, Peter;
- Turner, Malcolm W.;
- Atherton, David J.
Publication type:
Article
Neurofibromatosis (Von Recklinghausen Disease), Genetics, Cell Biology and Biochemistry (Book).
Published in:
1983
By:
- Atherton, David J.
Publication type:
Book Review
Clinical Genodermatology. Volumes I and 2.
Published in:
1982
By:
- Atherton, David J.
Publication type:
Book Review
An unusual N-terminal deletion of the laminin α3a isoform leads to the chronic granulation tissue disorder laryngo-onycho-cutaneous syndrome.
Published in:
Human Molecular Genetics, 2004, v. 13, n. 3, p. 365
By:
- 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, Roderic 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.
Publication type:
Article
An unusual N-terminal deletion of the laminin α3a isoform leads to the chronic granulation tissue disorder laryngo-onycho-cutaneous syndrome.
Published in:
Human Molecular Genetics, 2003, v. 12, n. 18, p. 2395, doi. 10.1093/hmg/ddg234
By:
- 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.
Publication type:
Article
Hay-Wells syndrome is caused by heterozygous missense mutations in the SAM domain of p63.
Published in:
Human Molecular Genetics, 2001, v. 10, n. 3, p. 221, doi. 10.1093/hmg/10.3.221
By:
- McGrath, John A.;
- Duijf, Pascal H.G.;
- Doetsch, Volker;
- Irvine, Alan D.;
- de Waal, Rob;
- Vanmolkot, Kaate R.J.;
- Wessagowit, Vesarat;
- Kelly, Alexander;
- Atherton, David J.;
- Griffiths, W. Andrew D.;
- Orlow, Seth J.;
- van Haeringen, Arie;
- Ausems, Margreet G.E.M.;
- Yang, Annie;
- McKeon, Frank;
- Bamshad, Michael A.;
- Brunner, Han G.;
- Hamel, Ben C.J.;
- van Bokhoven, Hans
Publication type:
Article

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