Zobrazeno 1 - 10
of 78
pro vyhledávání: '"J J, Cream"'
Publikováno v:
Clinical Genetics. 16:297-300
A study of the family of a patient who had an SLE-like syndrome and an extremely low serum C4 revealed an inheritance of C4 types and HLA region markers which indicated that the patient had 60--70% of "normal" C4 level prior to the onset of disease.
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
Autor:
S. C. M. Stern, J. J. Cream, B. Muller, A. Frankel, A. M. Farrell, D. Woodrow, K. El-Ghariani
Publikováno v:
Clinical and Experimental Dermatology. 24:19-22
We describe a 69-year-old woman who presented with purpura on the legs. Examination of a blood film revealed a homogenous population of abnormal lymphoid cells with villous projections. The immunophenotype was consistent with a diagnosis of splenic l
Publikováno v:
British Journal of Dermatology. 135:471-474
We report a 63-year-old woman who presented with an 8-week history of widespread indurated, purpuric lesions associated with weight loss of 7 kg and several episodes of epistaxis. A skin biopsy demonstrated a lymphocytic vasculitis with haemorrhage a
Publikováno v:
Clinical Endocrinology. 43:305-310
OBJECTIVE Acne vulgaris is androgen dependent but the hormonal mechanisms are unclear. Although there have been many studies of serum hormones in women with acne there are few studies in men and the results are conflicting. We have therefore carried
Autor:
B. Ramsay, I.M. Murray-Lyon, N.A. Theodorou, J. J. Cream, F.P. Paradinas, D F Woodrow, D. Sherman
Publikováno v:
Journal of the American Academy of Dermatology. 26:105-109
A patient is described who had generalized plane xanthomas, cutaneous vasculitis, peliosis hepatis, and intraabdominal giant lymph node hyperplasia of the plasma cell type. After excision of the abdominal mass, the xanthonnas resolved and the liver r
Autor:
R U, Sidwell, A, Sandison, J, Wing, H D, Fawcett, J-E, Seet, C, Fisher, T, Nardo, M, Stefanini, A R, Lehmann, J J, Cream
Publikováno v:
The British journal of dermatology. 155(1)
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 sensitivity of
Publikováno v:
British Journal of Dermatology. 135:110-112
The ectopic deposition of ova of Schistosoma haematobium within the dermis is very rare, even in countries where infection with this trematode is widespread. When it does occur, it usually affects the genital area. We report a patient who developed e
Publikováno v:
Clinical endocrinology. 50(3)
Acne vulgaris is androgen related and in some cases is associated with excess androgen production, which in men would be mainly testicular or adrenal in origin. Ordinarily, testosterone synthesis in the testis is controlled by serum LH. In order to a
Autor:
A M, Farrell, D C, Shanson, J S, Ross, N M, Roberts, C, Fry, J J, Cream, R C, Staughton, C B, Bunker
Publikováno v:
Clinical and experimental dermatology. 23(6)
We describe an outbreak of methicillin-resistant Staphylococcus aureus (MRSA) in a dermatology day-care unit and the methods used to determine the mechanism of spread and control it. The epidemic strain had a characteristic sensitivity pattern and wa