15 results on '"Saito, Hajime"'
Search Results
2. Outcomes of patients receiving additional esophagectomy after endoscopic resection for clinically mucosal, but pathologically submucosal, squamous cell carcinoma of the esophagus
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Motoyama, Satoru, Jin, Mario, Matsuhashi, Tamotsu, Nanjo, Hiroshi, Ishiyama, Koichi, Sato, Yusuke, Yoshino, Kei, Sasaki, Tomohiko, Wakita, Akiyuki, Saito, Hajime, Minamiya, Yoshihiro, Ohnishi, Hirohide, and Ogawa, Jun-ichi
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- 2013
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3. Tumoral CRP expression in thoracic esophageal squamous cell cancers is associated with poor outcomes
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Nakatsu, Toshinobu, Motoyama, Satoru, Maruyama, Kiyotomi, Usami, Shuetsu, Sato, Yusuke, Miura, Masatomo, Hinai, Yudai, Saito, Hajime, Minamiya, Yoshihiro, Murata, Katsuyuki, and Ogawa, Jun-ichi
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- 2012
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4. CRP Genetic Polymorphism Is Associated with Lymph Node Metastasis in Thoracic Esophageal Squamous Cell Cancer
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Motoyama, Satoru, Miura, Masatomo, Hinai, Yudai, Maruyama, Kiyotomi, Usami, Shuetsu, Saito, Hajime, Minamiya, Yoshihiro, Satoh, Shigeru, Murata, Katsuyuki, Suzuki, Toshio, and Ogawa, Jun-ichi
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- 2009
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5. REG Iα Promotes PD-L1 Expression in Esophageal Cancer Cells
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WAKITA, Akiyuki, MOTOYAMA, Satoru, SATO, Yusuke, KOYOTA, Souichi, YOSHINO, Kei, SASAKI, Tomohiko, IMAI, Kazuhiro, SAITO, Hajime, and MINAMIYA, Yoshihiro
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PD-L1 ,esophageal cancer ,REG Iα - Published
- 2015
6. Esophageal Cancer Patients Have a High Incidence of Severe Periodontitis and Preoperative Dental Care Reduces the Likelihood of Severe Pneumonia after Esophagectomy.
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Sato, Yusuke, Motoyama, Satoru, Takano, Hiroshi, Nakata, akira, Liu, Jiajia, Harimaya, Daiki, Todo, Naoto, Yoshino, Kei, Sasaki, Tomohiko, Wakita, akiyuki, Kawakita, Yuta, Imai, Kazuhiro, Saito, Hajime, Fukuda, Masayuki, and Minamiya, Yoshihiro
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DIAGNOSIS of esophageal cancer ,ESOPHAGEAL cancer risk factors ,PERIODONTITIS ,RISK factors of periodontal disease ,ESOPHAGECTOMY ,DISEASE risk factors - Abstract
Background: Poor oral health is a risk factor for causing upper aerodigestive tract tumors, including esophageal cancer. Our aim was to determine the periodontitis rate in our cohort of esophageal cancer patients. We also analyzed whether preoperative dental examination and care reduces the likelihood of severe pneumonia after esophagectomy. Study Design: Between 2003 and 2014, 529 esophageal cancer patients received esophagectomy at Akita University Hospital. We studied 232 patients who had preoperative dental examinations and care (dental care group) retrospectively and assessed the severity of their periodontitis. Thedental care group was compared to 297 patients who did not have preoperative dental care (control group) with respect to the incidence of severe pneumonia after esophagectomy. Results: Ninety-one patients (39.2%) in the dental care group were diagnosed with slight periodontitis and 69 (29.7%) were diagnosed with severe periodontitis. Among all the patients, 69 patients (13.0%) were diagnosed with grade 3B postoperative severe pneumonia. The dental care group had a significantly lower incidence of severe pneumonia than the control group. Moreover, multivariable logistic regression analysis revealed that anastomotic leakage, preoperative dental care, gender and %VC were correlated significantly with the occurrence of postoperative severe pneumonia. Conclusion: Preoperative dental examination and care by a dentist are essential to reduce the likelihood of postoperative severe pneumonia in esophageal cancer patients. [ABSTRACT FROM AUTHOR]
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- 2016
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7. Novel Candidate Biomarkers of Chemoradiosensitivity in Esophageal Squamous Cell Carcinoma: A Systematic Review.
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Sato, Yusuke, Motoyama, Satoru, Saito, Hajime, and Minamiya, Yoshihiro
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ESOPHAGEAL cancer ,BIOMARKERS ,SQUAMOUS cell carcinoma ,CANCER prognosis ,CANCER patients - Abstract
There is no doubt that, along with surgery, chemoradiotherapy is an important treatment for esophageal squamous cell carcinoma (ESCC). Patients who respond well to chemoradiotherapy obtain great benefits toward overcoming their cancer, and so a more favorable prognosis. On the other hand, patients who do not respond well have wasted valuable time and experienced severe toxicity and seriously diminished quality of life, only to have their cancer recur with an unfavorable prognosis. For this reason, a reliable biomarker of chemoradiosensitivity in ESCC has long been sought. In this review, we will enumerate recently reported candidate biomarkers of chemoradiosensitivity in ESCC that have the potential for future clinical application. [ABSTRACT FROM AUTHOR]
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- 2016
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8. Two cases of cisplatin-induced permanent renal failure following neoadjuvant chemotherapy for esophageal cancer.
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Sasaki, Tomohiko, Motoyama, Satoru, Komatsuda, Atsushi, Shibata, Hiroyuki, Sato, Yusuke, Yoshino, Kei, Wakita, Akiyuki, Saito, Hajime, Anbai, Akira, Jin, Mario, and Minamiya, Yoshihiro
- Abstract
Introduction We experienced two esophageal cancer patients who developed severe acute renal failure after neoadjuvant chemotherapy with cisplatin and 5-fluorourasil. Presentation of case After administration of cisplatin, their serum creatinine increased gradually until they required hemodialysis and their renal failure was permanent. In both cases, renal biopsy examination indicated partial recovery of the proximal tubule, but renal function did not recover. After these events, one patient underwent definitive radiotherapy and the other underwent esophagectomy for their esophageal cancers, while continuing dialysis. Both patients are alive without cancer recurrence. Discussion In these two cases of cisplatin-induced renal failure, renal biopsy examination showed only slight disorder of proximal tubules and tendency to recover. Conclusion Although cisplatin-related nephrotoxicity is a well-recognized complication, there have been few reports of renal failure requiring hemodialysis in cancer patients. In this report, we present their clinical courses and the pathological findings of cisplatin-related renal failure. [ABSTRACT FROM AUTHOR]
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- 2016
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9. Status of Involved Lymph Nodes and Direction of Metastatic Lymphatic Flow Between Submucosal and T2-4 Thoracic Squamous Cell Esophageal Cancers.
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Motoyama, Satoru, Maruyama, Kiyotomi, Sato, Yusuke, Usami, Shuetsu, Nakatsu, Toshinobu, Saito, Hajime, Minamiya, Yoshihiro, and Ogawa, Jun-ichi
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DISSECTION ,SURGERY ,LYMPH nodes ,LYMPHATICS ,SQUAMOUS cell carcinoma ,ESOPHAGEAL cancer - Abstract
Three-field lymph node dissection for thoracic esophageal cancer is associated with high morbidity and reduced quality of life after surgery. Consequently, minimized lymphadenectomy would be desirable, if appropriate. In the present study, we retrospectively analyzed the status of involved nodes and the direction of metastatic lymphatic flow from tumors into involved nodes to determine whether submucosal squamous cell esophageal cancers are potential candidates for minimized lymphadenectomy. We enrolled 199 patients who received esophagectomy with extensive lymph node dissection between 1989 and 2005 and retrospectively analyzed their prognoses, distribution of solitary metastatic lymph nodes, and the direction of metastatic lymphatic flow from the tumor, taking into consideration tumor location and depth. Of these patients with submucosal cancers, 83% had 1 or 2 involved nodes, and their esophageal cancer-specific 5-year survival rate was 66%. Solitary lymph node metastasis did not occur in neck lymph nodes in lower thoracic submucosal esophageal cancers, and the direction of metastatic lymphatic flow from the tumor was almost always in one direction. By contrast, T2–4 cancers with 2–4 involved nodes had bidirectional metastatic lymphatic flow from the tumor. There was a difference in the status of lymph node metastasis and the direction of metastatic lymphatic flow from tumors into involved nodes between submucosal and T2–4 thoracic squamous cell esophageal cancers. This analysis may be useful for developing an approach to minimized lymphadenectomy for thoracic esophageal cancers. [ABSTRACT FROM AUTHOR]
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- 2009
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10. Preoperative mapping of lymphatic drainage from the tumor using ferumoxide-enhanced magnetic resonance imaging in clinical submucosal thoracic squamous cell esophageal cancer.
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Motoyama, Satoru, Ishiyama, Koichi, Maruyama, Kiyotomi, Okuyama, Manabu, Sato, Yusuke, Hayashi, Kaori, Nanjo, Hiroshi, Saito, Hajime, Minamiya, Yoshihiro, and Ogawa, Jun-ichi
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OPERATIVE surgery ,MAGNETIC resonance imaging of cancer ,ESOPHAGEAL cancer ,METASTASIS - Abstract
Background: In thoracic esophageal cancer, lymph node metastases distribute widely from the neck to the abdominal area as a result of a complex periesophageal lymphatic network. The aim of the present study was to evaluate the potential clinical utility of a new method of mapping lymphatic drainage from tumors using ferumoxide-enhanced magnetic resonance imaging (MRI). Methods: Twenty-three patients with clinical submucosal thoracic squamous cell esophageal cancer were examined. Ferumoxides were injected endoscopically into the peritumoral submucosal layer, after which their appearance in the lymph nodes in the neck, superior mediastinum, and abdomen was evaluated using MRI. Results: Flux of ferumoxides from tumors was detected in all 23 patients. Among the 20 patients with middle and lower thoracic esophageal cancers, there was no lymphatic drainage to the neck in 5 (25%) patients, none to the neck and superior mediastinum in 4 (20%), and none to the abdomen in 2 (10%), which could enable the extent of lymph node dissection to be reduced. We diagnosed clinical negative lymph node metastasis (N0) in 17 patients; the remaining 6 patients were diagnosed with clinical lymph node metastasis. Two patients (12%) diagnosed clinical N0, showed pathologic lymph node metastasis. Ferumoxide-enhanced MRI detected an influx of contrast agent into the metastatic node in both patients. Conclusions: Ferumoxide-enhanced MRI lymphatic mapping enables detection of the direction and area of lymphatic flux. It thus has the potential to improve our ability to gauge the appropriate extent of treatment in clinical submucosal squamous cell esophageal cancer. [Copyright &y& Elsevier]
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- 2007
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11. Surgical Outcome of Colon Interposition by the Posterior Mediastinal Route for Thoracic Esophageal Cancer.
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Motoyama, Satoru, Kitamura, Michihiko, Saito, Reijiro, Maruyama, Kiyotomi, Sato, Yusuke, Hayashi, Kaori, Saito, Hajime, Minamiya, Yoshihiro, and Ogawa, Jun-ichi
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ESOPHAGEAL cancer ,CANCER patients ,CHEST diseases ,MEDICAL research - Abstract
Background: For thoracic esophageal cancer patients with a history of gastrectomy, esophageal reconstruction using segments of colon was often accomplished using the anterior mediastinal route to avoid fatal complications related to colon necrosis. Our aim was to review our experience with reconstruction by the posterior mediastinal route and assess the surgical outcomes. Methods: Between 1989 and August 2006, 34 esophageal cancer patients at Akita University Hospital underwent esophageal reconstruction accomplished by colon interposition by the posterior mediastinal route. Data from these patients were reviewed. Results: Colon conduits consisted of left colon segments in 4 patients and right colon segments in 30. The grafts were supplied with blood by the left colonic artery in 13 patients, the middle colonic artery in 20, and the right colonic artery in 1. The esophagocolic (pharyngocolic) anastomosis was located in the neck in 33 patients (97%) and in the thorax in 1. No patient died during the initial hospital stay. There were no instances of colon necrosis. An anastomotic fistula occurred in 3 patients (9%). Proximal anastomotic strictures occurred in 2 patients (6%). No late graft redundancies resulting in significant dysphagia occurred. Reductions in body weight did not differ from those seen when the gastric tube was used for reconstruction, and alimentary function was good after surgery. The 1-, 2-, 3-, and 5-year survival rates were 66%, 52%, 48%, and 48%, respectively. Conclusions: Colon interposition by the posterior mediastinal route provides a good outcome and is considered the route of first choice. [Copyright &y& Elsevier]
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- 2007
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12. Squamous cell carcinoma in an esophageal diverticulum below the aortic arch.
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Wakita, Akiyuki, Motoyama, Satoru, Sato, Yusuke, Yoshino, Kei, Sasaki, Tomohiko, Saito, Hajime, Minamiya, Yoshihiro, and Ogawa, Jun-ichi
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SQUAMOUS cell carcinoma ,ESOPHAGEAL cancer ,DIVERTICULUM ,THORACIC aorta ,DIVERTICULA of the hypopharynx ,VOCAL cord cancer - Abstract
Abstract: INTRODUCTION: Esophageal diverticula frequently arise from pharyngoesophageal transition area, tracheal bifurcation and epiphrenic region. Carcinoma arising from esophageal diverticulum is rarely seen. We report a patient with a squamous cell carcinoma arising within an esophageal diverticulum below the aortic arch. PRESENTATION OF CASE: A 70-year-old man was diagnosed to have a squamous cell carcinoma of the vocal cord with enlarged lymph nodes in the neck, as well as a squamous cell carcinoma arising within an esophageal diverticulum below the aortic arch. There have been no reported cases of esophageal cancer arising from a diverticulum below the aortic arch. Preoperative radiotherapy for the esophageal cancer and pharyngeal cancer was given, followed by surgery. The excised specimen of the esophageal diverticulum and its external appearance revealed that it lacked muscle fibers, with a type 0-IIa lesion arising from the diverticulum. Microscopic examination showed three lymph nodes at the superior mediastinum were positive for malignancy. Bilateral pleural dissemination was detected 7 months after esophagectomy. DISCUSSION: Cancer arising from an esophageal diverticulum is mainly found at an advanced stage because of delayed diagnosis. The absence of muscularis propia may lead to early invasion. Thus, cancers within an esophageal diverticulum are considered to be at a more advanced stage than similar cancers arising elsewhere. CONCLUSION: For detecting of cancer arising from an esophageal diverticulum, a high index of awareness is important. Delay in diagnosis makes surgical management difficult. [Copyright &y& Elsevier]
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- 2012
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13. IGFBP3 and BAG1 enhance radiation-induced apoptosis in squamous esophageal cancer cells
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Yoshino, Kei, Motoyama, Satoru, Koyota, Souichi, Shibuya, Kaori, Usami, Shuetsu, Maruyama, Kiyotomi, Saito, Hajime, Minamiya, Yoshihiro, Sugiyama, Toshihiro, and Ogawa, Jun-ichi
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PHYSIOLOGICAL effects of radiation , *APOPTOSIS , *SQUAMOUS cell carcinoma , *CANCER cells , *ESOPHAGEAL cancer , *GENE expression , *ANTINEOPLASTIC agents , *SMALL interfering RNA - Abstract
Abstract: Identification of reliable markers of radiosensitivity and the key molecules that enhance the susceptibility of esophageal cancer cells to anticancer treatments would be highly desirable. To identify molecules that confer radiosensitivity to esophageal squamous carcinoma cells, we assessed the radiosensitivities of the TE-5, TE-9 and TE-12 cloneA1 cell lines. TE-12 cloneA1 cells showed significantly greater susceptibility to radiotherapy at 5 and 10Gy than either TE-5 or TE-9 cells. Consistent with that finding, 24h after irradiation (5Gy), TE-12 cloneA1 cells showed higher levels of caspase 3/7 activity than TE-5 or TE-9 cells. When we used DNA microarrays to compare the gene expression profiles of TE-5 and TE-12 cloneA1 cells, we found that the mRNA and protein expression of insulin-like growth factor binding protein 3 (IGFBP3) and Bcl-2-associated athanogene 1 (BAG1) was five or more times higher in TE-12 cloneA1 cells than TE-5 cells. Conversely, knocking down expression of IGFBP3 and BAG1 mRNA in TE-12 cloneA1 cells using small interfering RNA (siRNA) significantly reduced radiosensitivity. These data suggest that IGFBP3 and BAG1 may be key markers of radiosensitivity that enhance the susceptibility of squamous cell esophageal cancer to radiotherapy. IGFBP3 and BAG1 may thus be useful targets for improved and more individualized treatments for patients with esophageal squamous cell carcinoma. [Copyright &y& Elsevier]
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- 2011
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14. Regenerating gene I regulates interleukin-6 production in squamous esophageal cancer cells
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Usami, Shuetsu, Motoyama, Satoru, Koyota, Souichi, Wang, Jingshu, Hayashi-Shibuya, Kaori, Maruyama, Kiyotomi, Takahashi, Naoko, Saito, Hajime, Minamiya, Yoshihiro, Takasawa, Shin, Ogawa, Jun-ichi, and Sugiyama, Toshihiro
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GENETIC regulation , *INTERLEUKIN-6 , *SQUAMOUS cell carcinoma , *CANCER cells , *ESOPHAGEAL cancer , *CYTOLOGY , *MESSENGER RNA , *CYTOKINES - Abstract
Abstract: Regenerating gene (REG) I plays important roles in cancer cell biology. The purpose of this study was to determine whether REG I affects cytokine production in cancer cells. We transfected TE-5 and TE-9 squamous esophageal cancer cells with REG Iα and Iβ and examined its effects on cytokine expression. We found that transfecting TE-5 and TE-9 cells with REG I Iα and Iβ led to significantly increased expression of interleukin (IL)-6 mRNA and protein, but it had little or no effect on expression of IL-2, IL-4, IL-5, IL-10, IL-12, IL-13, IL-17A, interferon-γ, tumor necrosis factor-α, granulocyte-colony stimulating factor or transforming growth factor-β1. The elevated IL-6 expression seen in REG Iα transfectants was silenced by small interfering RNA-mediated knockdown. These finding suggest that REG I may act through IL-6 to exert effects on squamous esophageal cancer cell biology. [Copyright &y& Elsevier]
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- 2010
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15. C-Reactive Protein 1059G>C Genetic Polymorphism Influences Serum C-Reactive Protein Levels after Esophagectomy in Patients with Thoracic Esophageal Cancer
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Motoyama, Satoru, Miura, Masatomo, Hinai, Yudai, Maruyama, Kiyotomi, Usami, Shuetsu, Nakatsu, Toshinobu, Saito, Hajime, Minamiya, Yoshihiro, Suzuki, Toshio, and Ogawa, Jun-ichi
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C-reactive protein , *GENETIC polymorphisms , *ESOPHAGECTOMY , *BLOOD proteins , *ESOPHAGEAL cancer , *CYTOKINES - Abstract
Background: Little is known about how C-reactive protein (CRP) genetic polymorphisms influence the rise in serum CRP levels seen after surgery. The purpose of this study was to assess the association between CRP polymorphisms and acute-phase serum CRP levels after esophagectomy for thoracic esophageal cancer. Study Design: We enrolled 110 patients who underwent curative esophagectomy without neoadjuvant treatment between 2003 and 2008. Using peripheral blood samples collected from the patients, polymorphisms for CRP, tumor necrosis factor, interferon-γ, tumor growth factor-β1, interleukin (IL)-1β, IL-1 receptor antagonist, IL-2, IL-4, IL-6, IL-6 receptor, IL-10, and IL-12β were all investigated to determine which, if any, affect postoperative serum CRP levels and clinical outcomes. Results: Although preoperative serum CRP levels did not differ, 12 hours after esophagectomy, serum CRP levels were significantly higher in patients carrying the CRP 1059G/G genotype than in those with the 1059G/C genotype (111 ± 35 mg/L versus 78 ± 17 mg/L; p = 0.0266), and after 36 hours CRP levels remained higher in those with the 1059G/G genotype (217 ± 63 mg/L versus 140 ± 51 mg/L; p = 0.0020). Logistic regression models revealed that patients carrying the CRP 1059G/G genotype had a significantly higher likelihood of a postesophagectomy increase in serum CRP, although the CRP 1059G>C genetic polymorphism had no effect on clinical outcomes. None of the other cytokine genetic polymorphisms influenced postoperative serum CRP levels. Conclusions: Our findings suggest that the CRP 1059G>C genetic polymorphism is 1 determinant of serum CRP levels after major surgery. [Copyright &y& Elsevier]
- Published
- 2009
- Full Text
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