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How to manage a task-oriented virtual assistant software project: an experience report Research Article

Shuyue LI, Jiaqi GUO, Yan GAO, Jianguang LOU, Dejian YANG, Yan XIAO, Yadong ZHOU, Ting LIU,lishuyue1221@stu.xjtu.edu.cn,jasperguo2013@stu.xjtu.edu.cn,yan.gao@microsoft.com,jlou@microsoft.com,dejian.yang@microsoft.com,yan.xiao@microsoft.com,ydzhou@xjtu.edu.cn,tingliu@mail.xjtu.edu.cn

Frontiers of Information Technology & Electronic Engineering 2022, Volume 23, Issue 5,   Pages 749-762 doi: 10.1631/FITEE.2100467

Abstract: Meanwhile, the management and experience related to the development of s are hardly studied or sharedTo bridge this knowledge gap, in this paper, we share our experience and the lessons that we have learned

Keywords: Experience report     Software project management     Virtual assistant     Machine learning    

Study of RDL-based data report in bridge structural health monitoring system

Zhang Xiaobin,Chen Weiguo

Strategic Study of CAE 2010, Volume 12, Issue 7,   Pages 110-112

Abstract: of traditional data reporting program, this article transformed the problems into multiple templates report

Keywords: structural health monitoring system     RDL     report definition language     data report    

Cushing’s syndrome during pregnancy caused by adrenal cortical adenoma: a case report and literature

Wei Wang,Fengyi Yuan,Dan Xu

Frontiers of Medicine 2015, Volume 9, Issue 3,   Pages 380-383 doi: 10.1007/s11684-015-0407-x

Abstract:

Cushing’s syndrome (CS) during pregnancy is a rare condition with significant maternal and fetal complications. A case of CS during the third trimester of pregnancy secondary to adrenocortical adenoma was reported. Literature review revealed the disadvantages of different treatments in this period. Besides the conservative treatment, surgery is recommended for CS during the third trimester of pregnancy secondary to adrenal adenoma, if an experienced surgeon is available.

Keywords: Cushing’s syndrome     pregnancy     adrenocortical adenoma    

Diagnosis and treatment of thyroglossal duct carcinoma: Report of three cases with review of literatures

GAO Yan, CHEN Yan, SUN Zhipeng, GUO Chuanbin, YU Guangyan, ZHAN Yi

Frontiers of Medicine 2008, Volume 2, Issue 1,   Pages 58-62 doi: 10.1007/s11684-008-0011-4

Abstract: Thyroglossal duct carcinoma, which is usually diagnosed postoperatively, is a rare malignant tumor arising in the thyroglossal duct cyst. The definitive diagnosis can be made only after microscopic examination. We retrospectively reviewed three cases of thyroglossal duct carcinoma diagnosed in Peking University School and Hospital of Stomatology from January 1986 to August 2006. Clinical and pathological features were investigated and the optimal treatment protocol was proposed. The constituent ratio of thyroglossal duct carcinoma among surgically excised thyroglossal duct lesions was 2.9%. The clinical presentation of thyroglossal duct carcinoma was very similar to that of its benign counterpart. Two cases were diagnosed as thyroglossal duct cyst prior to the operation, the remaining one as dermoid cyst. All three cases were diagnosed as papillary carcinoma of thyroid origin after microscopic examination. Primary thyroglossal duct carcinoma should conform to the following criteria: localization of the carcinoma to a clearly demonstrable thyroglossal duct cyst or tract; clinically or histologically confirmed absence of carcinoma of the thyroid gland. Papillary carcinoma is the most common histological type, which usually develops slowly with an excellent prognosis. The histological characteristics including: formation of papillary structure; nuclear morphological variations such as ground glass nuclei, pseudoinclusions, intranuclear grooves and filaments; concentrically calcified structures termed psammoma bodies which is regarded as a strong indication of papillary carcinoma; and positivity in immunohistological staining for thyroglobin. Sistrunk procedure of excision is the choice for treatment. A close follow-up is needed. In the presence of thyroid gland masses or cervical lymphadenopathy, thyroidectomy or neck dissection should be recommended. The effect of thyroid suppression therapy and radioactive iodine therapy is not conclusive.

Engineering Fronts in fields of Energy and Electrical Science and Technologies in the report of

Frontiers in Energy 2023, Volume 17, Issue 1,   Pages 5-8 doi: 10.1007/s11708-023-0868-6

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Salvage therapy with lenalidomide containing regimen for relapsed/refractory Castleman disease: a report

Xinping Zhou, Juying Wei, Yinjun Lou, Gaixiang Xu, Min Yang, Hui Liu, Liping Mao, Hongyan Tong, Jie Jin

Frontiers of Medicine 2017, Volume 11, Issue 2,   Pages 287-292 doi: 10.1007/s11684-017-0510-2

Abstract:

Castleman disease (CD) is an uncommon non-clonal lymphoproliferative disorder with unknown etiology. No standard therapy is recommended for relapsed/refractory CD patients, thus requiring development of novel experimental approaches. Our cohort of three adult patients with multicentric CD (MCD) were treated with refractory to traditional chemotherapy lenalidomide-containing regimens (10–25 mg lenalidomide perorally administered on days 1–21 in 28-day cycle) as second- to fourth-line treatment. Partial remission was achieved in first plasma-cell CD patient, who relapsed seven months after autologous hematopoietic stem cell transplantation and then failed to respond to four cycles of chemotherapy. Partial remission was obtained in second patient with CD and polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes syndrome. Third case showed complete remission with complete disappearance of pleural effusion and ascites and normalization of platelet count. To conclude, encouraging clinical responses were achieved in cohort of three patients with lenalidomide-based regimen, though long-term efficacy remains to be observed. We propose further investigation of therapeutic potential of this drug in treating MCD.

Keywords: Castleman disease     lenalidomide    

Pulmonary alveolar microlithiasis: an interesting case report with systematic review of Indian literature

Nidhya Ganesan,Marie Moses Ambroise,Anita Ramdas,King Herald Kisku,Kulwant Singh,Renu G’ Boy Varghese

Frontiers of Medicine 2015, Volume 9, Issue 2,   Pages 229-238 doi: 10.1007/s11684-015-0394-y

Abstract:

Pulmonary alveolar microlithiasis is a rare disease characterized by intra-alveolar presence of microliths. This study reports an interesting case of pulmonary alveolar microlithiasis and provides a systematic review of cases reported from India. A 23-year-old female presented with a history of cough, wheeze, chest pain, and episodic wheeze for five months. Pulmonary function tests demonstrated an obstructive pattern, and chest X-ray showed fine micronodular opacities predominantly involving the middle and lower zones of both lungs. Transbronchial lung biopsy revealed the diagnosis. She responded well to inhaled steroid therapy. A systematic review of literature was performed and identified 73 cases of pulmonary alveolar microlithiasis reported from India. The mean (SD) age of the patients was 28.8 (14.9) years, with an almost equal male:female ratio. Many patients were asymptomatic at presentation. Breathlessness and cough were the most common symptoms, and the disease progressed into respiratory failure associated with cor pulmonale. About one-third of the cases were initially misdiagnosed and treated as pulmonary tuberculosis. Extra-pulmonary manifestations and co-morbidities were also evident in our series. This systematic review helps to determine epidemiological and clinical characteristics of pulmonary alveolar microlithiasis. Further research is needed to elucidate the etiopathogenesis, diagnosis, and therapeutic options, which are beneficial in developing and identifying cost-effective treatment for pulmonary alveolar microlithiasis.

Keywords: pulmonary alveolar microlithiasis     alveolar microlithiasis     microliths     rare diseases    

Case report of neurofibromatosis type 1 combined with primary ciliary dyskinesia

Frontiers of Medicine 2021, Volume 15, Issue 6,   Pages 933-937 doi: 10.1007/s11684-021-0860-7

Abstract: Herein, we report a patient diagnosed with NF on the basis of the results of genetic testing who presented

Keywords: primary ciliary dyskinesia     neurofibromatosis     bronchiectasis     transmission electron microscopy     genetic sequencing    

Aneurysmal dilatation of the aortic sinuses of Valsalva — beyond Marfan syndrome: a single centre experience

Maryanne Caruana,Mary N. Sheppard,Wei Li

Frontiers of Medicine 2014, Volume 8, Issue 4,   Pages 419-426 doi: 10.1007/s11684-014-0383-6

Abstract:

Aneurysmal dilatation of the aortic sinuses of Valsalva has been most extensively documented in the setting of aortopathies, particularly Marfan syndrome. On the other hand, there is limited data in the literature about congenital sinus of Valsalva aneurysms outside this context. For the purpose of this review, we carried out a literature search on aneurysmal dilatation of the sinuses of Valsalva in Marfan syndrome, and compared this with congenital sinus of Valsalva aneurysms, also including data from a case series from our institution. In conclusion, there are differences in management of aortic dilatation in Marfan syndrome and congenital sinus of Valsalva aneurysms. Though less well-recognised, congenital aneurysms are often associated with significant morbidity and mortality and timely intervention is necessary.

Keywords: sinus of Valsalva aneurysms     Marfan syndrome     aortic dissection    

Taizhou’s COVID-19 prevention and control experience with telemedicine features

Cenyi Shao, Shijian Li, Feng Zhu, Dahai Zhao, Hui Shao, Haixiao Chen, Zhiruo Zhang

Frontiers of Medicine 2020, Volume 14, Issue 4,   Pages 506-510 doi: 10.1007/s11684-020-0811-8

Abstract: We summarize Taizhou’s COVID-19 prevention and control experience with telemedicine features, with a

Keywords: COVID-19     telemedicine     prevention experience    

Vein of Galen malformations - report of 2 cases and literature review

CAI Chunquan, ZHANG Qingjiang, SHEN Changhong

Frontiers of Medicine 2008, Volume 2, Issue 3,   Pages 317-322 doi: 10.1007/s11684-008-0061-7

Abstract: Vein of Galen malformations (VGMs) are rare, consisting approximately 1% of intracranial vascular malformations, but nearly one third of pediatric vascular malformations, which can cause severe morbidity and mortality in infants and older children, but more particularly in neonates. We presented 2 patients with VGMs which were confirmed by characteristic clinical symptoms and neuroradiological findings (including CT, MRI and/or angiography). One patient underwent embolization followed by CT, MRI and conventional angiography. The patient’s neurological and cognitive status was normal at present. The other neonate died of congestive heart failure 36 h after birth.

Keywords: underwent embolization     angiography     pediatric vascular     cognitive     characteristic    

Thinking and practice of accelerating transformation of traditional Chinese medicine from experience

Baoyan Liu, Yanhong Zhang, Jingqing Hu, Liyun He, Xuezhong Zhou

Frontiers of Medicine 2011, Volume 5, Issue 2,   Pages 163-170 doi: 10.1007/s11684-011-0143-9

Abstract: The gradual development of Chinese medicine is based on constant accumulation and summary of experiencethousands of years, with the development of evidence-based medicine, the bondage of the research methods of experienceThe rapid transition and transformation from experience medicine to evidence-based medicine have becomescientific and reliable evidence of Chinese medicine, as well as transform and develop Chinese medicine from experience

Keywords: Chinese medicine     experience medicine     evidence-based medicine     real world    

Mature cystic teratoma of the parotid gland: a case report and review of the literature

Lenan SHAO DMD, MD, Hanxiong GUAN MD, Jie WAN MS,

Frontiers of Medicine 2009, Volume 3, Issue 4,   Pages 503-506 doi: 10.1007/s11684-009-0076-8

Abstract: We report one case of mature cystic teratoma that presented as a tender, well-defined round mass in the

Keywords: teratoma     parotid gland    

Ventricular tachycardia in a disseminated MDR-TB patient: a case report and brief review of literature

Hui Li,Ran Li,Jiuxin Qu,Xiaomin Yu,Zhixin Cao,Yingmei Liu,Bin Cao

Frontiers of Medicine 2014, Volume 8, Issue 2,   Pages 259-263 doi: 10.1007/s11684-014-0321-7

Abstract:

Although significant breakthroughs have been achieved in tuberculosis management, we still encounter numerous difficulties in diagnosis and treatment of the disease. Additionally, a new challenge, multidrug-resistant tuberculosis (MDR-TB) with unspecific clinical presentation, often results in delayed diagnosis. In this paper, we reported a case of disseminated tuberculosis with rare presentation of ventricular fibrillation, which proved resistant to both isoniazid and rifampicin. A review of literature showed that ventricular fibrillation or tachycardia in tuberculosis patients with pericarditis or myocarditis has been sporadically reported in the past, but none has been conducted involving patients with MDR-TB infections.

Keywords: tuberculosis     MDR-TB     ventricular tachycardia    

Paratesticular fibrous pseudotumor: a report of five cases and literature review

Zhicheng Zhang,Jun Yang,Mingchao Li,Wei Cai,Qingquan Liu,Tao Wang,Xiaolin Guo,Shaogang Wang,Jihong Liu,Zhangqun Ye

Frontiers of Medicine 2014, Volume 8, Issue 4,   Pages 484-488 doi: 10.1007/s11684-014-0325-3

Abstract:

Paratesticular fibrous pseudotumor is a rare benign tumor that originates from intrascrotal tissue, such as tunica vaginalis, epididymis, or spermatic cord. Five cases of fibrous pseudotumor in our hospital were reviewed retrospectively, and the clinical manifestations were analyzed. Three cases of unilateral nodules, comprising one case located in the tunica vaginalis and two cases located in the epididymis, underwent local excision of the unilateral nodule. Two cases of diffuse incrassation in the tunica vaginalis underwent right radical orchiectomy. Postoperative pathological examination showed that all were fibrous pseudotumors. An average follow-up of 26 months showed uneventful results without recurrence for all patients. Fibrous pseudotumor is not a neoplasm but a reactive fibrous inflammatory hyperplasia. Definitive diagnosis requires pathological examination. Radical orchiectomy should be avoided when possible, and local excision should be performed because of the lack of obvious evidence of potential malignancy.

Keywords: fibroma     inflammation     scrotum     testicular neoplasm    

Title Author Date Type Operation

How to manage a task-oriented virtual assistant software project: an experience report

Shuyue LI, Jiaqi GUO, Yan GAO, Jianguang LOU, Dejian YANG, Yan XIAO, Yadong ZHOU, Ting LIU,lishuyue1221@stu.xjtu.edu.cn,jasperguo2013@stu.xjtu.edu.cn,yan.gao@microsoft.com,jlou@microsoft.com,dejian.yang@microsoft.com,yan.xiao@microsoft.com,ydzhou@xjtu.edu.cn,tingliu@mail.xjtu.edu.cn

Journal Article

Study of RDL-based data report in bridge structural health monitoring system

Zhang Xiaobin,Chen Weiguo

Journal Article

Cushing’s syndrome during pregnancy caused by adrenal cortical adenoma: a case report and literature

Wei Wang,Fengyi Yuan,Dan Xu

Journal Article

Diagnosis and treatment of thyroglossal duct carcinoma: Report of three cases with review of literatures

GAO Yan, CHEN Yan, SUN Zhipeng, GUO Chuanbin, YU Guangyan, ZHAN Yi

Journal Article

Engineering Fronts in fields of Energy and Electrical Science and Technologies in the report of

Journal Article

Salvage therapy with lenalidomide containing regimen for relapsed/refractory Castleman disease: a report

Xinping Zhou, Juying Wei, Yinjun Lou, Gaixiang Xu, Min Yang, Hui Liu, Liping Mao, Hongyan Tong, Jie Jin

Journal Article

Pulmonary alveolar microlithiasis: an interesting case report with systematic review of Indian literature

Nidhya Ganesan,Marie Moses Ambroise,Anita Ramdas,King Herald Kisku,Kulwant Singh,Renu G’ Boy Varghese

Journal Article

Case report of neurofibromatosis type 1 combined with primary ciliary dyskinesia

Journal Article

Aneurysmal dilatation of the aortic sinuses of Valsalva — beyond Marfan syndrome: a single centre experience

Maryanne Caruana,Mary N. Sheppard,Wei Li

Journal Article

Taizhou’s COVID-19 prevention and control experience with telemedicine features

Cenyi Shao, Shijian Li, Feng Zhu, Dahai Zhao, Hui Shao, Haixiao Chen, Zhiruo Zhang

Journal Article

Vein of Galen malformations - report of 2 cases and literature review

CAI Chunquan, ZHANG Qingjiang, SHEN Changhong

Journal Article

Thinking and practice of accelerating transformation of traditional Chinese medicine from experience

Baoyan Liu, Yanhong Zhang, Jingqing Hu, Liyun He, Xuezhong Zhou

Journal Article

Mature cystic teratoma of the parotid gland: a case report and review of the literature

Lenan SHAO DMD, MD, Hanxiong GUAN MD, Jie WAN MS,

Journal Article

Ventricular tachycardia in a disseminated MDR-TB patient: a case report and brief review of literature

Hui Li,Ran Li,Jiuxin Qu,Xiaomin Yu,Zhixin Cao,Yingmei Liu,Bin Cao

Journal Article

Paratesticular fibrous pseudotumor: a report of five cases and literature review

Zhicheng Zhang,Jun Yang,Mingchao Li,Wei Cai,Qingquan Liu,Tao Wang,Xiaolin Guo,Shaogang Wang,Jihong Liu,Zhangqun Ye

Journal Article