Zobrazeno 1 - 10
of 45
pro vyhledávání: '"W. A. D. Griffiths"'
Publikováno v:
Journal of the European Academy of Dermatology and Venereology. 27:e131-e135
Background Adult pityriasis rubra pilaris (PRP) type 1 is a rare chronic papulosquamous disorder with clinical and histological parallels with psoriasis. Treatment is challenging and recent case reports suggest a potential role for tumour necrosis fa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::071daf7b9e7ecbb9245c00ba6e022601
https://doi.org/10.1111/j.1468-3083.2012.04456.x
https://doi.org/10.1111/j.1468-3083.2012.04456.x
Autor:
Robert M.W. de Waal, Ben C.J. Hamel, Kaate R.J. Vanmolkot, Hans van Bokhoven, David J. Atherton, Volker Doetsch, W Andrew D Griffiths, John A. McGrath, Pascal H.G. Duijf, Annie Yang, Han G. Brunner, Arie van Haeringen, Seth J. Orlow, Frank McKeon, Alexander E. Kelly, Margreet G. E. M. Ausems, V Wessagowit, Alan D. Irvine, Michael A. Bamshad
Publikováno v:
Human Molecular Genetics, 10, 221--9
Scopus-Elsevier
Human Molecular Genetics, 10(3), 221-229. Oxford University Press
Human Molecular Genetics, 10, 3, pp. 221--9
Scopus-Elsevier
Human Molecular Genetics, 10(3), 221-229. Oxford University Press
Human Molecular Genetics, 10, 3, pp. 221--9
Item does not contain fulltext Hay-Wells syndrome, also known as ankyloblepharon-ectodermal dysplasia-clefting (AEC) syndrome (OMIM 106260), is a rare autosomal dominant disorder characterized by congenital ectodermal dysplasia, including alopecia, s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::50d19fcd157d9c29787edd7c79c0d3be
https://doi.org/10.1093/hmg/10.3.221
https://doi.org/10.1093/hmg/10.3.221
Publikováno v:
Clinical and Experimental Dermatology. 25:611-614
A 21-year-old woman presented with non-bullous congenital ichthyosiform erythroderma; she was born a collodion baby. Associated features were ocular albinism, anterior segment dysgenesis of both eyes and Noonan syndrome. X-linked ichthyosis (steroid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0c30fa4079acecdfc394b9d41f858b90
https://doi.org/10.1046/j.1365-2230.2000.00719.x
https://doi.org/10.1046/j.1365-2230.2000.00719.x
Autor:
V. A. Hill, W. A. D. Griffiths
Publikováno v:
Journal of Dermatological Treatment. 8:127-131
Three cases of classical type I pityriasis ruba pilaris (PRP) treated with zidovudine (AZT) are reported. All three patients were healthy and did not have human immunodeficiency virus (HIV) infection. Recently seven cases of PRP associated with HIV i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::47682cb3fbb51dddb7b551e7a1022884
https://doi.org/10.3109/09546639709160285
https://doi.org/10.3109/09546639709160285
Publikováno v:
Journal of the European Academy of Dermatology and Venereology : JEADV. 27(1)
Adult pityriasis rubra pilaris (PRP) type 1 is a rare chronic papulosquamous disorder with clinical and histological parallels with psoriasis. Treatment is challenging and recent case reports suggest a potential role for tumour necrosis factor (TNF)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::91a0cc098dc0287c4a66a6b3c96cf57e
https://pubmed.ncbi.nlm.nih.gov/22324561
https://pubmed.ncbi.nlm.nih.gov/22324561
Publikováno v:
Clinical and experimental dermatology. 36(2)
Summary Erythema gyratum repens (EGR) is a rare cutaneous eruption characterized by serpiginous morphology and a migrating scaly border. It is one of the most specific cutaneous paraneoplastic phenomena, and is associated with malignancy in most case
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dfb081491caa6aaa18b1eee2715ba95a
https://pubmed.ncbi.nlm.nih.gov/20637029
https://pubmed.ncbi.nlm.nih.gov/20637029
Autor:
Hiroshi Shimizu, P. H. McKee, J. S. Ross, W. A. D. Griffiths, Martin M. Black, N. P. Smith, Balbir S. Bhogal
Publikováno v:
Journal of Cutaneous Pathology. 19:212-216
We report three patients with pemphigoid nodularis. Patients were females aged 76, 71 and 50 years, and all had features of bullous pemphigoid together with prurigo-like lesions at some stage of their illness. In two cases, nodular lesions preceded t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::654aa975eb03c5f83a2d80a2cc8ef63c
https://doi.org/10.1111/j.1600-0560.1992.tb01661.x
https://doi.org/10.1111/j.1600-0560.1992.tb01661.x
Publikováno v:
Clinical and Experimental Dermatology. 24:428-430
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a47164b64a98b2ac5e2eb7f32d743805
https://doi.org/10.1046/j.1365-2230.1999.00522.x
https://doi.org/10.1046/j.1365-2230.1999.00522.x
Publikováno v:
British Journal of Dermatology. 141:544-546
Netherton's syndrome is a rare autosomal recessive condition with variable expression. It comprises an ichthyosiform dermatitis and erythroderma of variable intensity and manifestations, associated with hair abnormalities. The pathognomonic finding (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::85d73391046df21623250f02d1f2d178
https://doi.org/10.1046/j.1365-2133.1999.03056.x
https://doi.org/10.1046/j.1365-2133.1999.03056.x
Publikováno v:
The Lancet. Oncology. 6(11)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::68609aeabf7aa385e33c81edd0a49f0d
https://pubmed.ncbi.nlm.nih.gov/16257800
https://pubmed.ncbi.nlm.nih.gov/16257800