Zobrazeno 1 - 10
of 395
pro vyhledávání: '"J. Ormos"'
Autor:
P Szenohradszky, E Szederkényi, Béla Iványi, Zita Morvay, F Marofka, E. Csajbók, J. Ormos, G Smehak
Publikováno v:
Transplantation Proceedings. 31:2107-2111
Autor:
J. Ormos, Béla Iványi, Béla Bozóky, Tibor Krenács, László Krenács, Zoltan Laszik, Zsolt Rázga
Publikováno v:
Journal of Histotechnology. 14:75-80
Intracellular, extracellular, and bacterial antigens were demonstrated ultrastructurally by means of silver enhanced immunogold marker systems (IGSS method). Mild fixation provided a suitable compromise between the ultrastructural and antigenic prese
Publikováno v:
Pathology - Research and Practice. 187:178-183
The cellular infiltration in 42 needle and wedge biopsies of transplanted kidneys was investigated immunohistochemically. The percentages of helper/inducer (CD 4+) cells, suppressor/cytotoxic cells (CD 8+), B lymphocytes, macrophages, plasma cells (P
Publikováno v:
Zeitschrift für Gastroenterologie. 46
Publikováno v:
Transplantation proceedings. 30(5)
Publikováno v:
Orvosi hetilap. 138(42)
In two nephrology centres between 1983 and 1993 among 1545 kidney biopsies 34 cases of thin basement membrane nephropathy have been diagnosed. All patients had a varying degree of microscopic dysmorph haematuria, occasional slight proteinuria--except
Publikováno v:
Orvosi hetilap. 137(41)
The nail-patella syndrome is a hereditary disorder showing an autosomal dominant trait. It is characterized by a series of skeletal disorders and nephropathy. The skeletal defects and the renal involvement might occur separately. The usual clinical p
Publikováno v:
Orvosi hetilap. 135(45)
The correlation of B mode and Doppler sonographic parameters and diagnoses established by histological examination of graft biopsies, nephrectomies and clinical data are discussed. 48 histological samples from 36 patients were reevaluated. The maximu
Publikováno v:
Orvosi hetilap. 133(38)
IgG lambda type of monoclonal gammopathy and thin basement membrane nephropathy were established in a middle-aged man examined because of persistent haematuria, lambda light-chain proteinuria and moderately diminished renal function. A 10% level of p
Publikováno v:
Pediatric nephrology (Berlin, Germany). 6(1)
A 14-year-old boy with persistent proteinuria (1.6-4.0 g/day), microscopic haematuria, moderate hypertension, macrothrombocytopenia (giant platelets, platelet number 30 x 10(9)/l) and a familial sensorineural hearing loss (the father and the brother