Zobrazeno 1 - 10
of 66
pro vyhledávání: '"R B Gordon"'
Publikováno v:
American Journal of Roentgenology. 165:839-845
The purposes of this study were to analyze the CT features of scirrhous carcinoma of the gastrointestinal (GI) tract and to assess the usefulness of CT in detecting and staging these lesions.This is a retrospective evaluation of 31 proven cases of sc
Publikováno v:
Radiology. 195:131-134
Two percent glutaraldehyde on colonic mucosa may result in a toxic colitis, and the clinical features may mimic those of colonic ischemia. The study was performed to determine the radiologic appearance of glutaraldehyde-induced toxic colitis.A retros
Autor:
R B, GORDON
Publikováno v:
Educational focus. 17(3)
Publikováno v:
Radiology. 185:769-775
In 19 patients with closed-loop intestinal obstruction, including 16 patients with strangulating obstruction, the findings at examination with computed tomography (CT) were retrospectively correlated with the surgical and pathologic findings and eval
Publikováno v:
American Journal of Roentgenology. 154:499-503
The CT and radiologic findings in 11 patients (five with AIDS and six without AIDS) with ileocecal tuberculosis are described. On CT scans, five cases showed mild circumferential wall thickening of the terminal ileum and cecum, thickening of the ileo
Publikováno v:
American Journal of Roentgenology. 154:281-285
Pitfalls in CT diagnosis of acute diverticulitis were investigated in 16 patients with the disease who had misleading or equivocal CT features. The CT appearance was correlated with contrast enemas (13 cases) and with surgical assessment and patholog
Autor:
J P, Kraus, M, Janosík, V, Kozich, R, Mandell, V, Shih, M P, Sperandeo, G, Sebastio, R, de Franchis, G, Andria, L A, Kluijtmans, H, Blom, G H, Boers, R B, Gordon, P, Kamoun, M Y, Tsai, W D, Kruger, H G, Koch, T, Ohura, M, Gaustadnes
Publikováno v:
Human mutation. 13(5)
The major cause of homocystinuria is mutation of the gene encoding the enzyme cystathionine beta-synthase (CBS). Deficiency of CBS activity results in elevated levels of homocysteine as well as methionine in plasma and urine and decreased levels of c
Publikováno v:
Human mutation. 11(4)
RT-PCR and direct sequence analyses were used to define mutations in the cystathionine beta-synthase (CBS) gene in two unrelated male patients with vitamin B6 nonresponsive homocystinuria. Both patients were compound heterozygotes for CBS alleles con
Publikováno v:
AJR. American journal of roentgenology. 168(3)
The purpose of this study was to describe and analyze the CT features of small-bowel lymphoma, compare those features with the radiographic presentation in immunocompetent patients and patients with AIDS, and discuss the role of CT in the initial det
Publikováno v:
European journal of human genetics : EJHG. 5(1)
Homocystinuria, due to a deficiency of the enzyme cystathionine beta-synthase (CBS), is an inborn error of sulphur-amino acid metabolism. This is an autosomal recessive disease which results in hyperhomocysteinaemia and a wide range of clinical featu