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排序方式: 共有572条查询结果,搜索用时 421 毫秒
531.
532.
533.
Thoracic actinomycosis: CT findings 总被引:8,自引:0,他引:8
534.
Patellar tendinosis (jumper's knee): findings at histopathologic examination, US, and MR imaging. Victorian Institute of Sport Tendon Study Group 总被引:11,自引:0,他引:11
535.
Effect of dialysate calcium concentrations on intradialytic blood pressure course in cardiac-compromised patients 总被引:1,自引:0,他引:1
FM van der Sande EC Cheriex WH van Kuijk KM Leunissen 《American journal of kidney diseases》1998,32(1):125-131
To prevent hypercalcemia in the treatment of secondary hyperparathyroidism, low calcium (L-Ca) dialysate is advocated. However, changes in ionized calcium (i-Ca) levels have a pivotal role in myocardial contraction and could influence blood pressure stability during dialysis. Recently, our group found in patients with normal cardiac function a significant decrease in blood pressure (decrease in systolic blood pressure [DSBP]: -13 mm Hg and decrease in mean arterial pressure [DMAP]: -7 mm Hg) during dialysis with L-Ca dialysate compared with high calcium (H-Ca) dialysate, and this was mainly related to a decreased left ventricular contractility with use of L-Ca dialysate. On the basis of these data, it could be expected that changes in i-Ca levels during dialysis are of more clinical importance in cardiac-compromised patients (CCpts), New York Heart Association classifications III and IV. In this study, the effects of L-Ca dialysate (1.25 mmol/L) and H-Ca dialysate (1.75 mmol/L) on arterial blood pressure parameters (systolic [SBP], diastolic [DBP], and mean arterial blood pressure [MAP]), heart rate, stroke distance (SDist), and minute distance (MDist) during 3 hours of a standardized ultrafiltration/hemodialysis (UF+HD) in nine CCpts was investigated. i-Ca levels increased significantly with H-Ca dialysate UF+HD, whereas there was no change with L-Ca dialysate. SBP, DBP, and MAP decreased statistically and clinically significantly during UF+HD with L-Ca dialysate and were significantly lower with the use of L-Ca dialysate compared with H-Ca dialysate. SDist and MDist decreased significantly with L-Ca dialysate, whereas there were no changes in SDist and MDist with H-Ca dialysate. The predialysis and postdialysis index of systemic vascular resistance (SVRI) was similar between L-Ca dialysate and H-Ca dialysate use. Between the two groups, there were no significant differences in changes in SVRI. From this study, we can conclude that changes in i-Ca levels are a very important determinant of the blood pressure response during UF+HD in CCpts, and this response is mediated by changes in myocardial contractility. 相似文献
536.
Storage pool deficiency in cattle with the Chediak-Higashi syndrome results from an absence of dense granule precursors in their megakaryocytes 总被引:1,自引:0,他引:1
Platelets from cattle with the Chediak-Higashi syndrome (CHS) have a storage pool deficiency and virtual absence of platelet dense granules. Megakaryocytes (MKs) from five control (n = 135) and five CHS (n = 133) cattle were evaluated using standard transmission electron microscopy. Osmiophilic dense granules were not observed in control or CHS MKs. In MKs from normal cattle, clear vesicles of 200- to 650-nm diameter bounded by a sharp membrane were observed. They were easily differentiated from the demarcation membrane system, endoplasmic reticulum, and alpha granules. The clear vesicles were virtually absent in MKs from CHS cattle at all stages of maturation. MKs in bone marrow samples from two control (n = 91) and two CHS (n = 61) cattle that had been processed for the uranaffin reaction were also evaluated. The clear vesicles were replaced by uranaffin-positive granules in MKs from control cattle, but positive uranaffin granules were not observed in CHS MKs. These findings indicate that the platelet dense granule storage pool deficiency in CHS cattle results from an anatomic absence of dense granule precursors in maturing and mature CHS MKs. 相似文献
537.
Diadenosine 5',5'-p1,p4-tetraphosphate deficiency in blood platelets of the Chediak-Higashi syndrome
Diadenosine tetraphosphate (AP4A) is an unusual nucleotide found in a variety of cells, including platelets. It has been suggested that platelet AP4A is stored in the dense granules and is metabolically inactive. We have studied the AP4A content of blood platelets in two patients and three cattle with Chediak-Higashi syndrome (CHS), a hereditary platelet defect with dense granule deficiency. Acid-soluble extractions of whole blood and platelets were neutralized. The adenosine triphosphate (ATP) level was measured by luminescence technique. To measure the AP4A content, the neutralized extract was treated with phosphomonoesterase for removal of ATP. The AP4A content was then measured by coupling the phosphodiesterase and luciferase reaction. The AP4A content was 0.43 nmol/mg protein for normal human platelets and 0.004 nmol/mg protein for CHS platelets. The ATP/AP4A ratio was 67 for normal and 3,023 for CHS platelets. The whole blood AP4A was reduced by 89% in CHS patients who had only a slight decrease in ATP level (26% reduction). Similarly, bovine platelets with CHS showed a marked decrease of AP4A content and a moderate reduction of the ATP level. The platelet ATP/AP4A ratio was 351 and 3,133 for normal and CHS cattle, respectively. Results demonstrate a marked reduction of AP4A in CHS platelets and suggest that AP4A may be a useful marker for the measurement of dense granule content in platelets. 相似文献
538.
Induction of mutations in Ki-ras and INK4a in liver tumors of mice exposed in utero to 3-methylcholanthrene 总被引:2,自引:1,他引:1
An understanding of the basic mechanisms responsible for the pathogenesis
of liver neoplasms is needed in order to develop better therapeutic
strategies. The present study utilized a pharmacogenetic mouse model to
assess the role of cytochrome P4501A1 (Cyp1a1) in modulating genetic damage
to oncogenic and tumor suppressor loci following in utero exposure to the
polycyclic aromatic hydrocarbon, 3- methylcholanthrene (MC). Analysis of
the Ha-ras, Ki-ras, INK4a and p53 genes was carried out with lysates from
paraffin-embedded liver tissue from transplacentally-treated mice. The
lysates were subjected to DNA amplification by the PCR technique followed
by allele-specific oligonucleotide hybridization screening and SSCP
analysis. All of the 26 neoplasms screened (23 hepatocellular carcinomas,
two hepatocellular adenomas and one sarcoma) exhibited a GGC-->CGC
(GLY13-->ARG13) transversion at the Ki-ras gene locus. None of the
tumors had Ki-ras mutations at codon 12 of exon 1. Approximately 12% (3/26)
of the liver tumors exhibited point mutations in exon 1 of the INK4a gene,
with each of the three tumors exhibiting two point mutations. Analysis of
exon 2 of the INK4a gene showed the presence of a CCG-->CTG
(PRO73-->LEU73) transition in two of the 26 neoplasms. No mutations were
found in exons 1 or 2 of the Ha-ras gene, or in exons 5-8 of the p53 gene.
Analysis of tumor RNAs showed overexpression of Ha-ras, cip1 and c-jun in
approximately 38% of the liver tumor samples. The results of this study
suggest that mutagenic damage to oncogenes and tumor suppressor genes may
be critical factors in mediating transplacentally-induced liver
tumorigenesis. The fact that Ki-ras mutations were found in all of the
tumors suggests that mutation at this gene locus may be an early event in
liver tumor pathogenesis, while mutation in tumor suppressor genes may
occur later during tumor progression. These combined results are consistent
with the pathogenesis of cancer in humans.
相似文献
539.
540.
BACKGROUND: Noncomplement-fixing white cell antibodies have been demonstrated by the use of immunofluorescence flow cytometry against intact lymphocytes. However, such antibodies may be either HLA-specific or directed against other white cell antigens. Commercial enzyme-linked immunosorbent assay (ELISA) kits, using solubilized HLA molecules as targets, enable such HLA-specific antibodies to be detected in patients who are refractory to platelet transfusion, patients experiencing febrile transfusion reactions, and patients whose sera give nonspecific hemagglutination in indirect antiglobulin tests. STUDY DESIGN AND METHODS: Sera from all three groups of patients, previously screened for cytotoxic antibodies by using complement-dependent lymphocytotoxicity, were re-investigated with commercial ELISA kits for HLA antibody screening and identification using the manufacturers' recommended test methods. RESULTS: Non-complement fixing HLA antibodies were detected by ELISA in many sera that were lymphocytotoxicity test- negative; that is, 14 (17.5%) of 80 from refractory patients, 8 (23.5%) of 34 from those with febrile reactions, and 11 (22.4%) of 49 from those with nonspecific hemagglutination in the direct antiglobulin test. However, not all cytotoxic white cell antibodies were detectable by ELISA: only 19 (82.6%) of 23, 19 (67.8%) of 28, and 11 (73.6%) of 49, respectively in the three groups. Similarly, only 143 (79.4%) of 181 cytotoxic sera with clear-cut HLA-A or -B locus specificities were detectable by ELISA. CONCLUSION: ELISAs detect some but not all clinically significant HLA antibodies, irrespective of their ability to fix complement in vitro. 相似文献