Pesquisa | Biblioteca Virtual em Saúde

1.

Congenital anetoderma in a preterm infant.

Wain, E Mary; Mellerio, Jemima E; Robson, Alistair; Atherton, David J.

Pediatr Dermatol ; 25(6): 626-9, 2008.

Artigo em Inglês | MEDLINE | ID: mdl-19067869

2.

Complete maternal isodisomy of chromosome 3 in a child with recessive dystrophic epidermolysis bullosa but no other phenotypic abnormalities.

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.

J Invest Dermatol ; 126(9): 2039-43, 2006 Sep.

Artigo em Inglês | MEDLINE | ID: mdl-16710310

3.

Acrodermatitis enteropathica variant with borderline plasma zinc concentrations.

Paul, Siba Prosad; Vamvakiti, Ekaterini; Atherton, David J; Candy, David C A.

J Pediatr Gastroenterol Nutr ; 52(5): 630, 2011 May.

Artigo em Inglês | MEDLINE | ID: mdl-21502834

4.

Infantile haemangiomas.

Atherton, David J.

Early Hum Dev ; 82(12): 789-95, 2006 Dec.

Artigo em Inglês | MEDLINE | ID: mdl-17059871

5.

Understanding irritant napkin dermatitis.

Atherton, David J.

Int J Dermatol ; 55 Suppl 1: 7-9, 2016 Jul.

Artigo em Inglês | MEDLINE | ID: mdl-27311779

6.

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

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.

J Invest Dermatol ; 136(4): 770-778, 2016 Apr.

Artigo em Inglês | MEDLINE | ID: mdl-26778290

7.

Mycosis fungoides with a CD56+ immunophenotype.

Wain, E Mary; Orchard, Guy E; Mayou, Susan; Atherton, David J; Misch, Klaus J; Russell-Jones, Robin.

J Am Acad Dermatol ; 53(1): 158-63, 2005 Jul.

Artigo em Inglês | MEDLINE | ID: mdl-15965442

8.

Two cases of primarily palmoplantar keratoderma associated with novel mutations in keratin 1.

Terron-Kwiatkowski, Ana; Paller, Amy S; Compton, John; Atherton, David J; McLean, W H Irwin; Irvine, Alan D.

J Invest Dermatol ; 119(4): 966-71, 2002 Oct.

Artigo em Inglês | MEDLINE | ID: mdl-12406346

9.

Recurrent mutations in kindlin-1, a novel keratinocyte focal contact protein, in the autosomal recessive skin fragility and photosensitivity disorder, Kindler syndrome.

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.

J Invest Dermatol ; 122(1): 78-83, 2004 Jan.

Artigo em Inglês | MEDLINE | ID: mdl-14962093

10.

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

Atherton, David J.

Curr Med Res Opin ; 20(5): 645-9, 2004 May.

Artigo em Inglês | MEDLINE | ID: mdl-15140329

11.

Germline melanocortin-1-receptor genotype is associated with severity of cutaneous phenotype in congenital melanocytic nevi: a role for MC1R in human fetal development.

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.

J Invest Dermatol ; 132(8): 2026-32, 2012 Aug.

Artigo em Inglês | MEDLINE | ID: mdl-22572819

12.

Juvenile xanthogranuloma with presumed involvement of the optic disc and retina.

Hildebrand, Göran Darius; Timms, Chris; Thompson, Dorothy A; Atherton, David J; Malone, Marian; Levitt, Gill; Laidlaw, D Alistair H; Russell-Eggitt, Isabelle; Taylor, David S I.

Arch Ophthalmol ; 122(10): 1551-5, 2004 Oct.

Artigo em Inglês | MEDLINE | ID: mdl-15477475

13.

Clinical resolution of a neonatally eroded giant congenital melanocytic nevus.

Gass, Julia K; Grant, John W; Hall, Per N; Atherton, David J; Burrows, Nigel P.

Pediatr Dermatol ; 23(6): 567-70, 2006.

Artigo em Inglês | MEDLINE | ID: mdl-17156000

14.

Successful treatment of laryngeal stenosis in laryngo-onycho-cutaneous syndrome with topical mitomycin C.

Phillips, P Seamus; Amonoo-Kuofi, Kwame; Hore, Ian D B; Atherton, David J; Albert, David M.

Pediatr Dermatol ; 23(1): 75-7, 2006.

Artigo em Inglês | MEDLINE | ID: mdl-16445419

15.

Azathioprine as a treatment for severe atopic eczema in children with a partial thiopurine methyl transferase (TPMT) deficiency.

Murphy, Lesley-Ann; Atherton, David J.

Pediatr Dermatol ; 20(6): 531-4, 2003.

Artigo em Inglês | MEDLINE | ID: mdl-14651577

16.

Mutations in the gene encoding capillary morphogenesis protein 2 cause juvenile hyaline fibromatosis and infantile systemic hyalinosis.

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.

Am J Hum Genet ; 73(4): 791-800, 2003 Oct.

Artigo em Inglês | MEDLINE | ID: mdl-14508707

17.

An unusual N-terminal deletion of the laminin alpha3a isoform leads to the chronic granulation tissue disorder laryngo-onycho-cutaneous syndrome.

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; Smith, Frances J D; McGrath, John A; Phillips, Rodney J.

Hum Mol Genet ; 12(18): 2395-409, 2003 Sep 15.

Artigo em Inglês | MEDLINE | ID: mdl-12915477

18.

Loss of kindlin-1, a human homolog of the Caenorhabditis elegans actin-extracellular-matrix linker protein UNC-112, causes Kindler syndrome.

Siegel, Dawn H; Ashton, Gabrielle H S; Penagos, Homero G; Lee, James V; Feiler, Heidi S; Wilhelmsen, Kirk C; South, Andrew P; Smith, Frances J D; Prescott, Alan R; Wessagowit, Vesarat; Oyama, Noritaka; Akiyama, Masashi; Al Aboud, Daifullah; Al Aboud, Khalid; Al Githami, Ahmad; Al Hawsawi, Khalid; Al Ismaily, Abla; Al-Suwaid, Raouf; Atherton, David J; Caputo, Ruggero; Fine, Jo-David; Frieden, Ilona J; Fuchs, Elaine; Haber, Richard M; Harada, Takashi; Kitajima, Yasuo; Mallory, Susan B; Ogawa, Hideoki; Sahin, Sedef; Shimizu, Hiroshi; Suga, Yasushi; Tadini, Gianluca; Tsuchiya, Kikuo; Wiebe, Colin B; Wojnarowska, Fenella; Zaghloul, Adel B; Hamada, Takahiro; Mallipeddi, Rajeev; Eady, Robin A J; McLean, W H Irwin; McGrath, John A; Epstein, Ervin H.

Am J Hum Genet ; 73(1): 174-87, 2003 Jul.

Artigo em Inglês | MEDLINE | ID: mdl-12789646

19.

Topical corticosteroids in atopic dermatitis.

Atherton, David J.

BMJ ; 327(7421): 942-3, 2003 Oct 25.

Artigo em Inglês | MEDLINE | ID: mdl-14576221

20.

Infantile systemic hyalinosis: newly recognized disorder of collagen?

Glover, Mary T; Lake, Bryan D; Atherton, David J.

s.l; s.n; 1991. 7 p. ilus.

Não convencional em Inglês | SES-SP, SESSP-ILSLACERVO, SES-SP | ID: biblio-1241638

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Congenital anetoderma in a preterm infant.

Complete maternal isodisomy of chromosome 3 in a child with recessive dystrophic epidermolysis bullosa but no other phenotypic abnormalities.

Acrodermatitis enteropathica variant with borderline plasma zinc concentrations.

Infantile haemangiomas.

Understanding irritant napkin dermatitis.

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

Mycosis fungoides with a CD56+ immunophenotype.

Two cases of primarily palmoplantar keratoderma associated with novel mutations in keratin 1.

Recurrent mutations in kindlin-1, a novel keratinocyte focal contact protein, in the autosomal recessive skin fragility and photosensitivity disorder, Kindler syndrome.

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.

Juvenile xanthogranuloma with presumed involvement of the optic disc and retina.

Clinical resolution of a neonatally eroded giant congenital melanocytic nevus.

Successful treatment of laryngeal stenosis in laryngo-onycho-cutaneous syndrome with topical mitomycin C.

Azathioprine as a treatment for severe atopic eczema in children with a partial thiopurine methyl transferase (TPMT) deficiency.

Mutations in the gene encoding capillary morphogenesis protein 2 cause juvenile hyaline fibromatosis and infantile systemic hyalinosis.

An unusual N-terminal deletion of the laminin alpha3a isoform leads to the chronic granulation tissue disorder laryngo-onycho-cutaneous syndrome.

Loss of kindlin-1, a human homolog of the Caenorhabditis elegans actin-extracellular-matrix linker protein UNC-112, causes Kindler syndrome.

Topical corticosteroids in atopic dermatitis.

Infantile systemic hyalinosis: newly recognized disorder of collagen?