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Predatory Journals in Scientific Research: A Great Challenge 掠夺性科研期刊:一个巨大的挑战
Pub Date : 2023-01-10 DOI: 10.56557/jocrims/2023/v9i18135
N. Johnkennedy, Nwaokoro Joakin Chidozie
Predatory journals are publications that promote themselves as authentic scholarly journals but falsify their publishing procedures. Predatory journals or periodicals that falsely represent their publishing works while presenting themselves as legitimate scholarly journals. They are referred to as fake, dishonest or bogus journals. Many copyright or publication ethics violations, such like making false claims that review process is given, keeping secrets about article processing charges (APC's), misrepresenting editorial board members and others, all examples of parasitic techniques. Since they are growing more widespread around the world, predatory journals are examined in this review to help authors identify and steer well clear of them.
掠夺性期刊是将自己标榜为真正的学术期刊,但伪造出版程序的出版物。掠夺性期刊或期刊,谎称其出版作品,而自称为合法的学术期刊。它们被称为假的、不诚实的或伪造的期刊。许多违反版权或出版道德的行为,比如谎称审查过程是给定的,对文章处理费用(APC)保密,歪曲编辑委员会成员和其他人,都是寄生技术的例子。由于掠夺性期刊在世界范围内越来越普遍,本文对掠夺性期刊进行了研究,以帮助作者识别并避开它们。
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引用次数: 0
UTILIZATION OF OVATE PONTIC- A VIABLE SOLUTION IN ESTHETIC ZONE – REPORT OF TWO CASES 卵状桥的应用——美学区可行的解决方案——附两例报告
Pub Date : 2022-12-31 DOI: 10.56557/jocrims/2022/v8i18128
P. Mandal, Vineet Nair
Restoration of aesthetic along with maintenance of healthy gingival tissue is of utmost importance when treating the maxillary anterior region. Resorption of residual alveolar ridge or irregularities in soft tissue often complicate favourable relationship with the pontic, compromising the final aesthetic outcome. Various techniques were used to overcome this problem. Esthetic emergence profile was achieved in final prosthesis of all the following cases without any adverse consequences on a long term follow up. Apart from esthetics, clinically healthy, functional, and hygienic conditions can be established at ovate pontic sites if appropriate plaque control is performed. In this article we discuss two cases where missing tooth was replaced by provisional FPD with ovate pontic followed by final prosthesis after 6-7 weeks to achieve a natural emergence profile. Follow up is continuing till the publication of this article and the prosthesis and tissue health are perfectly fine.
在治疗上颌前牙区时,在保持牙龈组织健康的同时恢复美观是至关重要的。残留牙槽嵴的吸收或软组织的不规则性往往使与桥的良好关系复杂化,从而影响最终的美观效果。人们使用了各种技术来克服这个问题。在长期随访中,所有病例的最终假体都达到了美观的出现轮廓,没有任何不良后果。除了美观之外,如果进行适当的斑块控制,可以在卵形桥桥部位建立临床健康,功能和卫生条件。在这篇文章中,我们讨论了两个病例,在6-7周后用临时FPD和卵形桥代替缺失的牙齿,然后再进行最终的假体修复,以达到自然出现的效果。随访一直持续到本文发表,假体和组织健康状况完全良好。
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引用次数: 0
KIMURA’S DISEASE IN AN ASIAN MALE: A VERY RARE CAUSE OF LYMPHADENOPATHY 一名亚洲男性的木村氏病:一种非常罕见的淋巴结病
Pub Date : 2022-12-30 DOI: 10.56557/jocrims/2022/v8i18059
V. Goyal, Ruhi Dak, Vibhas Mohan Sood
The present case study highlights  Kimura’s Disease in an Asian Male. Kimura disease (KD) is a rare chronic inflammatory disorder of unknown etiology. It usually presents as subcutaneous mass in the head and neck region and is frequently associated with regional lymphadenopathy or salivary gland involvement. A study done at Dept of Internal Medicine ,American Institute Of Medical sciences, GBH general hospital, Udaipur, Rajasthan, India. A case report of a 13 year old male, admitted to GBH general Hospital on 1st January, 2023 with chief complains of swelling (painless) Left side of the  face below eye since 4 months and swelling under Rt. lobe of the ear since 3 months.On radiological examination, Kimura’s disease mimics other chronic and malignant diseases such as tuberculosis or lymphoma. This is an important study since it is a rare case and further research should be done in this area for further management and prompt diagnosis of such rare causes of upper body lymphadenopathy(frequently confused with malignancy),unless histopathology is clearly demonstrated.
本案例研究强调了一名亚洲男性的木村病。木村病是一种罕见的慢性炎症性疾病,病因不明。它通常表现为头颈部皮下肿块,常伴有局部淋巴结病或涎腺受累。这项研究是在印度拉贾斯坦邦乌代普尔GBH综合医院美国医学研究所内科部完成的。一例13岁男性患者,于2023年1月1日在GBH总医院住院,主诉为眼下左侧面部肿胀(无痛)4个月,耳垂下肿胀3个月。在放射学检查中,木村氏病类似于其他慢性和恶性疾病,如肺结核或淋巴瘤。这是一项重要的研究,因为它是一个罕见的病例,应该在该领域进行进一步的研究,以进一步管理和及时诊断这种罕见的上半身淋巴结病(经常与恶性肿瘤混淆),除非组织病理学得到明确证明。
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引用次数: 0
CONGENITAL UTERINE ANOMALY-BICORNUATE UTERUS WITH SUCCESSFUL PREGNANCIES OUTCOMES IN A TERTIARY HOSPITAL, SOUTHERN NIGERIA: CASE SERIES 先天性子宫异常-双角子宫与成功妊娠结局在三级医院,尼日利亚南部:病例系列
Pub Date : 2022-12-30 DOI: 10.56557/jocrims/2022/v8i18058
F. C. C. Wekere, P. Kua, L. Sapira-Ordu, S. Asikimabo-ofori, P. K. Gbeneol, R. S. Iwo-Amah, L. B. Lebara, Sandra U. Ibeabuchi, Sokeipirim E. Ikiroma, P. S. Abere, L. D. Ndii, Glory P. A. Briggs
Bicornuate uterus, a class IV Mullerian anomaly results from impairment in the fusion of the Mullerian duct. It is associated with both normal and many obstetric complications. We present two rare cases of bicornuate uterus with successful pregnancy outcomes among Nigerian ladies. The diagnoses of the bicornuate uterus were made incidentally during a routine antenatal ultrasound scan in their first pregnancies. These were confirmed intraoperatively and the patients were notified. In the first case, the foetal head occupied the cavity of the left horn and the breech in the cavity of the large right horn while in the second case, the right horn was empty and the foetus was in the left horn. These women with bicornuate uterus carried their pregnancies to term and had elective repeat caesarean sections with favourable foeto-maternal outcomes. The mothers and their babies are alive and doing well. Overall, the ladies had two and four successful pregnancy outcomes respectively. Women with a bicornuate uterus can achieve successful pregnancy outcomes despite the obstetric challenges of the anomaly. Thus, the index cases highlight that it is practically safe to forgo metroplasty in bicornuate uterus, in particular, asymptomatic women that had achieved successful pregnancies.
双角状子宫,IV级缪勒管异常,由缪勒管融合受损引起。它与正常和许多产科并发症有关。我们提出两例罕见的双角子宫与成功的妊娠结局在尼日利亚妇女。双角子宫的诊断是偶然的,在常规产前超声扫描在他们的第一次怀孕。这些在术中得到证实,并通知患者。在第一种情况下,胎儿头部占据了左角的腔,臀部占据了大右角的腔,而在第二种情况下,右角是空的,胎儿在左角。这些患有双角子宫的妇女将妊娠进行到足月,并进行选择性重复剖腹产,胎母结局良好。母亲和他们的孩子都活得很好。总的来说,这些女性分别有2次和4次成功怀孕。双角子宫妇女可以获得成功的妊娠结局,尽管产科的挑战异常。因此,指数病例强调,在双角子宫中放弃子宫成形术实际上是安全的,特别是那些无症状且成功怀孕的妇女。
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引用次数: 0
CLINICIANS DILEMMA: FALSELY UNDETECTED TSH LEVELS DUE TO TSH ISOFORM ON POPULAR COMMERCIAL IMMUNOASSAY IN INDIAN SUBJECT AND RETROSPECTIVE ANALYSIS 临床医生的困境:由于TSH异构体在印度流行的商业免疫分析和回顾性分析中错误地未检测TSH水平
Pub Date : 2022-01-06 DOI: 10.56557/jocrims/2022/v8i17572
Pawan Kumar, Parul Sharma, Megha Tomar, Ravi Tomar
Introduction: TSH is one of the most routinely measured tests the clinical laboratory to diagnose and monitor thyroid diseases. TSH as the preferred screening test as recommended by The American Thyroid Association and the American Association of Clinical Endocrinologists for diagnosing thyroid dysfunction. Third-generation Ultra serum TSH assays have a functional sensitivity of 0.001 uIU/mL and have been considered highest among biochemical assay for assessing thyroid disorders. However, as observed in many clinical laboratories sometimes results of TSH assays are discordant among different immunoassay platforms. Case Report: TSH values of a 56 years old male on Siemens Attelica while TSH was found to be elevated on Abbott Architect 1000 and Beckman Coulter DXI800. Retrospective analysis revealed few other cases (8/190) approx. 4.2 % showed discordant TSH values. This was found to be possibly because of mutation in TSH beta region (R55G). Conclusion: Our present study suggest that these individuals who shows <0.001 values on Siemens Attelica must be tested with other platforms to assure appropriate management of disease. Further, clinicians and laboratory staff need to be aware about TSH variants along with other reported interferences.
简介:TSH是临床实验室诊断和监测甲状腺疾病最常用的常规检测之一。TSH是美国甲状腺协会和美国临床内分泌学家协会推荐用于诊断甲状腺功能障碍的首选筛查试验。第三代Ultra血清TSH检测的功能灵敏度为0.001 uIU/mL,被认为是评估甲状腺疾病的生化检测中最高的。然而,正如在许多临床实验室中观察到的,有时不同免疫分析平台的TSH测定结果不一致。病例报告:56岁男性患者在Siemens Attelica上发现TSH值升高,在Abbott Architect 1000和Beckman Coulter DXI800上发现TSH值升高。回顾性分析显示其他病例(8/190)约为少数。4.2% TSH值不一致。这可能是由于TSH β区(R55G)突变所致。结论:我们目前的研究表明,这些在Siemens Attelica上显示<0.001值的个体必须在其他平台上进行测试,以确保适当的疾病管理。此外,临床医生和实验室工作人员需要了解TSH变异以及其他已报道的干扰。
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引用次数: 0
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Journal of Case Reports in Medical Science
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