Zobrazeno 1 - 10
of 96
pro vyhledávání: '"P J, Zilko"'
Publikováno v:
Musclenerve. 23(6)
A 10-year retrospective review was conducted to ascertain the prevalence of inclusion body myositis (IBM) in Western Australia. Seventeen patients with sporadic IBM aged 45-90 years were identified and the prevalence of IBM was calculated to be 9.3 x
Autor:
James McCluskey, V. J. McCann, R. L. Dawkins, D. Feeney, G. J. O'Neill, P. J. Zilko, P. H. Kay, F.T. Christiansen
Publikováno v:
Tissue Antigens. 21:159-160
Publikováno v:
Annals of neurology. 38(6)
The genetic predisposition to inclusion body myositis (IBM) is probably multifactorial. The deposition of the beta-amyloid protein is a characteristic histological feature of both IBM and Alzheimer's disease (AD). The epsilon 4 allele of apolipoprote
Publikováno v:
Australian and New Zealand Journal of Medicine. 10:39-43
Summary: Immunological status may predict clinical outcome in BCG treated melanoma. P. M. Reynolds. G. Grimsley. R. L. Dawkins, M. J. Byrne and P. J. Zilko. Aust. N.Z. J. Med., 1980, 10, pp. 39–43. Twenty-seven patients with surgically reseated sta
Publikováno v:
Proceedings of the Royal Society of Medicine. 70:118-122
Thirty-seven patients were studied before and during treatment with respect to immune status, clinical response and development of adverse effects and autoantibodies. The baseline immune status was not predictive in terms of the above features, apart
Publikováno v:
Australian and New Zealand Journal of Medicine. 16:329-335
Scleromyxedema (lichen myxedematosus) is a rare cutaneous manifestation in patients with idiopathic inflammatory myopathy. The clinical and histological findings in three patients with this association are presented. Two patients had a severe inflamm
Autor:
P. J. Zilko, Roger L. Dawkins
Publikováno v:
The American Journal of Medicine. 59:448-452
Described here is a 59 year old man with dermatomyositis and hypogammaglobulinemia. His muscle power improved after corticosteroid therapy, but extensive amyloidosis and repeated infections appeared. Bone marrow morphology suggested multiple myeloma,
Publikováno v:
Arthritis & Rheumatism. 24:743-746
Publikováno v:
The American Journal of Digestive Diseases. 20:1076-1080
This report documents a case of cystic lymphangiomyoma of the sigmoid colon in a 35-year-old woman who presented with symptoms of a protein-losing enteropathy. This case was unique in that it involved not only the colonic wall and mesentery but also
Publikováno v:
Clinical Immunology and Immunopathology. 14:222-230
Suppressor lymphocyte activity measured by a concanavalin A stimulation method was reduced in myasthenia gravis patients with HLA-B8 and DRW3. These patients also had cold reactive lymphocytotoxic antibodies but these two abnormalities did not correl