Zobrazeno 1 - 10
of 25
pro vyhledávání: '"R U, Sidwell"'
Autor:
J.-E. Seet, Alan R. Lehmann, Tiziana Nardo, Cyril Fisher, Heather Fawcett, Jonathan F. Wing, A Sandison, Miria Stefanini, J. J. Cream, R. U Sidwell
Publikováno v:
British Journal of Dermatology. 155:81-88
Background Xeroderma pigmentosum (XP) is an autosomal recessive disorder of, in most cases, defective nucleotide excision repair (NER) of ultraviolet radiation (UV)- and chemical-induced DNA damage. The condition is characterized by an increased sens
Publikováno v:
Clinical and Experimental Dermatology. 31:208-211
Erratum. Notice is given that it has been drawn to the attention of the journal that the dermal filler used in this case was erroneously identified as Artecoll®. The authors submitted this article in good faith on the strength of documentary evidenc
Trichophyton erinaceikerion barbae from a hedgehog with direct osculatory transfer to another person
Publikováno v:
Clinical and Experimental Dermatology. 39:38-40
We describe a case of kerion tinea barbae infection due to Trichophyton erinacei in a 37-year-old man. The infection had also been transferred to his partner by direct contact from kissing. T. erinacei is a zoophilic dermatophyte occasionally harbour
Autor:
Robert C.D Staughton, Nicholas Francis, R. U. Sidwell, Sophie A Grabczynska, Louise A Brueton
Publikováno v:
Journal of the American Academy of Dermatology. 50:53-56
Winchester syndrome is a rare genetic disorder, one of the inherited osteolysis disorders which are a group of diseases characterized by destruction and resorption of affected bones with consequent skeletal deformities and functional impairment. The
Publikováno v:
Pediatric Dermatology. 21:66-69
Neonatal hemangiomatosis is a well-recognized cause of left ventricular failure. We describe an infant with neonatal hemangiomatosis and an ostium secundum atrial septal defect who developed severe right heart failure. This was due to the combination
Publikováno v:
Archives of Disease in Childhood. 83:59-63
BACKGROUND Dystrophic epidermolysis bullosa (DEB) is an uncommon genetic disorder of the skin and mucosae. In 1996, we reported the occurrence of lethal dilated cardiomyopathy (DCM) in two affected children. METHODS In the past seven years we have ro
Autor:
James S.A. Green, Nerys M. Roberts, Nicholas Francis, R. U. Sidwell, K. L. Agnew, Christopher B Bunker, Victoria M. Yates, Nicholas Madden
Publikováno v:
Journal of Pediatric Surgery. 40:1329-1331
Granuloma annulare (GA) is a benign inflammatory disorder of unknown etiology characterized histologically by dermal palisading granulomas with central degeneration of collagen (necrobiosis). There is a rare subcutaneous clinical variant, this occurr
Publikováno v:
Clinical and Experimental Dermatology. 29:630-632
Dermalive, an injectable skin filler composed of a combination of synthetic hyaluronic acid and acrylic hydrogel particles was recently developed for soft tissue augmentation. Dermalive produces longer term results than temporary injectable fillers a
Publikováno v:
Clinical and Experimental Dermatology. 28:323-325
Publikováno v:
Clinical and Experimental Dermatology. 27:526-528