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Anti-diabetic Properties of Melissa officinalis and Saffron: Recent Advances and Discoveries 厚朴和藏红花抗糖尿病作用的研究进展
IF 0.1 Q4 Medicine Pub Date : 2023-10-01 DOI: 10.12996/gmj.2023.93
S. Sanaie, Behnam Sadigi, Reza Yarani, Nikolaj Travica, Zahra Yousefi, S. Shakouri, Alireza Ostadrahimi, M. Mobasseri, Fateme Tahmasbi, Mostafa Araj-khodaei
Aim: Diabetes mellitus is a chronic medical condition characterized by an accumulation of glucose in the bloodstream. Specifically, type 2 diabetes occurs when the body’s cells are unable to efficiently respond to insulin, the hormone responsible for transporting circulatory glucose into cells. In the advanced stages of the disease, the body may also not produce sufficient amounts of insulin. As the disease progresses, the symptoms become more severe and potentially lead to a series of comorbidities. Although several medications are used to treat and control type 2 diabetes, these medications may have serious side effects. Hence, the use of herbal medicine to alleviate type 2 diabetes has been studied and has attracted widespread interest. Our major goal is to examine these herbs' effectiveness and related mechanisms of action in treating type 2 diabetes. Method : We studied worldwide traditional medicines, old texts, and published literature for anti-diabetic effect of Melissa officinalis and saffron. Electronic databases comprising PubMed, Web of Science, Science Direct, Scopus and Google Scholar were searched to collect articles published between 1990 and 2022 years. Results : We confirmed that a variety of herbal therapies, including saffron and lemon balm (Melissa officinalis), had anti-diabetic activities based on the findings of various research. Conclusion: Saffron and Melissa officinalis have anti-diabetic properties.
目的:糖尿病是一种以血液中葡萄糖积聚为特征的慢性疾病。具体来说,当身体细胞无法有效地对胰岛素做出反应时,就会发生2型糖尿病,胰岛素是负责将循环葡萄糖输送到细胞中的激素。在疾病的晚期,身体也可能无法产生足够量的胰岛素。随着疾病的发展,症状变得更加严重,并可能导致一系列合并症。尽管有几种药物用于治疗和控制2型糖尿病,但这些药物可能会产生严重的副作用。因此,使用草药来缓解2型糖尿病已经得到了研究,并引起了广泛的兴趣。我们的主要目标是检查这些草药在治疗2型糖尿病方面的有效性和相关作用机制。方法:我们研究了世界各地的传统药物、旧文献和已发表的文献中关于梅丽莎·officinalis和藏红花抗糖尿病的作用。搜索包括PubMed、Web of Science、Science Direct、Scopus和Google Scholar在内的电子数据库,以收集1990年至2022年间发表的文章。结果:根据各种研究结果,我们证实了包括藏红花和柠檬风油精(Melissa officinalis)在内的多种草药疗法具有抗糖尿病活性。结论:藏红花和梅丽莎具有抗糖尿病作用。
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引用次数: 0
Evaluation of Interobserver and Intraobserver Differences of Graf Method in Developmental Hip Dysplasia Graf方法在发育性髋关节发育不良中观察者间和观察者内差异的评价
IF 0.1 Q4 Medicine Pub Date : 2023-10-01 DOI: 10.12996/gmj.2023.86
Gelişimsel Kalça, Displazisinde Graf, Yönteminin Gözlemciler, Arası ve, Gözlemci İçi, Farklılıklarının Değerlendirilmesi, H. Doğruel, A. C. Baymurat, Ismail Cengiz Tuncay, Hakan Atalar
Purpose: The aim of this study was to evaluate possible differences in hip ultrasonography (US) results between physicians working in different medical centers. Method: In this study, a total of 117 horizontal US images representing all sonographic types of developmental dysplasia of the hip (DDH) were utilized. Four experienced researchers independently measured the 117 US images at different times. The results obtained by each researcher were documented separately, including alpha and beta angles, Graf types. All of the collected data were analyzed statistically to assess for interobserver and intraobserver variability. Results: The study found that the average change between the alpha angles ranged from a minimum of 1 to a maximum of 4. The mean change between the beta angles was wider, ranging from a minimum of 1.8 to a maximum of 8.2. To evaluate the differences between the Graf hip typologies, paired groups were formed and Cohen's Kappa method was used. For the first group k= 0.661, for the second group k= 0.671, for the third group K= 0.647, for the fourth group k= 0, 718, k= 0.717 for the fifth group and k= 0.637 for the sixth group. Interobserver Kappa evaluation results (k=0.647) showed moderate and significant agreement. Conclusion: The results revealed a moderate to substantial level of agreement between the researchers. Based on these findings, it was concluded that the use of US for screening and follow-up of the Graf hip typing method should be performed by experienced professionals.
目的:本研究的目的是评估在不同医疗中心工作的医生之间髋关节超声(US)结果的可能差异。方法:在本研究中,共使用了117张水平超声图像,代表了所有类型的髋关节发育不良(DDH)。四位经验丰富的研究人员在不同时间独立测量了117张美国图像。每个研究人员获得的结果都被单独记录下来,包括阿尔法角和贝塔角,Graf类型。对所有收集的数据进行统计学分析,以评估观察者间和观察者内的变异性。结果:研究发现,α角之间的平均变化范围从最小值1到最大值4。β角之间的平均变化范围更广,最小值为1.8,最大值为8.2。为了评估Graf-hip类型之间的差异,形成了配对组,并使用了Cohen的Kappa方法。对于第一组k=0.661,对于第二组k=0.671,对于第三组k=0.647,对于第四组k=0718,对于第五组k=0.717,对于第六组k=0.637。观察者间Kappa评价结果(k=0.647)显示中度和显著一致。结论:研究结果显示,研究人员之间存在中度到实质性的一致性。基于这些发现,我们得出结论,使用US筛查和随访Graf髋关节分型方法应由经验丰富的专业人员进行。
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引用次数: 0
Do Routine Laboratory Parameters Predict the Disease Activity in Children with Behçet’s Disease? 常规实验室参数能预测behaperet病患儿的疾病活动性吗?
IF 0.1 Q4 Medicine Pub Date : 2023-10-01 DOI: 10.12996/gmj.2023.76
Deniz Gezgin, Sevcan A Yildirim¹, Bakkaloglu, Rutin Laboratuvar, Parametreleri Behçet, Hastalığı olan, Çocuklarda Hastalık, Aktivitesini Öngörüyor
Objective. Juvenile Behçet’s disease (jBD) is a multi-systemic inflammatory disorder characterized by recurrent episodes of oral and genital aphthae, and cutaneous, gastrointestinal, neurological, articular, ocular and vascular manifestations. The main aim of this study was to assess the value of routine laboratory parameters for predicting disease activity in children with jBD. Methods. The demographic features and laboratory findings, including white blood cell, neutrophil (NEU), lymphocyte (LYM) and platelet (PLT) counts, neutrophil/ lymphocyte ratio (NLR), platelet/ lymphocyte ratio (PLR), mean platelet volume/platelet ratio (MPR) values were retrospectively evaluated between jBD patients with active and inactive, and compared with those in healthy peers. Inactive jBD was accepted as the absence of any clinical symptoms, while active jBD was accepted as presence of at least two clinical symptoms related with jBD. Results. Thirty six patients with jBD, and 58 sex-and age-matched healthy children were enrolled into this study. Median age at diagnosis of jBD was 13 (min – max: 5-17) years. 12 patients had active and remaining 24 inactive disease at enrollment. Active jBD group had significantly higher mean values for NLR, PLR, and lower MPV compared to inactive patients (p= 0.026, p= 0.039, and p= 0.07, respectively). PLR was revealed as an independent factor for predicting disease activity in jBD patients (p= 0.035, OR [95% Cl] = 0.988 [0.978-0.999]). Conclusion. This study has shown that active jBD patients had increased values of NLR and PLR. Among them PLR was the possible risk predictor for disease activity. These parameters are easily accessible inflammatory markers that may help detecting active disease in the early phase to prevent complications and to guide the therapy.
目标。青少年behet病(jBD)是一种多系统炎症性疾病,其特征是口腔和生殖器溃疡的反复发作,以及皮肤、胃肠、神经、关节、眼部和血管的表现。本研究的主要目的是评估常规实验室参数对预测jBD患儿疾病活动性的价值。方法。回顾性评价活动性和非活动性jBD患者的人口统计学特征和实验室检查结果,包括白细胞、中性粒细胞(NEU)、淋巴细胞(LYM)和血小板(PLT)计数、中性粒细胞/淋巴细胞比率(NLR)、血小板/淋巴细胞比率(PLR)、平均血小板体积/血小板比率(MPR)值,并与健康同龄人进行比较。非活动性jBD被接受为没有任何临床症状,而活动性jBD被接受为存在至少两种与jBD相关的临床症状。结果。36名jBD患者和58名性别和年龄匹配的健康儿童参加了这项研究。诊断为jBD的中位年龄为13岁(最小-最大:5-17岁)。入组时,12例患者有活动性疾病,其余24例为非活动性疾病。与不活跃患者相比,活跃jBD组NLR、PLR和MPV的平均值均显著升高(p= 0.026、p= 0.039和p= 0.07)。PLR是预测jBD患者疾病活动性的独立因素(p= 0.035, OR [95% Cl] = 0.988[0.978-0.999])。结论。本研究显示活动期jBD患者NLR和PLR值升高。其中,PLR可能是疾病活动性的危险预测因子。这些参数是容易获得的炎症标志物,可能有助于在早期发现活动性疾病,以预防并发症并指导治疗。
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引用次数: 0
Solid Tumors other than Breast Cancer are Associated with Germ-line ATM Heterozygosity 癌症以外的实体瘤与种系ATM杂合性相关
IF 0.1 Q4 Medicine Pub Date : 2023-10-01 DOI: 10.12996/gmj.2023.87
MD Oktay Ünsal, O. Yazıcı, N. Özdemir, Büşra Güvercin, A. Özet, Mehmet Ali Ergün
Objective: It is known that ATM heterozygosity is associated with increased risk of cancer, especially for breast cancer. This report reveals the characteristics of the patients with solid tumors other than breast cancer, associated with Germ-line ATM heterozygosity. Methods: Patients with germline ATM heterozygous mutation, admitted to the Department of Medical Genetics between January 2020 to 2023 were evaluated retrospectively. Patients with a diagnosis of solid tumors other than breast cancer, being followed up for at least 6 months were included in the study. Data of the patients were examinated using the SPSS software version 23. Results: Median aged at cancer diagnosis of 36 patients were 52.5 (23-65) years. The median follow-up period was 29.5 (11-283) months. Colorectal cancer was the most common diagnosis (30.6%). At follow-up, second primary solid malignancy was diagnosed in 27.8% (10 patients) of the patients. The median time for development of second primary malignancy were 9 (3-156) months. Most common diagnosis of these 10 patients were breast cancer (80%-8 patients). Conclusion: Development of various solid tumors other than breast cancer related to Germ-line ATM heterozygosity highlights the importance of ATM linked to cancer susceptibility.
目的:ATM杂合性与癌症,特别是癌症的发病风险增加有关。本报告揭示了癌症以外的实体瘤患者与生殖系ATM杂合性相关的特征。方法:对2020年1月至2023年间入住医学遗传学系的种系ATM杂合突变患者进行回顾性评估。被诊断为癌症以外实体瘤的患者,至少随访6个月,纳入研究。使用SPSS软件版本23对患者的数据进行检查。结果:36例患者诊断为癌症的中位年龄为52.5(23-65)岁。中位随访期为29.5(11-283)个月。结直肠癌癌症是最常见的诊断(30.6%)。在随访中,27.8%(10例)的患者被诊断为第二原发性实体瘤。发展为第二原发性恶性肿瘤的中位时间为9(3-156)个月。这10例患者中最常见的诊断是乳腺癌症(80%-8例)。结论:与种系ATM杂合性相关的癌症以外的各种实体瘤的发展突出了ATM与癌症易感性相关的重要性。
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引用次数: 0
Prognostic Factors for Survival in Pediatric Diffuse Midline Gliomas: The Importance of T2 FLAIR Missmatch Sign and Nimotuzumab Therapy 影响儿童弥漫性中线胶质瘤生存的预后因素:T2 FLAIR不匹配征和尼莫单抗治疗的重要性
IF 0.1 Q4 Medicine Pub Date : 2023-10-01 DOI: 10.12996/gmj.2023.84
MD Arzu Okur, Ozge Vural, Merve Yazol, Büşra Topuz Turkcan, A. Börcek, F. Pınarlı, C. Karadeniz
Purpose: The aim of this study is to investigate the clinical and radiological features, especially the importance of the T2-FLAIR mismatch sign and the response to treatment of patients diagnosed with diffuse midline gliomas (DMG) in our center. Methods: Eighteen patients treated with a diagnosis of DMG between January 2008 and January 2021 in Gazi University Medical Faculty, Department of Pediatric Oncology were retrospectively evaluated. The radiologycal evaluation was made as T2-FLAIR mismatch sign positive or negative. After a tumor board review, the diagnosis of DMG was made clinically and radiologically and all patients received local radiotherapy. Nimotuzumab was given as monotherapy or in combination with other medications Results: T2-FLAIR mismatch sign was positive for twelve patients and median OS for patients with T2-FLAIR mismatch positive and negative were 12.5 months and 9.2 months respectively (p=0.77). Median PFS for patients with T2-FLAIR mismatch sign positive and negative were 10.6 months and 4.8 months respectively (p=0.84). After nimotuzumab therapy, there was 4 cases with PR (44.4%), and 1 patient with SD (11.1%). Median OS for patients who were treated with and without nimotuzumab were 16.5 and 6.2 months respectively (p<0.05). Median PFS for patients who were treated with and without nimotuzumab were 13.3 and 3.7 months respectively (p<0.05). Conclusion: In conclusion, DMGs have poor prognosis. In our study patients with T2-FLAIR mismatch sign positive had better prognosis so it can be used as an imaging marker for prognosis. Nimotuzumab therapy may be a promising treatment option for DMG.
目的:本研究的目的是研究我们中心诊断为弥漫性中线胶质瘤(DMG)患者的临床和放射学特征,特别是T2-FLAIR错配征的重要性以及对治疗的反应。方法:回顾性评估2008年1月至2021年1月在加孜大学医学院儿科肿瘤系接受诊断为DMG治疗的18名患者。放射组学评价为T2-FLAIR错配征阳性或阴性。在肿瘤委员会审查后,对DMG进行了临床和放射学诊断,所有患者都接受了局部放疗。结果:12例患者的T2-FLAIR错配征为阳性,T2-FLAIR错配征阳性和阴性患者的中位OS分别为12.5个月和9.2个月(p=0.77)。尼莫妥珠单抗治疗后,PR患者4例(44.4%),SD患者1例(11.1%)。接受和不接受尼莫妥珠mab治疗的患者的中位OS分别为16.5和6.2个月(p<0.05)。接受或不接受尼莫妥单抗治疗的患者中位PFS分别为13.3和3.7个月(p>0.05)。结论:总之,DMG预后较差。在我们的研究中,T2-FLAIR错配征阳性的患者预后较好,因此可以作为预后的影像学标志。尼莫单抗治疗DMG可能是一种很有前景的治疗选择。
{"title":"Prognostic Factors for Survival in Pediatric Diffuse Midline Gliomas: The Importance of T2 FLAIR Missmatch Sign and Nimotuzumab Therapy","authors":"MD Arzu Okur, Ozge Vural, Merve Yazol, Büşra Topuz Turkcan, A. Börcek, F. Pınarlı, C. Karadeniz","doi":"10.12996/gmj.2023.84","DOIUrl":"https://doi.org/10.12996/gmj.2023.84","url":null,"abstract":"Purpose: The aim of this study is to investigate the clinical and radiological features, especially the importance of the T2-FLAIR mismatch sign and the response to treatment of patients diagnosed with diffuse midline gliomas (DMG) in our center. Methods: Eighteen patients treated with a diagnosis of DMG between January 2008 and January 2021 in Gazi University Medical Faculty, Department of Pediatric Oncology were retrospectively evaluated. The radiologycal evaluation was made as T2-FLAIR mismatch sign positive or negative. After a tumor board review, the diagnosis of DMG was made clinically and radiologically and all patients received local radiotherapy. Nimotuzumab was given as monotherapy or in combination with other medications Results: T2-FLAIR mismatch sign was positive for twelve patients and median OS for patients with T2-FLAIR mismatch positive and negative were 12.5 months and 9.2 months respectively (p=0.77). Median PFS for patients with T2-FLAIR mismatch sign positive and negative were 10.6 months and 4.8 months respectively (p=0.84). After nimotuzumab therapy, there was 4 cases with PR (44.4%), and 1 patient with SD (11.1%). Median OS for patients who were treated with and without nimotuzumab were 16.5 and 6.2 months respectively (p<0.05). Median PFS for patients who were treated with and without nimotuzumab were 13.3 and 3.7 months respectively (p<0.05). Conclusion: In conclusion, DMGs have poor prognosis. In our study patients with T2-FLAIR mismatch sign positive had better prognosis so it can be used as an imaging marker for prognosis. Nimotuzumab therapy may be a promising treatment option for DMG.","PeriodicalId":42791,"journal":{"name":"Gazi Medical Journal","volume":null,"pages":null},"PeriodicalIF":0.1,"publicationDate":"2023-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"45381334","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Laryngeal Amyloidosis Case Series: Rare Cause of Hoarseness 喉淀粉样变病例系列:罕见的声音嘶哑原因
IF 0.1 Q4 Medicine Pub Date : 2023-07-01 DOI: 10.12996/gmj.2023.72
Bao Ling Wong, P. S. Heng, Chian Ling Tang, Nik Fariza Husna Nik Hassan
Background: Amyloidosis is defined as a group of diseases which resulted from abnormal extracellular deposition of insoluble protein, called amyloid. It can either presented as localized or with systemic involvement. Laryngeal amyloidosis is a very rare cause of dysphonia, accounting for only 0.2 to 1.2 percent of all benign laryngeal tumours. Objectives: To highlight the clinical presentations and raise awareness of laryngeal amyloidosis among otorhinolaryngology surgeons. An index of suspicion must be conveyed to the histopathologist in the request form for them to embark on a specific staining technique. Method: We discussed two cases of laryngeal amyloidosis, with their presentations, management and the follow up. Both cases were middle aged female. The diagnosis of laryngeal amyloidosis is only by histopathological as clinically it is very ambiguous. Conclusion: The mainstay of treatment for laryngeal amyloidosis is surgical debulking but it is not curative as complete removal of the diseased tissue is difficult. In addition, the treatment should be directed towards the maintenance of the airway and the improvement of the voice.
背景:淀粉样变性是一组由细胞外不溶性蛋白(淀粉样蛋白)异常沉积引起的疾病。它既可以表现为局部的,也可以表现为全身的。喉淀粉样变是一种非常罕见的引起发音障碍的原因,仅占所有良性喉部肿瘤的0.2%至1.2%。目的:提高耳鼻喉外科医生对喉淀粉样变的认识和临床表现。在请求表格中,必须向组织病理学家传达怀疑指数,以便他们开始使用特定的染色技术。方法:对2例喉淀粉样变的临床表现、治疗及随访进行分析。两例均为中年女性。喉淀粉样变的诊断仅通过组织病理学,因为临床上它是非常模糊的。结论:喉淀粉样变性的主要治疗方法是手术减容,但由于很难完全切除病变组织,因此无法治愈。此外,治疗应针对气道的维护和声音的改善。
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引用次数: 0
Managing a Ruptured Giant Abdominal Aortic Aneurysm with Aortocaval Fistula 主动脉腔瘘治疗破裂的巨大腹主动脉瘤
IF 0.1 Q4 Medicine Pub Date : 2023-07-01 DOI: 10.12996/gmj.2023.74
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引用次数: 0
The Effects of Cerium Oxide on Sevoflurane Anesthesia and its Relationship to Renal Injury in Rats 氧化铈对七氟醚麻醉大鼠的影响及其与肾损伤的关系
IF 0.1 Q4 Medicine Pub Date : 2023-07-01 DOI: 10.12996/gmj.2023.59
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引用次数: 0
The Evaluation of the Prevalence of Improper Medication Use in Patients Age of 65 and over in Internal Diseases and Neurology Intensive Care Units in Terms of Stopp-Start Criteria 基于停止-开始标准的内科及神经内科重症监护病房65岁及以上患者不当用药发生率评估
IF 0.1 Q4 Medicine Pub Date : 2023-07-01 DOI: 10.12996/gmj.2023.62
Özdağ Erdil, H. Z. Güney
Introduction: Physiological changes are seen in many systems in the body related to aging. Treatment modalities and drug prescribing processes need to be re-evaluated in the geriatric population. To elaborate on polypharmacy, the number of drugs the individual should use must also be defined effectively. Various criteria have been developed for prescribing and using drugs for elderly individuals. The most used of these criteria is called the Beers criteria. STOPP and START criteria are other criteria used. Material and Method: Our study aimed to retrospectively evaluate the prevalence of inappropriate drug use in patients aged 65 and over who were hospitalized in the Internal Medicine and Neurology Intensive Care Units of Ankara Atatürk Training and Research Hospital in terms of STOPP-START criteria. Results: Study group consists of 168 (58,3%) female and 120 (41,7%) male. A total of 727 diseases were diagnosed in 288 patients. 201 of these were "Cerebrovascular Diseases,” 153 were "Hypertension.” While the most common STOPP criterion main group and single criterion were antiplatelet anticoagulant agent group (35,7%), “Presence of a drug class causing duplication (Aiming optimum level with a single drug before adding a new agent) (23,2%)”, respectively. At the same time, the most common START criterion main group and single criterion were cardiovascular system group (94,5%), and “Statin therapy in patients who are near the end of life or who are not older than 85 years of age, with a history of coronary, cerebral or peripheral vascular disease”, respectively (70,2%). Conclusion: It is seen that the study results are generally similar to the national literature. There are partisan differences between the study results and the international literature. It is anticipated that these differences can be attributed to the diagnostic criteria used, study group selection, and study design differences.
引言:身体中许多系统都会出现与衰老有关的生理变化。需要对老年人群的治疗方式和药物处方过程进行重新评估。为了详细说明多药治疗,还必须有效地确定个人应使用的药物数量。为老年人开处方和使用药物制定了各种标准。这些标准中使用最多的被称为Beers标准。STOPP和START标准是使用的其他标准。材料和方法:我们的研究旨在根据STOP-START标准,回顾性评估在安卡拉阿塔图克训练研究医院内科和神经重症监护室住院的65岁及以上患者中不适当药物使用的患病率。结果:研究组包括168名(58.3%)女性和120名(41.7%)男性。288名患者共诊断出727种疾病。其中201项为“脑血管疾病”,153项为“高血压”而最常见的STOPP标准主要组和单一标准分别是抗血小板抗凝剂组(35,7%)、“存在导致重复的药物类别(在添加新药物之前用单一药物达到最佳水平)”(23,2%)。同时,最常见的START标准主要组和单一标准分别是心血管系统组(94.5%)和“对接近生命终点或年龄不超过85岁、有冠状动脉、脑血管或外周血管病史的患者进行他汀类药物治疗”(70.2%)。结论:研究结果与国内文献基本一致。研究结果与国际文献之间存在党派差异。预计这些差异可归因于所使用的诊断标准、研究组选择和研究设计的差异。
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引用次数: 0
Microsatellite Instability in Lung Adenocarcinoma 肺腺癌的微卫星不稳定性
IF 0.1 Q4 Medicine Pub Date : 2023-07-01 DOI: 10.12996/gmj.2023.70
{"title":"Microsatellite Instability in Lung Adenocarcinoma","authors":"","doi":"10.12996/gmj.2023.70","DOIUrl":"https://doi.org/10.12996/gmj.2023.70","url":null,"abstract":"","PeriodicalId":42791,"journal":{"name":"Gazi Medical Journal","volume":null,"pages":null},"PeriodicalIF":0.1,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"45189956","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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Gazi Medical Journal
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